{"id":497,"date":"2023-08-24T10:45:55","date_gmt":"2023-08-24T09:45:55","guid":{"rendered":"https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/?page_id=497"},"modified":"2023-08-24T11:38:12","modified_gmt":"2023-08-24T10:38:12","slug":"publications-2","status":"publish","type":"page","link":"https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/publications-2\/","title":{"rendered":"Publications"},"content":{"rendered":"<div id=\"pl-497\"  class=\"panel-layout\" ><div id=\"pg-497-0\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-497-0-0\"  class=\"panel-grid-cell\" ><div id=\"panel-497-0-0-0\" class=\"widget_text so-panel widget widget_custom_html panel-first-child panel-last-child\" data-index=\"0\" ><h3 class=\"widget-title\">Publications<\/h3><div class=\"textwidget custom-html-widget\"><div class=\"teachpress_pub_list\"><form name=\"tppublistform\" method=\"get\"><a name=\"tppubs\" id=\"tppubs\"><\/a><div class=\"teachpress_filter\"><select class=\"default\" name=\"yr\" id=\"yr\" tabindex=\"2\" onchange=\"teachpress_jumpMenu('parent',this, 'https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/publications-2\/?')\">\r\n                   <option value=\"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=#tppubs\">All years<\/option>\r\n                   <option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2026#tppubs\" >2026<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2025#tppubs\" >2025<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2024#tppubs\" >2024<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2023#tppubs\" >2023<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2022#tppubs\" >2022<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2021#tppubs\" >2021<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2020#tppubs\" >2020<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2019#tppubs\" >2019<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2018#tppubs\" >2018<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2017#tppubs\" >2017<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2016#tppubs\" >2016<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2015#tppubs\" >2015<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2014#tppubs\" >2014<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2013#tppubs\" >2013<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2012#tppubs\" >2012<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2011#tppubs\" >2011<\/option><option value = \"tgid=&amp;type=&amp;auth=&amp;usr=&amp;yr=2009#tppubs\" >2009<\/option>\r\n                <\/select><select class=\"default\" name=\"auth\" id=\"auth\" tabindex=\"5\" onchange=\"teachpress_jumpMenu('parent',this, 'https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/publications-2\/?')\">\r\n                   <option value=\"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=#tppubs\">All authors<\/option>\r\n                   <option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=262#tppubs\" > Aksi\u0107, Jelena M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=260#tppubs\" > Aksi\u0107, Marija S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=337#tppubs\" > Aleksi\u0107, Lidija<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=61#tppubs\" > Andelkovi\u0107, K. K.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=335#tppubs\" > An\u0111elkovi\u0107, Katarina<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=228#tppubs\" > Andrejevi\u0107, Tina P.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=376#tppubs\" > Aran\u0111elovi\u0107, Sandra<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=40#tppubs\" > Ara\u0161kov, J. B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=42#tppubs\" > Armakovi\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=136#tppubs\" > Armakovi\u0107, S. J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=227#tppubs\" > A\u0161anin, Darko P.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=318#tppubs\" > Babi\u0107, Biljana M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=380#tppubs\" > Bani\u0107, Nemanja<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=171#tppubs\" > Begovi\u0107, N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=119#tppubs\" > Beli\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=103#tppubs\" > Belo\u0161evi\u0107, S. K.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=253#tppubs\" > Belo\u0161evi\u0107, Svetlana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=299#tppubs\" > Belo\u0161evi\u0107, Svetlana K.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=39#tppubs\" > Benedekovi\u0107, G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=292#tppubs\" > Benedekovi\u0107, Goran<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=345#tppubs\" > Benedekovi\u0107, Goranm<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=209#tppubs\" > Bera, O.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=186#tppubs\" > Bihelovic, F.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=121#tppubs\" > Bjelogrli\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=85#tppubs\" > Blagojevi\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=50#tppubs\" > Blanu\u0161a, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=175#tppubs\" > Bogdanovi\u0107, G. A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=166#tppubs\" > Bogdanovi\u0107, G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=342#tppubs\" > Bogdanovi\u0107, Goran<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=346#tppubs\" > Bogdanovi\u0107, Gordana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=221#tppubs\" > Bogdanovi\u0107, Milica G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=305#tppubs\" > Bori\u0161ev, Ivana \u0110.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=201#tppubs\" > Br\u010deski, I. D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=197#tppubs\" > \u010ce\u0161ljevi\u0107, V. I.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=90#tppubs\" > Chylewska, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=182#tppubs\" > Cudina, O.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=374#tppubs\" > \u0106ulum, Andr\u00e9 Stephan<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=122#tppubs\" > Cvijeti\u0107, I.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=191#tppubs\" > Cvijeti\u0107, I. N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=48#tppubs\" > Dabi\u0107, P.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=113#tppubs\" > Deki\u0107, B. R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=257#tppubs\" > Deki\u0107, Biljana R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=23#tppubs\" > Deki\u0107, V. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=277#tppubs\" > Deki\u0107, Vidoslav S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=264#tppubs\" > Dimitrijevi\u0107, Marina V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=94#tppubs\" > Dimitrijevi\u0107, T.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=333#tppubs\" > Dimiza, Filitsa<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=168#tppubs\" > Divjakovi\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=349#tppubs\" > Divjakovi\u0107, Vladimir<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=6#tppubs\" > Djoki\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=242#tppubs\" > Djoki\u0107, Sanja<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=154#tppubs\" > Djordjevic, I. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=81#tppubs\" > Djuran, M. I.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=231#tppubs\" > Djuran, Milo\u0161 I.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=178#tppubs\" > Dobricic, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=378#tppubs\" > Doj\u010dinovi\u0107, Biljana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=88#tppubs\" > Donnard, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=198#tppubs\" > Dordevi\u0107, M. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=78#tppubs\" > Dra\u0161kovi\u0107, N. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=56#tppubs\" > Dra\u017ei\u0107, B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=160#tppubs\" > Elshaflu, H.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=127#tppubs\" > Emhemmed, F.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=30#tppubs\" > Ferenc, W.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=47#tppubs\" > Filipovi\u0107, N. R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=366#tppubs\" > Filipovi\u0107, Nenad R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=179#tppubs\" > Francuski, B. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=183#tppubs\" > Francuski, D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=36#tppubs\" > Francuz, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=293#tppubs\" > Francuz, Jovana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=120#tppubs\" > Gad\u017euri\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=298#tppubs\" > Gazdi\u0107, Dragana V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=263#tppubs\" > Gen\u010di\u0107, Marija S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=320#tppubs\" > Gili\u0107, Martina D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=76#tppubs\" > Gitari\u0107, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=377#tppubs\" > Gligorijevi\u0107, Nevenka<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=82#tppubs\" > Gli\u0161i\u0107, B. \u0110.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=232#tppubs\" > Gli\u0161i\u0107, Biljana \u0110.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=159#tppubs\" > Grubisic, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=109#tppubs\" > Gruden, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=89#tppubs\" > Gulea, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=115#tppubs\" > Gure\u0161i\u0107, D. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=309#tppubs\" > Gure\u0161i\u0107, Dejan M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=213#tppubs\" > Guzsv\u00e1ny, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=219#tppubs\" > Hawes, Chris S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=217#tppubs\" > Holl\u00f3, B. Barta<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=15#tppubs\" > Holl\u00f3, B. B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=27#tppubs\" > Holl\u00f3, B. Barta<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=202#tppubs\" > Holl\u00f3, B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=323#tppubs\" > Holl\u00f3, Berta Barta<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=222#tppubs\" > Holl\u00f3, Berta Barta<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=358#tppubs\" > Hozjan, Mi\u0161el<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=172#tppubs\" > Ivkovi\u0107, S. A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=208#tppubs\" > Ivkovi\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=180#tppubs\" > Jacevic, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=130#tppubs\" > Ja\u0107imovi\u0107, \u017d.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=18#tppubs\" > Ja\u0107imovi\u0107, \u017d. K.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=296#tppubs\" > Ja\u0107imovi\u0107, \u017deljko K.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=51#tppubs\" > Jagli\u010di\u0107, Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=37#tppubs\" > Jakimov, D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=350#tppubs\" > Jakimov, Dimitar<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=339#tppubs\" > Jakimov, Dimitar S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=311#tppubs\" > Jakimov, Dmitar<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=145#tppubs\" > Jakovljevi\u0107, K.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=74#tppubs\" > Janiak, C.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=301#tppubs\" > Janiak, Christoph<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=340#tppubs\" > Jani\u0107evi\u0107, Suzana C.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=278#tppubs\" > Jani\u0107evi\u0107, Suzana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=204#tppubs\" > Jani\u0107ijevi\u0107, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=86#tppubs\" > Janji\u0107, G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=126#tppubs\" > Janovi\u0107, B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=195#tppubs\" > Ja\u0161o, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=289#tppubs\" > Jeli\u0107, Miodrag G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=199#tppubs\" > Jeremi\u0107, D. A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=110#tppubs\" > Jeremi\u0107, D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=19#tppubs\" > Je\u0161i\u0107, L. S. Vojinovi\u0107<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=146#tppubs\" > Joksovi\u0107, M. D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=70#tppubs\" > Jovanovi\u0107, L.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=28#tppubs\" > Jovanovi\u0107, L. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=372#tppubs\" > Jovanovi\u0107, Ljiljana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=344#tppubs\" > Jovanovi\u0107, Ljiljana S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=267#tppubs\" > Jovanovic, Milos<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=268#tppubs\" > Jovanovic, Predrag<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=118#tppubs\" > Jovi\u0107, B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=225#tppubs\" > Jovi\u0107, Branislav D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=210#tppubs\" > Jovi\u010di\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=25#tppubs\" > Kahlenberg, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=279#tppubs\" > Kahlenberg, Volker<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=362#tppubs\" > Kallingal, Anoop<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=150#tppubs\" > Kanazir, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=52#tppubs\" > Karanovi\u0107, L.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=132#tppubs\" > Kastratovi\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=291#tppubs\" > Kesi\u0107, Jelena<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=33#tppubs\" > Kincses, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=73#tppubs\" > Knedel, T. -O.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=10#tppubs\" > Koji\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=240#tppubs\" > Koji\u0107, Vesna<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=308#tppubs\" > Koji\u0107, Vesna V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=281#tppubs\" > Kop, Tatjana J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=220#tppubs\" > Kordi\u0107, Branko B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=131#tppubs\" > Kosovi\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=312#tppubs\" > Kosti\u0107, Marijana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=49#tppubs\" > Kova\u010d, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=35#tppubs\" > Kova\u010devi\u0107, I.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=243#tppubs\" > Kova\u010devi\u0107, Ivana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=13#tppubs\" > Kremenovi\u0107, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=353#tppubs\" > Kremenovi\u0107, Aleksandar<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=141#tppubs\" > Krivoku\u0107a, A. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=143#tppubs\" > Krsti\u0107, N. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=17#tppubs\" > Krsti\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=295#tppubs\" > Krsti\u0107, Sanja<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=24#tppubs\" > Kr\u00fcger, B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=261#tppubs\" > Kr\u00fcger, Biljana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=71#tppubs\" > Kuzminac, I.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=108#tppubs\" > Kyne, S. H.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=212#tppubs\" > Lalovi\u0107, M. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=134#tppubs\" > Latinovi\u0107, N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=101#tppubs\" > Leovac, V. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=254#tppubs\" > Leovac, Vukadin M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=162#tppubs\" > Li, H.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=156#tppubs\" > Lolic, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=348#tppubs\" > Lon\u010dar, Eva<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=371#tppubs\" > Lozin\u0161ek, Matic<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=361#tppubs\" > Maciejewska, Natalia<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=26#tppubs\" > Magyari, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=91#tppubs\" > Makowski, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=355#tppubs\" > Malenov, Du\u0161an P.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=161#tppubs\" > Male\u0161evi\u0107, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=164#tppubs\" > Marinkovi\u0107, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=341#tppubs\" > Marinkovi\u0107, Emilija T. Pecev<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=124#tppubs\" > Markovi\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=153#tppubs\" > Markovi\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=271#tppubs\" > Maslak, Veselin<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=139#tppubs\" > Mati\u0107, I. Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=326#tppubs\" > Mati\u0107, Ivana Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=188#tppubs\" > Matovic, R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=332#tppubs\" > Medakovi\u0107, Vesna<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=331#tppubs\" > Mil\u010di\u0107, Milo\u0161<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=363#tppubs\" > Milivojac, Andrej Lj.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=144#tppubs\" > Milo\u0161ev, M. Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=169#tppubs\" > Milutinovi\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=315#tppubs\" > Mi\u0161kov-Paji\u0107, Vukoslava<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=60#tppubs\" > Miti\u0107, D. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=151#tppubs\" > Mladenovi\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=176#tppubs\" > Moln\u00e1r, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=32#tppubs\" > Mosolyg\u00f3, T.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=128#tppubs\" > Muller, C. D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=229#tppubs\" > Nenadovic, Marija<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=282#tppubs\" > Ne\u0161i\u0107, Marko<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=368#tppubs\" > Ne\u0161i\u0107, Milan S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=369#tppubs\" > Ne\u0161i\u0107, Milica D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=54#tppubs\" > Nikoli\u0107, M. A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=41#tppubs\" > Nikoli\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=95#tppubs\" > Novakovi\u0107, I.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=140#tppubs\" > Novakovi\u0107, I. T.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=325#tppubs\" > Novakovi\u0107, Irena<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=97#tppubs\" > Novakovi\u0107, S. B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=300#tppubs\" > Novakovi\u0107, Sla\u0111ana B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=184#tppubs\" > Novkovic, L.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=365#tppubs\" > Ognjanovi\u0107, Milo\u0161<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=31#tppubs\" > Osypiuk, D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=105#tppubs\" > Pa\u010devski, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=45#tppubs\" > Padr\u00f3n, J. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=117#tppubs\" > Papovi\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=214#tppubs\" > Papp, Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=64#tppubs\" > Pavi\u0107, A. B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=302#tppubs\" > Pavi\u0107, Aleksandar<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=174#tppubs\" > Pavlovi\u0107, R. Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=280#tppubs\" > Pavlovi\u0107, Radoslav Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=359#tppubs\" > Perdih, Franc<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=107#tppubs\" > Peri\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=148#tppubs\" > Perovi\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=275#tppubs\" > Petkovic, Milos<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=53#tppubs\" > Pet\u0159\u00ed\u010dek, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=196#tppubs\" > Petrovi\u0107, Z. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=328#tppubs\" > Pirkovi\u0107, Andrea<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=137#tppubs\" > Poleti, D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=2#tppubs\" > Popsavin, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=246#tppubs\" > Popsavin, Mirjana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=9#tppubs\" > Popsavin, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=245#tppubs\" > Popsavin, Velimir<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=157#tppubs\" > Portalone, G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=364#tppubs\" > Pregelj, Matej<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=334#tppubs\" > Psomas, George<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=65#tppubs\" > Radakovi\u0107, N. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=96#tppubs\" > Radanovi\u0107, D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=16#tppubs\" > Radanovi\u0107, M. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=223#tppubs\" > Radanovi\u0107, Mirjana M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=218#tppubs\" > Radnovi\u0107, Nikola D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=11#tppubs\" > Radovanovi\u0107, L.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=351#tppubs\" > Radovanovi\u0107, Lidija<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=20#tppubs\" > Radulovi\u0107, N. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=375#tppubs\" > Radulovi\u0107, Niko<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=256#tppubs\" > Radulovi\u0107, Niko S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=68#tppubs\" > Rai\u010devi\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=287#tppubs\" > Rai\u010devi\u0107, Vidak N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=255#tppubs\" > Rai\u010devi\u0107, Vidak<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=272#tppubs\" > Rakic, Srdjan<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=206#tppubs\" > Ratkovi\u0107, Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=356#tppubs\" > Regojevi\u0107, Marijana S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=22#tppubs\" > Risti\u0107, M. N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=258#tppubs\" > Risti\u0107, Milenko N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=114#tppubs\" > Risti\u0107, N. R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=310#tppubs\" > Risti\u0107, Novica R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=59#tppubs\" > Risti\u0107, P. G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=360#tppubs\" > Risti\u0107, Predrag G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=83#tppubs\" > Rodi\u0107, D. D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=43#tppubs\" > Rodi\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=5#tppubs\" > Rodi\u0107, M. V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=273#tppubs\" > Rodic, Marko<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=226#tppubs\" > Rodi\u0107, Marko V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=14#tppubs\" > Rogan, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=354#tppubs\" > Rogan, Jelena<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=319#tppubs\" > Rom\u010devi\u0107, Maja<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=322#tppubs\" > Rom\u010devi\u0107, Neboj\u0161a \u017d.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=189#tppubs\" > Saicic, R. N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=75#tppubs\" > Saka\u010d, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=290#tppubs\" > Sakellis, Elias<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=276#tppubs\" > Savic, Vladimir<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=21#tppubs\" > Sejmanovi\u0107, D. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=259#tppubs\" > Sejmanovi\u0107, Dragana M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=324#tppubs\" > Selakovi\u0107, Sne\u017eana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=192#tppubs\" > Sen\u0107anski, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=270#tppubs\" > Simic, Milena<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=200#tppubs\" > Simi\u0107, V. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=224#tppubs\" > \u0160kori\u0107, Du\u0161an \u0110.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=142#tppubs\" > Sladi\u0107, D. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=193#tppubs\" > Sladi\u0107, D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=66#tppubs\" > \u0160mit, B. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=173#tppubs\" > \u0160mit, B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=286#tppubs\" > \u0160mit, Biljana M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=163#tppubs\" > \u0160oji\u0107, N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=63#tppubs\" > Soldatovi\u0107, T. V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=170#tppubs\" > Spasojevi\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=34#tppubs\" > Spengler, G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=330#tppubs\" > Spremo-Potparevi\u0107, Biljana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=129#tppubs\" > Srdi\u0107-Raji\u0107, T.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=347#tppubs\" > Srdi\u0107-Raji\u0107, Tatjana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=307#tppubs\" > Sre\u0107o-Zelenovi\u0107, Bojana M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=62#tppubs\" > Stani\u0107, P. B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=379#tppubs\" > Stani\u0107, Petar B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=57#tppubs\" > Stani\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=306#tppubs\" > Stanisavljevi\u0107, Sla\u0111ana M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=111#tppubs\" > Stankovi\u0107, D. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=77#tppubs\" > Stanojevi\u0107, I. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=147#tppubs\" > Stanojkovi\u0107, T.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=327#tppubs\" > Stanojkovi\u0107, Tatjana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=283#tppubs\" > Stepanovi\u0107, Olivera<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=304#tppubs\" > \u0160tetin, Na\u0111a<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=79#tppubs\" > Stevanovi\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=294#tppubs\" > Stevanovi\u0107, Milena<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=373#tppubs\" > Stojanovi\u0107, Nikola<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=265#tppubs\" > Stojanovi\u0107-Radi\u0107, Zorica Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=194#tppubs\" > Strikovi\u0107, Z.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=207#tppubs\" > Sukdolak, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=99#tppubs\" > \u0160umar-Ristovi\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=336#tppubs\" > \u0160umar-Ristovi\u0107, Maja<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=1#tppubs\" > Svir\u010dev, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=241#tppubs\" > Svir\u010dev, Milo\u0161<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=55#tppubs\" > Sz\u00e9cs\u00e9nyi, K. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=29#tppubs\" > Sz\u00e9cs\u00e9nyi, K. M\u00e9sz\u00e1ros<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=177#tppubs\" > Sz\u00e9cs\u00e9nyi, K. M\u00e9sz\u00e1saros<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=133#tppubs\" > Szil\u00e1gyi, I. M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=58#tppubs\" > Tanaskovi\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=269#tppubs\" > Tasic, Gordana<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=149#tppubs\" > Te\u0161i\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=205#tppubs\" > Todorovi\u0107, N.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=285#tppubs\" > Todorovi\u0107, Nina<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=46#tppubs\" > Todorovi\u0107, T. R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=367#tppubs\" > Todorovi\u0107, Tamara R.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=266#tppubs\" > Tomic, Tatjana Ilic<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=211#tppubs\" > Tomi\u0107, Z. D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=321#tppubs\" > Traji\u0107, Jelena<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=106#tppubs\" > Tribus, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=152#tppubs\" > Trifunovi\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=185#tppubs\" > Trmcic, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=216#tppubs\" > Vajdle, O.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=303#tppubs\" > Vasiljevi\u0107, Branka<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=190#tppubs\" > Verbi\u0107, T. \u017d.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=44#tppubs\" > Vi\u0161njevac, A.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=181#tppubs\" > Vladimirov, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=274#tppubs\" > Vlahovic, Filip<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=102#tppubs\" > Vojinovi\u0107-Je\u0161i\u0107, L. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=135#tppubs\" > Vojinovi\u0107-Je\u0161i\u0107, L.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=288#tppubs\" > Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=343#tppubs\" > Vojinovi\u0107-Je\u0161i\u0107, Ljiljana. S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=80#tppubs\" > Vojnovi\u0107, S.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=230#tppubs\" > Vojnovic, Sandra<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=116#tppubs\" > Vrane\u0161, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=203#tppubs\" > Vu\u010dkovi\u0107, G.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=123#tppubs\" > Vuj\u010di\u0107, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=155#tppubs\" > Vukasinovic, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=87#tppubs\" > Vuli\u0107, P.