Jeremić, Dejan

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Authority KeyName Variants
orcid::0000-0001-9950-0803
  • Jeremić, Dejan (26)
Projects
Structure-properties relationships of natural and synthetic molecules and their metal complexes Rational design and synthesis of biologically active and coordination compounds and functional materials, relevant for (bio)nanotechnology
Sinteza, analiza i aktivnost novih organskih polidentatnih liganada i njihovih kompleksa sa d-metalima Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200026 (University of Belgrade, Institute of Chemistry, Technology and Metallurgy - IChTM)
Reinforcement of the Faculty of Chemistry, University of Belgrade, towards becoming a Center of Excellence in the region of WB for Molecular Biotechnology and Food research Application of advanced oxidation processes and nanostructured oxide materials for the removal of pollutants from the environment, development and optimisation of instrumental techniques for efficiency monitoring
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200168 (University of Belgrade, Faculty of Chemistry) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200175 (Institute of Technical Sciences of SASA, Belgrade)
Magbiovin project (FP7-ERAChairs-Pilot Call-2013, Grant agreement: 621375) Mechanistic studies of the reactions of transition metal ion complexes with biologically relevant molecules
Bioactive natural products as potential sources of new pharmaceuticals and food supplements Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200116 (University of Belgrade, Faculty of Agriculture)
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200288 (Innovation Center of the Faculty of Chemistry) Simultaneous Bioremediation and Soilification of Degraded Areas to Preserve Natural Resources of Biologically Active Substances, and Development and Production of Biomaterials and Dietetic Products
Zero- to Three-Dimensional Nanostructures for Application in Electronics and Renewable Energy Sources: Synthesis, Characterization and Processing Synthesis, characterization and activity of organic and coordination composition and their application in (bio) nanotechnology
Interakcije prirodnih proizvoda i njihovih analoga sa proteinima i nukleinskim kiselinama Istraživanje dejstava modifikatora biološkog odgovora u fiziološkim i patološkim stanjima
Farmakodinamska i farmakogenetska istraživanja novih lekova i prediktivna/prognostička vrednost farmakoterapije u onkologiji NSF PREM award DMR 11523617
Project F133 funded by the Serbian Academy of Sciences and Arts Provincial Secretarial and Technological Development of Vojvodina, Republic of Serbia

Author's Bibliography

Multiferroic heterostructure BaTiO3/ε-Fe2O3composite obtained by in situ reaction

Filipović, Suzana; Obradović, Nina; Anđelković, Ljubica; Olćan, Dragan; Petrović, Jovana P.; Mirković, Marija; Pavlović, Vladimir B.; Jeremić, Dejan; Vlahović, Branislav; Đorđević, Antonije

(ETRAN Society, 2021)

TY  - JOUR
AU  - Filipović, Suzana
AU  - Obradović, Nina
AU  - Anđelković, Ljubica
AU  - Olćan, Dragan
AU  - Petrović, Jovana P.
AU  - Mirković, Marija
AU  - Pavlović, Vladimir B.
AU  - Jeremić, Dejan
AU  - Vlahović, Branislav
AU  - Đorđević, Antonije
PY  - 2021
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4511
AB  - Solid-state reaction between BaTiO3and Fe2O3was used to produce a multiferroic heterostructure composite. Commercial BaTiO3and Fe(NO3)3•9H2O were suspended in ethanol for 30 minutes in an ultrasound bath. The prepared mixture was thermally processed at 300°C for 6 h. Sintering at 1300 °C for 1 h resulted in a mixture of different phases, BaTiO3, BaFe12O19and Ba12Ti28Fe15O84, which were confirmed by x-ray powder diffraction. A dense microstructure with a small volume fraction of closed porosity was indicated by the scanning electron microscopy, while a homogeneous distribution of Fe ions over BaTiO3phase was visible from energy dispersive spectroscopy mapping. Doping of BaTiO3with Fe2O3resulted in formation of magnetic hexaferrite phases, as confirmed by dielectric measurements that showed a broadened maximum of the permittivity measured as a function of temperature. © 2021 Authors. Published by association for ETRAN Society.
PB  - ETRAN Society
T2  - Science of Sintering
T2  - Science of Sintering
T1  - Multiferroic heterostructure BaTiO3/ε-Fe2O3composite obtained by in situ reaction
VL  - 53
IS  - 1
SP  - 1
EP  - 8
DO  - 10.2298/SOS2101001F
ER  - 
@article{
author = "Filipović, Suzana and Obradović, Nina and Anđelković, Ljubica and Olćan, Dragan and Petrović, Jovana P. and Mirković, Marija and Pavlović, Vladimir B. and Jeremić, Dejan and Vlahović, Branislav and Đorđević, Antonije",
year = "2021",
abstract = "Solid-state reaction between BaTiO3and Fe2O3was used to produce a multiferroic heterostructure composite. Commercial BaTiO3and Fe(NO3)3•9H2O were suspended in ethanol for 30 minutes in an ultrasound bath. The prepared mixture was thermally processed at 300°C for 6 h. Sintering at 1300 °C for 1 h resulted in a mixture of different phases, BaTiO3, BaFe12O19and Ba12Ti28Fe15O84, which were confirmed by x-ray powder diffraction. A dense microstructure with a small volume fraction of closed porosity was indicated by the scanning electron microscopy, while a homogeneous distribution of Fe ions over BaTiO3phase was visible from energy dispersive spectroscopy mapping. Doping of BaTiO3with Fe2O3resulted in formation of magnetic hexaferrite phases, as confirmed by dielectric measurements that showed a broadened maximum of the permittivity measured as a function of temperature. © 2021 Authors. Published by association for ETRAN Society.",
publisher = "ETRAN Society",
journal = "Science of Sintering, Science of Sintering",
title = "Multiferroic heterostructure BaTiO3/ε-Fe2O3composite obtained by in situ reaction",
volume = "53",
number = "1",
pages = "1-8",
doi = "10.2298/SOS2101001F"
}
Filipović, S., Obradović, N., Anđelković, L., Olćan, D., Petrović, J. P., Mirković, M., Pavlović, V. B., Jeremić, D., Vlahović, B.,& Đorđević, A.. (2021). Multiferroic heterostructure BaTiO3/ε-Fe2O3composite obtained by in situ reaction. in Science of Sintering
ETRAN Society., 53(1), 1-8.
https://doi.org/10.2298/SOS2101001F
Filipović S, Obradović N, Anđelković L, Olćan D, Petrović JP, Mirković M, Pavlović VB, Jeremić D, Vlahović B, Đorđević A. Multiferroic heterostructure BaTiO3/ε-Fe2O3composite obtained by in situ reaction. in Science of Sintering. 2021;53(1):1-8.
doi:10.2298/SOS2101001F .
Filipović, Suzana, Obradović, Nina, Anđelković, Ljubica, Olćan, Dragan, Petrović, Jovana P., Mirković, Marija, Pavlović, Vladimir B., Jeremić, Dejan, Vlahović, Branislav, Đorđević, Antonije, "Multiferroic heterostructure BaTiO3/ε-Fe2O3composite obtained by in situ reaction" in Science of Sintering, 53, no. 1 (2021):1-8,
https://doi.org/10.2298/SOS2101001F . .

