[dr Jelena M. Poljarevic]

Hemijski fakultet, Studentski trg 12-16, Beograd
Katedra za opštu i neorgansku hemiju

Telefon:   011-3336736

Telefon (lokalni):   736

Laboratorija:   525

E-mail:   jelenal@chem.bg.ac.rs

Lični podaci

Datum i mesto rođenja: 19.12.1983.godine, Kruševac. Udata, majka dvoje dece. Jezici koje koristi: srpski (maternji) i engleski.

Obrazovanje i usavršavanja

2002-2007: Osnovne studije - Hemijske nauke / Univerzitet u Beogradu - Hemijski fakultet (Beograd)

2007-2015: Doktorat - Hemijske nauke / Univerzitet u Beogradu - Hemijski fakultet (Beograd)

Kretanje u službi

2008-2010: Saradnik u nastavi / Univerzitet u Beogradu - Hemijski fakultet (Beograd)

2010-2018: Asistent / Univerzitet u Beogradu - Hemijski fakultet (Beograd)

2018: Docent / Univerzitet u Beogradu - Hemijski fakultet (Beograd)

Oblasti naučnog interesovanja

Koordinaciona hemija, boineorganska hemija

Nagrade i priznanja

2016: Stipendija za postodktorske studije Ministarstva prosvete, nauke i tehnološkog razvoja Rebuplike Srbije

Ostale aktivnosti

Član Srpskog hemijskog društva od 2008.

Angažman u nastavi

Učešće u naučnoistraživačkim projektima

Aktivni projekti:

  • 2020-2021: Pionirska inovacija vlažnih maramica za bebe: ekološki orijentisani, održivi koncept za bebinu kožu – PoC-5087
    vrsta projekta:   domaći inovacioni
    projekat finansira:   Fond za inovacionu delatnost Republike Srbije (Beograd)

Završeni projekti:

  • 2011: Racionalni dizajn i sinteza biološki aktivnih i koordinacionih jedinjenja i funkcionalnih materijala, relevantnih u (bio) nanotehnologiji – 172035
    vrsta projekta:   domaći fundamentalni
    projekat finansira:   Ministarstvo za nauku i tehnološki razvoj Republike Srbije (Beograd)

Brojevi za identifikaciju autora

Izabrane reference

M.V. Dimitrijević, Lj.E. Mihajlović-Lalić, S. Grgurić-Šipka, T.M. Mihajlov-Krstev, D.L. Miladinović, J.M. Poljarević, Synthesis, chemical characterization, and antimicrobial potency of picolinate-based halfsandwich Ru(II) complexes, J. Coord. Chem., 76, 783, (2023). https://doi.org/10.1080/00958972.2023.2195965

T. Petrović, N. Gligorijević, F. Belaj, S. Aranđelović, Lj.E. Mihajlović-Lalić, S. Grgurić-Šipka, J. Poljarević, Drug combination study of novel oxorhenium(V) complexes, J. Inorg. Biochem., 2022, 231, 111807. https://doi.org/10.1016/j.jinorgbio.2022.111807

Lj.E. Mihajlović-Lalić, J. Poljarević, S. Grgurić-Šipka, Metal complexes with α-picolinic acid frameworks and their antitumor activity, Inorg. Chim. Acta, 2021, 527, 120582. https://doi.org/10.1016/j.ica.2021.120582

J.P. Mészáros, G. Németi, J.M. Poljarevic, T. Holczbauer, N.V. May, É.A. Enyedy, Effect of the additional carboxyl group in half-sandwich organometallic 2,4-dipicolinate complexes on solution speciation and structure, Eur. J. Inorg. Chem., 2021, 2021 (19) 1858. https://doi.org/10.1002/ejic.202100122


J.P. Mészáros, H. Geisler, J.M. Poljarević, A. Roller, M.S. Legina, M. Hejl, M.A. Jakupec, B.K. Keppler, W. Kandioller, É.A. Enyedy, Naphthoquinones of natural origin: aqueous chemistry and coordination to half-sandwich organometallic cations, J. Organomet. Chem., 2020, 907, 121070. https://doi.org/10.1016/j.jorganchem.2019.121070