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=284#tppubs\" > Wang, Xiuze<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=72#tppubs\" > Wrodnigg, T.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=215#tppubs\" > Zbiljic, J.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=338#tppubs\" > Zelenovi\u0107, Bojana Sre\u0107o<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=244#tppubs\" > Zelenovi\u0107, Bojana Sre\u0107o<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=329#tppubs\" > \u017divkovi\u0107, Lada<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=138#tppubs\" > \u017divkovi\u0107, M. B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=67#tppubs\" > \u017divkovi\u0107, M. D.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=104#tppubs\" > \u017divkovi\u0107-Radovanovi\u0107, V.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=317#tppubs\" > \u017divkovi\u0107-Radovanovi\u0107, Vukosava<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=187#tppubs\" > Zlatar, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=370#tppubs\" > Zlatkovi\u0107, Dragan B.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=158#tppubs\" > Zlatovic, M.<\/option><option value = \"tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=357#tppubs\" > Zori\u0107, Mihajlo Z.<\/option>\r\n                <\/select><\/div><\/form><div class=\"tablenav\"><div class=\"tablenav-pages\"><span class=\"displaying-num\">113 entries<\/span> <a class=\"page-numbers button disabled\">&laquo;<\/a> <a class=\"page-numbers button disabled\">&lsaquo;<\/a> 1 of 3 <a href=\"https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/publications-2\/?limit=2&amp;tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=&amp;tsr=#tppubs\" title=\"next page\" class=\"page-numbers button\">&rsaquo;<\/a> <a href=\"https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/publications-2\/?limit=3&amp;tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=&amp;tsr=#tppubs\" title=\"last page\" class=\"page-numbers button\">&raquo;<\/a> <\/div><\/div><div class=\"teachpress_publication_list\"><h3 class=\"tp_h3\" id=\"tp_h3_2026\">2026<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">113.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rai\u010devi\u0107, Vidak;  Aran\u0111elovi\u0107, Sandra;  Gligorijevi\u0107, Nevenka;  Doj\u010dinovi\u0107, Biljana;  Rodi\u0107, Marko;  \u0106ulum, Andr\u00e9 Stephan;  Radulovi\u0107, Niko<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('114','tp_links')\" style=\"cursor:pointer;\">ROS-mediated antiproliferative effects of dihydrotestosterone-derived ferrocene\u2013steroid conjugates toward human cancer cell lines of variable androgen dependence<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">European Journal of Medicinal Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 302, <\/span><span class=\"tp_pub_additional_issue\">iss. 2026, <\/span><span class=\"tp_pub_additional_pages\">pp. 118276, <\/span><span class=\"tp_pub_additional_year\">2026<\/span>, <span class=\"tp_pub_additional_isbn\">ISBN: 0223-5234<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_114\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('114','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_114\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('114','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_114\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{nokey,<br \/>\r\ntitle = {ROS-mediated antiproliferative effects of dihydrotestosterone-derived ferrocene\u2013steroid conjugates toward human cancer cell lines of variable androgen dependence},<br \/>\r\nauthor = {Vidak Rai\u010devi\u0107 and Sandra Aran\u0111elovi\u0107 and Nevenka Gligorijevi\u0107 and Biljana Doj\u010dinovi\u0107 and Marko Rodi\u0107 and Andr\u00e9 Stephan \u0106ulum and Niko Radulovi\u0107},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523425010414},<br \/>\r\ndoi = {10.1016\/j.ejmech.2025.118276},<br \/>\r\nisbn = {0223-5234},<br \/>\r\nyear  = {2026},<br \/>\r\ndate = {2026-01-15},<br \/>\r\nurldate = {2026-01-15},<br \/>\r\njournal = {European Journal of Medicinal Chemistry},<br \/>\r\nvolume = {302},<br \/>\r\nissue = {2026},<br \/>\r\npages = {118276},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('114','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_114\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523425010414\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523425010414\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523425010414<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.ejmech.2025.118276\" title=\"Follow DOI:10.1016\/j.ejmech.2025.118276\" target=\"_blank\">doi:10.1016\/j.ejmech.2025.118276<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('114','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2025\">2025<\/h3><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_number\">112.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rai\u010devi\u0107, Vidak;  Radulovi\u0107, Niko S.;  Bani\u0107, Nemanja;  Leovac, Vukadin M.;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('116','tp_links')\" style=\"cursor:pointer;\">Competing hydrogen bonding and acyclic \u03c0-stacking between hydrogen-bridged quasi-rings in Z- and E-methyl pyruvate semicarbazone: a quantitative interaction energy analysis <\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_year\">2025<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_116\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('116','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_116\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('116','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_116\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('116','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_116\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Competing hydrogen bonding and acyclic \u03c0-stacking between hydrogen-bridged quasi-rings in Z- and E-methyl pyruvate semicarbazone: a quantitative interaction energy analysis },<br \/>\r\nauthor = { Vidak Rai\u010devi\u0107 and Niko S. Radulovi\u0107 and Nemanja Bani\u0107 and Vukadin M. Leovac and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/ce\/d5ce00911a},<br \/>\r\ndoi = {10.1039\/D5CE00911A},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-11-04},<br \/>\r\nurldate = {2025-11-04},<br \/>\r\njournal = {CrystEngComm},<br \/>\r\nabstract = {The competition between hydrogen bonding and stacking interactions in the solid-state packing of Z- and E-isomers of methyl pyruvate semicarbazone (1-Z and 1-E) is quantitatively analyzed using a combination of X-ray crystallography, density functional theory (DFT), and energy vector diagrams (EVDs). The E-isomer forms dimers stabilized by resonance-assisted hydrogen bonds (RAHBs) with an interaction energy of \u221270.4 kJ mol\u22121, which serve as the building units (BUs) of its columnar-layered crystal structure. In contrast, the Z-isomer exhibits weaker RAHBs (\u221261.7 kJ mol\u22121) and relies more heavily on dispersion-driven stacking interactions between hydrogen-bridged quasi-rings, resulting in a distinct layered motif. Solution NMR studies confirm intramolecular hydrogen bonding in 1-Z and present evidence of self-association. This work highlights the delicate balance between classical hydrogen bonds and stacking forces in directing crystal packing, with implications for the design of hydrazone-based functional materials.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('116','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_116\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The competition between hydrogen bonding and stacking interactions in the solid-state packing of Z- and E-isomers of methyl pyruvate semicarbazone (1-Z and 1-E) is quantitatively analyzed using a combination of X-ray crystallography, density functional theory (DFT), and energy vector diagrams (EVDs). The E-isomer forms dimers stabilized by resonance-assisted hydrogen bonds (RAHBs) with an interaction energy of \u221270.4 kJ mol\u22121, which serve as the building units (BUs) of its columnar-layered crystal structure. In contrast, the Z-isomer exhibits weaker RAHBs (\u221261.7 kJ mol\u22121) and relies more heavily on dispersion-driven stacking interactions between hydrogen-bridged quasi-rings, resulting in a distinct layered motif. Solution NMR studies confirm intramolecular hydrogen bonding in 1-Z and present evidence of self-association. This work highlights the delicate balance between classical hydrogen bonds and stacking forces in directing crystal packing, with implications for the design of hydrazone-based functional materials.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('116','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_116\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/ce\/d5ce00911a\" title=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/ce\/d5ce00911a\" target=\"_blank\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/ce\/d5ce00911a<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1039\/D5CE00911A\" title=\"Follow DOI:10.1039\/D5CE00911A\" target=\"_blank\">doi:10.1039\/D5CE00911A<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('116','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">111.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Stani\u0107, Petar B.;  Rodi\u0107, Marko V.;  \u0160mit, Biljana M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('115','tp_links')\" style=\"cursor:pointer;\">5-(2-Methylsulfanylethyl)-3-prop-2-enyl-2-sulfanylideneimidazolidin-4-one <\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Molbank, <\/span><span class=\"tp_pub_additional_volume\">vol. 2025, <\/span><span class=\"tp_pub_additional_issue\">iss. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. M2057, <\/span><span class=\"tp_pub_additional_year\">2025<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_115\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('115','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_115\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('115','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_115\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('115','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_115\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{nokey,<br \/>\r\ntitle = {5-(2-Methylsulfanylethyl)-3-prop-2-enyl-2-sulfanylideneimidazolidin-4-one },<br \/>\r\nauthor = { Petar B. Stani\u0107 and Marko V. Rodi\u0107 and Biljana M. \u0160mit },<br \/>\r\nurl = {https:\/\/www.mdpi.com\/1422-8599\/2025\/3\/M2057},<br \/>\r\ndoi = {10.3390\/M2057},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-09-04},<br \/>\r\nurldate = {2025-09-04},<br \/>\r\njournal = {Molbank},<br \/>\r\nvolume = {2025},<br \/>\r\nissue = {3},<br \/>\r\npages = {M2057},<br \/>\r\nabstract = {An amino acid-derived 2-thiohydantoin, 5-(2-methylsulfanylethyl)-3-prop-2-enyl-2-sulfanylideneimidazolidin-4-one, obtained from l-methionine, was synthesized in a two-step reaction protocol with allyl isothiocyanate. The compound was obtained in an 82% yield and was fully structurally characterized by NMR and IR spectroscopy. The crystal structure, molecular packing, and intermolecular interactions were characterized by X-ray diffraction analysis.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('115','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_115\" style=\"display:none;\"><div class=\"tp_abstract_entry\">An amino acid-derived 2-thiohydantoin, 5-(2-methylsulfanylethyl)-3-prop-2-enyl-2-sulfanylideneimidazolidin-4-one, obtained from l-methionine, was synthesized in a two-step reaction protocol with allyl isothiocyanate. The compound was obtained in an 82% yield and was fully structurally characterized by NMR and IR spectroscopy. The crystal structure, molecular packing, and intermolecular interactions were characterized by X-ray diffraction analysis.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('115','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_115\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.mdpi.com\/1422-8599\/2025\/3\/M2057\" title=\"https:\/\/www.mdpi.com\/1422-8599\/2025\/3\/M2057\" target=\"_blank\">https:\/\/www.mdpi.com\/1422-8599\/2025\/3\/M2057<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/M2057\" title=\"Follow DOI:10.3390\/M2057\" target=\"_blank\">doi:10.3390\/M2057<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('115','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">110.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Ne\u0161i\u0107, Milan S.;  Ne\u0161i\u0107, Milica D.;  Zlatkovi\u0107, Dragan B.;  Rodi\u0107, Marko V.;  Lozin\u0161ek, Matic;  Radulovi\u0107, Niko S.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('112','tp_links')\" style=\"cursor:pointer;\">One-Step Introduction of Nitrogen-Containing Functional Groups onto Aryl Methyl Ketones: Synthesis of \u03b1-Iminoamidines with Tunable Biorelevant Properties<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">The Journal of Organic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 90, <\/span><span class=\"tp_pub_additional_number\">no. 27, <\/span><span class=\"tp_pub_additional_pages\">pp. 9319-9326, <\/span><span class=\"tp_pub_additional_year\">2025<\/span><span class=\"tp_pub_additional_note\">, (PMID: 40468847)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_112\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('112','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_112\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('112','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_112\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('112','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_112\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{doi:10.1021\/acs.joc.5c00224,<br \/>\r\ntitle = {One-Step Introduction of Nitrogen-Containing Functional Groups onto Aryl Methyl Ketones: Synthesis of \u03b1-Iminoamidines with Tunable Biorelevant Properties},<br \/>\r\nauthor = {Milan S. Ne\u0161i\u0107 and Milica D. Ne\u0161i\u0107 and Dragan B. Zlatkovi\u0107 and Marko V. Rodi\u0107 and Matic Lozin\u0161ek and Niko S. Radulovi\u0107},<br \/>\r\nurl = {https:\/\/doi.org\/10.1021\/acs.joc.5c00224<br \/>\r\nhttps:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.5c00224<br \/>\r\nhttps:\/\/pubs.acs.org\/cms\/10.1021\/joceah.2025.90.issue-27\/asset\/joceah.2025.90.issue-27.xlargecover.jpg, Issue Cover Page},<br \/>\r\ndoi = {10.1021\/acs.joc.5c00224},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-06-05},<br \/>\r\nurldate = {2025-06-05},<br \/>\r\njournal = {The Journal of Organic Chemistry},<br \/>\r\nvolume = {90},<br \/>\r\nnumber = {27},<br \/>\r\npages = {9319-9326},<br \/>\r\nabstract = {In this work, we report a straightforward one-step oxidative method for introducing three nitrogen atoms into aryl methyl ketones, yielding \u03b1-iminoamidines. Minor changes to the reaction conditions or workup, or subsequent simple transformations, unlock a variety of nitrogen-rich scaffolds. Physicochemical data show tunable basicity and lipophilicity\u2500key traits for medicinal chemistry. The scaffold also supports axial stereoisomerism, adding stereochemical diversity.},<br \/>\r\nnote = {PMID: 40468847},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('112','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_112\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In this work, we report a straightforward one-step oxidative method for introducing three nitrogen atoms into aryl methyl ketones, yielding \u03b1-iminoamidines. Minor changes to the reaction conditions or workup, or subsequent simple transformations, unlock a variety of nitrogen-rich scaffolds. Physicochemical data show tunable basicity and lipophilicity\u2500key traits for medicinal chemistry. The scaffold also supports axial stereoisomerism, adding stereochemical diversity.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('112','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_112\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1021\/acs.joc.5c00224\" title=\"https:\/\/doi.org\/10.1021\/acs.joc.5c00224\" target=\"_blank\">https:\/\/doi.org\/10.1021\/acs.joc.5c00224<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.5c00224\" title=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.5c00224\" target=\"_blank\">https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.5c00224<\/a><\/li><li><i class=\"fas fa-file-image\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/pubs.acs.org\/cms\/10.1021\/joceah.2025.90.issue-27\/asset\/joceah.2025.90.issue-27.xlargecover.jpg\" title=\"Issue Cover Page\" target=\"_blank\">Issue Cover Page<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1021\/acs.joc.5c00224\" title=\"Follow DOI:10.1021\/acs.joc.5c00224\" target=\"_blank\">doi:10.1021\/acs.joc.5c00224<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('112','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">109.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Risti\u0107, Predrag G.;  Maciejewska, Natalia;  Kallingal, Anoop;  Rodi\u0107, Marko V.;  Milivojac, Andrej Lj.;  Pregelj, Matej;  Ognjanovi\u0107, Milo\u0161;  Filipovi\u0107, Nenad R.;  Todorovi\u0107, Tamara R.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('111','tp_links')\" style=\"cursor:pointer;\">Structural patterns and cytotoxic activity of dinuclear Cu(II), Ni(II) and Cd(II) complexes with pyridine-based malonic acid dihydrazone<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Polyhedron, <\/span><span class=\"tp_pub_additional_pages\">pp. 117523, <\/span><span class=\"tp_pub_additional_year\">2025<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 0277-5387<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_111\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('111','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_111\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('111','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_111\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('111','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_111\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{RISTIC2025117523,<br \/>\r\ntitle = {Structural patterns and cytotoxic activity of dinuclear Cu(II), Ni(II) and Cd(II) complexes with pyridine-based malonic acid dihydrazone},<br \/>\r\nauthor = {Predrag G. Risti\u0107 and Natalia Maciejewska and Anoop Kallingal and Marko V. Rodi\u0107 and Andrej Lj. Milivojac and Matej Pregelj and Milo\u0161 Ognjanovi\u0107 and Nenad R. Filipovi\u0107 and Tamara R. Todorovi\u0107},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538725001378},<br \/>\r\ndoi = {https:\/\/doi.org\/10.1016\/j.poly.2025.117523},<br \/>\r\nissn = {0277-5387},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-04-01},<br \/>\r\nurldate = {2025-01-01},<br \/>\r\njournal = {Polyhedron},<br \/>\r\npages = {117523},<br \/>\r\nabstract = {A dinuclear Cu(II) complex, [Cu2(L)(H2L)](ClO4)2\u00b74H2O (Cu-1), with a condensation derivative of 2-acetylpyridine and malonic acid dihydrazide (H2L), was obtained through a direct synthesis. After recrystallization, the single-crystalline product was characterized by single crystal X-ray diffraction analysis, EPR, UV\/Vis and IR spectroscopy. In the resulting dimeric Cu(II) complex, one ligand molecule is coordinated in its dianionic form, while the other is coordinated in its neutral form. Both ligands adopt a bis-tridentate coordination mode through an NNO donor atom set. Perchlorate ions and water molecules are in the outer coordination sphere, consistent with the conductometric measurement. The coordination geometry around the Cu(II) ion is distorted octahedral. Comparative structural analysis using FIM (Full interaction map) methodology and Hirshfeld surface analysis, along with 2D fingerprint plots of intermolecular interactions revealed significant structural differences among Cu-1 and previously synthesized Ni(II) complexes [Ni2(HL)H2L](ClO4)3\u22193DMSO (Ni-1) and [Ni2(H2L)2](ClO4)4\u22194DMSO\u00b7EtOH (Ni-2), as well as Cd(II) complex [Cd2(H2O)2(H2L)2](ClO4)4\u00b74H2O (Cd-1). Finally, the cytotoxic activities of these dinuclear complexes were evaluated with comparisons drawn based on their half-maximal inhibitory concentration values.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('111','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_111\" style=\"display:none;\"><div class=\"tp_abstract_entry\">A dinuclear Cu(II) complex, [Cu2(L)(H2L)](ClO4)2\u00b74H2O (Cu-1), with a condensation derivative of 2-acetylpyridine and malonic acid dihydrazide (H2L), was obtained through a direct synthesis. After recrystallization, the single-crystalline product was characterized by single crystal X-ray diffraction analysis, EPR, UV\/Vis and IR spectroscopy. In the resulting dimeric Cu(II) complex, one ligand molecule is coordinated in its dianionic form, while the other is coordinated in its neutral form. Both ligands adopt a bis-tridentate coordination mode through an NNO donor atom set. Perchlorate ions and water molecules are in the outer coordination sphere, consistent with the conductometric measurement. The coordination geometry around the Cu(II) ion is distorted octahedral. Comparative structural analysis using FIM (Full interaction map) methodology and Hirshfeld surface analysis, along with 2D fingerprint plots of intermolecular interactions revealed significant structural differences among Cu-1 and previously synthesized Ni(II) complexes [Ni2(HL)H2L](ClO4)3\u22193DMSO (Ni-1) and [Ni2(H2L)2](ClO4)4\u22194DMSO\u00b7EtOH (Ni-2), as well as Cd(II) complex [Cd2(H2O)2(H2L)2](ClO4)4\u00b74H2O (Cd-1). Finally, the cytotoxic activities of these dinuclear complexes were evaluated with comparisons drawn based on their half-maximal inhibitory concentration values.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('111','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_111\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538725001378\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538725001378\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538725001378<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/https:\/\/doi.org\/10.1016\/j.poly.2025.117523\" title=\"Follow DOI:https:\/\/doi.org\/10.1016\/j.poly.2025.117523\" target=\"_blank\">doi:https:\/\/doi.org\/10.1016\/j.poly.2025.117523<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('111','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">108.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Regojevi\u0107, Marijana S.;  Zori\u0107, Mihajlo Z.;  Radnovi\u0107, Nikola D.;  Bogdanovi\u0107, Milica G.;  Holl\u00f3, Berta Barta;  Rodi\u0107, Marko V.;  Rai\u010devi\u0107, Vidak;  Bori\u0161ev, Ivana \u0110.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Hozjan, Mi\u0161el;  Perdih, Franc;  Radanovi\u0107, Mirjana M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('110','tp_links')\" style=\"cursor:pointer;\">Anion-directed synthesis of copper(I\/II) complexes with a Schiff base derived from 2-(diphenylphosphino)benzaldehyde and aminoguanidine<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Molecular Structure, <\/span><span class=\"tp_pub_additional_volume\">vol. 1336, <\/span><span class=\"tp_pub_additional_pages\">pp. 142051, <\/span><span class=\"tp_pub_additional_year\">2025<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 0022-2860<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_110\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('110','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_110\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('110','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_110\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('110','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_110\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{REGOJEVIC2025142051,<br \/>\r\ntitle = {Anion-directed synthesis of copper(I\/II) complexes with a Schiff base derived from 2-(diphenylphosphino)benzaldehyde and aminoguanidine},<br \/>\r\nauthor = {Marijana S. Regojevi\u0107 and Mihajlo Z. Zori\u0107 and Nikola D. Radnovi\u0107 and Milica G. Bogdanovi\u0107 and Berta Barta Holl\u00f3 and Marko V. Rodi\u0107 and Vidak Rai\u010devi\u0107 and Ivana \u0110. Bori\u0161ev and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Mi\u0161el Hozjan and Franc Perdih and Mirjana M. Radanovi\u0107},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0022286025007367},<br \/>\r\ndoi = {https:\/\/doi.org\/10.1016\/j.molstruc.2025.142051},<br \/>\r\nissn = {0022-2860},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-03-19},<br \/>\r\nurldate = {2025-01-01},<br \/>\r\njournal = {Journal of Molecular Structure},<br \/>\r\nvolume = {1336},<br \/>\r\npages = {142051},<br \/>\r\nabstract = {Condensation of aminoguanidine hydrochloride and 2-(diphenylphosphino)benzaldehyde yielded a new Schiff base derivative with the formula (HL)Cl\u00b7H2O. In addition to the usual methods for identification and characterization, such as spectroscopic and thermal analyses, as well as crystal structure determination, its coordination properties were thoroughly investigated. The reaction of methanolic solutions of copper(II) salts (chloride, bromide, and nitrate) with the ligand resulted in the formation of diverse products. In the reaction of copper(II) chloride and the ligand, two complexes were formed, viz. (HLO)2[CuIICl4] (1) and [CuI(HL)Cl2] (2). During the formation of 1, the diphenylphosphino residue of the ligand underwent oxidation. The reaction between the bromide salt and the ligand led to the formation of a mixture of two complexes with [CuI(HL)(Br\/Cl)Br] (3) as the dominant product and only a few crystals of [CuI(HL)(\u03bc-Br\/Cl)(Br\/Cl)2] (4). An interesting feature of these compounds is the substitutional disorder of two halide anions in different coordination sites. A similar phenomenon occurs in [CuI2(HL)2(\u03bc-Cl)(\u03bc-NO3)ClX], where X = Cl, NO3 (5), which is formed under the same reaction conditions when the nitrate salt is used. All the complexes were characterized by elemental analysis, FTIR, UV-Vis, SC-XRD, PXRD, and TG-MS, except for complex 4 due to its low yield. Additionally, the antioxidant capacity of 1, 2, 3 and 5 was investigated in vitro, with the copper(I) complexes exhibiting greater activity.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('110','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_110\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Condensation of aminoguanidine hydrochloride and 2-(diphenylphosphino)benzaldehyde yielded a new Schiff base derivative with the formula (HL)Cl\u00b7H2O. In addition to the usual methods for identification and characterization, such as spectroscopic and thermal analyses, as well as crystal structure determination, its coordination properties were thoroughly investigated. The reaction of methanolic solutions of copper(II) salts (chloride, bromide, and nitrate) with the ligand resulted in the formation of diverse products. In the reaction of copper(II) chloride and the ligand, two complexes were formed, viz. (HLO)2[CuIICl4] (1) and [CuI(HL)Cl2] (2). During the formation of 1, the diphenylphosphino residue of the ligand underwent oxidation. The reaction between the bromide salt and the ligand led to the formation of a mixture of two complexes with [CuI(HL)(Br\/Cl)Br] (3) as the dominant product and only a few crystals of [CuI(HL)(\u03bc-Br\/Cl)(Br\/Cl)2] (4). An interesting feature of these compounds is the substitutional disorder of two halide anions in different coordination sites. A similar phenomenon occurs in [CuI2(HL)2(\u03bc-Cl)(\u03bc-NO3)ClX], where X = Cl, NO3 (5), which is formed under the same reaction conditions when the nitrate salt is used. All the complexes were characterized by elemental analysis, FTIR, UV-Vis, SC-XRD, PXRD, and TG-MS, except for complex 4 due to its low yield. Additionally, the antioxidant capacity of 1, 2, 3 and 5 was investigated in vitro, with the copper(I) complexes exhibiting greater activity.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('110','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_110\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0022286025007367\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0022286025007367\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0022286025007367<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/https:\/\/doi.org\/10.1016\/j.molstruc.2025.142051\" title=\"Follow DOI:https:\/\/doi.org\/10.1016\/j.molstruc.2025.142051\" target=\"_blank\">doi:https:\/\/doi.org\/10.1016\/j.molstruc.2025.142051<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('110','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">107.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Jani\u0107evi\u0107, Suzana C.;  Deki\u0107, Vidoslav S.;  Deki\u0107, Biljana R.;  Marinkovi\u0107, Emilija T. Pecev;  Radulovi\u0107, Niko S.;  Bogdanovi\u0107, Milica G.;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('107','tp_links')\" style=\"cursor:pointer;\">The crystal structure of (E)-3-((E)-3-(4-ethoxy-3-methoxyphenyl)-1-hydroxyallylidene) chroman-2,4-dione, C21H18O6<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Zeitschrift f\u00fcr Kristallographie - New Crystal Structures, <\/span><span class=\"tp_pub_additional_volume\">vol. 240, <\/span><span class=\"tp_pub_additional_issue\">iss. 2, <\/span><span class=\"tp_pub_additional_pages\">pp. 199-201, <\/span><span class=\"tp_pub_additional_year\">2025<\/span>, <span class=\"tp_pub_additional_isbn\">ISBN: 2197-4578<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_107\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('107','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_107\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('107','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_107\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('107','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_107\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{nokey,<br \/>\r\ntitle = {The crystal structure of (E)-3-((E)-3-(4-ethoxy-3-methoxyphenyl)-1-hydroxyallylidene) chroman-2,4-dione, C21H18O6},<br \/>\r\nauthor = {Suzana C. Jani\u0107evi\u0107 and Vidoslav S. Deki\u0107 and Biljana R. Deki\u0107 and Emilija T. Pecev Marinkovi\u0107 and Niko S. Radulovi\u0107 and Milica G. Bogdanovi\u0107 and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2024-0419\/html},<br \/>\r\ndoi = {10.1515\/ncrs-2024-0419},<br \/>\r\nisbn = {2197-4578},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-02-27},<br \/>\r\nurldate = {2024-12-23},<br \/>\r\njournal = {Zeitschrift f\u00fcr Kristallographie - New Crystal Structures},<br \/>\r\nvolume = {240},<br \/>\r\nissue = {2},<br \/>\r\npages = {199-201},<br \/>\r\nabstract = {C21H18O6, triclinic, P -1 (no. 2), a = 7.2187(4)\u202f\u00c5, b = 9.3833(7)\u202f\u00c5, c = 13.6874(13)\u202f\u00c5, \u03b1 = 85.933(7)\u00b0, \u03b2 = 81.991(7)\u00b0, \u03b3 = 69.983(7)\u00b0, V = 862.35(12)\u202f\u00c53, Z = 2, Rgt(F) = 0.0418, wRref(F2) = 0.1233, T = 295(2)\u202fK.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('107','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_107\" style=\"display:none;\"><div class=\"tp_abstract_entry\">C21H18O6, triclinic, P -1 (no. 2), a = 7.2187(4)\u202f\u00c5, b = 9.3833(7)\u202f\u00c5, c = 13.6874(13)\u202f\u00c5, \u03b1 = 85.933(7)\u00b0, \u03b2 = 81.991(7)\u00b0, \u03b3 = 69.983(7)\u00b0, V = 862.35(12)\u202f\u00c53, Z = 2, Rgt(F) = 0.0418, wRref(F2) = 0.1233, T = 295(2)\u202fK.