The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods

Šuljagić, Marija; Vulić, Predrag; Jeremić, Dejan; Pavlović, Vladimir B.; Filipović, Suzana; Kilanski, Lukasz; Lewinska, Sabina; Slawska-Waniewska, Anna; Milenković, Milica R.; Nikolić, Aleksandar S.; Anđelković, Ljubica

(Elsevier, 2021)

TY  - JOUR
AU  - Šuljagić, Marija
AU  - Vulić, Predrag
AU  - Jeremić, Dejan
AU  - Pavlović, Vladimir B.
AU  - Filipović, Suzana
AU  - Kilanski, Lukasz
AU  - Lewinska, Sabina
AU  - Slawska-Waniewska, Anna
AU  - Milenković, Milica R.
AU  - Nikolić, Aleksandar S.
AU  - Anđelković, Ljubica
PY  - 2021
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4271
AB  - To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.
PB  - Elsevier
T2  - Materials Research Bulletin
T1  - The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods
VL  - 134
SP  - 111117
DO  - 10.1016/j.materresbull.2020.111117
ER  - 
@article{
author = "Šuljagić, Marija and Vulić, Predrag and Jeremić, Dejan and Pavlović, Vladimir B. and Filipović, Suzana and Kilanski, Lukasz and Lewinska, Sabina and Slawska-Waniewska, Anna and Milenković, Milica R. and Nikolić, Aleksandar S. and Anđelković, Ljubica",
year = "2021",
abstract = "To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.",
publisher = "Elsevier",
journal = "Materials Research Bulletin",
title = "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods",
volume = "134",
pages = "111117",
doi = "10.1016/j.materresbull.2020.111117"
}
Šuljagić, M., Vulić, P., Jeremić, D., Pavlović, V. B., Filipović, S., Kilanski, L., Lewinska, S., Slawska-Waniewska, A., Milenković, M. R., Nikolić, A. S.,& Anđelković, L.. (2021). The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin
Elsevier., 134, 111117.
https://doi.org/10.1016/j.materresbull.2020.111117
Šuljagić M, Vulić P, Jeremić D, Pavlović VB, Filipović S, Kilanski L, Lewinska S, Slawska-Waniewska A, Milenković MR, Nikolić AS, Anđelković L. The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin. 2021;134:111117.
doi:10.1016/j.materresbull.2020.111117 .
Šuljagić, Marija, Vulić, Predrag, Jeremić, Dejan, Pavlović, Vladimir B., Filipović, Suzana, Kilanski, Lukasz, Lewinska, Sabina, Slawska-Waniewska, Anna, Milenković, Milica R., Nikolić, Aleksandar S., Anđelković, Ljubica, "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods" in Materials Research Bulletin, 134 (2021):111117,
https://doi.org/10.1016/j.materresbull.2020.111117 . .
4
3

Structure and properties of nanocrystalline tetragonal BaTiO3 prepared by combustion solid state synthesis

Filipović, S.; Anđelković, Ljubica; Jeremić, Dejan; Vulić, P.; Nikolić, A. S.; Marković, S.; Paunović, V.; Lević, Steva M.; Pavlović, Vladimir B.

(Association for ETRAN Society, 2020)

