
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:format>111 str.</dc:format>
  <dc:format>5251588 bytes</dc:format>
  <dc:title xml:lang="srp">Sinteza, karakterizacija, antimikrobni i citotoksični efekti kompleksa Mn(II), Zn(II) i Bi(III) sa hidrazonskim derivatima žirarovog P i T reagensa : doktorska disertacija</dc:title>
  <dc:rights>All rights reserved</dc:rights>
  <dc:subject xml:lang="srp">kompleksi d-metala, kristalna struktura, antimikrobna aktivnost, citotoksični efekat, teorijski proračuni</dc:subject>
  <dc:subject xml:lang="eng">d-metal complexes, crystal structure, antimicrobial activity, cytotoxic effect, theoretical calculations</dc:subject>
  <dc:date>2022</dc:date>
  <dc:creator id="https://plus.cobiss.net/cobiss/sr/sr/conor/96775945">Stevanović, Nevena, 1992-</dc:creator>
  <dc:language>srp</dc:language>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/12473191">Anđelković, Katarina, 1957-</dc:contributor>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/32564327">Čobeljić, Božidar, 1983-</dc:contributor>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/14048103">Šumar Ristović, Maja, 1971-</dc:contributor>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/10884455">Vujčić, Miroslava, 1961-</dc:contributor>
  <dc:description xml:lang="srp">U ovom radu opisana je sinteza, karakterizacija i kristalna struktura kompleksa 1,nastalog između jona Zn(II) i (E)-1-(2-okso-2-(2-(hinolin-2-ilmetilen)hidrazinil)etil)piridin--ijum-hlorida (HL1Cl) i kompleksa 2, 3, 4 i 5, nastalih između jona Cu(II), Mn(II), Zn(II) iBi(III) sa (E)-N,N,N-trimetil-2-okso-2-(2-(1-(tiazol-2-il)etiliden)hidrazinil)etan-1-aminijumhloridom (HL2Cl). Svi kompleksi okarakterisani su rendgenskom strukturnom analizom,elementalnom analizom i IC spektroskopijom.U slučaju kompleksa 1 ligand HL1Cl koordinovan je u deprotonovanom obliku prekohinolinskog atoma azota, azometinskog atoma azota i karbonilnog atoma kiseonika. LigandHL2Cl u kompleksima 2–4 koordinovan je u deprotonovanom formalno neutralnomcviterjonskom obliku preko NNO donorskog seta atoma, dok u kompleksu 5 ostaje uprotonovanoj formi.Ispitana je antimikrobna aktivnost, test na račićima Artemia salina i DPPH test na svimkompleksima. Antimikrobna aktivnost je ispitana na pet sojeva Gram-pozitivnih i pet sojevaGram-negativnih bakterija, dva soja kvasaca i jednom soju gljivica. Određena je i citotoksičnaaktivnost prema pet malignih ćelijskih linija (HeLa, A375, MCF7, PC-3 i A549) i jednojnormalnoj ćelijskoj liniji (HaCaT). Nije ispitivana citotoksična aktivnost kompleksa 5 uslednjegove hidrolize u rastvoru DMSO.Kompleks 1 pokazao je značajnu antibakterijsku aktivnost posebno premaGram-negativnim bakterijama, sa aktivnošću sličnoj hloramfenikolu, dok je dinuklearnikompleks 3 pokazao antifungalnu aktivnost sličnog intenziteta sa amfotericinom B.Kompleksi 2 i 3 pokazali su značajnu citotoksičnu aktivnost, pri čemu je aktivnost kompleksa3 tek neznatno slabija od one koju pokazuje cisplatin prema ćelijama MCF7.</dc:description>
  <dc:description xml:lang="eng">In this work synthesis, characterization and crystal structures of 1, Zn(II) complex([ZnL1(NCS)2]), with (E)-1-(2-oxo-2-(2-(quinolin-2-ylmethylene)hydrazinyl)ethyl)pyridin--1-ium chloride (HL1Cl) and 2, 3, 4 and 5, Cu(II), Mn(II), Zn(II) and Bi(III) complexes with(E)-N,N,N-trimethyl-2-oxo-2-(2-(1-(thiazol-2-yl)ethylidene)hydrazinyl)ethan-1-aminiumchloride (HL2Cl) are represented. All complexes are characterized by X-ray crystallographicanalysis, elemental analysis and IR spectroscopy.In case of complex 1 hydrazone ligand HL1Cl is coordinated in deprotonated formthrough the quinoline nitrogen, azomethine nitrogen and carbonyl oxygen atoms. Hydrazoneligand HL2Cl in complexes 2–4 is coordinated in deprotonated formally neutral zwitter-ionicform via NNO donor set atoms, while in complex 5 it remains in protonated form.Antimicrobial activity, brine shrimp assay and DPPH radical scavenging activity of allcomplexes was evaluated. Antimicrobial activity was tested against a five Gram-negative andfive Gram-positive bacteria, two yeasts and one fungal strain. Cytotoxic activity against fivemalignant cancer cell lines (HeLa, A375, MCF7, PC-3 and A549) and normal cell line HaCaTwas tested as well. Due to hydrolysis that is occurring in DMSO solution of complex 5, thiscomplex was not tested for cytotoxic activity.Complex 1 showed a significant antibacterial activity especially towards Gram-negativebacteria, with intensity similar to chloramphenicol, while the binuclear Mn(II) complex (3)showed antifungal activity of similar intensity as amphotericin B. Complexes 2 and 3 showeda significant cytotoxic activity. The activity of Mn(II) complex (3) is only slightly weaker thanthat of cisplatin against breast cancer MCF7 cells. </dc:description>
  <dc:description xml:lang="srp">Hemija -  Neorganska hemija / Chemistry - Inorganic chemistry  Datum odbrane: 28.09.2022. </dc:description>
  <dc:type>info:eu-repo/semantics/bachelorThesis</dc:type>
  <dc:identifier>https://phaidrabg.bg.ac.rs/o:28081</dc:identifier>
  <dc:identifier>cobiss:108554761</dc:identifier>
  <dc:identifier>thesis:8988</dc:identifier>
</oai_dc:dc>