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('107','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_107\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2024-0419\/html\" title=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2024-0419\/html\" target=\"_blank\">https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2024-0419\/html<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1515\/ncrs-2024-0419\" title=\"Follow DOI:10.1515\/ncrs-2024-0419\" target=\"_blank\">doi:10.1515\/ncrs-2024-0419<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('107','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">106.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rai\u010devi\u0107, Vidak;  Jovanovi\u0107, Ljiljana;  Rodi\u0107, Marko V.;  Stojanovi\u0107, Nikola;  \u0106ulum, Andr\u00e9 Stephan;  Radulovi\u0107, Niko<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('113','tp_links')\" style=\"cursor:pointer;\">Homopregnane-type ferrocene-steroid conjugates exhibit immunomodulatory activity<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Bioorganic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 155, <\/span><span class=\"tp_pub_additional_pages\">pp. 108129, <\/span><span class=\"tp_pub_additional_year\">2025<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 0045-2068<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_113\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('113','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_113\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('113','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_113\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('113','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_113\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{RAICEVIC2025108129,<br \/>\r\ntitle = {Homopregnane-type ferrocene-steroid conjugates exhibit immunomodulatory activity},<br \/>\r\nauthor = {Vidak Rai\u010devi\u0107 and Ljiljana Jovanovi\u0107 and Marko V. Rodi\u0107 and Nikola Stojanovi\u0107 and Andr\u00e9 Stephan \u0106ulum and Niko Radulovi\u0107},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206825000094},<br \/>\r\ndoi = {10.1016\/j.bioorg.2025.108129},<br \/>\r\nissn = {0045-2068},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-02-01},<br \/>\r\nurldate = {2025-01-01},<br \/>\r\njournal = {Bioorganic Chemistry},<br \/>\r\nvolume = {155},<br \/>\r\npages = {108129},<br \/>\r\nabstract = {Numerous compounds with useful biological activities were previously prepared by tethering ferrocene to natural product scaffolds. Some conjugates of ferrocene and steroids in particular were demonstrated to act as both potent and selective antiproliferative agents. Motivated by a lack of structural diversity in the pregnane series of conjugates, we performed chemical modifications of several naturally occurring progestogens, their biosynthetic precursors and chemically related derivatives so as to obtain conjugates 1\u20138, in which the steroid skeleton and ferrocene core are linked by the steroid sidechain. All compounds were characterized by 1D and 2D NMR, IR, UV\u2013Vis, and HRMS; conjugate 7 was also analyzed by single-crystal X-ray diffraction. A cyclic voltammetric investigation of the electrochemical properties of 1\u20138 was performed. While none of the conjugates exhibited high cytotoxicity toward rat splenocytes, they were nevertheless found to enlist different types of immunomodulatory responses, most arising from the introduction of the ferrocene core.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('113','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_113\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Numerous compounds with useful biological activities were previously prepared by tethering ferrocene to natural product scaffolds. Some conjugates of ferrocene and steroids in particular were demonstrated to act as both potent and selective antiproliferative agents. Motivated by a lack of structural diversity in the pregnane series of conjugates, we performed chemical modifications of several naturally occurring progestogens, their biosynthetic precursors and chemically related derivatives so as to obtain conjugates 1\u20138, in which the steroid skeleton and ferrocene core are linked by the steroid sidechain. All compounds were characterized by 1D and 2D NMR, IR, UV\u2013Vis, and HRMS; conjugate 7 was also analyzed by single-crystal X-ray diffraction. A cyclic voltammetric investigation of the electrochemical properties of 1\u20138 was performed. While none of the conjugates exhibited high cytotoxicity toward rat splenocytes, they were nevertheless found to enlist different types of immunomodulatory responses, most arising from the introduction of the ferrocene core.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('113','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_113\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206825000094\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206825000094\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206825000094<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.bioorg.2025.108129\" title=\"Follow DOI:10.1016\/j.bioorg.2025.108129\" target=\"_blank\">doi:10.1016\/j.bioorg.2025.108129<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('113','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2024\">2024<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">105.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Belo\u0161evi\u0107, Svetlana;  Novakovi\u0107, Sla\u0111ana B.;  Rodi\u0107, Marko V.;  Leovac, Vukadin M.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Bogdanovi\u0107, Goran;  Radanovi\u0107, Mirjana M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('108','tp_links')\" style=\"cursor:pointer;\">Introducing a novel crystal form of pyruvic acid thiosemicarbazone and its sodium salt <\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 89, <\/span><span class=\"tp_pub_additional_issue\">iss. 7-8, <\/span><span class=\"tp_pub_additional_pages\">pp. 1011-1023, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 1820-7421 \/ 0352-5139<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_108\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('108','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_108\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('108','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_108\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('108','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_108\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{nokey,<br \/>\r\ntitle = {Introducing a novel crystal form of pyruvic acid thiosemicarbazone and its sodium salt },<br \/>\r\nauthor = {Svetlana Belo\u0161evi\u0107 and Sla\u0111ana B. Novakovi\u0107 and Marko V. Rodi\u0107 and Vukadin M. Leovac and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Goran Bogdanovi\u0107 and Mirjana M. Radanovi\u0107},<br \/>\r\nurl = {https:\/\/www.shd-pub.org.rs\/index.php\/JSCS\/article\/view\/12896},<br \/>\r\ndoi = {10.2298\/JSC240417050B },<br \/>\r\nissn = {1820-7421 \/ 0352-5139},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-08-12},<br \/>\r\nurldate = {2024-08-12},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {89},<br \/>\r\nissue = {7-8},<br \/>\r\npages = {1011-1023},<br \/>\r\nabstract = {The reaction of thiosemicarbazide and sodium pyruvate has been thoroughly studied and the novel crystal form of pyruvic acid thiosemicarbazone (H2pt) and its sodium salt were obtained. Compounds were characterized by IR spectra, melting points, elemental analysis and conductometric measurements, as well as single-crystal X-ray analysis. A detailed comparative analysis of crystal structures of these compounds is given, as well as comparison with some of the earlier known complexes containing H2pt. The two novel crystal structures exhibit notably different hydrogen bonding patterns, mutually and in comparison with previously reported crystal form of H2pt. All crystal structures are stabilized by extensive network of N\u2013H...O, O\u2013H...O and N\u2013H...S hydrogen bonds. The cyclic hydrogen bonding motif involving the thioureido moieties of the ligand is the only one which repeats in each structure.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('108','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_108\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The reaction of thiosemicarbazide and sodium pyruvate has been thoroughly studied and the novel crystal form of pyruvic acid thiosemicarbazone (H2pt) and its sodium salt were obtained. Compounds were characterized by IR spectra, melting points, elemental analysis and conductometric measurements, as well as single-crystal X-ray analysis. A detailed comparative analysis of crystal structures of these compounds is given, as well as comparison with some of the earlier known complexes containing H2pt. The two novel crystal structures exhibit notably different hydrogen bonding patterns, mutually and in comparison with previously reported crystal form of H2pt. All crystal structures are stabilized by extensive network of N\u2013H...O, O\u2013H...O and N\u2013H...S hydrogen bonds. The cyclic hydrogen bonding motif involving the thioureido moieties of the ligand is the only one which repeats in each structure.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('108','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_108\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.shd-pub.org.rs\/index.php\/JSCS\/article\/view\/12896\" title=\"https:\/\/www.shd-pub.org.rs\/index.php\/JSCS\/article\/view\/12896\" target=\"_blank\">https:\/\/www.shd-pub.org.rs\/index.php\/JSCS\/article\/view\/12896<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.2298\/JSC240417050B \" title=\"Follow DOI:10.2298\/JSC240417050B \" target=\"_blank\">doi:10.2298\/JSC240417050B <\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('108','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">104.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Jovanovi\u0107, Predrag;  Jovanovi\u0107, Milo\u0161;  Petkovic, Milo\u0161;  Simi\u0107, Milena;  Tasi\u0107, Gordana;  Rodi\u0107, Marko V.;  Raki\u0107, Srdjan;  Vlahovi\u0107, Filip;  Savi\u0107, Vladimir<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('106','tp_links')\" style=\"cursor:pointer;\">Three Component Cascade Processes Involving Palladium Catalyzed Transformations\/Dipolar Cycloadditions for the Synthesis of Angular Heterotriquinane Derivatives<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Advanced Synthesis &amp; Catalysis, <\/span><span class=\"tp_pub_additional_volume\">vol. 366, <\/span><span class=\"tp_pub_additional_issue\">iss. 17, <\/span><span class=\"tp_pub_additional_pages\">pp. 3564-3571, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 1615-4150<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_106\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('106','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_106\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('106','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_106\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('106','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_106\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{https:\/\/doi.org\/10.1002\/adsc.202400253,<br \/>\r\ntitle = {Three Component Cascade Processes Involving Palladium Catalyzed Transformations\/Dipolar Cycloadditions for the Synthesis of Angular Heterotriquinane Derivatives},<br \/>\r\nauthor = {Predrag Jovanovi\u0107 and Milo\u0161 Jovanovi\u0107 and Milo\u0161 Petkovic and Milena Simi\u0107 and Gordana Tasi\u0107 and Marko V. Rodi\u0107 and Srdjan Raki\u0107 and Filip Vlahovi\u0107 and Vladimir Savi\u0107},<br \/>\r\nurl = {https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/adsc.202400253},<br \/>\r\ndoi = {https:\/\/doi.org\/10.1002\/adsc.202400253},<br \/>\r\nissn = {1615-4150},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-07-04},<br \/>\r\nurldate = {2024-07-18},<br \/>\r\njournal = {Advanced Synthesis & Catalysis},<br \/>\r\nvolume = {366},<br \/>\r\nissue = {17},<br \/>\r\npages = {3564-3571},<br \/>\r\nabstract = {Abstract Combining chemical reactivities of allenes and oximes created a methodology for the preparation of heterocyclic triquinane-type skeletons via a cascade process constructing four bonds in a single step. The initial reaction of allene moiety promoted by Pd-catalysis, affording \u03c0-allyl Pd-species, was followed by two additional transformations - nucleophilic displacement and dipolar cycloaddition - to furnish the product highly stereoselectively in moderate to good yields. For the process to be efficient, it was necessary to use a dipolarophilic component as a solvent. Intriguingly, while the reaction with cyclopentanone derived oxime progressed through the whole cascade, with cyclohexanone analogue it stopped at the nitrone stage, requiring an additional step to yield similar type of products. Some aspects of the studied cascade were examined by DFT.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('106','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_106\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Abstract Combining chemical reactivities of allenes and oximes created a methodology for the preparation of heterocyclic triquinane-type skeletons via a cascade process constructing four bonds in a single step. The initial reaction of allene moiety promoted by Pd-catalysis, affording \u03c0-allyl Pd-species, was followed by two additional transformations - nucleophilic displacement and dipolar cycloaddition - to furnish the product highly stereoselectively in moderate to good yields. For the process to be efficient, it was necessary to use a dipolarophilic component as a solvent. Intriguingly, while the reaction with cyclopentanone derived oxime progressed through the whole cascade, with cyclohexanone analogue it stopped at the nitrone stage, requiring an additional step to yield similar type of products. Some aspects of the studied cascade were examined by DFT.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('106','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_106\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/adsc.202400253\" title=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/adsc.202400253\" target=\"_blank\">https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/adsc.202400253<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/https:\/\/doi.org\/10.1002\/adsc.202400253\" title=\"Follow DOI:https:\/\/doi.org\/10.1002\/adsc.202400253\" target=\"_blank\">doi:https:\/\/doi.org\/10.1002\/adsc.202400253<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('106','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">103.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Djoki\u0107, Sanja;  Benedekovi\u0107, Goran;  Kesi\u0107, Jelena;  Rodi\u0107, Marko V.;  Popsavin, Mirjana;  Popsavin, Velimir;  Francuz, Jovana<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('109','tp_links')\" style=\"cursor:pointer;\"> First total synthesis of asperilactone B. Revision of absolute stereochemistry of asperilactones B and C<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Organic &amp; Biomolecular Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 22, <\/span><span class=\"tp_pub_additional_issue\">iss. 24, <\/span><span class=\"tp_pub_additional_pages\">pp. 4864-4867, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>, <span class=\"tp_pub_additional_isbn\">ISBN: 1477-0539<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_109\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('109','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_109\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('109','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_109\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{nokey,<br \/>\r\ntitle = { First total synthesis of asperilactone B. Revision of absolute stereochemistry of asperilactones B and C},<br \/>\r\nauthor = {Sanja Djoki\u0107 and Goran Benedekovi\u0107 and Jelena Kesi\u0107 and Marko V. Rodi\u0107 and Mirjana Popsavin and Velimir Popsavin and Jovana Francuz},<br \/>\r\nurl = {https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/ob\/d4ob00583j},<br \/>\r\ndoi = {10.1039\/D4OB00583J},<br \/>\r\nisbn = {1477-0539},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-05-10},<br \/>\r\nurldate = {2024-05-10},<br \/>\r\njournal = {Organic & Biomolecular Chemistry},<br \/>\r\nvolume = {22},<br \/>\r\nissue = {24},<br \/>\r\npages = {4864-4867},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('109','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_109\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/ob\/d4ob00583j\" title=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/ob\/d4ob00583j\" target=\"_blank\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/ob\/d4ob00583j<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1039\/D4OB00583J\" title=\"Follow DOI:10.1039\/D4OB00583J\" target=\"_blank\">doi:10.1039\/D4OB00583J<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('109','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">102.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Popsavin, Mirjana;  Djoki\u0107, Sanja;  Kova\u010devi\u0107, Ivana;  Stanisavljevi\u0107, Sla\u0111ana M.;  Koji\u0107, Vesna;  Rodi\u0107, Marko V.;  Aleksi\u0107, Lidija;  Kesi\u0107, Jelena;  Zelenovi\u0107, Bojana Sre\u0107o;  Popsavin, Velimir;  Jakimov, Dimitar S.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('105','tp_links')\" style=\"cursor:pointer;\">Synthesis and biological activity of thiophene bioisosteres of natural styryl lactone goniofufurone and related compounds<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">European Journal of Medicinal Chemistry, <\/span><span class=\"tp_pub_additional_pages\">pp. 116340, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_105\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('105','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_105\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('105','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_105\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('105','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_105\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{nokey,<br \/>\r\ntitle = {Synthesis and biological activity of thiophene bioisosteres of natural styryl lactone goniofufurone and related compounds},<br \/>\r\nauthor = {Mirjana Popsavin and Sanja Djoki\u0107 and Ivana Kova\u010devi\u0107 and Sla\u0111ana M. Stanisavljevi\u0107 and Vesna Koji\u0107 and Marko V. Rodi\u0107 and Lidija Aleksi\u0107 and Jelena Kesi\u0107 and Bojana {Sre\u0107o Zelenovi\u0107} and Velimir Popsavin and Dimitar S. Jakimov},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523424002204},<br \/>\r\ndoi = {10.1016\/j.ejmech.2024.116340},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-03-21},<br \/>\r\njournal = {European Journal of Medicinal Chemistry},<br \/>\r\npages = {116340},<br \/>\r\nabstract = {Ten new thiophene derivatives related to goniofufurone have been obtained by multistep synthesis starting from d-glucose. The critical step of the synthesis was the Grignard reaction of 2-thienyl magnesium bromide with a protected dialdose, yielding the C-5 epimeric thiophene derivatives 9 and 10. The mixture was oxidized to the 5-keto derivative 11, which after deprotection was converted to the corresponding keto-lactone 14. Stereoselective reduction of 14 afforded the thiophene mimic of goniofufurone 3. Esterification of 3 with cinnamic or 4-fluorocinnamic acid gave hybrids 5\u20137. Synthesized analogues were evaluated for their in vitro cytotoxicity against several tumour cell lines. The vast majority of them showed better activity than lead 1. In the culture of K562\u202fcells, compound 3 was more active than the commercial antitumour drug doxorubicin. Structural features of analogues important for their antiproliferative activities were identified by SAR analysis. Pro-apoptotic potential examination of compound 3 on the K562\u202fcell line was performed using flow cytometry, double fluorescence staining and apoptotic morphology screening. Results show that this derivative induces cell membrane disruptions attributable to apoptosis and induces the apoptotic morphology, but decreasing simultaneously the population of cells in the subG1 phase of the cell cycle. The results further suggest that analogue 3 achieves strong cytotoxicity without causing DNA fragmentation. This is clearly indicated by the relatively low incidence of micronuclei, as well as the SAR analysis of all biological effects.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('105','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_105\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Ten new thiophene derivatives related to goniofufurone have been obtained by multistep synthesis starting from d-glucose. The critical step of the synthesis was the Grignard reaction of 2-thienyl magnesium bromide with a protected dialdose, yielding the C-5 epimeric thiophene derivatives 9 and 10. The mixture was oxidized to the 5-keto derivative 11, which after deprotection was converted to the corresponding keto-lactone 14. Stereoselective reduction of 14 afforded the thiophene mimic of goniofufurone 3. Esterification of 3 with cinnamic or 4-fluorocinnamic acid gave hybrids 5\u20137. Synthesized analogues were evaluated for their in vitro cytotoxicity against several tumour cell lines. The vast majority of them showed better activity than lead 1. In the culture of K562\u202fcells, compound 3 was more active than the commercial antitumour drug doxorubicin. Structural features of analogues important for their antiproliferative activities were identified by SAR analysis. Pro-apoptotic potential examination of compound 3 on the K562\u202fcell line was performed using flow cytometry, double fluorescence staining and apoptotic morphology screening. Results show that this derivative induces cell membrane disruptions attributable to apoptosis and induces the apoptotic morphology, but decreasing simultaneously the population of cells in the subG1 phase of the cell cycle. The results further suggest that analogue 3 achieves strong cytotoxicity without causing DNA fragmentation. This is clearly indicated by the relatively low incidence of micronuclei, as well as the SAR analysis of all biological effects.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('105','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_105\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523424002204\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523424002204\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523424002204<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.ejmech.2024.116340\" title=\"Follow DOI:10.1016\/j.ejmech.2024.116340\" target=\"_blank\">doi:10.1016\/j.ejmech.2024.116340<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('105','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">101.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Selakovi\u0107, Sne\u017eana;  Rodi\u0107, Marko V.;  Novakovi\u0107, Irena;  Mati\u0107, Ivana Z.;  Stanojkovi\u0107, Tatjana;  Pirkovi\u0107, Andrea;  \u017divkovi\u0107, Lada;  Spremo-Potparevi\u0107, Biljana;  Mil\u010di\u0107, Milo\u0161;  Medakovi\u0107, Vesna;  Dimiza, Filitsa;  Psomas, George;  An\u0111elkovi\u0107, Katarina;  \u0160umar-Ristovi\u0107, Maja<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('104','tp_links')\" style=\"cursor:pointer;\">Cu(II) complexes with a salicylaldehyde derivative and \u03b1-diimines as co-ligands: synthesis, characterization, biological activity. Experimental and theoretical approach<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Dalton Transactions, <\/span><span class=\"tp_pub_additional_volume\">vol. 53, <\/span><span class=\"tp_pub_additional_issue\">iss. 6, <\/span><span class=\"tp_pub_additional_pages\">pp. 2770-2788 , <\/span><span class=\"tp_pub_additional_year\">2024<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 1477-9234<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_104\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('104','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_104\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('104','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_104\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('104','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_104\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{2024Selakovic,<br \/>\r\ntitle = {Cu(II) complexes with a salicylaldehyde derivative and \u03b1-diimines as co-ligands: synthesis, characterization, biological activity. Experimental and theoretical approach},<br \/>\r\nauthor = {Sne\u017eana Selakovi\u0107 and Marko V. Rodi\u0107 and Irena Novakovi\u0107 and Ivana Z. Mati\u0107 and Tatjana Stanojkovi\u0107 and Andrea Pirkovi\u0107 and Lada \u017divkovi\u0107 and Biljana Spremo-Potparevi\u0107 and Milo\u0161 Mil\u010di\u0107 and Vesna Medakovi\u0107 and Filitsa Dimiza and George Psomas and Katarina An\u0111elkovi\u0107 and Maja \u0160umar-Ristovi\u0107},<br \/>\r\nurl = {https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/dt\/d3dt03862a},<br \/>\r\ndoi = {10.1039\/D3DT03862A},<br \/>\r\nissn = {1477-9234},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-02-14},<br \/>\r\nurldate = {2024-02-14},<br \/>\r\njournal = {Dalton Transactions},<br \/>\r\nvolume = {53},<br \/>\r\nissue = {6},<br \/>\r\npages = {2770-2788 },<br \/>\r\nabstract = {Copper(II) complexes with an \u03b1-diimine show a wide variety of biological activities, such as antibacterial, antifungal, antioxidant and anticancer. In this work, we synthesized and structurally characterized two novel Cu(II) complexes with methyl 3-formyl-4-hydroxybenzoate (HL) and \u03b1-diimines: 2,2\u2032-bipyridine (bipy) and 1,10-phenanthroline (phen). Crystal structure analysis shows that the formulas of the compounds are [Cu(bipy)(L)(BF4)] (1) and [Cu(phen)(L)(H2O)](BF4)\u00b7H2O (2), with BF4\u2212 as a ligand in complex 1, which is rarely coordinated to metals. Both complexes have a square pyramidal geometry, while DFT calculations showed that the most stable structures of complexes 1 and 2 in a water\/DMSO mixture are square-planar derivatives [Cu(bipy)(L)]+ and [Cu(phen)(L)]+. The antibacterial activity of compounds was evaluated in vitro on four Gram-negative and four Gram-positive bacterial strains. Complex 2 showed greater antibacterial activity towards all bacterial strains comparable to the control compound Amikacin. Complex 2 exerted a strong cytotoxic effect against the tested cancer cell lines (IC50 values ranging from 0.32 to 0.44 \u03bcM). Both complexes caused apoptotic cell death in HeLa cells and a noticeable in vitro antiangiogenic effect. In the concentration range of 5 to 100 \u03bcM, the complexes showed the absence of a genotoxic effect and displayed a protective effect against oxidative DNA damage induced by H2O2 in human peripheral blood cells. The interaction between the compounds and calf\u2013thymus DNA was evaluated by diverse techniques suggesting a tight binding, which was also confirmed by molecular docking. In addition, it was found that the complexes bind tightly and reversibly to bovine and human serum albumin.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('104','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_104\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Copper(II) complexes with an \u03b1-diimine show a wide variety of biological activities, such as antibacterial, antifungal, antioxidant and anticancer. In this work, we synthesized and structurally characterized two novel Cu(II) complexes with methyl 3-formyl-4-hydroxybenzoate (HL) and \u03b1-diimines: 2,2\u2032-bipyridine (bipy) and 1,10-phenanthroline (phen). Crystal structure analysis shows that the formulas of the compounds are [Cu(bipy)(L)(BF4)] (1) and [Cu(phen)(L)(H2O)](BF4)\u00b7H2O (2), with BF4\u2212 as a ligand in complex 1, which is rarely coordinated to metals. Both complexes have a square pyramidal geometry, while DFT calculations showed that the most stable structures of complexes 1 and 2 in a water\/DMSO mixture are square-planar derivatives [Cu(bipy)(L)]+ and [Cu(phen)(L)]+. The antibacterial activity of compounds was evaluated in vitro on four Gram-negative and four Gram-positive bacterial strains. Complex 2 showed greater antibacterial activity towards all bacterial strains comparable to the control compound Amikacin. Complex 2 exerted a strong cytotoxic effect against the tested cancer cell lines (IC50 values ranging from 0.32 to 0.44 \u03bcM). Both complexes caused apoptotic cell death in HeLa cells and a noticeable in vitro antiangiogenic effect. In the concentration range of 5 to 100 \u03bcM, the complexes showed the absence of a genotoxic effect and displayed a protective effect against oxidative DNA damage induced by H2O2 in human peripheral blood cells. The interaction between the compounds and calf\u2013thymus DNA was evaluated by diverse techniques suggesting a tight binding, which was also confirmed by molecular docking. In addition, it was found that the complexes bind tightly and reversibly to bovine and human serum albumin.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('104','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_104\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/dt\/d3dt03862a\" title=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/dt\/d3dt03862a\" target=\"_blank\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/dt\/d3dt03862a<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1039\/D3DT03862A\" title=\"Follow DOI:10.1039\/D3DT03862A\" target=\"_blank\">doi:10.1039\/D3DT03862A<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('104','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">100.