TY  - JOUR
AU  - Filipović, S.
AU  - Anđelković, Ljubica
AU  - Jeremić, Dejan
AU  - Vulić, P.
AU  - Nikolić, A. S.
AU  - Marković, S.
AU  - Paunović, V.
AU  - Lević, Steva M.
AU  - Pavlović, Vladimir B.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4301
AB  - Barium titanate (BaTiO3) attracts high scientific and technological attention due to good dielectric and electromechanical properties. Although BaTiO3 is one of the most frequently investigated ferroelectric materials, the need for finding new and/or improved synthesis methods of this material still exists. In this paper, a novel, mild synthesis route for producing tetragonal BaTiO3 from barium nitrate and Ti-oxalate precursor is presented. Morphology of the prepared and subsequently sintered BaTiO3 was determined by SEM. Particle size distribution of the as prepared powder was monitored by the laser diffraction. The phase composition, structure and lattice dynamics were investigated by XRD and Raman spectroscopy. Finally, dielectric parameters were determined in the temperature range from 30 to 180ºC, and within a variety of frequencies. Curie temperature was detected at 130ºC.
PB  - Association for ETRAN Society
T2  - Science of Sintering
T1  - Structure and properties of nanocrystalline tetragonal BaTiO3 prepared by combustion solid state synthesis
VL  - 52
IS  - 3
SP  - 257
EP  - 268
DO  - 10.2298/SOS2003257F
ER  - 
@article{
author = "Filipović, S. and Anđelković, Ljubica and Jeremić, Dejan and Vulić, P. and Nikolić, A. S. and Marković, S. and Paunović, V. and Lević, Steva M. and Pavlović, Vladimir B.",
year = "2020",
abstract = "Barium titanate (BaTiO3) attracts high scientific and technological attention due to good dielectric and electromechanical properties. Although BaTiO3 is one of the most frequently investigated ferroelectric materials, the need for finding new and/or improved synthesis methods of this material still exists. In this paper, a novel, mild synthesis route for producing tetragonal BaTiO3 from barium nitrate and Ti-oxalate precursor is presented. Morphology of the prepared and subsequently sintered BaTiO3 was determined by SEM. Particle size distribution of the as prepared powder was monitored by the laser diffraction. The phase composition, structure and lattice dynamics were investigated by XRD and Raman spectroscopy. Finally, dielectric parameters were determined in the temperature range from 30 to 180ºC, and within a variety of frequencies. Curie temperature was detected at 130ºC.",
publisher = "Association for ETRAN Society",
journal = "Science of Sintering",
title = "Structure and properties of nanocrystalline tetragonal BaTiO3 prepared by combustion solid state synthesis",
volume = "52",
number = "3",
pages = "257-268",
doi = "10.2298/SOS2003257F"
}
Filipović, S., Anđelković, L., Jeremić, D., Vulić, P., Nikolić, A. S., Marković, S., Paunović, V., Lević, S. M.,& Pavlović, V. B.. (2020). Structure and properties of nanocrystalline tetragonal BaTiO3 prepared by combustion solid state synthesis. in Science of Sintering
Association for ETRAN Society., 52(3), 257-268.
https://doi.org/10.2298/SOS2003257F
Filipović S, Anđelković L, Jeremić D, Vulić P, Nikolić AS, Marković S, Paunović V, Lević SM, Pavlović VB. Structure and properties of nanocrystalline tetragonal BaTiO3 prepared by combustion solid state synthesis. in Science of Sintering. 2020;52(3):257-268.
doi:10.2298/SOS2003257F .
Filipović, S., Anđelković, Ljubica, Jeremić, Dejan, Vulić, P., Nikolić, A. S., Marković, S., Paunović, V., Lević, Steva M., Pavlović, Vladimir B., "Structure and properties of nanocrystalline tetragonal BaTiO3 prepared by combustion solid state synthesis" in Science of Sintering, 52, no. 3 (2020):257-268,
https://doi.org/10.2298/SOS2003257F . .
1

One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles

Jeremić, Dejan; Anđelković, Ljubica; Milenković, Milica R.; Šuljagić, Marija; Šumar-Ristović, Maja; Ostojić, Sanja; Nikolić, Aleksandar S.; Vulić, Predrag; Brčeski, Ilija; Pavlović, Vladimir B.

(2020)

TY  - JOUR
AU  - Jeremić, Dejan
AU  - Anđelković, Ljubica
AU  - Milenković, Milica R.
AU  - Šuljagić, Marija
AU  - Šumar-Ristović, Maja
AU  - Ostojić, Sanja
AU  - Nikolić, Aleksandar S.
AU  - Vulić, Predrag
AU  - Brčeski, Ilija
AU  - Pavlović, Vladimir B.
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4306
AB  - This work is the first report of a very simple and fast one-pot synthesis of nickel oxide (NiO) and hematite (α-Fe2O3) nanoparticles by thermal decomposition of transition metal aqua complexes with camphor sulfonate anions. Obtained nanopowders were characterized by X-ray powder diffraction, Fourier transform IR analysis, scanning electron microscopy, and Energy-dispersive X-ray spectroscopy. X-ray powder diffraction confirmed the formation of high purity NiO and α-Fe2O3 crystal phases. In the case of α-Fe2O3, about five times larger average crystallite size was obtained. Fourier transform IR spectra of synthesized materials showed characteristic peaks for NiO and α-Fe2O3 nanostructures. To visualize the morphology and the chemical composition of the final products Scanning electron microscopy and Energy-dispersive X-ray spectroscopy were performed. The thermogravimetric analysis was done for a better understanding of the general thermal behavior of precursor compounds. This easy-to-perform and fast preparation method opens a broad range of obtained materials’ usage, particularly due to its economic viability
T2  - Science of Sintering
T1  - One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles
VL  - 52
IS  - 4
SP  - 481
EP  - 490
DO  - 10.2298/SOS2004481J
ER  - 
@article{
author = "Jeremić, Dejan and Anđelković, Ljubica and Milenković, Milica R. and Šuljagić, Marija and Šumar-Ristović, Maja and Ostojić, Sanja and Nikolić, Aleksandar S. and Vulić, Predrag and Brčeski, Ilija and Pavlović, Vladimir B.",
year = "2020",
abstract = "This work is the first report of a very simple and fast one-pot synthesis of nickel oxide (NiO) and hematite (α-Fe2O3) nanoparticles by thermal decomposition of transition metal aqua complexes with camphor sulfonate anions. Obtained nanopowders were characterized by X-ray powder diffraction, Fourier transform IR analysis, scanning electron microscopy, and Energy-dispersive X-ray spectroscopy. X-ray powder diffraction confirmed the formation of high purity NiO and α-Fe2O3 crystal phases. In the case of α-Fe2O3, about five times larger average crystallite size was obtained. Fourier transform IR spectra of synthesized materials showed characteristic peaks for NiO and α-Fe2O3 nanostructures. To visualize the morphology and the chemical composition of the final products Scanning electron microscopy and Energy-dispersive X-ray spectroscopy were performed. The thermogravimetric analysis was done for a better understanding of the general thermal behavior of precursor compounds. This easy-to-perform and fast preparation method opens a broad range of obtained materials’ usage, particularly due to its economic viability",
journal = "Science of Sintering",
title = "One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles",
volume = "52",
number = "4",
pages = "481-490",
doi = "10.2298/SOS2004481J"
}
Jeremić, D., Anđelković, L., Milenković, M. R., Šuljagić, M., Šumar-Ristović, M., Ostojić, S., Nikolić, A. S., Vulić, P., Brčeski, I.,& Pavlović, V. B.. (2020). One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles. in Science of Sintering, 52(4), 481-490.
https://doi.org/10.2298/SOS2004481J
Jeremić D, Anđelković L, Milenković MR, Šuljagić M, Šumar-Ristović M, Ostojić S, Nikolić AS, Vulić P, Brčeski I, Pavlović VB. One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles. in Science of Sintering. 2020;52(4):481-490.
doi:10.2298/SOS2004481J .
Jeremić, Dejan, Anđelković, Ljubica, Milenković, Milica R., Šuljagić, Marija, Šumar-Ristović, Maja, Ostojić, Sanja, Nikolić, Aleksandar S., Vulić, Predrag, Brčeski, Ilija, Pavlović, Vladimir B., "One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles" in Science of Sintering, 52, no. 4 (2020):481-490,
https://doi.org/10.2298/SOS2004481J . .
1
1
3