 

S. Misirlic-Dencic, J. Poljarevic, A.M. Isakovic, T. Sabo, I. Markovic, V. Trajkovic, Current development of metal complexes with diamine ligands as potential anticancer agents, Curr. Med. Chem., 2020, 27 (3), 380. https://doi.org/10.2174/0929867325666181031114306

 

M. Pavlović, A. Tadić, N. Gligorijević, J. Poljarević*, T. Petrović, B. Dojčinović, A. Savić, S. Radulović, S. Grgurić-Šipka, S. Aranđelović, Synthesis, chemical characterization, PARP inhibition, DNA binding and cellular uptake of novel ruthenium(II)-arene complexes bearing benzamide derivatives in human breast cancer cells, J. Inorg. Biochem., 2020, 210, 111155. https://doi.org/10.1016/j.jinorgbio.2020.111155 

 

J.P. Mészáros, J.M. Poljarević, I. Szatmári, O. Csuvik, F. Fülöp, N. Szoboszlai, G. Spengler, É.A. Enyedy, An 8-hydroxyquinoline-proline hybrid with multidrug resistance reversal activity and the solution chemistry of its half-sandwich organometallic Ru and Rh complexes, Dalton Trans., 2020, 49 (23), 7977. https://doi.org/10.1039/d0dt01256d

 

B. Tubić, V. Dobričić, J. Poljarević, A. Savić, T. Sabo, B. Marković, Estimation of passive gastrointestinal absorption and membrane retention using PAMPA test, quantitative structure-permeability and quantitative structure-retention relationship analyses of ethylenediamine-N,N'-di-2-(3-cyclohexyl)propanoic acid and 1,3-propanediamine-N,N'-di-2-(3-cyclohexyl)propanoic acid derivatives, J. Pharmaceut. Biomed., 2020, 184, 113213. https://doi.org/10.1016/j.jpba.2020.113213 

 

J.P. Mészáros, J.M. Poljarevic, G.T. Gál, N.V. May, G. Spengler, É.A. Enyedy, Comparative solution and structural studies of half-sandwich rhodium and ruthenium complexes bearing curcumin and acetylacetone, J. Inorg. Biochem., 2019, 195, 91. https://doi.org/10.1016/j.jinorgbio.2019.02.015

 

Jelena M. Poljarević, G. Tamás Gál, Nóra V. May, Gabriella Spengler, Orsolya Dömötör, Aleksandar R. Savić, Sanja Grgurić-Šipka, Éva A. Enyedy, Comparative solution equilibrium and structural studies of half-sandwich ruthenium(II)(η6-toluene) complexes of picolinate derivatives; Journal of Inorganic Biochemistry 181 (2018) 74–85.

A. Tadić, J. Poljarević, M. Krstić, M. Kajzerberger, S. Aranđelović, S. Radulović, C. Kakoulidou, A.N. Papadopoulos, G. Psomas, S. Grgurić-Šipka, Ruthenium-arene complexes with NSAIDs: Synthesis, characterization and bioactivity, New J. Chem., 2018, 42 (4), 3001. https://doi.org/10.1039/c7nj04416j

Lj.E. Mihajlović-Lalić, D. Stanković, J. Poljarevíc, T.J. Sabo, D. Manojlović, Voltammetric study of antitumor efficient ethylenediamine-type of ligands, J. Electrochem. Soc., 2018, 165 (10), G123. https://doi.org/10.1149/2.1121810jes

A.M. Isakovic, S.M. Petricevic, S.M. Ristic, D.M. Popadic, T.K. Kravic-Stevovic, N.S. Zogovic, J.M. Poljarevic, T.V. Zivanovic Radnic, T.J. Sabo, A.J. Isakovic, I.D. Markovic, V.S. Trajkovic, S.T. Misirlic-Dencic, In vitro and in vivo antimelanoma effect of ethyl ester cyclohexyl analog of ethylenediamine dipropanoic acid, Melanoma Res., 2018, 28 (1), 8. https://doi.org/10.1097/CMR.0000000000000409