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radnovi\u0107, Nikola D.;  \u0160tetin, Na\u0111a;  Radanovi\u0107, Mirjana M.;  Bori\u0161ev, Ivana \u0110.;  Rodi\u0107, Marko V.;  Ja\u0107imovi\u0107, \u017deljko K.;  Holl\u00f3, Berta Barta<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('101','tp_links')\" style=\"cursor:pointer;\">Two isomers of a novel Ag(I) complex with pyrazole-type ligand\u2014synthesis, structural, thermal, and antioxidative characterization<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Inorganics, <\/span><span class=\"tp_pub_additional_volume\">vol. 12, <\/span><span class=\"tp_pub_additional_issue\">iss. 1, <\/span><span class=\"tp_pub_additional_pages\">pp. 4, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 2304-6740<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_101\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('101','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_101\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('101','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_101\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('101','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_101\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{inorganics12010004,<br \/>\r\ntitle = {Two isomers of a novel Ag(I) complex with pyrazole-type ligand\u2014synthesis, structural, thermal, and antioxidative characterization},<br \/>\r\nauthor = {Nikola D. Radnovi\u0107 and Na\u0111a \u0160tetin and Mirjana M. Radanovi\u0107 and Ivana \u0110. Bori\u0161ev and Marko V. Rodi\u0107 and \u017deljko K. Ja\u0107imovi\u0107 and Berta Barta Holl\u00f3},<br \/>\r\nurl = {https:\/\/www.mdpi.com\/2304-6740\/12\/1\/4},<br \/>\r\ndoi = {10.3390\/inorganics12010004},<br \/>\r\nissn = {2304-6740},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-01-01},<br \/>\r\nurldate = {2024-01-01},<br \/>\r\njournal = {Inorganics},<br \/>\r\nvolume = {12},<br \/>\r\nissue = {1},<br \/>\r\npages = {4},<br \/>\r\nabstract = {The synthesis of the first Ag(I) complexes with ethyl-5-amino-1-methyl-1H-pyrazole-4-carboxylate (L) is presented. The reaction of AgClO4 with the ligand in a molar ratio of 1:1 gives a bis(ligand) complex [AgL2]ClO4 (1) in the presence of 4-formylbenzonitrile, monoperiodic polymer [AgL2]ClO4n (2). Characterization involved IR spectroscopy, conductometric measurements, thermogravimetric analysis, antioxidant tests, powder, and single crystal X-ray diffraction. Structural analysis revealed ligand coordination in a monodentate manner through the nitrogen atom of the pyrazole ring in both complexes. Complex 1 displayed a linear coordination environment for Ag(I), whereas, in complex 2, square-planar coordination was achieved with the additional involvement of two oxygen atoms from bridging perchlorate anions. Notably, the thermal properties of both isomers are found to be nearly identical. The significant antioxidant activity of the isomer with a reverse-oriented pyrazole-type ligand suggests its potential relevance in biological studies.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('101','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_101\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The synthesis of the first Ag(I) complexes with ethyl-5-amino-1-methyl-1H-pyrazole-4-carboxylate (L) is presented. The reaction of AgClO4 with the ligand in a molar ratio of 1:1 gives a bis(ligand) complex [AgL2]ClO4 (1) in the presence of 4-formylbenzonitrile, monoperiodic polymer [AgL2]ClO4n (2). Characterization involved IR spectroscopy, conductometric measurements, thermogravimetric analysis, antioxidant tests, powder, and single crystal X-ray diffraction. Structural analysis revealed ligand coordination in a monodentate manner through the nitrogen atom of the pyrazole ring in both complexes. Complex 1 displayed a linear coordination environment for Ag(I), whereas, in complex 2, square-planar coordination was achieved with the additional involvement of two oxygen atoms from bridging perchlorate anions. Notably, the thermal properties of both isomers are found to be nearly identical. The significant antioxidant activity of the isomer with a reverse-oriented pyrazole-type ligand suggests its potential relevance in biological studies.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('101','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_101\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.mdpi.com\/2304-6740\/12\/1\/4\" title=\"https:\/\/www.mdpi.com\/2304-6740\/12\/1\/4\" target=\"_blank\">https:\/\/www.mdpi.com\/2304-6740\/12\/1\/4<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/inorganics12010004\" title=\"Follow DOI:10.3390\/inorganics12010004\" target=\"_blank\">doi:10.3390\/inorganics12010004<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('101','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2023\">2023<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">99.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kosti\u0107, Marijana;  Rodi\u0107, Marko V.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Radanovi\u0107, Mirjana M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('103','tp_links')\" style=\"cursor:pointer;\">Synthesis and structural analysis of tetranuclear Zn(II) complex with 2,3-dihydroxybenzaldehyde-aminoguanidine<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 88, <\/span><span class=\"tp_pub_additional_issue\">iss. 12, <\/span><span class=\"tp_pub_additional_pages\">pp. 1253-1264, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 1820-7421<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_103\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('103','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_103\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('103','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_103\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('103','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_103\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{2023Kosti\u0107,<br \/>\r\ntitle = {Synthesis and structural analysis of tetranuclear Zn(II) complex with 2,3-dihydroxybenzaldehyde-aminoguanidine},<br \/>\r\nauthor = {Marijana Kosti\u0107 and Marko V. Rodi\u0107 and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Mirjana M. Radanovi\u0107},<br \/>\r\nurl = {https:\/\/doiserbia.nb.rs\/Article.aspx?id=0352-51392300067K},<br \/>\r\ndoi = {10.2298\/JSC230808067K },<br \/>\r\nissn = {1820-7421},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-12-19},<br \/>\r\nurldate = {2023-12-19},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {88},<br \/>\r\nissue = {12},<br \/>\r\npages = {1253-1264},<br \/>\r\nabstract = {Here we report a new Schiff base of aminoguanidine and 2,3-dihyd\u00adroxybenzaldehyde (H2L) and its physicochemical characterization, along with an investigation into its coordination affinities towards zinc. By reacting zinc acetate with the chloride salt of the ligand in the MeCN\u2013H2O solution, yellow single-crystals of tetranuclear, centrosymmetric complex, with the formula [Zn2(\u00b5-L)(\u00b5-OAc)2]2\u22192MeCN, were obtained. The complex was characterized by IR spectroscopy, conductometry, elemental analysis, and single-crystal X-ray diffraction analysis. Notably, both nitrogen atoms of the aminoguanidine residue coordinate to the same zinc atom, while both deprotonated phenyl oxy\u00adgen atoms achieve bridging coordination. Furthermore, two acetate anions bridge adjacent zinc atoms in addition to the Schiff base anion. Meaningful insights into the hierarchy and significance of intermolecular interactions within the crystal structure were gained by estimating the energies using the CrystalExplorer model. The calculations revealed that the crystal structure can be classified as a layer type, with notably stronger interactions occurring along the [001] and [011] directions.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('103','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_103\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Here we report a new Schiff base of aminoguanidine and 2,3-dihyd\u00adroxybenzaldehyde (H2L) and its physicochemical characterization, along with an investigation into its coordination affinities towards zinc. By reacting zinc acetate with the chloride salt of the ligand in the MeCN\u2013H2O solution, yellow single-crystals of tetranuclear, centrosymmetric complex, with the formula [Zn2(\u00b5-L)(\u00b5-OAc)2]2\u22192MeCN, were obtained. The complex was characterized by IR spectroscopy, conductometry, elemental analysis, and single-crystal X-ray diffraction analysis. Notably, both nitrogen atoms of the aminoguanidine residue coordinate to the same zinc atom, while both deprotonated phenyl oxy\u00adgen atoms achieve bridging coordination. Furthermore, two acetate anions bridge adjacent zinc atoms in addition to the Schiff base anion. Meaningful insights into the hierarchy and significance of intermolecular interactions within the crystal structure were gained by estimating the energies using the CrystalExplorer model. The calculations revealed that the crystal structure can be classified as a layer type, with notably stronger interactions occurring along the [001] and [011] directions.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('103','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_103\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doiserbia.nb.rs\/Article.aspx?id=0352-51392300067K\" title=\"https:\/\/doiserbia.nb.rs\/Article.aspx?id=0352-51392300067K\" target=\"_blank\">https:\/\/doiserbia.nb.rs\/Article.aspx?id=0352-51392300067K<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.2298\/JSC230808067K \" title=\"Follow DOI:10.2298\/JSC230808067K \" target=\"_blank\">doi:10.2298\/JSC230808067K <\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('103','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">98.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radnovi\u0107, Nikola D.;  Hawes, Chris S.;  Kordi\u0107, Branko B.;  Bogdanovi\u0107, Milica G.;  Holl\u00f3, Berta Barta;  Radanovi\u0107, Mirjana M.;  \u0160kori\u0107, Du\u0161an \u0110.;  Jovi\u0107, Branislav D.;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('77','tp_links')\" style=\"cursor:pointer;\">Synthesis, characterization, and impact of water on the stability of postmodified Schiff base containing metal\u2013organic frameworks<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Inorganics, <\/span><span class=\"tp_pub_additional_volume\">vol. 11, <\/span><span class=\"tp_pub_additional_issue\">iss. 11, <\/span><span class=\"tp_pub_additional_pages\">pp. 432, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 2304-6740<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_77\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('77','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_77\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('77','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_77\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('77','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_77\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{inorganics11110432,<br \/>\r\ntitle = {Synthesis, characterization, and impact of water on the stability of postmodified Schiff base containing metal\u2013organic frameworks},<br \/>\r\nauthor = {Nikola D. Radnovi\u0107 and Chris S. Hawes and Branko B. Kordi\u0107 and Milica G. Bogdanovi\u0107 and Berta {Barta Holl\u00f3} and Mirjana M. Radanovi\u0107 and Du\u0161an \u0110. \u0160kori\u0107 and Branislav D. Jovi\u0107 and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.mdpi.com\/2304-6740\/11\/11\/432},<br \/>\r\ndoi = {10.3390\/inorganics11110432},<br \/>\r\nissn = {2304-6740},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-11-08},<br \/>\r\nurldate = {2023-11-08},<br \/>\r\njournal = {Inorganics},<br \/>\r\nvolume = {11},<br \/>\r\nissue = {11},<br \/>\r\npages = {432},<br \/>\r\nabstract = {In this study, the synthesis of a Schiff base containing metal-organic frameworks (MOFs) of the UiO-67 family has been investigated. MOFs featuring free amine groups were successfully synthesized under mild solvothermal conditions using 2-amino-[1,1&prime;-biphenyl]-4,4&prime;-dicarboxylic acid and 2,2&prime;-diamino-[1,1&prime;-biphenyl]-4,4&prime;-dicarboxylic acid as bridging ligands, resulting in MOFs with amine groups covalently linked to the bridging ligands. Both types of functionalized MOFs were post-synthetically modified with 4-formylbenzonitrile that resulted in imine formation. All the obtained compounds were characterized by PXRD, TGA, DTA, BET, NMR, and FTIR spectroscopy, while stability in water was monitored with SEM, EDS, and UV-VIS spectroscopy.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('77','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_77\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In this study, the synthesis of a Schiff base containing metal&amp;ndash;organic frameworks (MOFs) of the UiO-67 family has been investigated. MOFs featuring free amine groups were successfully synthesized under mild solvothermal conditions using 2-amino-[1,1&amp;prime;-biphenyl]-4,4&amp;prime;-dicarboxylic acid and 2,2&amp;prime;-diamino-[1,1&amp;prime;-biphenyl]-4,4&amp;prime;-dicarboxylic acid as bridging ligands, resulting in MOFs with amine groups covalently linked to the bridging ligands. Both types of functionalized MOFs were post-synthetically modified with 4-formylbenzonitrile that resulted in imine formation. All the obtained compounds were characterized by PXRD, TGA, DTA, BET, NMR, and FTIR spectroscopy, while stability in water was monitored with SEM, EDS, and UV&amp;ndash;VIS spectroscopy.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('77','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_77\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.mdpi.com\/2304-6740\/11\/11\/432\" title=\"https:\/\/www.mdpi.com\/2304-6740\/11\/11\/432\" target=\"_blank\">https:\/\/www.mdpi.com\/2304-6740\/11\/11\/432<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/inorganics11110432\" title=\"Follow DOI:10.3390\/inorganics11110432\" target=\"_blank\">doi:10.3390\/inorganics11110432<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('77','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">97.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> A\u0161anin, Darko P.;  Andrejevi\u0107, Tina P.;  Nenadovic, Marija;  Rodi\u0107, Marko V.;  Vojnovic, Sandra;  Djuran, Milo\u0161 I.;  Gli\u0161i\u0107, Biljana \u0110.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('78','tp_links')\" style=\"cursor:pointer;\">Comparative study of antimicrobial potential and DNA\/BSA binding affinity of silver(I) and gold(III) coordination compounds with 1,6-naphthyridine<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Polyhedron, <\/span><span class=\"tp_pub_additional_volume\">vol. 244, <\/span><span class=\"tp_pub_additional_pages\">pp. 116585, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 0277-5387<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_78\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('78','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_78\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('78','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_78\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('78','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_78\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{ASANIN2023116585,<br \/>\r\ntitle = {Comparative study of antimicrobial potential and DNA\/BSA binding affinity of silver(I) and gold(III) coordination compounds with 1,6-naphthyridine},<br \/>\r\nauthor = {Darko P. A\u0161anin and Tina P. Andrejevi\u0107 and Marija Nenadovic and Marko V. Rodi\u0107 and Sandra Vojnovic and Milo\u0161 I. Djuran and Biljana \u0110. Gli\u0161i\u0107},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538723003078},<br \/>\r\ndoi = {https:\/\/doi.org\/10.1016\/j.poly.2023.116585},<br \/>\r\nissn = {0277-5387},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-11-01},<br \/>\r\nurldate = {2023-01-01},<br \/>\r\njournal = {Polyhedron},<br \/>\r\nvolume = {244},<br \/>\r\npages = {116585},<br \/>\r\nabstract = {In the present study, synthesis of silver(I) and gold(III) coordination compounds with 1,6-naphthyridine (1,6-naph), [Ag(1,6-naph)(H2O)](BF4)n (1) and [AuCl3(1,6-naph)] (2), was reported. The methods used for the structural characterization of a new compound 1 included IR, NMR (1H and 13C) and UV\u2013Vis spectroscopy, cyclic voltammetry and single-crystal X-ray diffraction analysis. The crystallographic results showed that compound 1 represents silver(I) coordination polymer, in which 1,6-naph ligand acts as a bidentate bridging ligand connecting two Ag(I) ions via its N1 and N6 nitrogen atoms, while the third coordination site of the metal ion is occupied by the water oxygen atom, resulted in a T-shape geometry. Compounds 1 and 2 were evaluated in vitro for antimicrobial activity against five bacterial and two Candida species, while their cytotoxicity was tested on the normal human lung fibroblast cell line (MRC-5). Compound 1 has manifested a remarkable antifungal activity on both tested Candida strains (C. albicans and C. parapsilosis) with minimal inhibitory concentrations (MICs) of 1.43 and 11.38\u00a0\u00b5M (0.49 and 3.9\u00a0\u00b5g\/mL), respectively, while no significant antimicrobial activity was observed for 2. Moreover, silver(I) coordination polymer 1 inhibits the hyphae formation of C. albicans at subinhibitory concentration. The binding affinity of both compounds 1 and 2 with calf thymus DNA (ct-DNA) and bovine serum albumin (BSA) was studied by fluorescence spectroscopy, indicating their ability to interact with these biomolecules, with compound 2 being more reactive.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('78','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_78\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In the present study, synthesis of silver(I) and gold(III) coordination compounds with 1,6-naphthyridine (1,6-naph), [Ag(1,6-naph)(H2O)](BF4)n (1) and [AuCl3(1,6-naph)] (2), was reported. The methods used for the structural characterization of a new compound 1 included IR, NMR (1H and 13C) and UV\u2013Vis spectroscopy, cyclic voltammetry and single-crystal X-ray diffraction analysis. The crystallographic results showed that compound 1 represents silver(I) coordination polymer, in which 1,6-naph ligand acts as a bidentate bridging ligand connecting two Ag(I) ions via its N1 and N6 nitrogen atoms, while the third coordination site of the metal ion is occupied by the water oxygen atom, resulted in a T-shape geometry. Compounds 1 and 2 were evaluated in vitro for antimicrobial activity against five bacterial and two Candida species, while their cytotoxicity was tested on the normal human lung fibroblast cell line (MRC-5). Compound 1 has manifested a remarkable antifungal activity on both tested Candida strains (C. albicans and C. parapsilosis) with minimal inhibitory concentrations (MICs) of 1.43 and 11.38\u00a0\u00b5M (0.49 and 3.9\u00a0\u00b5g\/mL), respectively, while no significant antimicrobial activity was observed for 2. Moreover, silver(I) coordination polymer 1 inhibits the hyphae formation of C. albicans at subinhibitory concentration. The binding affinity of both compounds 1 and 2 with calf thymus DNA (ct-DNA) and bovine serum albumin (BSA) was studied by fluorescence spectroscopy, indicating their ability to interact with these biomolecules, with compound 2 being more reactive.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('78','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_78\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538723003078\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538723003078\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538723003078<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/https:\/\/doi.org\/10.1016\/j.poly.2023.116585\" title=\"Follow DOI:https:\/\/doi.org\/10.1016\/j.poly.2023.116585\" target=\"_blank\">doi:https:\/\/doi.org\/10.1016\/j.poly.2023.116585<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('78','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">96.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Aksi\u0107, Jelena M.;  Gen\u010di\u0107, Marija S.;  Radulovi\u0107, Niko S.;  Dimitrijevi\u0107, Marina V.;  Stojanovi\u0107-Radi\u0107, Zorica Z.;  Tomic, Tatjana Ilic;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('86','tp_links')\" style=\"cursor:pointer;\">Bioisosteric ferrocenyl 1,3-thiazolidine-4-carboxylic acid derivatives: In vitro antiproliferative and antimicrobial evaluations<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Bioorganic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 139, <\/span><span class=\"tp_pub_additional_pages\">pp. 106708, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_86\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('86','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_86\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('86','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_86\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Aksi\u01072023,<br \/>\r\ntitle = {Bioisosteric ferrocenyl 1,3-thiazolidine-4-carboxylic acid derivatives: In vitro antiproliferative and antimicrobial evaluations},<br \/>\r\nauthor = {Jelena M. Aksi\u0107 and Marija S. Gen\u010di\u0107 and Niko S. Radulovi\u0107 and Marina V. Dimitrijevi\u0107 and Zorica Z. Stojanovi\u0107-Radi\u0107 and Tatjana Ilic Tomic and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206823003693},<br \/>\r\ndoi = {10.1016\/j.bioorg.2023.106708},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-10-01},<br \/>\r\nurldate = {2023-01-01},<br \/>\r\njournal = {Bioorganic Chemistry},<br \/>\r\nvolume = {139},<br \/>\r\npages = {106708},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('86','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_86\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206823003693\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206823003693\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0045206823003693<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.bioorg.2023.106708\" title=\"Follow DOI:10.1016\/j.bioorg.2023.106708\" target=\"_blank\">doi:10.1016\/j.bioorg.2023.106708<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('86','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">95.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Jovanovi\u0107, Milo\u0161;  Jovanovi\u0107, Predrag;  Tasi\u0107, Gordana;  Simi\u0107, Milena;  Maslak, Veselin;  Raki\u0107, Srdjan;  Rodi\u0107, Marko V.;  Vlahovi\u0107, Filip;  Petkovi\u0107, Milo\u0161;  Savi\u0107, Vladimir<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('87','tp_links')\" style=\"cursor:pointer;\">Regio- and stereoselective, intramolecular [2+2] cycloaddition of allenes, promoted by visible light photocatalysis<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Advanced Synthesis and Catalysis, <\/span><span class=\"tp_pub_additional_volume\">vol. 365, <\/span><span class=\"tp_pub_additional_issue\">iss. 15, <\/span><span class=\"tp_pub_additional_pages\">pp. 2516 \u2013 2523, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_87\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('87','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_87\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('87','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_87\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('87','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_87\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Jovanovic20232516,<br \/>\r\ntitle = {Regio- and stereoselective, intramolecular [2+2] cycloaddition of allenes, promoted by visible light photocatalysis},<br \/>\r\nauthor = {Milo\u0161 Jovanovi\u0107 and Predrag Jovanovi\u0107 and Gordana Tasi\u0107 and Milena Simi\u0107 and Veselin Maslak and Srdjan Raki\u0107 and Marko V. Rodi\u0107 and Filip Vlahovi\u0107 and Milo\u0161 Petkovi\u0107 and Vladimir Savi\u0107},<br \/>\r\nurl = {https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.202300301},<br \/>\r\ndoi = {10.1002\/adsc.202300301},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-08-10},<br \/>\r\nurldate = {2023-08-10},<br \/>\r\njournal = {Advanced Synthesis and Catalysis},<br \/>\r\nvolume = {365},<br \/>\r\nissue = {15},<br \/>\r\npages = {2516 \u2013 2523},<br \/>\r\nabstract = {Enallenylamides have been utilized for the synthesis of heterobicycle[4.2.0]octane derivatives via Ir\/h\u03bd promoted [2+2] cycloaddition reaction. The reaction specifically targets the distal double bond of the allene moiety, and results in the exclusive formation of the trans product. The process is conducted at room temperature and under an inert atmosphere. An extensive study on the substituent propensities during the cycloaddition step revealed variable effects. Electron-withdrawing groups conjugated with the double bond participating in the cycloaddition either hindered the process or reduced its yield. Conversely, electron-donating substituents enhanced the efficiency, resulting in product yields ranging from 60% to 88%. Our study also demonstrated the influence of protecting groups on the reaction pathway.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('87','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_87\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Enallenylamides have been utilized for the synthesis of heterobicycle[4.2.0]octane derivatives via Ir\/h\u03bd promoted [2+2] cycloaddition reaction. The reaction specifically targets the distal double bond of the allene moiety, and results in the exclusive formation of the trans product. The process is conducted at room temperature and under an inert atmosphere. An extensive study on the substituent propensities during the cycloaddition step revealed variable effects. Electron-withdrawing groups conjugated with the double bond participating in the cycloaddition either hindered the process or reduced its yield. Conversely, electron-donating substituents enhanced the efficiency, resulting in product yields ranging from 60% to 88%. Our study also demonstrated the influence of protecting groups on the reaction pathway.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('87','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_87\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.202300301\" title=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.202300301\" target=\"_blank\">https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.202300301<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1002\/adsc.202300301\" title=\"Follow DOI:10.1002\/adsc.202300301\" target=\"_blank\">doi:10.1002\/adsc.202300301<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('87','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">94.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Koji\u0107, Vesna;  Svir\u010dev, Milo\u0161;  Djoki\u0107, Sanja;  Kova\u010devi\u0107, Ivana;  Rodi\u0107, Marko V.;  Zelenovi\u0107, Bojana Sre\u0107o;  Popsavin, Velimir;  Popsavin, Mirjana<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('80','tp_links')\" style=\"cursor:pointer;\">Synthesis and antiproliferative activity of new thiazole hybrids with [3.3.0]furofuranone or tetrahydrofuran scaffolds <\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 88, <\/span><span class=\"tp_pub_additional_issue\">iss. 5, <\/span><span class=\"tp_pub_additional_pages\">pp. 467-479, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_isbn\">ISBN: 2683-3867<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_80\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('80','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_80\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('80','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_80\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('80','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_80\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{1,<br \/>\r\ntitle = {Synthesis and antiproliferative activity of new thiazole hybrids with [3.3.0]furofuranone or tetrahydrofuran scaffolds },<br \/>\r\nauthor = {Vesna Koji\u0107 and Milo\u0161 Svir\u010dev and Sanja Djoki\u0107 and Ivana Kova\u010devi\u0107 and Marko V. Rodi\u0107 and Bojana Sre\u0107o Zelenovi\u0107 and Velimir Popsavin and Mirjana Popsavin },<br \/>\r\nurl = {https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392300002K},<br \/>\r\ndoi = {https:\/\/doi.org\/10.2298\/JSC221130002K },<br \/>\r\nisbn = {2683-3867},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-04-14},<br \/>\r\nurldate = {2023-04-14},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {88},<br \/>\r\nissue = {5},<br \/>\r\npages = {467-479},<br \/>\r\nabstract = {New thiazole hybrids were synthesized and evaluated for their in vitro cytotoxicity against a panel of human malignant cell lines. The key steps in the synthesis of hybrids 3\u20137 involved the initial condensation of appropriate aldo\u00adnonitriles with cysteine ethyl ester hydrochloride, followed by subsequent treatment of resulting thiazolines with diazabicycloundecene to form the thiaz\u00adole ring. Bioiso\u00adsteres 8 and 14 have been prepared after the stereoselective addition of 2-(tri\u00admethylsilyl)thiazole to the hemiacetals obtained by periodate cleavage of terminal diol functionality in the suitably protected d-glucose der\u00adivatives. The obtained analogues showed various antiproliferative activities in the cultures of several tumour cell lines. Hybrid 6 was the most potent in HeLa cells, exhibiting more than 10 and 4 times stronger activity than both leads 1 and 2, respectively. The most active compound in Raji cells was hybrid 12, which was nearly 2-fold more potent than the clinical antitumour drug doxo\u00adrubicin. All analogues were more potent in A549 cells with respect to lead 1, while compounds 6 and 7 were slightly more active than doxorubicin. Prelim\u00adinary structure\u2013activity relationship analysis revealed that the presence of a cinnamate group at the C-3 pos\u00adition in analogues of type 7 increases the act\u00adivity of resulting molecular hybrids.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('80','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_80\" style=\"display:none;\"><div class=\"tp_abstract_entry\">New thiazole hybrids were synthesized and evaluated for their in vitro cytotoxicity against a panel of human malignant cell lines. The key steps in the synthesis of hybrids 3\u20137 involved the initial condensation of appropriate aldo\u00adnonitriles with cysteine ethyl ester hydrochloride, followed by subsequent treatment of resulting thiazolines with diazabicycloundecene to form the thiaz\u00adole ring. Bioiso\u00adsteres 8 and 14 have been prepared after the stereoselective addition of 2-(tri\u00admethylsilyl)thiazole to the hemiacetals obtained by periodate cleavage of terminal diol functionality in the suitably protected d-glucose der\u00adivatives. The obtained analogues showed various antiproliferative activities in the cultures of several tumour cell lines. Hybrid 6 was the most potent in HeLa cells, exhibiting more than 10 and 4 times stronger activity than both leads 1 and 2, respectively. The most active compound in Raji cells was hybrid 12, which was nearly 2-fold more potent than the clinical antitumour drug doxo\u00adrubicin. All analogues were more potent in A549 cells with respect to lead 1, while compounds 6 and 7 were slightly more active than doxorubicin. Prelim\u00adinary structure\u2013activity relationship analysis revealed that the presence of a cinnamate group at the C-3 pos\u00adition in analogues of type 7 increases the act\u00adivity of resulting molecular hybrids.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('80','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_80\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392300002K\" title=\"https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392300002K\" target=\"_blank\">https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392300002K<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/https:\/\/doi.org\/10.2298\/JSC221130002K \" title=\"Follow DOI:https:\/\/doi.org\/10.2298\/JSC221130002K \" target=\"_blank\">doi:https:\/\/doi.org\/10.2298\/JSC221130002K <\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('80','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">93.