Supplementary data for the article: Perić, M.; Kyne, S. H.; Gruden, M.; Rodić, M.; Jeremić, D.; Stanković, D. M.; Brčeski, I. Synthesis, Structural and DFT Analysis of a Binuclear Nickel(II) Complex with the 1,4-Bis[2-[2-(Diphenylphosphino)Benzylidene]]Phthalazinylhydrazone Ligand. Monatshefte fur Chemie 2019, 150 (7), 1241–1248. https://doi.org/10.1007/s00706-019-02405-7

Perić, Marko; Kyne, Sara H.; Gruden-Pavlović, Maja; Rodić, Marko; Jeremić, Dejan; Stanković, Dalibor; Brčeski, Ilija

(Springer-Verlag GmbH Austria, 2019)

TY  - DATA
AU  - Perić, Marko
AU  - Kyne, Sara H.
AU  - Gruden-Pavlović, Maja
AU  - Rodić, Marko
AU  - Jeremić, Dejan
AU  - Stanković, Dalibor
AU  - Brčeski, Ilija
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3317
PB  - Springer-Verlag GmbH Austria
T2  - Monatshefte fur Chemie
T1  - Supplementary data for the article: Perić, M.; Kyne, S. H.; Gruden, M.; Rodić, M.; Jeremić, D.; Stanković, D. M.; Brčeski, I. Synthesis, Structural and DFT Analysis of a Binuclear Nickel(II) Complex with the 1,4-Bis[2-[2-(Diphenylphosphino)Benzylidene]]Phthalazinylhydrazone Ligand. Monatshefte fur Chemie 2019, 150 (7), 1241–1248. https://doi.org/10.1007/s00706-019-02405-7
ER  - 
@misc{
author = "Perić, Marko and Kyne, Sara H. and Gruden-Pavlović, Maja and Rodić, Marko and Jeremić, Dejan and Stanković, Dalibor and Brčeski, Ilija",
year = "2019",
publisher = "Springer-Verlag GmbH Austria",
journal = "Monatshefte fur Chemie",
title = "Supplementary data for the article: Perić, M.; Kyne, S. H.; Gruden, M.; Rodić, M.; Jeremić, D.; Stanković, D. M.; Brčeski, I. Synthesis, Structural and DFT Analysis of a Binuclear Nickel(II) Complex with the 1,4-Bis[2-[2-(Diphenylphosphino)Benzylidene]]Phthalazinylhydrazone Ligand. Monatshefte fur Chemie 2019, 150 (7), 1241–1248. https://doi.org/10.1007/s00706-019-02405-7"
}
Perić, M., Kyne, S. H., Gruden-Pavlović, M., Rodić, M., Jeremić, D., Stanković, D.,& Brčeski, I.. (2019). Supplementary data for the article: Perić, M.; Kyne, S. H.; Gruden, M.; Rodić, M.; Jeremić, D.; Stanković, D. M.; Brčeski, I. Synthesis, Structural and DFT Analysis of a Binuclear Nickel(II) Complex with the 1,4-Bis[2-[2-(Diphenylphosphino)Benzylidene]]Phthalazinylhydrazone Ligand. Monatshefte fur Chemie 2019, 150 (7), 1241–1248. https://doi.org/10.1007/s00706-019-02405-7. in Monatshefte fur Chemie
Springer-Verlag GmbH Austria..
Perić M, Kyne SH, Gruden-Pavlović M, Rodić M, Jeremić D, Stanković D, Brčeski I. Supplementary data for the article: Perić, M.; Kyne, S. H.; Gruden, M.; Rodić, M.; Jeremić, D.; Stanković, D. M.; Brčeski, I. Synthesis, Structural and DFT Analysis of a Binuclear Nickel(II) Complex with the 1,4-Bis[2-[2-(Diphenylphosphino)Benzylidene]]Phthalazinylhydrazone Ligand. Monatshefte fur Chemie 2019, 150 (7), 1241–1248. https://doi.org/10.1007/s00706-019-02405-7. in Monatshefte fur Chemie. 2019;..
Perić, Marko, Kyne, Sara H., Gruden-Pavlović, Maja, Rodić, Marko, Jeremić, Dejan, Stanković, Dalibor, Brčeski, Ilija, "Supplementary data for the article: Perić, M.; Kyne, S. H.; Gruden, M.; Rodić, M.; Jeremić, D.; Stanković, D. M.; Brčeski, I. Synthesis, Structural and DFT Analysis of a Binuclear Nickel(II) Complex with the 1,4-Bis[2-[2-(Diphenylphosphino)Benzylidene]]Phthalazinylhydrazone Ligand. Monatshefte fur Chemie 2019, 150 (7), 1241–1248. https://doi.org/10.1007/s00706-019-02405-7" in Monatshefte fur Chemie (2019).

Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand

Perić, Marko; Kyne, Sara H.; Gruden, Maja; Rodić, Marko; Jeremić, Dejan; Stanković, Dalibor; Brčeski, Ilija

(Springer-Verlag GmbH Austria, 2019)

TY  - JOUR
AU  - Perić, Marko
AU  - Kyne, Sara H.
AU  - Gruden, Maja
AU  - Rodić, Marko
AU  - Jeremić, Dejan
AU  - Stanković, Dalibor
AU  - Brčeski, Ilija
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3316
AB  - In this work we present the synthesis, and experimental and theoretical analysis of a binuclear nickel(II) complex coordinated to a new phthalazine dihydrazone-based ligand. Single-crystal X-ray diffraction analysis of the metal complex shows that the coordination geometry around each nickel(II) atom is distorted octahedral. DFT calculations predict that the magnetic exchange coupling constant of the binuclear nickel(II) complex is predominantly anti-ferromagnetic.
PB  - Springer-Verlag GmbH Austria
T2  - Monatshefte fur Chemie
T1  - Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand
VL  - 150
IS  - 7
SP  - 1241
EP  - 1248
DO  - 10.1007/s00706-019-02405-7
ER  - 
@article{
author = "Perić, Marko and Kyne, Sara H. and Gruden, Maja and Rodić, Marko and Jeremić, Dejan and Stanković, Dalibor and Brčeski, Ilija",
year = "2019",
abstract = "In this work we present the synthesis, and experimental and theoretical analysis of a binuclear nickel(II) complex coordinated to a new phthalazine dihydrazone-based ligand. Single-crystal X-ray diffraction analysis of the metal complex shows that the coordination geometry around each nickel(II) atom is distorted octahedral. DFT calculations predict that the magnetic exchange coupling constant of the binuclear nickel(II) complex is predominantly anti-ferromagnetic.",
publisher = "Springer-Verlag GmbH Austria",
journal = "Monatshefte fur Chemie",
title = "Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand",
volume = "150",
number = "7",
pages = "1241-1248",
doi = "10.1007/s00706-019-02405-7"
}
Perić, M., Kyne, S. H., Gruden, M., Rodić, M., Jeremić, D., Stanković, D.,& Brčeski, I.. (2019). Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand. in Monatshefte fur Chemie
Springer-Verlag GmbH Austria., 150(7), 1241-1248.
https://doi.org/10.1007/s00706-019-02405-7
Perić M, Kyne SH, Gruden M, Rodić M, Jeremić D, Stanković D, Brčeski I. Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand. in Monatshefte fur Chemie. 2019;150(7):1241-1248.
doi:10.1007/s00706-019-02405-7 .
Perić, Marko, Kyne, Sara H., Gruden, Maja, Rodić, Marko, Jeremić, Dejan, Stanković, Dalibor, Brčeski, Ilija, "Synthesis, structural and DFT analysis of a binuclear nickel(II) complex with the 1,4-bis[2-[2-(diphenylphosphino)benzylidene]]phthalazinylhydrazone ligand" in Monatshefte fur Chemie, 150, no. 7 (2019):1241-1248,
https://doi.org/10.1007/s00706-019-02405-7 . .
1
1

Mechanochemically synthesized cobalt-ferrite and starch-coated cobalt-ferrite nanoparticles as efficient adsorbents for hexavalent chromium removal

Šuljagić, Marija; Jeremić, Dejan; Milenković, Milica R.; Nikolić, Aleksandar S.; Anđelković, Ljubica

(Belgrade : Institute of Technical Sciences of SASA, 2019)

TY  - CONF
AU  - Šuljagić, Marija
AU  - Jeremić, Dejan
AU  - Milenković, Milica R.
AU  - Nikolić, Aleksandar S.
AU  - Anđelković, Ljubica
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3786
AB  - Cobalt-ferrite (CoFe2O4) and starch-coated CoFe2O4 nanoparticles were prepared by the
mechanochemical method and carefully chosen as adsorbents for Cr(VI) removal from
wastewater. The kinetic study, adsorption isotherms and influence of pH, contact time and
interfering ions were investigated to have deeper insight into adsorbent quality. UV/Vis
spectroscopy confirmed that the dominant adsorption mechanism is the electrostatic
attraction at lower pH values. The study showed there was no significant change in
adsorption efficiency for starch-coated nanoparticles. However, starch as a natural and
biocompatible compound can enhance nanoparticles water dispersibility. The advantage of
such materials is that saturation time does not exceed 20 minutes. Therefore, the as-prepared
and starch-coated CoFe2O4 presents very efficient material for application in the field of
water remediation.
PB  - Belgrade : Institute of Technical Sciences of SASA
C3  - Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia
T1  - Mechanochemically synthesized cobalt-ferrite and starch-coated cobalt-ferrite nanoparticles as efficient adsorbents for hexavalent chromium removal
SP  - 70
EP  - 70
ER  - 
@conference{
author = "Šuljagić, Marija and Jeremić, Dejan and Milenković, Milica R. and Nikolić, Aleksandar S. and Anđelković, Ljubica",
year = "2019",
abstract = "Cobalt-ferrite (CoFe2O4) and starch-coated CoFe2O4 nanoparticles were prepared by the
mechanochemical method and carefully chosen as adsorbents for Cr(VI) removal from
wastewater. The kinetic study, adsorption isotherms and influence of pH, contact time and
interfering ions were investigated to have deeper insight into adsorbent quality. UV/Vis
spectroscopy confirmed that the dominant adsorption mechanism is the electrostatic
attraction at lower pH values. The study showed there was no significant change in
adsorption efficiency for starch-coated nanoparticles. However, starch as a natural and
biocompatible compound can enhance nanoparticles water dispersibility. The advantage of
such materials is that saturation time does not exceed 20 minutes. Therefore, the as-prepared
and starch-coated CoFe2O4 presents very efficient material for application in the field of
water remediation.",
publisher = "Belgrade : Institute of Technical Sciences of SASA",
journal = "Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia",
title = "Mechanochemically synthesized cobalt-ferrite and starch-coated cobalt-ferrite nanoparticles as efficient adsorbents for hexavalent chromium removal",
pages = "70-70"
}
Šuljagić, M., Jeremić, D., Milenković, M. R., Nikolić, A. S.,& Anđelković, L.. (2019). Mechanochemically synthesized cobalt-ferrite and starch-coated cobalt-ferrite nanoparticles as efficient adsorbents for hexavalent chromium removal. in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia
Belgrade : Institute of Technical Sciences of SASA., 70-70.
Šuljagić M, Jeremić D, Milenković MR, Nikolić AS, Anđelković L. Mechanochemically synthesized cobalt-ferrite and starch-coated cobalt-ferrite nanoparticles as efficient adsorbents for hexavalent chromium removal. in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia. 2019;:70-70..
Šuljagić, Marija, Jeremić, Dejan, Milenković, Milica R., Nikolić, Aleksandar S., Anđelković, Ljubica, "Mechanochemically synthesized cobalt-ferrite and starch-coated cobalt-ferrite nanoparticles as efficient adsorbents for hexavalent chromium removal" in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia (2019):70-70.