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Deki\u0107, Vidoslav S.;  Deki\u0107, Biljana R.;  Sejmanovi\u0107, Dragana M.;  Jani\u0107evi\u0107, Suzana;  Kr\u00fcger, Biljana;  Kahlenberg, Volker;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('88','tp_links')\" style=\"cursor:pointer;\">The crystal structure of (Z)-3-(1-(2-((E)-4-isopropylbenzylidene)hydrazinyl)ethylidene) chroman-2,4-dione, C21H20N2O3<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Zeitschrift fur Kristallographie - New Crystal Structures, <\/span><span class=\"tp_pub_additional_volume\">vol. 238, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 521 \u2013 524, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_88\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('88','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_88\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('88','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_88\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('88','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_88\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Deki\u01072023521,<br \/>\r\ntitle = {The crystal structure of (Z)-3-(1-(2-((E)-4-isopropylbenzylidene)hydrazinyl)ethylidene) chroman-2,4-dione, C21H20N2O3},<br \/>\r\nauthor = {Vidoslav S. Deki\u0107 and Biljana R. Deki\u0107 and Dragana M. Sejmanovi\u0107 and Suzana Jani\u0107evi\u0107 and Biljana Kr\u00fcger and Volker Kahlenberg and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0062\/html?lang=en},<br \/>\r\ndoi = {10.1515\/ncrs-2023-0062},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-04-13},<br \/>\r\nurldate = {2023-01-01},<br \/>\r\njournal = {Zeitschrift fur Kristallographie - New Crystal Structures},<br \/>\r\nvolume = {238},<br \/>\r\nnumber = {3},<br \/>\r\npages = {521 \u2013 524},<br \/>\r\nabstract = {C21H20N2O3, monoclinic, P21\/c (no. 14), a = 6.8892(3) \u00c5, b = 21.8269(13) \u00c5, c = 35.1144(19) \u00c5, \u03b2 = 90.344(5)\u00b0, V = 5280.1(5) \u00c53, Z = 12, R gt(F) = 0.0672, wR ref(F 2) = 0.1460, T = 170(2) K.<br \/>\r\nCCDC no.: 2246347},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('88','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_88\" style=\"display:none;\"><div class=\"tp_abstract_entry\">C21H20N2O3, monoclinic, P21\/c (no. 14), a = 6.8892(3) \u00c5, b = 21.8269(13) \u00c5, c = 35.1144(19) \u00c5, \u03b2 = 90.344(5)\u00b0, V = 5280.1(5) \u00c53, Z = 12, R gt(F) = 0.0672, wR ref(F 2) = 0.1460, T = 170(2) K.<br \/>\r\nCCDC no.: 2246347<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('88','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_88\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0062\/html?lang=en\" title=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0062\/html?lang=en\" target=\"_blank\">https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0062\/html?lang=en<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1515\/ncrs-2023-0062\" title=\"Follow DOI:10.1515\/ncrs-2023-0062\" target=\"_blank\">doi:10.1515\/ncrs-2023-0062<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('88','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">92.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Belo\u0161evi\u0107, Svetlana;  Leovac, Vukadin M.;  Radanovi\u0107, Mirjana M.;  Bogdanovi\u0107, Milica G.;  Radnovi\u0107, Nikola D.;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('82','tp_links')\" style=\"cursor:pointer;\">Crystal structure of trans-diaqua-bis(methyl methylcarbamohydrazonothioato-\u03ba2N,N\u2032) nickel(II) iodide semihydrate, C6H22N6O2NiS2I2\u00b70.5H2O<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Zeitschrift fur Kristallographie - New Crystal Structures, <\/span><span class=\"tp_pub_additional_volume\">vol. 238, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 475 \u2013 477, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 2197-4578<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_82\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('82','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_82\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('82','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_82\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('82','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_82\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Belo\u0161evi\u01072023475,<br \/>\r\ntitle = {Crystal structure of trans-diaqua-bis(methyl methylcarbamohydrazonothioato-\u03ba2N,N\u2032) nickel(II) iodide semihydrate, C6H22N6O2NiS2I2\u00b70.5H2O},<br \/>\r\nauthor = {Svetlana Belo\u0161evi\u0107 and Vukadin M. Leovac and Mirjana M. Radanovi\u0107 and Milica G. Bogdanovi\u0107 and Nikola D. Radnovi\u0107 and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0040\/html},<br \/>\r\ndoi = {10.1515\/ncrs-2023-0040},<br \/>\r\nissn = {2197-4578},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-03-14},<br \/>\r\nurldate = {2023-01-01},<br \/>\r\njournal = {Zeitschrift fur Kristallographie - New Crystal Structures},<br \/>\r\nvolume = {238},<br \/>\r\nnumber = {3},<br \/>\r\npages = {475 \u2013 477},<br \/>\r\nabstract = {C6H23I2N6NiO2.50S2, monoclinic, C2\/c (no. 15), a = 8.2282(4) \u00c5, b = 21.9200(7) \u00c5, c = 11.4906(4) \u00c5, \u03b2 = 109.451(4)\u00b0, V = 1954.19(14) \u00c53, Z = 4, Rgt (F) = 0.0322, wRref (F 2) = 0.1113, T = 295.<br \/>\r\nCCDC no.: 2244689},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('82','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_82\" style=\"display:none;\"><div class=\"tp_abstract_entry\">C6H23I2N6NiO2.50S2, monoclinic, C2\/c (no. 15), a = 8.2282(4) \u00c5, b = 21.9200(7) \u00c5, c = 11.4906(4) \u00c5, \u03b2 = 109.451(4)\u00b0, V = 1954.19(14) \u00c53, Z = 4, Rgt (F) = 0.0322, wRref (F 2) = 0.1113, T = 295.<br \/>\r\nCCDC no.: 2244689<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('82','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_82\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0040\/html\" title=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0040\/html\" target=\"_blank\">https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2023-0040\/html<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1515\/ncrs-2023-0040\" title=\"Follow DOI:10.1515\/ncrs-2023-0040\" target=\"_blank\">doi:10.1515\/ncrs-2023-0040<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('82','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">91.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Babi\u0107, Biljana M.;  Rom\u010devi\u0107, Maja;  Gili\u0107, Martina D.;  Traji\u0107, Jelena;  Radanovi\u0107, Mirjana M.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Rodi\u0107, Marko V.;  Rom\u010devi\u0107, Neboj\u0161a \u017d.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('81','tp_links')\" style=\"cursor:pointer;\">Phonon assisted charge transfer in complexes of Zn(II) and Cd(II) with 2-acetylpyridine-aminoguanidine<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optical Materials, <\/span><span class=\"tp_pub_additional_volume\">vol. 136, <\/span><span class=\"tp_pub_additional_pages\">pp. 113445, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_81\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('81','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_81\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('81','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_81\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('81','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_81\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Babic2023,<br \/>\r\ntitle = {Phonon assisted charge transfer in complexes of Zn(II) and Cd(II) with 2-acetylpyridine-aminoguanidine},<br \/>\r\nauthor = {Biljana M. Babi\u0107 and Maja Rom\u010devi\u0107 and Martina D. Gili\u0107 and Jelena Traji\u0107 and Mirjana M. Radanovi\u0107 and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Marko V. Rodi\u0107 and Neboj\u0161a \u017d. Rom\u010devi\u0107},<br \/>\r\nurl = {https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0925346723000162},<br \/>\r\ndoi = {10.1016\/j.optmat.2023.113445},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-02-01},<br \/>\r\nurldate = {2023-02-01},<br \/>\r\njournal = {Optical Materials},<br \/>\r\nvolume = {136},<br \/>\r\npages = {113445},<br \/>\r\nabstract = {Metal complexes with some Schiff bases, as one of the most widely used groups of ligands, have a wide field of application. In order to find a material with the required optical properties, it is very important to examine the material characteristics as a function of the type of chelating ligand, metal, and the ions present as coligands. In this paper, the synthesis of two new complexes of 2-acetylpyridine-aminoguanidine (L) with zinc(II) and cadmium(II), viz. [Zn(L)(NCO)2] and [{Cd(L)Cl(\u03bc-NCO)}2] is described. Their structural characterization was provided by using SC-XRD. Spectroscopic characterization of these two new complexes and two previously synthesized complexes - [Zn(L)(NSC)2] and [Cd(L)Cl2] are performed. Their phonon structure was determined based on the IR transmission and Raman spectra. The range of Raman modes with significantly increased intensities was registered (1000-1700 cm\u22121), the same range for all four samples. Also, the registered photoluminescence and energy transfers were analyzed and three photoluminescence peaks (E1, E2, E3) were determined. It was concluded that phonons with significantly increased intensities participate in transitions from the E1 state to the energy levels in the range from E2 to E3. The strength of the peaks was significantly affected by replacing one [Cl]- with the [NCO]- ligand. The addition of the second [NCO]- ligand increases the photoluminescence over the entire measured range. The analysis performed helps to understand the issues related to the electron-phonon interaction. Also, the perspectives for the application of metal complexes with various ligands are expanding.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('81','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_81\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Metal complexes with some Schiff bases, as one of the most widely used groups of ligands, have a wide field of application. In order to find a material with the required optical properties, it is very important to examine the material characteristics as a function of the type of chelating ligand, metal, and the ions present as coligands. In this paper, the synthesis of two new complexes of 2-acetylpyridine-aminoguanidine (L) with zinc(II) and cadmium(II), viz. [Zn(L)(NCO)2] and [{Cd(L)Cl(\u03bc-NCO)}2] is described. Their structural characterization was provided by using SC-XRD. Spectroscopic characterization of these two new complexes and two previously synthesized complexes - [Zn(L)(NSC)2] and [Cd(L)Cl2] are performed. Their phonon structure was determined based on the IR transmission and Raman spectra. The range of Raman modes with significantly increased intensities was registered (1000-1700 cm\u22121), the same range for all four samples. Also, the registered photoluminescence and energy transfers were analyzed and three photoluminescence peaks (E1, E2, E3) were determined. It was concluded that phonons with significantly increased intensities participate in transitions from the E1 state to the energy levels in the range from E2 to E3. The strength of the peaks was significantly affected by replacing one [Cl]- with the [NCO]- ligand. The addition of the second [NCO]- ligand increases the photoluminescence over the entire measured range. The analysis performed helps to understand the issues related to the electron-phonon interaction. Also, the perspectives for the application of metal complexes with various ligands are expanding.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('81','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_81\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0925346723000162\" title=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0925346723000162\" target=\"_blank\">https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0925346723000162<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.optmat.2023.113445\" title=\"Follow DOI:10.1016\/j.optmat.2023.113445\" target=\"_blank\">doi:10.1016\/j.optmat.2023.113445<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('81','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">90.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radnovi\u0107, Nikola D.;  Deki\u0107, Biljana R.;  Risti\u0107, Milenko N.;  Sejmanovi\u0107, Dragana M.;  Aksi\u0107, Marija S.;  Kr\u00fcger, Biljana;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('84','tp_links')\" style=\"cursor:pointer;\">The crystal structure of 3-(1-(2-(4-hydroxy-3,5-dimethoxybenzylidene)hydrazinyl)ethylidene)chroman-2,4-dione dihydrate, C20H22N2O8<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Zeitschrift fur Kristallographie - New Crystal Structures, <\/span><span class=\"tp_pub_additional_volume\">vol. 238, <\/span><span class=\"tp_pub_additional_number\">no. 2, <\/span><span class=\"tp_pub_additional_pages\">pp. 171 \u2013 173, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 2197-4578<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_84\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('84','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_84\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('84','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_84\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('84','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_84\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Radnovi\u01072023171,<br \/>\r\ntitle = {The crystal structure of 3-(1-(2-(4-hydroxy-3,5-dimethoxybenzylidene)hydrazinyl)ethylidene)chroman-2,4-dione dihydrate, C20H22N2O8},<br \/>\r\nauthor = {Nikola D. Radnovi\u0107 and Biljana R. Deki\u0107 and Milenko N. Risti\u0107 and Dragana M. Sejmanovi\u0107 and Marija S. Aksi\u0107 and Biljana Kr\u00fcger and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0594\/html},<br \/>\r\ndoi = {10.1515\/ncrs-2022-0594},<br \/>\r\nissn = {2197-4578},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-01-24},<br \/>\r\nurldate = {2023-01-01},<br \/>\r\njournal = {Zeitschrift fur Kristallographie - New Crystal Structures},<br \/>\r\nvolume = {238},<br \/>\r\nnumber = {2},<br \/>\r\npages = {171 \u2013 173},<br \/>\r\nabstract = {C20H22N2O8, monoclinic, P21\/c (no. 14), a = 8.7634(8) \u00c5, b = 17.9290(18) \u00c5, c = 12.8437(9) \u00c5, \u03b2 = 100.013(8)\u00b0, V = 1987.3(3) \u00c53, Z = 4, Rgt(F) = 0.0401, wRref(F2) = 0.1026, T = 170 K.<br \/>\r\nCCDC no.: 2234050},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('84','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_84\" style=\"display:none;\"><div class=\"tp_abstract_entry\">C20H22N2O8, monoclinic, P21\/c (no. 14), a = 8.7634(8) \u00c5, b = 17.9290(18) \u00c5, c = 12.8437(9) \u00c5, \u03b2 = 100.013(8)\u00b0, V = 1987.3(3) \u00c53, Z = 4, Rgt(F) = 0.0401, wRref(F2) = 0.1026, T = 170 K.<br \/>\r\nCCDC no.: 2234050<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('84','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_84\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0594\/html\" title=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0594\/html\" target=\"_blank\">https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0594\/html<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1515\/ncrs-2022-0594\" title=\"Follow DOI:10.1515\/ncrs-2022-0594\" target=\"_blank\">doi:10.1515\/ncrs-2022-0594<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('84','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">89.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rai\u010devi\u0107, Vidak;  Radnovi\u0107, Nikola D.;  Rodi\u0107, Marko V.;  Radulovi\u0107, Niko S.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('83','tp_links')\" style=\"cursor:pointer;\">The crystal structure of 3-hydroxy-2-nitroestra-1,3,5(10)-trien-17-one, C18H21NO4<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Zeitschrift fur Kristallographie - New Crystal Structures, <\/span><span class=\"tp_pub_additional_volume\">vol. 238, <\/span><span class=\"tp_pub_additional_number\">no. 2, <\/span><span class=\"tp_pub_additional_pages\">pp. 277 \u2013 280, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 2197-4578<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_83\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('83','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_83\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('83','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_83\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('83','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_83\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Rai\u010devi\u01072023277,<br \/>\r\ntitle = {The crystal structure of 3-hydroxy-2-nitroestra-1,3,5(10)-trien-17-one, C18H21NO4},<br \/>\r\nauthor = {Vidak Rai\u010devi\u0107 and Nikola D. Radnovi\u0107 and Marko V. Rodi\u0107 and Niko S. Radulovi\u0107},<br \/>\r\nurl = {https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0602\/html},<br \/>\r\ndoi = {10.1515\/ncrs-2022-0602},<br \/>\r\nissn = {2197-4578},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-01-24},<br \/>\r\nurldate = {2023-01-01},<br \/>\r\njournal = {Zeitschrift fur Kristallographie - New Crystal Structures},<br \/>\r\nvolume = {238},<br \/>\r\nnumber = {2},<br \/>\r\npages = {277 \u2013 280},<br \/>\r\nabstract = {C18H21NO4, orthorhombic, C2221 (no. 20), a = 10.6891(2) \u00c5, b = 11.8375(2) \u00c5, c = 25.4410(4) \u00c5, V = 3219.11(10) \u00c53, Z = 8, Rgt(F) = 0.0483, wRref(F2) = 0.1449, T = 295 K.<br \/>\r\nCCDC no.: 2236340},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('83','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_83\" style=\"display:none;\"><div class=\"tp_abstract_entry\">C18H21NO4, orthorhombic, C2221 (no. 20), a = 10.6891(2) \u00c5, b = 11.8375(2) \u00c5, c = 25.4410(4) \u00c5, V = 3219.11(10) \u00c53, Z = 8, Rgt(F) = 0.0483, wRref(F2) = 0.1449, T = 295 K.<br \/>\r\nCCDC no.: 2236340<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('83','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_83\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0602\/html\" title=\"https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0602\/html\" target=\"_blank\">https:\/\/www.degruyter.com\/document\/doi\/10.1515\/ncrs-2022-0602\/html<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1515\/ncrs-2022-0602\" title=\"Follow DOI:10.1515\/ncrs-2022-0602\" target=\"_blank\">doi:10.1515\/ncrs-2022-0602<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('83','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">88.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Stanisavljevi\u0107, Sla\u0111ana M.;  Sre\u0107o-Zelenovi\u0107, Bojana M.;  Popsavin, Mirjana;  Rodi\u0107, Marko V.;  Popsavin, Velimir;  Koji\u0107, Vesna V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('79','tp_links')\" style=\"cursor:pointer;\">Divergent synthesis and antitumour activity of novel conformationally constrained (\u2212)-muricatacin analogues<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 88, <\/span><span class=\"tp_pub_additional_issue\">iss. 2, <\/span><span class=\"tp_pub_additional_pages\">pp. 113-121, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>, <span class=\"tp_pub_additional_isbn\">ISBN: 0352-5139<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_79\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('79','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_79\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('79','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_79\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('79','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_79\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{nokey,<br \/>\r\ntitle = {Divergent synthesis and antitumour activity of novel conformationally constrained (\u2212)-muricatacin analogues},<br \/>\r\nauthor = {Sla\u0111ana M. Stanisavljevi\u0107 and Bojana M. Sre\u0107o-Zelenovi\u0107 and Mirjana Popsavin and Marko V. Rodi\u0107 and Velimir Popsavin and Vesna V. Koji\u0107 },<br \/>\r\nurl = {https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392200069S},<br \/>\r\ndoi = {https:\/\/doi.org\/10.2298\/JSC220613069S},<br \/>\r\nisbn = {0352-5139},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-01-12},<br \/>\r\nurldate = {2023-01-12},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {88},<br \/>\r\nissue = {2},<br \/>\r\npages = {113-121},<br \/>\r\nabstract = {Four novel conformationally restricted (\u2013)-muricatacin analogues, bearing a methoxy group at the C-5 position and with an alkoxymethyl group \u0430s the C-7 side chain, have been synthesised and their in vitro antiproliferative activity was evaluated against a panel of seven human tumour cell lines, as well as a single normal cell line. All analogues (9\u201312) showed diverse antiproliferative effects against all tested human malignant cell lines, but were devoid of any significant cytotoxicity towards the normal foetal lung fibroblasts (MRC-5). A structure\u2013activity relationship study reveals that the introduction of tetrahydrofuran ring, the replacement of C-8 methylene group in the side chain of muricatacin analogues with the O-8 ether functionality, as well as the length of side chain may be beneficial for the antiproliferative effects of these lactones. All novel analogues were more potent than lead compound, (\u2013)-muricatacin, against HL-60 cell line. },<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('79','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_79\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Four novel conformationally restricted (\u2013)-muricatacin analogues, bearing a methoxy group at the C-5 position and with an alkoxymethyl group \u0430s the C-7 side chain, have been synthesised and their in vitro antiproliferative activity was evaluated against a panel of seven human tumour cell lines, as well as a single normal cell line. All analogues (9\u201312) showed diverse antiproliferative effects against all tested human malignant cell lines, but were devoid of any significant cytotoxicity towards the normal foetal lung fibroblasts (MRC-5). A structure\u2013activity relationship study reveals that the introduction of tetrahydrofuran ring, the replacement of C-8 methylene group in the side chain of muricatacin analogues with the O-8 ether functionality, as well as the length of side chain may be beneficial for the antiproliferative effects of these lactones. All novel analogues were more potent than lead compound, (\u2013)-muricatacin, against HL-60 cell line. <\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('79','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_79\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392200069S\" title=\"https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392200069S\" target=\"_blank\">https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0352-51392200069S<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/https:\/\/doi.org\/10.2298\/JSC220613069S\" title=\"Follow DOI:https:\/\/doi.org\/10.2298\/JSC220613069S\" target=\"_blank\">doi:https:\/\/doi.org\/10.2298\/JSC220613069S<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('79','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">87.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pavlovi\u0107, Radoslav Z.;  Kop, Tatjana J.;  Ne\u0161i\u0107, Marko;  Stepanovi\u0107, Olivera;  Wang, Xiuze;  Todorovi\u0107, Nina;  Rodi\u0107, Marko V.;  \u0160mit, Biljana M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('89','tp_links')\" style=\"cursor:pointer;\">On the selectivity in the synthesis of 3-fluoropiperidines using BF3-activated hypervalent iodine reagents<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Organic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 88, <\/span><span class=\"tp_pub_additional_number\">no. 15, <\/span><span class=\"tp_pub_additional_pages\">pp. 10946 \u2013 10959, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_89\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('89','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_89\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('89','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_89\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('89','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_89\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Pavlovi\u0107202310946,<br \/>\r\ntitle = {On the selectivity in the synthesis of 3-fluoropiperidines using BF3-activated hypervalent iodine reagents},<br \/>\r\nauthor = {Radoslav Z. Pavlovi\u0107 and Tatjana J. Kop and Marko Ne\u0161i\u0107 and Olivera Stepanovi\u0107 and Xiuze Wang and Nina Todorovi\u0107 and Marko V. Rodi\u0107 and Biljana M. \u0160mit},<br \/>\r\nurl = {https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.joc.3c00944},<br \/>\r\ndoi = {10.1021\/acs.joc.3c00944},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-01-01},<br \/>\r\nurldate = {2023-01-01},<br \/>\r\njournal = {Journal of Organic Chemistry},<br \/>\r\nvolume = {88},<br \/>\r\nnumber = {15},<br \/>\r\npages = {10946 \u2013 10959},<br \/>\r\nabstract = {Fluorinated piperidines find wide applications, most notably in the development of novel therapies and agrochemicals. Cyclization of alkenyl N-tosylamides promoted by BF3-activated aryliodine(III) carboxylates is an attractive strategy to construct 3-fluoropiperidines, but it suffers from selectivity issues arising from competitive oxoaminations and the inability to easily modulate the reactions diastereoselectivity. Herein, we report an itemized optimization of the reaction conditions carried out on both cyclic and acyclic substrates and outline the origins of substrate- and reagent-based stereo-, regio-, and chemoselectivity. Extensive mechanistic studies encompassing multinuclear NMR spectroscopy, deuterium labeling, rearrangements on stereodefined substrates, and careful structural analyses (NMR and X-ray) of the reaction products are performed. This revealed the processes and interactions crucial for achieving controlled preparation of 3-fluoropiperidines using I(III) chemistry and has provided an advanced understanding of the reaction mechanism. In brief, we propose that BF3-coordinated I(III) reagents attack C\u2550C to produce the corresponding iodiranium(III) ion, which then undergoes diastereodetermining 5-exo-cyclization. Transiently formed pyrrolidines with an exocyclic \u03c3-alkyl-I(III) moiety can further undergo aziridinium ion formation or reductive ligand coupling processes, which dictate not only the final product\u2019s ring size but also the chemoselectivity. Importantly, the selectivity of the reaction depends on the nature of the ligand bound to I(III) and the presence of electrolytes such as TBABF4. Reported findings will facilitate the usage of ArI(III)-dicarboxylates in the reliable construction of fluorinated azaheterocycles.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('89','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_89\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Fluorinated piperidines find wide applications, most notably in the development of novel therapies and agrochemicals. Cyclization of alkenyl N-tosylamides promoted by BF3-activated aryliodine(III) carboxylates is an attractive strategy to construct 3-fluoropiperidines, but it suffers from selectivity issues arising from competitive oxoaminations and the inability to easily modulate the reactions diastereoselectivity. Herein, we report an itemized optimization of the reaction conditions carried out on both cyclic and acyclic substrates and outline the origins of substrate- and reagent-based stereo-, regio-, and chemoselectivity. Extensive mechanistic studies encompassing multinuclear NMR spectroscopy, deuterium labeling, rearrangements on stereodefined substrates, and careful structural analyses (NMR and X-ray) of the reaction products are performed. This revealed the processes and interactions crucial for achieving controlled preparation of 3-fluoropiperidines using I(III) chemistry and has provided an advanced understanding of the reaction mechanism. In brief, we propose that BF3-coordinated I(III) reagents attack C\u2550C to produce the corresponding iodiranium(III) ion, which then undergoes diastereodetermining 5-exo-cyclization. Transiently formed pyrrolidines with an exocyclic \u03c3-alkyl-I(III) moiety can further undergo aziridinium ion formation or reductive ligand coupling processes, which dictate not only the final product\u2019s ring size but also the chemoselectivity. Importantly, the selectivity of the reaction depends on the nature of the ligand bound to I(III) and the presence of electrolytes such as TBABF4. Reported findings will facilitate the usage of ArI(III)-dicarboxylates in the reliable construction of fluorinated azaheterocycles.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('89','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_89\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.joc.3c00944\" title=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.joc.3c00944\" target=\"_blank\">https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.joc.3c00944<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1021\/acs.joc.3c00944\" title=\"Follow DOI:10.1021\/acs.joc.3c00944\" target=\"_blank\">doi:10.1021\/acs.joc.3c00944<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('89','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2022\">2022<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">86.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kesi\u0107, Jelena;  Kova\u010devi\u0107, Ivana;  Popsavin, Mirjana;  Benedekovi\u0107, Goran;  Rodi\u0107, Marko V.;  Koji\u0107, Vesna;  Popsavin, Velimir<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('92','tp_links')\" style=\"cursor:pointer;\">The first total synthesis and revision of absolute stereochemistry of natural cytotoxic lactone cleistanolate<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Bioorganic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 128, <\/span><span class=\"tp_pub_additional_pages\">pp. 106073, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 1090-2120<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_92\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('92','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_92\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('92','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_92\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Kesi\u01072022,<br \/>\r\ntitle = {The first total synthesis and revision of absolute stereochemistry of natural cytotoxic lactone cleistanolate},<br \/>\r\nauthor = {Jelena Kesi\u0107 and Ivana Kova\u010devi\u0107 and Mirjana Popsavin and Goran Benedekovi\u0107 and Marko V. Rodi\u0107 and Vesna Koji\u0107 and Velimir Popsavin},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85135509887&doi=10.1016%2fj.bioorg.2022.106073&partnerID=40&md5=b294f4f0c277de0e79bab1b7f2a0a309},<br \/>\r\ndoi = {10.1016\/j.bioorg.2022.106073},<br \/>\r\nissn = {1090-2120},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-11-01},<br \/>\r\nurldate = {2022-01-01},<br \/>\r\njournal = {Bioorganic Chemistry},<br \/>\r\nvolume = {128},<br \/>\r\npages = {106073},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('92','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_92\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85135509887&amp;doi=10.1016%2fj.bioorg.2022.106073&amp;partnerID=40&amp;md5=b294f4f0c277de0e79bab1b7f2a0a309\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85135509887&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85135509887&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.bioorg.2022.106073\" title=\"Follow DOI:10.1016\/j.bioorg.2022.106073\" target=\"_blank\">doi:10.1016\/j.bioorg.2022.106073<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('92','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">85.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Djoki\u0107, Sanja;  Francuz, Jovana;  Popsavin, Mirjana;  Rodi\u0107, Marko V.;  Koji\u0107, Vesna;  Stevanovi\u0107, Milena;  Popsavin, Velimir<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('93','tp_links')\" style=\"cursor:pointer;\">Natural product protulactone A: Total synthesis from D-galactose, X-ray analysis and biological evaluation<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Bioorganic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 127, <\/span><span class=\"tp_pub_additional_pages\">pp. 105980, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 1090-2120<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_93\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('93','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_93\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('93','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_93\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('93','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_93\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Djoki\u01072022,<br \/>\r\ntitle = {Natural product protulactone A: Total synthesis from D-galactose, X-ray analysis and biological evaluation},<br \/>\r\nauthor = {Sanja Djoki\u0107 and Jovana Francuz and Mirjana Popsavin and Marko V. Rodi\u0107 and Vesna Koji\u0107 and Milena Stevanovi\u0107 and Velimir Popsavin},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132916402&doi=10.1016%2fj.bioorg.2022.105980&partnerID=40&md5=dd4d2159d96c140eaf2ba8d88bd8399c},<br \/>\r\ndoi = {10.1016\/j.bioorg.2022.105980},<br \/>\r\nissn = {1090-2120},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-10-01},<br \/>\r\nurldate = {2022-01-01},<br \/>\r\njournal = {Bioorganic Chemistry},<br \/>\r\nvolume = {127},<br \/>\r\npages = {105980},<br \/>\r\nabstract = {Synthesis of protulactone A (PLA, 1) and twelve of its analogues have been achieved starting from d-galactose. PLA was isolated in the crystalline state, and its crystal structure was determined utilizing X-ray crystallography, which confirmed the assumed stereochemistry at all stereocenters. All tested compounds displayed antiproliferative activity against a panel of tumour cell lines, and all of them were non-cytotoxic toward the normal cells (MRC-5). Natural product PLA (1) was the most active against the K562 and MCF-7 cell lines (IC50 6.52 and 2.20 \u03bcM, respectively). Some of the synthesized derivatives showed very potent cytotoxicity, especially analogues 11, 13 and 15 (IC50 1.08\u20131.14 \u03bcM against MCF-7), and 9 and 14 (IC50 1.29 and 1.64 \u03bcM against K562). SAR analysis indicated important structural motifs for antiproliferative activity. Unfortunately, PLA (1), its C-7 epimer (2) and demethylated analogue (3) did not display a significant antimicrobial activity (two Gram-positive and two Gram-negative bacteria and one fungal strain) and they also cannot affect the ability to modulate bacterial communication.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('93','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_93\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Synthesis of protulactone A (PLA, 1) and twelve of its analogues have been achieved starting from d-galactose. PLA was isolated in the crystalline state, and its crystal structure was determined utilizing X-ray crystallography, which confirmed the assumed stereochemistry at all stereocenters. All tested compounds displayed antiproliferative activity against a panel of tumour cell lines, and all of them were non-cytotoxic toward the normal cells (MRC-5). Natural product PLA (1) was the most active against the K562 and MCF-7 cell lines (IC50 6.52 and 2.20 \u03bcM, respectively). Some of the synthesized derivatives showed very potent cytotoxicity, especially analogues 11, 13 and 15 (IC50 1.08\u20131.14 \u03bcM against MCF-7), and 9 and 14 (IC50 1.29 and 1.64 \u03bcM against K562). SAR analysis indicated important structural motifs for antiproliferative activity. Unfortunately, PLA (1), its C-7 epimer (2) and demethylated analogue (3) did not display a significant antimicrobial activity (two Gram-positive and two Gram-negative bacteria and one fungal strain) and they also cannot affect the ability to modulate bacterial communication.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('93','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_93\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132916402&amp;doi=10.1016%2fj.bioorg.2022.105980&amp;partnerID=40&amp;md5=dd4d2159d96c140eaf2ba8d88bd8399c\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132916402&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132916402&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.bioorg.2022.105980\" title=\"Follow DOI:10.1016\/j.bioorg.2022.105980\" target=\"_blank\">doi:10.1016\/j.bioorg.2022.105980<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('93','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">84.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Svir\u010dev, Milo\u0161;  Popsavin, Mirjana;  Pavi\u0107, Aleksandar;  Vasiljevi\u0107, Branka;  Rodi\u0107, Marko V.;  Djoki\u0107, Sanja;  Kesi\u0107, Jelena;  Zelenovi\u0107, Bojana Sre\u0107o;  Popsavin, Velimir;  Koji\u0107, Vesna<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('1','tp_links')\" style=\"cursor:pointer;\">Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Bioorganic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 121, <\/span><span class=\"tp_pub_additional_pages\">pp. 105691, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 00452068<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_1\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('1','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_1\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('1','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_1\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('1','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_1\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Svircev2022,<br \/>\r\ntitle = {Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity},<br \/>\r\nauthor = {Milo\u0161 Svir\u010dev and Mirjana Popsavin and Aleksandar Pavi\u0107 and Branka Vasiljevi\u0107 and Marko V. Rodi\u0107 and Sanja Djoki\u0107 and Jelena Kesi\u0107 and Bojana Sre\u0107o Zelenovi\u0107 and Velimir Popsavin and Vesna Koji\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124994961&doi=10.1016%2fj.bioorg.2022.105691&partnerID=40&md5=2271acd655f2ea616c6a7514a96ce797},<br \/>\r\ndoi = {10.1016\/j.bioorg.2022.105691},<br \/>\r\nissn = {00452068},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-04-01},<br \/>\r\nurldate = {2022-04-01},<br \/>\r\njournal = {Bioorganic Chemistry},<br \/>\r\nvolume = {121},<br \/>\r\npages = {105691},<br \/>\r\npublisher = {Academic Press Inc.},<br \/>\r\nabstract = {The synthesis of several new goniofufurone bioisosteres was achieved in which the phenyl residue was replaced by a thiazole ring. The key steps of the synthesis included the initial condensation of cyanohydrin benzoates with cysteine ethyl ester hydrochloride, followed by the subsequent reaction of resulting C-4\u2032 epimeric thiazolines with DBU, to introduce 5-deoxy functionality and to elaborate the thiazole ring in one step. Synthesized compounds showed potent growth inhibitory effects against selected human tumour cell lines, especially bioisostere 4, which in the culture of MCF-7 cells displayed the highest activity (IC50 = 0.19 nM) of all compounds under evaluation. This molecule exhibited 64474-fold higher antiproliferative activity than lead 2 and was1053-fold more active than the commercial antitumour agent doxorubicin in the culture of MCF-7 cells. The structural features of the tested compounds responsible for their antiproliferative activity have been identified by preliminary SAR analysis. The toxicity of the most active compound 4 was assessed by an in vivo experiment in a zebrafish model (Danio rerio), whereupon it was found non-toxic at any of the tested concentrations up to 125 \u03bcM. \u00a9 2022 Elsevier Inc.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('1','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_1\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The synthesis of several new goniofufurone bioisosteres was achieved in which the phenyl residue was replaced by a thiazole ring. The key steps of the synthesis included the initial condensation of cyanohydrin benzoates with cysteine ethyl ester hydrochloride, followed by the subsequent reaction of resulting C-4\u2032 epimeric thiazolines with DBU, to introduce 5-deoxy functionality and to elaborate the thiazole ring in one step. Synthesized compounds showed potent growth inhibitory effects against selected human tumour cell lines, especially bioisostere 4, which in the culture of MCF-7 cells displayed the highest activity (IC50 = 0.19 nM) of all compounds under evaluation. This molecule exhibited 64474-fold higher antiproliferative activity than lead 2 and was1053-fold more active than the commercial antitumour agent doxorubicin in the culture of MCF-7 cells. The structural features of the tested compounds responsible for their antiproliferative activity have been identified by preliminary SAR analysis. The toxicity of the most active compound 4 was assessed by an in vivo experiment in a zebrafish model (Danio rerio), whereupon it was found non-toxic at any of the tested concentrations up to 125 \u03bcM. \u00a9 2022 Elsevier Inc.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('1','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_1\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124994961&amp;doi=10.1016%2fj.bioorg.2022.105691&amp;partnerID=40&amp;md5=2271acd655f2ea616c6a7514a96ce797\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124994961&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124994961&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.bioorg.2022.105691\" title=\"Follow DOI:10.1016\/j.bioorg.2022.105691\" target=\"_blank\">doi:10.1016\/j.bioorg.2022.105691<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('1','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">83.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radovanovi\u0107, Lidija;  Malenov, Du\u0161an P.;  Rodi\u0107, Marko V.;  Kremenovi\u0107, Aleksandar;  Rogan, Jelena<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('2','tp_links')\" style=\"cursor:pointer;\">Crystallographic, spectroscopic, thermal and computational studies of polymeric cobalt(II)\u2013mellitate complex with 2,2\u2032-bipyridine<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Molecular Structure, <\/span><span class=\"tp_pub_additional_volume\">vol. 1252, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 00222860<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_2\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('2','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_2\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('2','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_2\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('2','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_2\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Radovanovic2022,<br \/>\r\ntitle = {Crystallographic, spectroscopic, thermal and computational studies of polymeric cobalt(II)\u2013mellitate complex with 2,2\u2032-bipyridine},<br \/>\r\nauthor = {Lidija Radovanovi\u0107 and Du\u0161an P. Malenov and Marko V. Rodi\u0107 and Aleksandar Kremenovi\u0107 and Jelena Rogan},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85121665875&doi=10.1016%2fj.molstruc.2021.132202&partnerID=40&md5=8fae8ed663c6a1e5f032492a3fd15d56},<br \/>\r\ndoi = {10.1016\/j.molstruc.2021.132202},<br \/>\r\nissn = {00222860},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-03-15},<br \/>\r\nurldate = {2022-03-15},<br \/>\r\njournal = {Journal of Molecular Structure},<br \/>\r\nvolume = {1252},<br \/>\r\npublisher = {Elsevier B.V.},<br \/>\r\nabstract = {Orange single crystals of new polymeric cobalt(II) complex [Co(bipy)(H2O)4]2[Co(\u03bc-mell)(H2O)2]\u00b710H2On, 1, were synthesized by slow evaporation method at room temperature (bipy = 2,2\u2032-bipyridine},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('2','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_2\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Orange single crystals of new polymeric cobalt(II) complex [Co(bipy)(H2O)4]2[Co(\u03bc-mell)(H2O)2]\u00b710H2On, 1, were synthesized by slow evaporation method at room temperature (bipy = 2,2\u2032-bipyridine<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('2','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_2\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85121665875&amp;doi=10.1016%2fj.molstruc.2021.132202&amp;partnerID=40&amp;md5=8fae8ed663c6a1e5f032492a3fd15d56\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85121665875&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85121665875&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.molstruc.2021.132202\" title=\"Follow DOI:10.1016\/j.molstruc.2021.132202\" target=\"_blank\">doi:10.1016\/j.molstruc.2021.132202<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('2','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">82.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Holl\u00f3, B. B.;  Radanovi\u0107, M. M.;  Rodi\u0107, M. V.;  Krsti\u0107, S.;  Ja\u0107imovi\u0107, \u017d. K.;  Je\u0161i\u0107, L. S. Vojinovi\u0107<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('3','tp_links')\" style=\"cursor:pointer;\">Synthesis, Physicochemical, Thermal and Antioxidative Properties of Zn(II) Coordination Compounds with Pyrazole-Type Ligand<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Inorganics, <\/span><span class=\"tp_pub_additional_volume\">vol. 10, <\/span><span class=\"tp_pub_additional_number\">no. 2, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 23046740<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_3\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('3','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_3\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('3','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_3\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('3','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_3\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Hollo2022,<br \/>\r\ntitle = {Synthesis, Physicochemical, Thermal and Antioxidative Properties of Zn(II) Coordination Compounds with Pyrazole-Type Ligand},<br \/>\r\nauthor = {B. B. Holl\u00f3 and M. M. Radanovi\u0107 and M. V. Rodi\u0107 and S. Krsti\u0107 and \u017d. K. Ja\u0107imovi\u0107 and L. S. Vojinovi\u0107 Je\u0161i\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&doi=10.3390%2finorganics10020020&partnerID=40&md5=9c0f5c8fb034d20838c7ae1eee7a43f2},<br \/>\r\ndoi = {10.3390\/inorganics10020020},<br \/>\r\nissn = {23046740},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\njournal = {Inorganics},<br \/>\r\nvolume = {10},<br \/>\r\nnumber = {2},<br \/>\r\npublisher = {MDPI},<br \/>\r\nabstract = {The reactions of pyrazole derivative, i.e., ethyl-5-amino-1-methyl-1H-pyrazole-4-carboxylate (L) with zinc halogenides in methanolic solution and zinc nitrate and zinc acetate in acetonic solution are described. The formulae of synthesized compounds are ZnL2 Cl2 (1), [ZnL2 Br2 ] (2), ZnL2 I2\u00b70.5MeOH (3), [Zn(L)2 (H2 O)4 ](NO3 )2 (4), and ZnL(OAc)2 2 (5). Two complexes are obtained in form of single crystals: [ZnL2 Br2 ] (2) and [Zn(L)2 (H2 O)4 ](NO3 )2 (4). Their crystal and molecular structure were determined by single-crystal X-ray structure analysis. The FTIR spectra of compounds prove the complex formation with all five zinc salts. The complexes are characterized by conducto-metric and thermoanalytical measurements, and their antioxidative activity was also tested by the scavenging effect on the DPPH radical. Conductometric results, solvolytic stability, and antioxidative activity of the compounds are in correlation. \u00a9 2022 by the authors. Licensee MDPI, Basel, Switzerland.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('3','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_3\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The reactions of pyrazole derivative, i.e., ethyl-5-amino-1-methyl-1H-pyrazole-4-carboxylate (L) with zinc halogenides in methanolic solution and zinc nitrate and zinc acetate in acetonic solution are described. The formulae of synthesized compounds are ZnL2 Cl2 (1), [ZnL2 Br2 ] (2), ZnL2 I2\u00b70.5MeOH (3), [Zn(L)2 (H2 O)4 ](NO3 )2 (4), and ZnL(OAc)2 2 (5). Two complexes are obtained in form of single crystals: [ZnL2 Br2 ] (2) and [Zn(L)2 (H2 O)4 ](NO3 )2 (4). Their crystal and molecular structure were determined by single-crystal X-ray structure analysis. The FTIR spectra of compounds prove the complex formation with all five zinc salts. The complexes are characterized by conducto-metric and thermoanalytical measurements, and their antioxidative activity was also tested by the scavenging effect on the DPPH radical. Conductometric results, solvolytic stability, and antioxidative activity of the compounds are in correlation. \u00a9 2022 by the authors. Licensee MDPI, Basel, Switzerland.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('3','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_3\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&amp;doi=10.3390%2finorganics10020020&amp;partnerID=40&amp;md5=9c0f5c8fb034d20838c7ae1eee7a43f2\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&amp;doi=10.3390%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&amp;doi=10.3390%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/inorganics10020020\" title=\"Follow DOI:10.3390\/inorganics10020020\" target=\"_blank\">doi:10.3390\/inorganics10020020<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('3','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">81.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Bogdanovi\u0107, Milica G.;  Radnovi\u0107, Nikola D.;  Holl\u00f3, Berta Barta;  Radanovi\u0107, Mirjana M.;  Kordi\u0107, Branko B.;  Rai\u010devi\u0107, Vidak N.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('90','tp_links')\" style=\"cursor:pointer;\">Polymeric Copper(II) Complexes with a Newly Synthesized Biphenyldicarboxylic Acid Schiff Base Ligand\u2014Synthesis, Structural and Thermal Characterization<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Inorganics, <\/span><span class=\"tp_pub_additional_volume\">vol. 10, <\/span><span class=\"tp_pub_additional_number\">no. 12, <\/span><span class=\"tp_pub_additional_year\">2022<\/span><span class=\"tp_pub_additional_note\">, (All Open Access, Gold Open Access)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_90\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('90','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_90\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('90','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_90\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Bogdanovi\u01072022,<br \/>\r\ntitle = {Polymeric Copper(II) Complexes with a Newly Synthesized Biphenyldicarboxylic Acid Schiff Base Ligand\u2014Synthesis, Structural and Thermal Characterization},<br \/>\r\nauthor = {Milica G. Bogdanovi\u0107 and Nikola D. Radnovi\u0107 and Berta Barta Holl\u00f3 and Mirjana M. Radanovi\u0107 and Branko B. Kordi\u0107 and Vidak N. Rai\u010devi\u0107 and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85144668410&doi=10.3390%2finorganics10120261&partnerID=40&md5=1f3a85c1b3d7884299a366a87faa7338},<br \/>\r\ndoi = {10.3390\/inorganics10120261},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\njournal = {Inorganics},<br \/>\r\nvolume = {10},<br \/>\r\nnumber = {12},<br \/>\r\nnote = {All Open Access, Gold Open Access},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('90','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_90\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85144668410&amp;doi=10.3390%2finorganics10120261&amp;partnerID=40&amp;md5=1f3a85c1b3d7884299a366a87faa7338\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85144668410&amp;doi=10.3390%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85144668410&amp;doi=10.3390%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/inorganics10120261\" title=\"Follow DOI:10.3390\/inorganics10120261\" target=\"_blank\">doi:10.3390\/inorganics10120261<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('90','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">80.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radanovi\u0107, Mirjana M.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Jeli\u0107, Miodrag G.;  Sakellis, Elias;  Holl\u00f3, Berta Barta;  Leovac, Vukadin M.;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('91','tp_links')\" style=\"cursor:pointer;\">Synthesis, Structures, and Photoluminescence of Two Novel Zinc(II) Compounds Containing 2-Acetylpyridine-aminoguanidine<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Inorganics, <\/span><span class=\"tp_pub_additional_volume\">vol. 10, <\/span><span class=\"tp_pub_additional_issue\">iss. 10, <\/span><span class=\"tp_pub_additional_pages\">pp. 147, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 2304-6740<\/span><span class=\"tp_pub_additional_note\">, (Open Access)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_91\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('91','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_91\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('91','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_91\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Radanovi\u01072022,<br \/>\r\ntitle = {Synthesis, Structures, and Photoluminescence of Two Novel Zinc(II) Compounds Containing 2-Acetylpyridine-aminoguanidine},<br \/>\r\nauthor = {Mirjana M. Radanovi\u0107 and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Miodrag G. Jeli\u0107 and Elias Sakellis and Berta Barta Holl\u00f3 and Vukadin M. Leovac and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85140650259&doi=10.3390%2finorganics10100147&partnerID=40&md5=60465235d621d70e75c8bfd5ba0f4fbb},<br \/>\r\ndoi = {10.3390\/inorganics10100147},<br \/>\r\nissn = {2304-6740},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\nurldate = {2022-01-01},<br \/>\r\njournal = {Inorganics},<br \/>\r\nvolume = {10},<br \/>\r\nissue = {10},<br \/>\r\npages = {147},<br \/>\r\nnote = {Open Access},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('91','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_91\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85140650259&amp;doi=10.3390%2finorganics10100147&amp;partnerID=40&amp;md5=60465235d621d70e75c8bfd5ba0f4fbb\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85140650259&amp;doi=10.3390%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85140650259&amp;doi=10.3390%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/inorganics10100147\" title=\"Follow DOI:10.3390\/inorganics10100147\" target=\"_blank\">doi:10.3390\/inorganics10100147<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('91','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">79.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radulovi\u0107, Niko S.;  Sejmanovi\u0107, Dragana M.;  Risti\u0107, Milenko N.;  Deki\u0107, Vidoslav S.;  Kr\u00fcger, Biljana;  Kahlenberg, Volker;  Rodi\u0107, Marko V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('94','tp_links')\" style=\"cursor:pointer;\">The crystal structure of 3-(1-(2-((5-methylthiophen-2-yl)methylene)hydrazinyl)ethylidene)chroman-2,4-dione, C17H14N2O3S<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Zeitschrift fur Kristallographie - New Crystal Structures, <\/span><span class=\"tp_pub_additional_volume\">vol. 237, <\/span><span class=\"tp_pub_additional_number\">no. 5, <\/span><span class=\"tp_pub_additional_pages\">pp. 775 \u2013 777, <\/span><span class=\"tp_pub_additional_year\">2022<\/span><span class=\"tp_pub_additional_note\">, (All Open Access, Gold Open Access)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_94\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('94','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_94\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('94','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_94\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Radulovi\u01072022775,<br \/>\r\ntitle = {The crystal structure of 3-(1-(2-((5-methylthiophen-2-yl)methylene)hydrazinyl)ethylidene)chroman-2,4-dione, C17H14N2O3S},<br \/>\r\nauthor = {Niko S. Radulovi\u0107 and Dragana M. Sejmanovi\u0107 and Milenko N. Risti\u0107 and Vidoslav S. Deki\u0107 and Biljana Kr\u00fcger and Volker Kahlenberg and Marko V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&doi=10.1515%2fncrs-2022-0225&partnerID=40&md5=1865a4b07541746d0bfa2b057d2f4a93},<br \/>\r\ndoi = {10.1515\/ncrs-2022-0225},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\njournal = {Zeitschrift fur Kristallographie - New Crystal Structures},<br \/>\r\nvolume = {237},<br \/>\r\nnumber = {5},<br \/>\r\npages = {775 \u2013 777},<br \/>\r\nnote = {All Open Access, Gold Open Access},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('94','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_94\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&amp;doi=10.1515%2fncrs-2022-0225&amp;partnerID=40&amp;md5=1865a4b07541746d0bfa2b057d2f4a93\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&amp;doi=10.1515%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&amp;doi=10.1515%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1515\/ncrs-2022-0225\" title=\"Follow DOI:10.1515\/ncrs-2022-0225\" target=\"_blank\">doi:10.1515\/ncrs-2022-0225<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('94','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">78.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Holl\u00f3, Berta Barta;  Radanovi\u0107, Mirjana M.;  Rodi\u0107, Marko V.;  Krsti\u0107, Sanja;  Ja\u0107imovi\u0107, \u017deljko K.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('95','tp_links')\" style=\"cursor:pointer;\">Synthesis, Physicochemical, Thermal and Antioxidative Properties of Zn(II) Coordination Compounds with Pyrazole-Type Ligand<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Inorganics, <\/span><span class=\"tp_pub_additional_volume\">vol. 10, <\/span><span class=\"tp_pub_additional_number\">no. 2, <\/span><span class=\"tp_pub_additional_year\">2022<\/span><span class=\"tp_pub_additional_note\">, (All Open Access, Gold Open Access)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_95\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('95','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_95\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('95','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_95\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Holl\u00f32022b,<br \/>\r\ntitle = {Synthesis, Physicochemical, Thermal and Antioxidative Properties of Zn(II) Coordination Compounds with Pyrazole-Type Ligand},<br \/>\r\nauthor = {Berta Barta Holl\u00f3 and Mirjana M. Radanovi\u0107 and Marko V. Rodi\u0107 and Sanja Krsti\u0107 and \u017deljko K. Ja\u0107imovi\u0107 and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&doi=10.3390%2finorganics10020020&partnerID=40&md5=9c0f5c8fb034d20838c7ae1eee7a43f2},<br \/>\r\ndoi = {10.3390\/inorganics10020020},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\nurldate = {2022-01-01},<br \/>\r\njournal = {Inorganics},<br \/>\r\nvolume = {10},<br \/>\r\nnumber = {2},<br \/>\r\nnote = {All Open Access, Gold Open Access},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('95','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_95\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&amp;doi=10.3390%2finorganics10020020&amp;partnerID=40&amp;md5=9c0f5c8fb034d20838c7ae1eee7a43f2\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&amp;doi=10.3390%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85124509428&amp;doi=10.3390%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/inorganics10020020\" title=\"Follow DOI:10.3390\/inorganics10020020\" target=\"_blank\">doi:10.3390\/inorganics10020020<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('95','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">77.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rodi\u0107, Marko V.;  Radanovi\u0107, Mirjana M.;  Gazdi\u0107, Dragana V.;  Leovac, Vukadin M.;  Holl\u00f3, Berta Barta;  Rai\u010devi\u0107, Vidak;  Belo\u0161evi\u0107, Svetlana K.;  Kr\u00fcger, Biljana;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('96','tp_links')\" style=\"cursor:pointer;\">Reactions of copper(II) bromide with 2,6-diacetylpyridine bis(phenylhydrazone) (L) \u2013 Molecular and crystal structures of L and its mixed-valence complex [CuIIL2][CuI2Br4]; [\u0420\u0415\u0410\u041a\u0426\u0418\u0408\u0415 \u0411\u0410\u041a\u0410\u0420(II)-\u0411\u0420\u041e\u041c\u0418\u0414\u0410 \u0421\u0410 \u0411\u0418\u0421(\u0424\u0415\u041d\u0418\u041b\u0425\u0418\u0414\u0420\u0410\u0417\u041e\u041d\u041e\u041c) 2,6-\u0414\u0418\u0410\u0426\u0415\u0422\u0418\u041b\u041f\u0418\u0420\u0418\u0414\u0418\u041d\u0410 (L) \u2013 \u041c\u041e\u041b\u0415\u041a\u0423\u041b\u0421\u041a\u0410 \u0418 \u041a\u0420\u0418\u0421\u0422\u0410\u041b\u041d\u0410 \u0421\u0422\u0420\u0423\u041a\u0422\u0423\u0420\u0410 L \u0418 \u040a\u0415\u0413\u041e\u0412\u041e\u0413 \u041c\u0415\u0428\u041e\u0412\u0418\u0422\u041e-\u0412\u0410\u041b\u0415\u041d\u0422\u041d\u041e\u0413 \u041a\u041e\u041c\u041f\u041b\u0415\u041a\u0421\u0410 [CuIIL2][CuI2Br4]]<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 87, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 307 \u2013 320, <\/span><span class=\"tp_pub_additional_year\">2022<\/span><span class=\"tp_pub_additional_note\">, (All Open Access, Gold Open Access)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_96\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('96','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_96\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('96','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_96\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Rodi\u01072022307,<br \/>\r\ntitle = {Reactions of copper(II) bromide with 2,6-diacetylpyridine bis(phenylhydrazone) (L) \u2013 Molecular and crystal structures of L and its mixed-valence complex [CuIIL2][CuI2Br4]; [\u0420\u0415\u0410\u041a\u0426\u0418\u0408\u0415 \u0411\u0410\u041a\u0410\u0420(II)-\u0411\u0420\u041e\u041c\u0418\u0414\u0410 \u0421\u0410 \u0411\u0418\u0421(\u0424\u0415\u041d\u0418\u041b\u0425\u0418\u0414\u0420\u0410\u0417\u041e\u041d\u041e\u041c) 2,6-\u0414\u0418\u0410\u0426\u0415\u0422\u0418\u041b\u041f\u0418\u0420\u0418\u0414\u0418\u041d\u0410 (L) \u2013 \u041c\u041e\u041b\u0415\u041a\u0423\u041b\u0421\u041a\u0410 \u0418 \u041a\u0420\u0418\u0421\u0422\u0410\u041b\u041d\u0410 \u0421\u0422\u0420\u0423\u041a\u0422\u0423\u0420\u0410 L \u0418 \u040a\u0415\u0413\u041e\u0412\u041e\u0413 \u041c\u0415\u0428\u041e\u0412\u0418\u0422\u041e-\u0412\u0410\u041b\u0415\u041d\u0422\u041d\u041e\u0413 \u041a\u041e\u041c\u041f\u041b\u0415\u041a\u0421\u0410 [CuIIL2][CuI2Br4]]},<br \/>\r\nauthor = {Marko V. Rodi\u0107 and Mirjana M. Radanovi\u0107 and Dragana V. Gazdi\u0107 and Vukadin M. Leovac and Berta Barta Holl\u00f3 and Vidak Rai\u010devi\u0107 and Svetlana K. Belo\u0161evi\u0107 and Biljana Kr\u00fcger and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85139601680&doi=10.2298%2fJSC211127112R&partnerID=40&md5=110d3cdcc21d5a7781c0021163d1c64c},<br \/>\r\ndoi = {10.2298\/JSC211127112R},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {87},<br \/>\r\nnumber = {3},<br \/>\r\npages = {307 \u2013 320},<br \/>\r\nnote = {All Open Access, Gold Open Access},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('96','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_96\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85139601680&amp;doi=10.2298%2fJSC211127112R&amp;partnerID=40&amp;md5=110d3cdcc21d5a7781c0021163d1c64c\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85139601680&amp;doi=10.2298%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85139601680&amp;doi=10.2298%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.2298\/JSC211127112R\" title=\"Follow DOI:10.2298\/JSC211127112R\" target=\"_blank\">doi:10.2298\/JSC211127112R<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('96','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">76.