A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch

Anđelković, Ljubica; Šuljagić, Marija; Lakić, Mladen; Jeremić, Dejan; Vulić, Predrag J.; Nikolić, Aleksandar S.

(Elsevier Sci Ltd, Oxford, 2018)

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Lakić, Mladen
AU  - Jeremić, Dejan
AU  - Vulić, Predrag J.
AU  - Nikolić, Aleksandar S.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2171
AB  - Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch
VL  - 44
IS  - 12
SP  - 14163
EP  - 14168
DO  - 10.1016/j.ceramint.2018.05.018
UR  - Kon_3502
ER  - 
@article{
author = "Anđelković, Ljubica and Šuljagić, Marija and Lakić, Mladen and Jeremić, Dejan and Vulić, Predrag J. and Nikolić, Aleksandar S.",
year = "2018",
abstract = "Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch",
volume = "44",
number = "12",
pages = "14163-14168",
doi = "10.1016/j.ceramint.2018.05.018",
url = "Kon_3502"
}
Anđelković, L., Šuljagić, M., Lakić, M., Jeremić, D., Vulić, P. J.,& Nikolić, A. S.. (2018). A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International
Elsevier Sci Ltd, Oxford., 44(12), 14163-14168.
https://doi.org/10.1016/j.ceramint.2018.05.018
Kon_3502
Anđelković L, Šuljagić M, Lakić M, Jeremić D, Vulić PJ, Nikolić AS. A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International. 2018;44(12):14163-14168.
doi:10.1016/j.ceramint.2018.05.018
Kon_3502 .
Anđelković, Ljubica, Šuljagić, Marija, Lakić, Mladen, Jeremić, Dejan, Vulić, Predrag J., Nikolić, Aleksandar S., "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch" in Ceramics International, 44, no. 12 (2018):14163-14168,
https://doi.org/10.1016/j.ceramint.2018.05.018 .,
Kon_3502 .
34
33
34

A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch

Anđelković, Ljubica; Šuljagić, Marija; Lakić, Mladen; Jeremić, Dejan; Vulić, Predrag J.; Nikolić, Aleksandar S.

(Elsevier Sci Ltd, Oxford, 2018)

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Šuljagić, Marija
AU  - Lakić, Mladen
AU  - Jeremić, Dejan
AU  - Vulić, Predrag J.
AU  - Nikolić, Aleksandar S.
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3149
AB  - Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch
VL  - 44
IS  - 12
SP  - 14163
EP  - 14168
DO  - 10.1016/j.ceramint.2018.05.018
UR  - Kon_3502
ER  - 
@article{
author = "Anđelković, Ljubica and Šuljagić, Marija and Lakić, Mladen and Jeremić, Dejan and Vulić, Predrag J. and Nikolić, Aleksandar S.",
year = "2018",
abstract = "Zinc-ferrite, nickel-ferrite and mixed nickel-zinc ferrites were successfully synthesized via the thermal decomposition method from acetylacetonate complexes. To control the particle size and enhance dispersibility in an aqueous medium, starch, a natural and biocompatible compound, was used for the first time for coating such magnetic powders. X-ray powder diffraction (XRPD) was performed to study the structural properties of all samples. The presence of a single-phase spinel structure as well as the cation distribution in both sites of all investigated magnetic powders was confirmed. The values of unit cell parameters obtained from the results of the Rietveld analysis decreased, while the average crystallite size increased with increasing Ni2+ content. The average microstrain parameters unambiguously showed a change in the spinel structure with cation distribution. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) analyses were also utilized to characterize the synthesized materials, corroborating the XRPD data. The obtained results indicated that functionalization by starch was successfully achieved.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch",
volume = "44",
number = "12",
pages = "14163-14168",
doi = "10.1016/j.ceramint.2018.05.018",
url = "Kon_3502"
}
Anđelković, L., Šuljagić, M., Lakić, M., Jeremić, D., Vulić, P. J.,& Nikolić, A. S.. (2018). A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International
Elsevier Sci Ltd, Oxford., 44(12), 14163-14168.
https://doi.org/10.1016/j.ceramint.2018.05.018
Kon_3502
Anđelković L, Šuljagić M, Lakić M, Jeremić D, Vulić PJ, Nikolić AS. A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch. in Ceramics International. 2018;44(12):14163-14168.
doi:10.1016/j.ceramint.2018.05.018
Kon_3502 .
Anđelković, Ljubica, Šuljagić, Marija, Lakić, Mladen, Jeremić, Dejan, Vulić, Predrag J., Nikolić, Aleksandar S., "A study of the structural and morphological properties of Ni-ferrite, Zn-ferrite and Ni-Zn-ferrites functionalized with starch" in Ceramics International, 44, no. 12 (2018):14163-14168,
https://doi.org/10.1016/j.ceramint.2018.05.018 .,
Kon_3502 .
35
33
34

Novel silver(I) compounds with 1-adamantanamine

Jeremić, Dejan; Đorđević, Milena; Miletić, Srđan B.; Anđelković, Ljubica; Sladić, Dušan; Brčeski, Ilija

(Serbian Chemical Soc, Belgrade, 2018)