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Francuz, Jovana;  Djoki\u0107, Sanja;  Popsavin, Mirjana;  Rodi\u0107, Marko V.;  Koji\u0107, Vesna;  Kr\u00fcger, Biljana;  Popsavin, Velimir<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('97','tp_links')\" style=\"cursor:pointer;\">New Synthetic Approach to Protulactone A and Structural Analogues<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Synlett, <\/span><span class=\"tp_pub_additional_volume\">vol. 34, <\/span><span class=\"tp_pub_additional_number\">no. 14, <\/span><span class=\"tp_pub_additional_pages\">pp. 1699 \u2013 1703, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_97\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('97','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_97\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('97','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_97\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Francuz20221699,<br \/>\r\ntitle = {New Synthetic Approach to Protulactone A and Structural Analogues},<br \/>\r\nauthor = {Jovana Francuz and Sanja Djoki\u0107 and Mirjana Popsavin and Marko V. Rodi\u0107 and Vesna Koji\u0107 and Biljana Kr\u00fcger and Velimir Popsavin},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85146462642&doi=10.1055%2fs-0042-1751400&partnerID=40&md5=28e3368b0c800e04aa68db19c53dab1f},<br \/>\r\ndoi = {10.1055\/s-0042-1751400},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\njournal = {Synlett},<br \/>\r\nvolume = {34},<br \/>\r\nnumber = {14},<br \/>\r\npages = {1699 \u2013 1703},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('97','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_97\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85146462642&amp;doi=10.1055%2fs-0042-1751400&amp;partnerID=40&amp;md5=28e3368b0c800e04aa68db19c53dab1f\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85146462642&amp;doi=10.1055%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85146462642&amp;doi=10.1055%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1055\/s-0042-1751400\" title=\"Follow DOI:10.1055\/s-0042-1751400\" target=\"_blank\">doi:10.1055\/s-0042-1751400<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('97','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">75.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radanovi\u0107, Mirjana M.;  Novakovi\u0107, Sla\u0111ana B.;  Rodi\u0107, Marko V.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Janiak, Christoph;  Leovac, Vukadin M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('98','tp_links')\" style=\"cursor:pointer;\">Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine \u2013 A novel coordination mode; [\u0421\u0418\u041d\u0422\u0415\u0417\u0410 \u0418 \u041a\u0410\u0420\u0410\u041a\u0422\u0415\u0420\u0418\u0417\u0410\u0426\u0418\u0408\u0410 \u041a\u041e\u041c\u041f\u041b\u0415\u041a\u0421\u0410 Cd(II) \u0421\u0410 2-\u0410\u0426\u0415\u0422\u0418\u041b\u041f\u0418\u0420\u0418\u0414\u0418\u041d-\u0410\u041c\u0418\u041d\u041e\u0413\u0412\u0410\u041d\u0418\u0414\u0418\u041d\u041e\u041c \u2013 \u041d\u041e\u0412\u0418 \u041d\u0410\u0427\u0418\u041d \u041a\u041e\u041e\u0420\u0414\u0418\u041d\u0410\u0426\u0418\u0408\u0415]<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 87, <\/span><span class=\"tp_pub_additional_number\">no. 11, <\/span><span class=\"tp_pub_additional_pages\">pp. 1259 \u2013 1272, <\/span><span class=\"tp_pub_additional_year\">2022<\/span><span class=\"tp_pub_additional_note\">, (All Open Access, Gold Open Access, Green Open Access)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_98\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('98','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_98\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('98','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_98\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Radanovi\u010720221259,<br \/>\r\ntitle = {Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine \u2013 A novel coordination mode; [\u0421\u0418\u041d\u0422\u0415\u0417\u0410 \u0418 \u041a\u0410\u0420\u0410\u041a\u0422\u0415\u0420\u0418\u0417\u0410\u0426\u0418\u0408\u0410 \u041a\u041e\u041c\u041f\u041b\u0415\u041a\u0421\u0410 Cd(II) \u0421\u0410 2-\u0410\u0426\u0415\u0422\u0418\u041b\u041f\u0418\u0420\u0418\u0414\u0418\u041d-\u0410\u041c\u0418\u041d\u041e\u0413\u0412\u0410\u041d\u0418\u0414\u0418\u041d\u041e\u041c \u2013 \u041d\u041e\u0412\u0418 \u041d\u0410\u0427\u0418\u041d \u041a\u041e\u041e\u0420\u0414\u0418\u041d\u0410\u0426\u0418\u0408\u0415]},<br \/>\r\nauthor = {Mirjana M. Radanovi\u0107 and Sla\u0111ana B. Novakovi\u0107 and Marko V. Rodi\u0107 and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Christoph Janiak and Vukadin M. Leovac},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85162091937&doi=10.2298%2fJSC220613072R&partnerID=40&md5=ace14c6b5ccd5c35c02b15eaa21c1185},<br \/>\r\ndoi = {10.2298\/JSC220613072R},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {87},<br \/>\r\nnumber = {11},<br \/>\r\npages = {1259 \u2013 1272},<br \/>\r\nnote = {All Open Access, Gold Open Access, Green Open Access},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('98','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_98\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85162091937&amp;doi=10.2298%2fJSC220613072R&amp;partnerID=40&amp;md5=ace14c6b5ccd5c35c02b15eaa21c1185\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85162091937&amp;doi=10.2298%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85162091937&amp;doi=10.2298%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.2298\/JSC220613072R\" title=\"Follow DOI:10.2298\/JSC220613072R\" target=\"_blank\">doi:10.2298\/JSC220613072R<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('98','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_misc\"><div class=\"tp_pub_number\">74.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Svir\u010dev, Milo\u0161;  Popsavin, Mirjana;  Pavi\u0107, Aleksandar;  Vasiljevi\u0107, Branka;  Rodi\u0107, Marko V.;  Djoki\u0107, Sanja;  Kesi\u0107, Jelena;  Zelenovi\u0107, Bojana Sre\u0107o;  Popsavin, Velimir;  Koji\u0107, Vesna<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('99','tp_links')\" style=\"cursor:pointer;\">Corrigendum to \u201cDesign, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity\u201d [Bioorg. Chem. 121 (2022) 105691] (Bioorganic Chemistry (2022) 121, (S0045206822000967), (10.1016\/j.bioorg.2022.105691))<\/a> <span class=\"tp_pub_type tp_  misc\">Miscellaneous<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_year\">2022<\/span><span class=\"tp_pub_additional_note\">, (All Open Access, Green Open Access)<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_99\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('99','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_99\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('99','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_99\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@misc{Svir\u010dev2022b,<br \/>\r\ntitle = {Corrigendum to \u201cDesign, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity\u201d [Bioorg. Chem. 121 (2022) 105691] (Bioorganic Chemistry (2022) 121, (S0045206822000967), (10.1016\/j.bioorg.2022.105691))},<br \/>\r\nauthor = {Milo\u0161 Svir\u010dev and Mirjana Popsavin and Aleksandar Pavi\u0107 and Branka Vasiljevi\u0107 and Marko V. Rodi\u0107 and Sanja Djoki\u0107 and Jelena Kesi\u0107 and Bojana Sre\u0107o Zelenovi\u0107 and Velimir Popsavin and Vesna Koji\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132934770&doi=10.1016%2fj.bioorg.2022.105984&partnerID=40&md5=650da1fa4f8f13392ae2897c4862990f},<br \/>\r\ndoi = {10.1016\/j.bioorg.2022.105984},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\nurldate = {2022-01-01},<br \/>\r\njournal = {Bioorganic Chemistry},<br \/>\r\nvolume = {127},<br \/>\r\nnote = {All Open Access, Green Open Access},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {misc}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('99','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_99\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132934770&amp;doi=10.1016%2fj.bioorg.2022.105984&amp;partnerID=40&amp;md5=650da1fa4f8f13392ae2897c4862990f\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132934770&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132934770&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.bioorg.2022.105984\" title=\"Follow DOI:10.1016\/j.bioorg.2022.105984\" target=\"_blank\">doi:10.1016\/j.bioorg.2022.105984<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('99','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">73.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Radulovi\u0107, N. S.;  Sejmanovi\u0107, D. M.;  Risti\u0107, M. N.;  Deki\u0107, V. S.;  Kr\u00fcger, B.;  Kahlenberg, V.;  Rodi\u0107, M. V.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('4','tp_links')\" style=\"cursor:pointer;\">The crystal structure of 3-(1-(2-((5-methylthiophen-2-yl)methylene)hydrazinyl)ethylidene)chroman-2,4-dione, C17H14N2O3S<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Zeitschrift fur Kristallographie - New Crystal Structures, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 14337266<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_4\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('4','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_4\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('4','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_4\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('4','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_4\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Radulovic2022,<br \/>\r\ntitle = {The crystal structure of 3-(1-(2-((5-methylthiophen-2-yl)methylene)hydrazinyl)ethylidene)chroman-2,4-dione, C17H14N2O3S},<br \/>\r\nauthor = {N. S. Radulovi\u0107 and D. M. Sejmanovi\u0107 and M. N. Risti\u0107 and V. S. Deki\u0107 and B. Kr\u00fcger and V. Kahlenberg and M. V. Rodi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&doi=10.1515%2fncrs-2022-0225&partnerID=40&md5=1865a4b07541746d0bfa2b057d2f4a93},<br \/>\r\ndoi = {10.1515\/ncrs-2022-0225},<br \/>\r\nissn = {14337266},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\njournal = {Zeitschrift fur Kristallographie - New Crystal Structures},<br \/>\r\npublisher = {De Gruyter Open Ltd},<br \/>\r\nabstract = {C17H14N2O3S, monoclinic, P21\/c (no. 14)},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('4','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_4\" style=\"display:none;\"><div class=\"tp_abstract_entry\">C17H14N2O3S, monoclinic, P21\/c (no. 14)<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('4','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_4\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&amp;doi=10.1515%2fncrs-2022-0225&amp;partnerID=40&amp;md5=1865a4b07541746d0bfa2b057d2f4a93\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&amp;doi=10.1515%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85132875131&amp;doi=10.1515%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1515\/ncrs-2022-0225\" title=\"Follow DOI:10.1515\/ncrs-2022-0225\" target=\"_blank\">doi:10.1515\/ncrs-2022-0225<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('4','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">72.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Magyari, J.;  Holl\u00f3, B. Barta;  Rodi\u0107, M. V.;  Jovanovi\u0107, L. S.;  Sz\u00e9cs\u00e9nyi, K. M\u00e9sz\u00e1ros;  Ferenc, W.;  Osypiuk, D.;  Mosolyg\u00f3, T.;  Kincses, A.;  Spengler, G.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('5','tp_links')\" style=\"cursor:pointer;\">Synthesis, characterization, thermal properties and biological activity of diazine-ring containing hydrazones and their metal complexes<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Thermal Analysis and Calorimetry, <\/span><span class=\"tp_pub_additional_volume\">vol. 147, <\/span><span class=\"tp_pub_additional_number\">no. 1, <\/span><span class=\"tp_pub_additional_pages\">pp. 229-242, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 13886150<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_5\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('5','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_5\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('5','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_5\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('5','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_5\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Magyari2022229,<br \/>\r\ntitle = {Synthesis, characterization, thermal properties and biological activity of diazine-ring containing hydrazones and their metal complexes},<br \/>\r\nauthor = {J. Magyari and B. {Barta Holl\u00f3} and M. V. Rodi\u0107 and L. S. Jovanovi\u0107 and K. M\u00e9sz\u00e1ros Sz\u00e9cs\u00e9nyi and W. Ferenc and D. Osypiuk and T. Mosolyg\u00f3 and A. Kincses and G. Spengler},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85091076453&doi=10.1007%2fs10973-020-10194-z&partnerID=40&md5=8cea031dadc72dc4c2d80cfbf7cc5fe5},<br \/>\r\ndoi = {10.1007\/s10973-020-10194-z},<br \/>\r\nissn = {13886150},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-01-01},<br \/>\r\nurldate = {2022-01-01},<br \/>\r\njournal = {Journal of Thermal Analysis and Calorimetry},<br \/>\r\nvolume = {147},<br \/>\r\nnumber = {1},<br \/>\r\npages = {229-242},<br \/>\r\npublisher = {Springer Science and Business Media B.V.},<br \/>\r\nabstract = {New coordination compounds have been synthesized by reacting Zn(II) and Co(II) nitrate or acetate in the presence of triethylamine with Schiff-base ligands containing diazine-ring, pyridine-2-carbaldehyde phthalazine-1-hydrazone, HzPYH, and di(2-pyridyl)ketone 3-chloro-pyridazine-6-hydrazone, HpDPKH. Complexes of [Co(HzPY)2]\u00b73.4H2O, [Zn(HzPY)2] and [Co(HpDPK)2]NO3\u00b7H2O were obtained. The crystal and the molecular structure of [Co(HzPY)2]\u00b73.4H2O were determined using X-ray diffraction structure analysis. The compounds were characterized by elemental analysis, FT-IR and UV\u2013Vis spectral data, conductivity and magnetic measurements, too. Except for the diamagnetic Co(III) compound with a nitrate counter-ion, [Co(HpDPK)2]NO3\u00b7H2O, all the complexes are neutral-type. The magnetic moment of [Co(HzPY)2]\u00b73.4H2O indicated a low-spin octahedral complex which is relatively rear amongst octahedral Co(II) complexes. Hence, its magnetic moment was measured in the temperature range of 3\u2013300\u00a0K. To obtain products in the form of single crystals and\/or to increase the yield, the reactions were carried out in solutions with different solvents or recrystallized from solvent mixtures. To determine the nature of the solvent (if any) in the crystalline products and to gain better insight into the decomposition mechanism, coupled TG\u2013MS measurements were carried out. The desolvated compounds were stable at relatively high temperatures (&gt; 200\u00a0\u00b0C). The cytotoxic, antiproliferative and efflux pump inhibitory effects of the compounds were tested in multidrug-resistant mouse T-lymphoma cells to study their effect on the suppression of MDR. The antibacterial activity of the compounds was also tested. The results of the antibacterial tests were analysed to understand better the effect of the central atoms and the structure on a specific activity. \u00a9 2020, Akad\u00e9miai Kiad\u00f3, Budapest, Hungary.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('5','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_5\" style=\"display:none;\"><div class=\"tp_abstract_entry\">New coordination compounds have been synthesized by reacting Zn(II) and Co(II) nitrate or acetate in the presence of triethylamine with Schiff-base ligands containing diazine-ring, pyridine-2-carbaldehyde phthalazine-1-hydrazone, HzPYH, and di(2-pyridyl)ketone 3-chloro-pyridazine-6-hydrazone, HpDPKH. Complexes of [Co(HzPY)2]\u00b73.4H2O, [Zn(HzPY)2] and [Co(HpDPK)2]NO3\u00b7H2O were obtained. The crystal and the molecular structure of [Co(HzPY)2]\u00b73.4H2O were determined using X-ray diffraction structure analysis. The compounds were characterized by elemental analysis, FT-IR and UV\u2013Vis spectral data, conductivity and magnetic measurements, too. Except for the diamagnetic Co(III) compound with a nitrate counter-ion, [Co(HpDPK)2]NO3\u00b7H2O, all the complexes are neutral-type. The magnetic moment of [Co(HzPY)2]\u00b73.4H2O indicated a low-spin octahedral complex which is relatively rear amongst octahedral Co(II) complexes. Hence, its magnetic moment was measured in the temperature range of 3\u2013300\u00a0K. To obtain products in the form of single crystals and\/or to increase the yield, the reactions were carried out in solutions with different solvents or recrystallized from solvent mixtures. To determine the nature of the solvent (if any) in the crystalline products and to gain better insight into the decomposition mechanism, coupled TG\u2013MS measurements were carried out. The desolvated compounds were stable at relatively high temperatures (&amp;gt; 200\u00a0\u00b0C). The cytotoxic, antiproliferative and efflux pump inhibitory effects of the compounds were tested in multidrug-resistant mouse T-lymphoma cells to study their effect on the suppression of MDR. The antibacterial activity of the compounds was also tested. The results of the antibacterial tests were analysed to understand better the effect of the central atoms and the structure on a specific activity. \u00a9 2020, Akad\u00e9miai Kiad\u00f3, Budapest, Hungary.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('5','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_5\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85091076453&amp;doi=10.1007%2fs10973-020-10194-z&amp;partnerID=40&amp;md5=8cea031dadc72dc4c2d80cfbf7cc5fe5\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85091076453&amp;doi=10.1007%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85091076453&amp;doi=10.1007%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1007\/s10973-020-10194-z\" title=\"Follow DOI:10.1007\/s10973-020-10194-z\" target=\"_blank\">doi:10.1007\/s10973-020-10194-z<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('5','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2021\">2021<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">71.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Nikoli\u0107, M. A.;  Sz\u00e9cs\u00e9nyi, K. M.;  Dra\u017ei\u0107, B.;  Rodi\u0107, M. V.;  Stani\u0107, V.;  Tanaskovi\u0107, S.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('9','tp_links')\" style=\"cursor:pointer;\">Binuclear Co(II) complexes with macrocycle and carboxylato ligands: structure, cytotoxicity and thermal behavior<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Molecular Structure, <\/span><span class=\"tp_pub_additional_volume\">vol. 1236, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 00222860<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_9\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('9','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_9\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('9','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_9\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('9','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_9\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Nikolic2021,<br \/>\r\ntitle = {Binuclear Co(II) complexes with macrocycle and carboxylato ligands: structure, cytotoxicity and thermal behavior},<br \/>\r\nauthor = {M. A. Nikoli\u0107 and K. M. Sz\u00e9cs\u00e9nyi and B. Dra\u017ei\u0107 and M. V. Rodi\u0107 and V. Stani\u0107 and S. Tanaskovi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85103121670&doi=10.1016%2fj.molstruc.2021.130133&partnerID=40&md5=91bc9d98954b3d1645b45f794daf0507},<br \/>\r\ndoi = {10.1016\/j.molstruc.2021.130133},<br \/>\r\nissn = {00222860},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-01-01},<br \/>\r\njournal = {Journal of Molecular Structure},<br \/>\r\nvolume = {1236},<br \/>\r\npublisher = {Elsevier B.V.},<br \/>\r\nabstract = {In vitro cytotoxic evaluation, formation constants and thermal stability of four mixed-ligand Co(II) complexes with tpmc = N,N',N\",N'\"-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraazacyclotetradecane and carboxylate\/dicarboxylate co-ligands of formulas [Co2(benz)2tpmc](ClO4)2\u20223H2O (1), benz\u2013 = benzoate anion; [Co2(L)tpmc](ClO4)2\u2022nH2O},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('9','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_9\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In vitro cytotoxic evaluation, formation constants and thermal stability of four mixed-ligand Co(II) complexes with tpmc = N,N',N\",N'\"-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraazacyclotetradecane and carboxylate\/dicarboxylate co-ligands of formulas [Co2(benz)2tpmc](ClO4)2\u20223H2O (1), benz\u2013 = benzoate anion; [Co2(L)tpmc](ClO4)2\u2022nH2O<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('9','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_9\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85103121670&amp;doi=10.1016%2fj.molstruc.2021.130133&amp;partnerID=40&amp;md5=91bc9d98954b3d1645b45f794daf0507\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85103121670&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85103121670&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.molstruc.2021.130133\" title=\"Follow DOI:10.1016\/j.molstruc.2021.130133\" target=\"_blank\">doi:10.1016\/j.molstruc.2021.130133<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('9','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">70.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Risti\u0107, P. G.;  Rodi\u0107, M. V.;  Filipovi\u0107, N. R.;  Miti\u0107, D. M.;  An\u0111elkovi\u0107, K. K.;  Todorovi\u0107, T. R.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('10','tp_links')\" style=\"cursor:pointer;\">Structural study of Pt(II) and Pd(II) complexes with quinoline-2-carboxaldehyde thiosemicarbazone<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 86, <\/span><span class=\"tp_pub_additional_number\">no. 4, <\/span><span class=\"tp_pub_additional_pages\">pp. 393-406, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 03525139<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_10\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('10','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_10\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('10','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_10\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('10','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_10\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Ristic2021393,<br \/>\r\ntitle = {Structural study of Pt(II) and Pd(II) complexes with quinoline-2-carboxaldehyde thiosemicarbazone},<br \/>\r\nauthor = {P. G. Risti\u0107 and M. V. Rodi\u0107 and N. R. Filipovi\u0107 and D. M. Miti\u0107 and K. K. An\u0111elkovi\u0107 and T. R. Todorovi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85106476575&doi=10.2298%2fJSC201126079R&partnerID=40&md5=e021927d5625fcdaa636a1154c53c19b},<br \/>\r\ndoi = {10.2298\/JSC201126079R},<br \/>\r\nissn = {03525139},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-01-01},<br \/>\r\nurldate = {2021-01-01},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {86},<br \/>\r\nnumber = {4},<br \/>\r\npages = {393-406},<br \/>\r\npublisher = {Serbian Chemical Society},<br \/>\r\nabstract = {Two square-planar complexes, [PtLCl] (1) and [PdLCl] (2), were synthesized with quinoline-2-carboxaldehyde thiosemicarbazone ligand (HL), and characterized by IR and NMR spectroscopy and single crystal X-ray diffraction analysis. In both complexes, L- is coordinated tridentately via the same donor atom set, while the fourth coordination site is occupied by a chloride ion. However, the complexes are not isostructural due to different types of non-covalent intermolecular interactions. These interactions were analyzed using Hirshfeld surfaces and two-dimensional fingerprint plots. \u00a9 2021 Serbian Chemical Society. All rights reserved.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('10','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_10\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Two square-planar complexes, [PtLCl] (1) and [PdLCl] (2), were synthesized with quinoline-2-carboxaldehyde thiosemicarbazone ligand (HL), and characterized by IR and NMR spectroscopy and single crystal X-ray diffraction analysis. In both complexes, L- is coordinated tridentately via the same donor atom set, while the fourth coordination site is occupied by a chloride ion. However, the complexes are not isostructural due to different types of non-covalent intermolecular interactions. These interactions were analyzed using Hirshfeld surfaces and two-dimensional fingerprint plots. \u00a9 2021 Serbian Chemical Society. All rights reserved.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('10','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_10\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85106476575&amp;doi=10.2298%2fJSC201126079R&amp;partnerID=40&amp;md5=e021927d5625fcdaa636a1154c53c19b\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85106476575&amp;doi=10.2298%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85106476575&amp;doi=10.2298%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.2298\/JSC201126079R\" title=\"Follow DOI:10.2298\/JSC201126079R\" target=\"_blank\">doi:10.2298\/JSC201126079R<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('10','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">69.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Dabi\u0107, P.;  Kahlenberg, V.;  Kr\u00fcger, B.;  Rodi\u0107, M.;  Kova\u010d, S.;  Blanu\u0161a, J.;  Jagli\u010di\u0107, Z.;  Karanovi\u0107, L.;  Pet\u0159\u00ed\u010dek, V.;  Kremenovi\u0107, A.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('8','tp_links')\" style=\"cursor:pointer;\">Low-temperature phase transition and magnetic properties of K3YbSi2O7<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials, <\/span><span class=\"tp_pub_additional_volume\">vol. 77, <\/span><span class=\"tp_pub_additional_pages\">pp. 584-593, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 20525192<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_8\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('8','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_8\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('8','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_8\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('8','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_8\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Dabic2021584,<br \/>\r\ntitle = {Low-temperature phase transition and magnetic properties of K3YbSi2O7},<br \/>\r\nauthor = {P. Dabi\u0107 and V. Kahlenberg and B. Kr\u00fcger and M. Rodi\u0107 and S. Kova\u010d and J. Blanu\u0161a and Z. Jagli\u010di\u0107 and L. Karanovi\u0107 and V. Pet\u0159\u00ed\u010dek and A. Kremenovi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85112075570&doi=10.1107%2fS2052520621006077&partnerID=40&md5=a72ff2112d139c1104d82f8f772b2dbe},<br \/>\r\ndoi = {10.1107\/S2052520621006077},<br \/>\r\nissn = {20525192},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-01-01},<br \/>\r\njournal = {Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials},<br \/>\r\nvolume = {77},<br \/>\r\npages = {584-593},<br \/>\r\npublisher = {International Union of Crystallography},<br \/>\r\nabstract = {The new ambient-temperature hexagonal (space group P63 \/mmc) polymorph of tripotassium ytterbium(III) disilicate (\u03b2-K3YbSi2O7) has been synthesized by the high-temperature flux method and subsequently structurally characterized. In the course of the temperature-dependent single-crystal diffraction experiments, a phase transformation of \u03b2-K3YbSi2O7 to a novel low-temperature orthorhombic phase (\u03b2\u2032-K3YbSi2O7, space group Cmcm) has been observed at about 210K. \u03b2-K3YbSi2O7 is isostructural with K3ErSi2O7, whereas \u03b2\u2032-K3YbSi2O7 adopts a new type of structure. Both compounds can be built up from a regular alternation of layers of two types, which are parallel to the (001) plane. In the octahedral layer, YbO6 octahedra are isolated and linked by K1O6+3 polyhedra. The second, slightly thicker sorosilicate layer is formed by a combination of Si2O7 dimers and K2O6+3 polyhedra. The boundary between the layers is a pseudo-kagome oxide sheet based on 3.6.3.6 meshes. The phase transition is due to a tilt of the two SiO4 tetrahedra forming a single dimer which induces a decrease of the Si - O - Si angle between bridging Si - O bonds from 180\u00b0 (dictated by symmetry in space group P63\/mmc) to \u2243164\u00b0. Magnetic characterization indicates that K3YbSi2O7 remains paramagnetic down to 2K, showing no apparent influence of the phase transformation on its magnetic properties. Analysis of the magnetization data revealed the positions of the three lowest crystal field levels of the Yb3+ cations, as well as the corresponding projections of their angular momentum on the direction of the magnetic field. \u00a9 2021 International Union of Crystallography. All rights reserved.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('8','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_8\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The new ambient-temperature hexagonal (space group P63 \/mmc) polymorph of tripotassium ytterbium(III) disilicate (\u03b2-K3YbSi2O7) has been synthesized by the high-temperature flux method and subsequently structurally characterized. In the course of the temperature-dependent single-crystal diffraction experiments, a phase transformation of \u03b2-K3YbSi2O7 to a novel low-temperature orthorhombic phase (\u03b2\u2032-K3YbSi2O7, space group Cmcm) has been observed at about 210K. \u03b2-K3YbSi2O7 is isostructural with K3ErSi2O7, whereas \u03b2\u2032-K3YbSi2O7 adopts a new type of structure. Both compounds can be built up from a regular alternation of layers of two types, which are parallel to the (001) plane. In the octahedral layer, YbO6 octahedra are isolated and linked by K1O6+3 polyhedra. The second, slightly thicker sorosilicate layer is formed by a combination of Si2O7 dimers and K2O6+3 polyhedra. The boundary between the layers is a pseudo-kagome oxide sheet based on 3.6.3.6 meshes. The phase transition is due to a tilt of the two SiO4 tetrahedra forming a single dimer which induces a decrease of the Si - O - Si angle between bridging Si - O bonds from 180\u00b0 (dictated by symmetry in space group P63\/mmc) to \u2243164\u00b0. Magnetic characterization indicates that K3YbSi2O7 remains paramagnetic down to 2K, showing no apparent influence of the phase transformation on its magnetic properties. Analysis of the magnetization data revealed the positions of the three lowest crystal field levels of the Yb3+ cations, as well as the corresponding projections of their angular momentum on the direction of the magnetic field. \u00a9 2021 International Union of Crystallography. All rights reserved.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('8','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_8\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85112075570&amp;doi=10.1107%2fS2052520621006077&amp;partnerID=40&amp;md5=a72ff2112d139c1104d82f8f772b2dbe\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85112075570&amp;doi=10.1107%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85112075570&amp;doi=10.1107%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1107\/S2052520621006077\" title=\"Follow DOI:10.1107\/S2052520621006077\" target=\"_blank\">doi:10.1107\/S2052520621006077<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('8','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">68.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Ara\u0161kov, J. B.;  Nikoli\u0107, M.;  Armakovi\u0107, S.;  Armakovi\u0107, S.;  Rodi\u0107, M.;  Vi\u0161njevac, A.;  Padr\u00f3n, J. M.;  Todorovi\u0107, T. R.;  Filipovi\u0107, N. R.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('7','tp_links')\" style=\"cursor:pointer;\">Structural, antioxidant, antiproliferative and in\u2012silico study of pyridine-based hydrazonyl\u2012selenazoles and their sulphur isosteres<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Molecular Structure, <\/span><span class=\"tp_pub_additional_volume\">vol. 1240, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 00222860<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_7\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('7','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_7\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('7','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_7\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('7','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_7\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Araskov2021,<br \/>\r\ntitle = {Structural, antioxidant, antiproliferative and in\u2012silico study of pyridine-based hydrazonyl\u2012selenazoles and their sulphur isosteres},<br \/>\r\nauthor = {J. B. Ara\u0161kov and M. Nikoli\u0107 and S. Armakovi\u0107 and S. Armakovi\u0107 and M. Rodi\u0107 and A. Vi\u0161njevac and J. M. Padr\u00f3n and T. R. Todorovi\u0107 and N. R. Filipovi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85105531083&doi=10.1016%2fj.molstruc.2021.130512&partnerID=40&md5=38165898ced20fcdedfe78321018129c},<br \/>\r\ndoi = {10.1016\/j.molstruc.2021.130512},<br \/>\r\nissn = {00222860},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-01-01},<br \/>\r\njournal = {Journal of Molecular Structure},<br \/>\r\nvolume = {1240},<br \/>\r\npublisher = {Elsevier B.V.},<br \/>\r\nabstract = {To evaluate the impact of chalcogen atom type, we performed a comparative study of antioxidant capacity and antiproliferative activity of a focused library of three pyridine-based hydrazonyl-1,3-selenazoles and their sulfur isosteres in five antioxidant assays and in six human solid tumor cell lines, respectively. In-silico calculations were further used to check pharmacokinetic profiles of investigated compounds such as drug-likeness parameters and interaction with water. Generally, selenium compounds appear to be more potent in comparison to sulfur isosteres in the performed essays. \u00a9 2021 Elsevier B.V.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('7','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_7\" style=\"display:none;\"><div class=\"tp_abstract_entry\">To evaluate the impact of chalcogen atom type, we performed a comparative study of antioxidant capacity and antiproliferative activity of a focused library of three pyridine-based hydrazonyl-1,3-selenazoles and their sulfur isosteres in five antioxidant assays and in six human solid tumor cell lines, respectively. In-silico calculations were further used to check pharmacokinetic profiles of investigated compounds such as drug-likeness parameters and interaction with water. Generally, selenium compounds appear to be more potent in comparison to sulfur isosteres in the performed essays. \u00a9 2021 Elsevier B.V.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('7','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_7\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85105531083&amp;doi=10.1016%2fj.molstruc.2021.130512&amp;partnerID=40&amp;md5=38165898ced20fcdedfe78321018129c\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85105531083&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85105531083&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.molstruc.2021.130512\" title=\"Follow DOI:10.1016\/j.molstruc.2021.130512\" target=\"_blank\">doi:10.1016\/j.molstruc.2021.130512<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('7','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">67.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kova\u010devi\u0107, Ivana;  Kesi\u0107, Jelena;  Popsavin, Mirjana;  Francuz, Jovana;  Koji\u0107, Vesna;  Jakimov, Dmitar;  Rodi\u0107, Marko V.;  Zelenovi\u0107, Bojana Sre\u0107o;  Benedekovi\u0107, Goran;  Popsavin, Velimir<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('6','tp_links')\" style=\"cursor:pointer;\">Asymmetric synthesis and biological evaluation of (+)-cardiobutanolide, (\u2212)-3-deoxycardiobutanolide and analogues as antiproliferative agents<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Tetrahedron, <\/span><span class=\"tp_pub_additional_volume\">vol. 97, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 00404020<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_6\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('6','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_6\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('6','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_6\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('6','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_6\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Kovacevic2021,<br \/>\r\ntitle = {Asymmetric synthesis and biological evaluation of (+)-cardiobutanolide, (\u2212)-3-deoxycardiobutanolide and analogues as antiproliferative agents},<br \/>\r\nauthor = {Ivana Kova\u010devi\u0107 and Jelena Kesi\u0107 and Mirjana Popsavin and Jovana Francuz and Vesna Koji\u0107 and Dmitar Jakimov and Marko V. Rodi\u0107 and Bojana Sre\u0107o Zelenovi\u0107 and Goran Benedekovi\u0107 and Velimir Popsavin},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85113549818&doi=10.1016%2fj.tet.2021.132408&partnerID=40&md5=42599acc79b24d5aa98450fedc233316},<br \/>\r\ndoi = {10.1016\/j.tet.2021.132408},<br \/>\r\nissn = {00404020},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-01-01},<br \/>\r\nurldate = {2021-01-01},<br \/>\r\njournal = {Tetrahedron},<br \/>\r\nvolume = {97},<br \/>\r\npublisher = {Elsevier Ltd},<br \/>\r\nabstract = {Two natural products, (+)-cardiobutanolide and (\u2212)-3-deoxycardiobutanolide, as well as five new analogues, were synthesized in several steps that included zinc-mediated THF ring opening, subsequent stereoselective olefination, and final Sharpless asymmetric dihydroxylation. In vitro antitumour activities of these compounds were evaluated against a panel of eight human tumour cell lines and one normal cell line. Some of compounds displayed powerful effects against tumour cells, but none of them were active toward normal cells. A SAR study revealed that the change of configuration at the C-6 and C-7 position of (+)-cardiobutanolide decreases antitumour activity of analogues. It also appears that the presence of a hydroxyl group at the C-3 position increases the activity of this type of lactones. A comparison of activities of conformationally rigid lactone goniofufurone with that of more flexible cardiobutanolide and 3-deoxycardiobutanolide indicates that steric flexibility has a positive effect on cytotoxicity. It was also confirmed that removal of the phenyl group may result in analogues of higher activity. Flow cytometry analysis revealed that the synthesized compounds did not induce apoptosis and necrosis of K562 cells. However, Western blot analysis showed that all compounds but one had an increased Bax\/Bcl-2 protein expression ratio. \u00a9 2021 Elsevier Ltd},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('6','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_6\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Two natural products, (+)-cardiobutanolide and (\u2212)-3-deoxycardiobutanolide, as well as five new analogues, were synthesized in several steps that included zinc-mediated THF ring opening, subsequent stereoselective olefination, and final Sharpless asymmetric dihydroxylation. In vitro antitumour activities of these compounds were evaluated against a panel of eight human tumour cell lines and one normal cell line. Some of compounds displayed powerful effects against tumour cells, but none of them were active toward normal cells. A SAR study revealed that the change of configuration at the C-6 and C-7 position of (+)-cardiobutanolide decreases antitumour activity of analogues. It also appears that the presence of a hydroxyl group at the C-3 position increases the activity of this type of lactones. A comparison of activities of conformationally rigid lactone goniofufurone with that of more flexible cardiobutanolide and 3-deoxycardiobutanolide indicates that steric flexibility has a positive effect on cytotoxicity. It was also confirmed that removal of the phenyl group may result in analogues of higher activity. Flow cytometry analysis revealed that the synthesized compounds did not induce apoptosis and necrosis of K562 cells. However, Western blot analysis showed that all compounds but one had an increased Bax\/Bcl-2 protein expression ratio. \u00a9 2021 Elsevier Ltd<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('6','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_6\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85113549818&amp;doi=10.1016%2fj.tet.2021.132408&amp;partnerID=40&amp;md5=42599acc79b24d5aa98450fedc233316\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85113549818&amp;doi=10.1016%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85113549818&amp;doi=10.1016%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.tet.2021.132408\" title=\"Follow DOI:10.1016\/j.tet.2021.132408\" target=\"_blank\">doi:10.1016\/j.tet.2021.132408<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('6','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2020\">2020<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">66.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rodi\u0107, Marko V.;  Mi\u0161kov-Paji\u0107, Vukoslava;  Leovac, Vukadin M.;  Radanovi\u0107, Mirjana M.;  Vojinovi\u0107-Je\u0161i\u0107, Ljiljana S.;  Belo\u0161evi\u0107, Svetlana K.;  Ja\u0107imovi\u0107, \u017deljko K.;  \u017divkovi\u0107-Radovanovi\u0107, Vukosava<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('19','tp_links')\" style=\"cursor:pointer;\">First cobalt complexes with methyl pyruvate semi\/thiosemicarbazone \u2013 Synthesis, physicochemical and structural characterization<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of the Serbian Chemical Society, <\/span><span class=\"tp_pub_additional_volume\">vol. 85, <\/span><span class=\"tp_pub_additional_number\">no. 4, <\/span><span class=\"tp_pub_additional_pages\">pp. 453-466, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 03525139<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_19\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('19','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_19\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('19','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_19\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('19','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_19\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Rodic2020453,<br \/>\r\ntitle = {First cobalt complexes with methyl pyruvate semi\/thiosemicarbazone \u2013 Synthesis, physicochemical and structural characterization},<br \/>\r\nauthor = {Marko V. Rodi\u0107 and Vukoslava Mi\u0161kov-Paji\u0107 and Vukadin M. Leovac and Mirjana M. Radanovi\u0107 and Ljiljana S. Vojinovi\u0107-Je\u0161i\u0107 and Svetlana K. Belo\u0161evi\u0107 and \u017deljko K. Ja\u0107imovi\u0107 and Vukosava \u017divkovi\u0107-Radovanovi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85086851131&doi=10.2298%2fJSC191219010R&partnerID=40&md5=7da26483f34febbe78a651c3165c0b0d},<br \/>\r\ndoi = {10.2298\/JSC191219010R},<br \/>\r\nissn = {03525139},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-01-01},<br \/>\r\nurldate = {2020-01-01},<br \/>\r\njournal = {Journal of the Serbian Chemical Society},<br \/>\r\nvolume = {85},<br \/>\r\nnumber = {4},<br \/>\r\npages = {453-466},<br \/>\r\npublisher = {Serbian Chemical Society},<br \/>\r\nabstract = {In the reaction of acetone solutions of CoX2\u2219nH2O (X = Cl, Br) with methyl pyruvate semi\/thiosemicarbazone (Hmps, Hmpt) the first Co(II) complexes with these ligands, i.e., [Co(Hmps)(H2O)X2] (X = Cl (1), Br (2)), [Co(Hmpt)2][CoCl4]\u22192H2\u041e (3) and [Co(Hmpt)2]Br2\u2219Me2CO (4) were obtained. Complexes 1 and 2 represent the first examples of metal complexes of Hmps. All the obtained compounds were characterized by elemental analysis, conductometry, magnetic measurements, and IR spectra, and for complexes 2\u20134, single crystal X-ray diffraction analysis was also performed. The effective magnetic moments were close to the upper limit (5 \u03bcB) for complexes 1 and 2, and close to the lower limit (4.4 \u03bcB) for complexes 3 and 4, and as such are characteristic for high-spin Co(II) complexes. Structural analysis showed that both ligands coordinate in a neutral form in a tridentate manner, via the ester oxygen, imine nitrogen and the oxygen atom of the ureido (Hmps), or the sulfur atom of the thioureido group (Hmpt). The central metal atoms are situated in a deformed octahedral coordination environment. Complex 2 has cis-Br configuration, while complexes 3 and 4 have mer-configuration. \u00a9 2020 Serbian Chemical Society. All rights reserved.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('19','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_19\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In the reaction of acetone solutions of CoX2\u2219nH2O (X = Cl, Br) with methyl pyruvate semi\/thiosemicarbazone (Hmps, Hmpt) the first Co(II) complexes with these ligands, i.e., [Co(Hmps)(H2O)X2] (X = Cl (1), Br (2)), [Co(Hmpt)2][CoCl4]\u22192H2\u041e (3) and [Co(Hmpt)2]Br2\u2219Me2CO (4) were obtained. Complexes 1 and 2 represent the first examples of metal complexes of Hmps. All the obtained compounds were characterized by elemental analysis, conductometry, magnetic measurements, and IR spectra, and for complexes 2\u20134, single crystal X-ray diffraction analysis was also performed. The effective magnetic moments were close to the upper limit (5 \u03bcB) for complexes 1 and 2, and close to the lower limit (4.4 \u03bcB) for complexes 3 and 4, and as such are characteristic for high-spin Co(II) complexes. Structural analysis showed that both ligands coordinate in a neutral form in a tridentate manner, via the ester oxygen, imine nitrogen and the oxygen atom of the ureido (Hmps), or the sulfur atom of the thioureido group (Hmpt). The central metal atoms are situated in a deformed octahedral coordination environment. Complex 2 has cis-Br configuration, while complexes 3 and 4 have mer-configuration. \u00a9 2020 Serbian Chemical Society. All rights reserved.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('19','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_19\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85086851131&amp;doi=10.2298%2fJSC191219010R&amp;partnerID=40&amp;md5=7da26483f34febbe78a651c3165c0b0d\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85086851131&amp;doi=10.2298%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85086851131&amp;doi=10.2298%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.2298\/JSC191219010R\" title=\"Follow DOI:10.2298\/JSC191219010R\" target=\"_blank\">doi:10.2298\/JSC191219010R<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('19','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">65.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rai\u010devi\u0107, V.;  Radulovi\u0107, N. S.;  Jovanovi\u0107, L.;  Rodi\u0107, M.;  Kuzminac, I.;  Jakimov, D.;  Wrodnigg, T.;  Knedel, T. -O.;  Janiak, C.;  Saka\u010d, M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('12','tp_links')\" style=\"cursor:pointer;\">Ferrocenylmethylation of estrone and estradiol: Structure, electrochemistry, and antiproliferative activity of new ferrocene\u2013steroid conjugates<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Applied Organometallic Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 34, <\/span><span class=\"tp_pub_additional_number\">no. 10, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 02682605<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_12\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('12','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_12\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('12','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_12\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('12','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_12\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Raicevic2020,<br \/>\r\ntitle = {Ferrocenylmethylation of estrone and estradiol: Structure, electrochemistry, and antiproliferative activity of new ferrocene\u2013steroid conjugates},<br \/>\r\nauthor = {V. Rai\u010devi\u0107 and N. S. Radulovi\u0107 and L. Jovanovi\u0107 and M. Rodi\u0107 and I. Kuzminac and D. Jakimov and T. Wrodnigg and T. -O. Knedel and C. Janiak and M. Saka\u010d},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85087436567&doi=10.1002%2faoc.5889&partnerID=40&md5=b753e6cb8ef41cb2c96ee52bd8d0172b},<br \/>\r\ndoi = {10.1002\/aoc.5889},<br \/>\r\nissn = {02682605},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-01-01},<br \/>\r\nurldate = {2020-01-01},<br \/>\r\njournal = {Applied Organometallic Chemistry},<br \/>\r\nvolume = {34},<br \/>\r\nnumber = {10},<br \/>\r\npublisher = {John Wiley and Sons Ltd},<br \/>\r\nabstract = {Conjugates of ferrocene with steroidal estrogens as selective antiproliferative agents against hormone-dependent breast cancer cells are believed to be limited by the inherent estrogenicity of the conjugates. Motivated by a significant cytotoxicity of the ester of ferrocenecarboxylic acid and the phenolic group of estradiol toward such a cell line, we decided to explore other a-ring-tethered ferrocene\u2013estra-1,3,5(10)-triene conjugates; in this study, ferrocenylmethylation of estradiol and estrone with (ferrocenylmethyl)trimethylammonium iodide in the presence of potassium carbonate yielded five new compounds (1\u20135). In dimethylformamide, only O-alkylated products formed (1 and 3), while a mixture of O- and C-alkylated products was obtained when methanol was used (2, 4, and 5 in addition to 1 and 3). All compounds were characterized using 1D and 2D NMR, IR, UV\u2013Vis, and high-resolution mass spectrometry. Two of the conjugates, a 3-O- and a 4-C-alkylated derivative of estrone (3 and 4, respectively), were also analyzed using single-crystal X-ray diffraction. A cyclic voltammetric investigation of the electrochemical properties of 1\u20135 was performed. While some of the compounds were shown to have a slight-to-moderate antiproliferative activity against at least one of the six tested human tumor cell lines and were nontoxic to (the noncancerous) fetal human fibroblasts, compound 2 (4-(ferrocenylmethyl)estra-1,3,5(10)-triene-3,17\u03b2-diol) with an IC50 value of 0.34 \u03bcM was found to be more active against the hormone-dependent breast cancer cell line MCF-7 than doxorubicin. These results suggest that a-ring substitution of steroidal estrogens is a plausible strategy for preparing other ferrocene\u2013steroid conjugates acting against tumor cells. \u00a9 2020 John Wiley & Sons, Ltd.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('12','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_12\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Conjugates of ferrocene with steroidal estrogens as selective antiproliferative agents against hormone-dependent breast cancer cells are believed to be limited by the inherent estrogenicity of the conjugates. Motivated by a significant cytotoxicity of the ester of ferrocenecarboxylic acid and the phenolic group of estradiol toward such a cell line, we decided to explore other a-ring-tethered ferrocene\u2013estra-1,3,5(10)-triene conjugates; in this study, ferrocenylmethylation of estradiol and estrone with (ferrocenylmethyl)trimethylammonium iodide in the presence of potassium carbonate yielded five new compounds (1\u20135). In dimethylformamide, only O-alkylated products formed (1 and 3), while a mixture of O- and C-alkylated products was obtained when methanol was used (2, 4, and 5 in addition to 1 and 3). All compounds were characterized using 1D and 2D NMR, IR, UV\u2013Vis, and high-resolution mass spectrometry. Two of the conjugates, a 3-O- and a 4-C-alkylated derivative of estrone (3 and 4, respectively), were also analyzed using single-crystal X-ray diffraction. A cyclic voltammetric investigation of the electrochemical properties of 1\u20135 was performed. While some of the compounds were shown to have a slight-to-moderate antiproliferative activity against at least one of the six tested human tumor cell lines and were nontoxic to (the noncancerous) fetal human fibroblasts, compound 2 (4-(ferrocenylmethyl)estra-1,3,5(10)-triene-3,17\u03b2-diol) with an IC50 value of 0.34 \u03bcM was found to be more active against the hormone-dependent breast cancer cell line MCF-7 than doxorubicin. These results suggest that a-ring substitution of steroidal estrogens is a plausible strategy for preparing other ferrocene\u2013steroid conjugates acting against tumor cells. \u00a9 2020 John Wiley &amp; Sons, Ltd.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('12','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_12\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85087436567&amp;doi=10.1002%2faoc.5889&amp;partnerID=40&amp;md5=b753e6cb8ef41cb2c96ee52bd8d0172b\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85087436567&amp;doi=10.1002%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85087436567&amp;doi=10.1002%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1002\/aoc.5889\" title=\"Follow DOI:10.1002\/aoc.5889\" target=\"_blank\">doi:10.1002\/aoc.5889<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('12','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_number\">64.<\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Dimitrijevi\u0107, T.;  Novakovi\u0107, I.;  Radanovi\u0107, D.;  Novakovi\u0107, S. B.;  Rodi\u0107, M. V.;  An\u0111elkovi\u0107, K. K.;  \u0160umar-Ristovi\u0107, M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" onclick=\"teachpress_pub_showhide('18','tp_links')\" style=\"cursor:pointer;\">Synthesis, spectral and structural characterization and biological activity of Cu(II) complexes with 4-(diethylamino)salicylaldehyde and \u03b1-diimines<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Coordination Chemistry, <\/span><span class=\"tp_pub_additional_volume\">vol. 73, <\/span><span class=\"tp_pub_additional_number\">no. 4, <\/span><span class=\"tp_pub_additional_pages\">pp. 702-716, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>, <span class=\"tp_pub_additional_issn\">ISSN: 00958972<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_18\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('18','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_18\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('18','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_18\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('18','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_18\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Dimitrijevic2020702,<br \/>\r\ntitle = {Synthesis, spectral and structural characterization and biological activity of Cu(II) complexes with 4-(diethylamino)salicylaldehyde and \u03b1-diimines},<br \/>\r\nauthor = {T. Dimitrijevi\u0107 and I. Novakovi\u0107 and D. Radanovi\u0107 and S. B. Novakovi\u0107 and M. V. Rodi\u0107 and K. K. An\u0111elkovi\u0107 and M. \u0160umar-Ristovi\u0107},<br \/>\r\nurl = {https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85082422790&doi=10.1080%2f00958972.2020.1740212&partnerID=40&md5=b8a926444671986ceaa42f76e5769067},<br \/>\r\ndoi = {10.1080\/00958972.2020.1740212},<br \/>\r\nissn = {00958972},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-01-01},<br \/>\r\nurldate = {2020-01-01},<br \/>\r\njournal = {Journal of Coordination Chemistry},<br \/>\r\nvolume = {73},<br \/>\r\nnumber = {4},<br \/>\r\npages = {702-716},<br \/>\r\npublisher = {Taylor and Francis Ltd.},<br \/>\r\nabstract = {In this article, synthesis, spectral and X-ray structure characterization, antimicrobial activity and Brine shrimp test of two new Cu(II) complexes with a salicylaldehyde derivative have been reported. Complexes [Cu(L)(bipy)]BF4\u00b70.5H2O and [Cu2(L)2(phen)2](BF4)2 were obtained in the reaction of Cu(BF4)2\u00b76H2O, deprotonated 4-(diethylamino)\u22122-hydroxybenzaldehyde ligand (L) and \u03b1-diimine (2,2\u2019-bipyridine or 1,10-phenanthroline). The complex with bipyridine is mononuclear, containing one L and one bipyridine ligand in a distorted square-planar cation with a BF4 \u2212 anion and lattice water molecule, whereas the complex with phenanthroline is a dinuclear centrosymmetric dimeric cation, containing two L ligands along with two phenanthroline ligands and BF4 \u2212 anions. The coordination geometry of each Cu(II) ion can be described as an elongated square pyramid. MS-ESI spectroscopy indicated that [Cu2(L)2(phen)2](BF4)2 is mononuclear in DMSO solution. In vitro antibacterial and antifungal activity was tested against four Gram-positive, four Gram-negative bacteria and three fungal strains. Complexes showed significantly stronger antibacterial activities than parent ligands. The mononuclear phenanthroline complex in solution showed very good antimicrobial activity, which is comparable to the activity of the standard antibiotic amikacin against all tested bacterial strains. The same complex has better antifungal activity than fluconazole, which was used as a standard. Results of the brine shrimp test indicate that both complexes have good toxicity against Artemia nauplii. \u00a9 2020, \u00a9 2020 Informa UK Limited, trading as Taylor & Francis Group.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('18','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_18\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In this article, synthesis, spectral and X-ray structure characterization, antimicrobial activity and Brine shrimp test of two new Cu(II) complexes with a salicylaldehyde derivative have been reported. Complexes [Cu(L)(bipy)]BF4\u00b70.5H2O and [Cu2(L)2(phen)2](BF4)2 were obtained in the reaction of Cu(BF4)2\u00b76H2O, deprotonated 4-(diethylamino)\u22122-hydroxybenzaldehyde ligand (L) and \u03b1-diimine (2,2\u2019-bipyridine or 1,10-phenanthroline). The complex with bipyridine is mononuclear, containing one L and one bipyridine ligand in a distorted square-planar cation with a BF4 \u2212 anion and lattice water molecule, whereas the complex with phenanthroline is a dinuclear centrosymmetric dimeric cation, containing two L ligands along with two phenanthroline ligands and BF4 \u2212 anions. The coordination geometry of each Cu(II) ion can be described as an elongated square pyramid. MS-ESI spectroscopy indicated that [Cu2(L)2(phen)2](BF4)2 is mononuclear in DMSO solution. In vitro antibacterial and antifungal activity was tested against four Gram-positive, four Gram-negative bacteria and three fungal strains. Complexes showed significantly stronger antibacterial activities than parent ligands. The mononuclear phenanthroline complex in solution showed very good antimicrobial activity, which is comparable to the activity of the standard antibiotic amikacin against all tested bacterial strains. The same complex has better antifungal activity than fluconazole, which was used as a standard. Results of the brine shrimp test indicate that both complexes have good toxicity against Artemia nauplii. \u00a9 2020, \u00a9 2020 Informa UK Limited, trading as Taylor &amp; Francis Group.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('18','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_18\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85082422790&amp;doi=10.1080%2f00958972.2020.1740212&amp;partnerID=40&amp;md5=b8a926444671986ceaa42f76e5769067\" title=\"https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85082422790&amp;doi=10.1080%[...]\" target=\"_blank\">https:\/\/www.scopus.com\/inward\/record.uri?eid=2-s2.0-85082422790&amp;doi=10.1080%[...]<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1080\/00958972.2020.1740212\" title=\"Follow DOI:10.1080\/00958972.2020.1740212\" target=\"_blank\">doi:10.1080\/00958972.2020.1740212<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('18','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><\/div><div class=\"tablenav\"><div class=\"tablenav-pages\"><span class=\"displaying-num\">113 entries<\/span> <a class=\"page-numbers button disabled\">&laquo;<\/a> <a class=\"page-numbers button disabled\">&lsaquo;<\/a> 1 of 3 <a href=\"https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/publications-2\/?limit=2&amp;tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=&amp;tsr=#tppubs\" title=\"next page\" class=\"page-numbers button\">&rsaquo;<\/a> <a href=\"https:\/\/personal.pmf.uns.ac.rs\/marko.rodic\/publications-2\/?limit=3&amp;tgid=&amp;yr=&amp;type=&amp;usr=&amp;auth=&amp;tsr=#tppubs\" title=\"last page\" class=\"page-numbers button\">&raquo;<\/a> <\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"<p>Publications All years 20262025202420232022202120202019201820172016201520142013201220112009 All authors Aksi\u0107, Jelena M. 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