TY  - JOUR
AU  - Jeremić, Dejan
AU  - Đorđević, Milena
AU  - Miletić, Srđan B.
AU  - Anđelković, Ljubica
AU  - Sladić, Dušan
AU  - Brčeski, Ilija
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2178
AB  - In this work, three novel silver(I) complexes with an almost completely rigid and bulky monodentate ligand, 1-adamantanamine, were synthesized. The aliphatic amine, 1-adamantanamine, is the sole electron donor ligand in these complexes. In addition to spectroscopic characterization, the basic biological activities of the new compounds were investigated and their minimum inhibitory concentrations were determined. The antifungal and antibacterial activities indicate that these compounds could potentially be applied as new therapeutics.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Novel silver(I) compounds with 1-adamantanamine
VL  - 83
IS  - 6
SP  - 699
EP  - 705
DO  - 10.2298/JSC171114041J
UR  - Kon_3509
ER  - 
@article{
author = "Jeremić, Dejan and Đorđević, Milena and Miletić, Srđan B. and Anđelković, Ljubica and Sladić, Dušan and Brčeski, Ilija",
year = "2018",
abstract = "In this work, three novel silver(I) complexes with an almost completely rigid and bulky monodentate ligand, 1-adamantanamine, were synthesized. The aliphatic amine, 1-adamantanamine, is the sole electron donor ligand in these complexes. In addition to spectroscopic characterization, the basic biological activities of the new compounds were investigated and their minimum inhibitory concentrations were determined. The antifungal and antibacterial activities indicate that these compounds could potentially be applied as new therapeutics.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Novel silver(I) compounds with 1-adamantanamine",
volume = "83",
number = "6",
pages = "699-705",
doi = "10.2298/JSC171114041J",
url = "Kon_3509"
}
Jeremić, D., Đorđević, M., Miletić, S. B., Anđelković, L., Sladić, D.,& Brčeski, I.. (2018). Novel silver(I) compounds with 1-adamantanamine. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 83(6), 699-705.
https://doi.org/10.2298/JSC171114041J
Kon_3509
Jeremić D, Đorđević M, Miletić SB, Anđelković L, Sladić D, Brčeski I. Novel silver(I) compounds with 1-adamantanamine. in Journal of the Serbian Chemical Society. 2018;83(6):699-705.
doi:10.2298/JSC171114041J
Kon_3509 .
Jeremić, Dejan, Đorđević, Milena, Miletić, Srđan B., Anđelković, Ljubica, Sladić, Dušan, Brčeski, Ilija, "Novel silver(I) compounds with 1-adamantanamine" in Journal of the Serbian Chemical Society, 83, no. 6 (2018):699-705,
https://doi.org/10.2298/JSC171114041J .,
Kon_3509 .
3
3
4

Cytotoxicity and antiviral activity of palladium(II) and platinum(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone

Simic, Vera; Kolarević, Stoimir; Brčeski, Ilija; Jeremić, Dejan; Vuković-Gačić, Branka

(Tubitak Scientific & Technical Research Council Turkey, Ankara, 2016)

TY  - JOUR
AU  - Simic, Vera
AU  - Kolarević, Stoimir
AU  - Brčeski, Ilija
AU  - Jeremić, Dejan
AU  - Vuković-Gačić, Branka
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2269
AB  - Metal coordination compounds have an important role in the development of novel drugs. Using the resazurin microtitration assay we assessed the cytotoxicity and antiviral activity of the ligand 2-(diphenylphosphino) benzaldehyde 1-adamantoylhydrazone and its Pd(II) and Pt(II) complexes. Cytotoxicity was tested in A549 human lung adenocarcinoma epithelial cells. We observed that the ligand displayed a more pronounced cytotoxic activity than the platinum-based drug, carboplatin. Morphological evaluation of A549 cells treated with the ligand by acridine orange and ethidium bromide double staining revealed the presence of signs of apoptosis. Antiviral activity against poliovirus type 1 was assessed by examination of the cytopathic effect (CPE) in Hep-2 cells. Cells that were exposed to the 19 mu M ligand before infection displayed a maximal significant reduction (by 24.42 +/- 1.49%) of the CPE. This was likely due to the inhibition of virus receptors and prevention of viral adsorption. Treatment with 17 mu M Pt(II) complex after viral infection caused a maximal significant reduction (by 30.52 +/- 3.12%) of the CPE, presumably through an effect on viral replication. The results indicate that the ligand should be viewed as a potential anticancer agent. The ligand and the Pt(II) complex show promising results for further investigation of antiviral activity.
PB  - Tubitak Scientific & Technical Research Council Turkey, Ankara
T2  - Turkish Journal of Biology
T1  - Cytotoxicity and antiviral activity of palladium(II) and platinum(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone
VL  - 40
IS  - 3
SP  - 661
EP  - 669
DO  - 10.3906/biy-1503-23
UR  - Kon_3085
ER  - 
@article{
author = "Simic, Vera and Kolarević, Stoimir and Brčeski, Ilija and Jeremić, Dejan and Vuković-Gačić, Branka",
year = "2016",
abstract = "Metal coordination compounds have an important role in the development of novel drugs. Using the resazurin microtitration assay we assessed the cytotoxicity and antiviral activity of the ligand 2-(diphenylphosphino) benzaldehyde 1-adamantoylhydrazone and its Pd(II) and Pt(II) complexes. Cytotoxicity was tested in A549 human lung adenocarcinoma epithelial cells. We observed that the ligand displayed a more pronounced cytotoxic activity than the platinum-based drug, carboplatin. Morphological evaluation of A549 cells treated with the ligand by acridine orange and ethidium bromide double staining revealed the presence of signs of apoptosis. Antiviral activity against poliovirus type 1 was assessed by examination of the cytopathic effect (CPE) in Hep-2 cells. Cells that were exposed to the 19 mu M ligand before infection displayed a maximal significant reduction (by 24.42 +/- 1.49%) of the CPE. This was likely due to the inhibition of virus receptors and prevention of viral adsorption. Treatment with 17 mu M Pt(II) complex after viral infection caused a maximal significant reduction (by 30.52 +/- 3.12%) of the CPE, presumably through an effect on viral replication. The results indicate that the ligand should be viewed as a potential anticancer agent. The ligand and the Pt(II) complex show promising results for further investigation of antiviral activity.",
publisher = "Tubitak Scientific & Technical Research Council Turkey, Ankara",
journal = "Turkish Journal of Biology",
title = "Cytotoxicity and antiviral activity of palladium(II) and platinum(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone",
volume = "40",
number = "3",
pages = "661-669",
doi = "10.3906/biy-1503-23",
url = "Kon_3085"
}
Simic, V., Kolarević, S., Brčeski, I., Jeremić, D.,& Vuković-Gačić, B.. (2016). Cytotoxicity and antiviral activity of palladium(II) and platinum(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone. in Turkish Journal of Biology
Tubitak Scientific & Technical Research Council Turkey, Ankara., 40(3), 661-669.
https://doi.org/10.3906/biy-1503-23
Kon_3085
Simic V, Kolarević S, Brčeski I, Jeremić D, Vuković-Gačić B. Cytotoxicity and antiviral activity of palladium(II) and platinum(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone. in Turkish Journal of Biology. 2016;40(3):661-669.
doi:10.3906/biy-1503-23
Kon_3085 .
Simic, Vera, Kolarević, Stoimir, Brčeski, Ilija, Jeremić, Dejan, Vuković-Gačić, Branka, "Cytotoxicity and antiviral activity of palladium(II) and platinum(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone" in Turkish Journal of Biology, 40, no. 3 (2016):661-669,
https://doi.org/10.3906/biy-1503-23 .,
Kon_3085 .
7
11
11

Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products

Jović, Milica; Manojlović, Dragan D.; Stanković, Dalibor; Gašić, Uroš M.; Jeremić, Dejan; Brčeski, Ilija; Roglić, Goran

(Wiley-Blackwell, Hoboken, 2015)

TY  - JOUR
AU  - Jović, Milica
AU  - Manojlović, Dragan D.
AU  - Stanković, Dalibor
AU  - Gašić, Uroš M.
AU  - Jeremić, Dejan
AU  - Brčeski, Ilija
AU  - Roglić, Goran
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3366
AB  - The aim of this paper was the development and optimization of an electrochemical method for the degradation of two triketone herbicides, mesotrione, and sulcotrione, in a two-electrode undivided electrochemical cell equipped with commercially available, non-modified, electrode materials. The electrochemical parameters studied included five different electrode systems (Zr/Pt, Pd/Pt, C/Pt, Nb/Pt, and Ti/Pt), current densities (27.66, 55.33, ..., 110.66 mA.cm(-2)) and pH values (3, 7, and 9) in 0.05 M sodium sulfate as supporting electrolyte. The electrical energy consumption and chemical oxygen demand were calculated for optimal conditions. The degradation efficiency was determined by high performance liquid chromatography (HPLC) equipped with a diode array detector, while the degradation products for both pesticides were identified and compared by ultra-high performance liquid chromatography (UHPLC)-mass spectrometry. The results could lead to an accurate estimate of their effect on the environment. A real water sample was used to study the influence of organic matter on pesticide degradation. Based on the results obtained the electrochemical treatment could be used for the successful removal of triketone herbicides from contaminated water.
PB  - Wiley-Blackwell, Hoboken
T2  - CLEAN - Soil Air Water
T1  - Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products
VL  - 43
IS  - 7
SP  - 1093
EP  - 1099
DO  - 10.1002/clen.201300951
ER  - 
@article{
author = "Jović, Milica and Manojlović, Dragan D. and Stanković, Dalibor and Gašić, Uroš M. and Jeremić, Dejan and Brčeski, Ilija and Roglić, Goran",
year = "2015",
abstract = "The aim of this paper was the development and optimization of an electrochemical method for the degradation of two triketone herbicides, mesotrione, and sulcotrione, in a two-electrode undivided electrochemical cell equipped with commercially available, non-modified, electrode materials. The electrochemical parameters studied included five different electrode systems (Zr/Pt, Pd/Pt, C/Pt, Nb/Pt, and Ti/Pt), current densities (27.66, 55.33, ..., 110.66 mA.cm(-2)) and pH values (3, 7, and 9) in 0.05 M sodium sulfate as supporting electrolyte. The electrical energy consumption and chemical oxygen demand were calculated for optimal conditions. The degradation efficiency was determined by high performance liquid chromatography (HPLC) equipped with a diode array detector, while the degradation products for both pesticides were identified and compared by ultra-high performance liquid chromatography (UHPLC)-mass spectrometry. The results could lead to an accurate estimate of their effect on the environment. A real water sample was used to study the influence of organic matter on pesticide degradation. Based on the results obtained the electrochemical treatment could be used for the successful removal of triketone herbicides from contaminated water.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "CLEAN - Soil Air Water",
title = "Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products",
volume = "43",
number = "7",
pages = "1093-1099",
doi = "10.1002/clen.201300951"
}
Jović, M., Manojlović, D. D., Stanković, D., Gašić, U. M., Jeremić, D., Brčeski, I.,& Roglić, G.. (2015). Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products. in CLEAN - Soil Air Water
Wiley-Blackwell, Hoboken., 43(7), 1093-1099.
https://doi.org/10.1002/clen.201300951
Jović M, Manojlović DD, Stanković D, Gašić UM, Jeremić D, Brčeski I, Roglić G. Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products. in CLEAN - Soil Air Water. 2015;43(7):1093-1099.
doi:10.1002/clen.201300951 .
Jović, Milica, Manojlović, Dragan D., Stanković, Dalibor, Gašić, Uroš M., Jeremić, Dejan, Brčeski, Ilija, Roglić, Goran, "Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products" in CLEAN - Soil Air Water, 43, no. 7 (2015):1093-1099,
https://doi.org/10.1002/clen.201300951 . .
1
2
2
2

Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products

Jović, Milica; Manojlović, Dragan D.; Stanković, Dalibor; Gašić, Uroš M.; Jeremić, Dejan; Brčeski, Ilija; Roglić, Goran

(Wiley-Blackwell, Hoboken, 2015)

TY  - JOUR
AU  - Jović, Milica
AU  - Manojlović, Dragan D.
AU  - Stanković, Dalibor
AU  - Gašić, Uroš M.
AU  - Jeremić, Dejan
AU  - Brčeski, Ilija
AU  - Roglić, Goran
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1744
AB  - The aim of this paper was the development and optimization of an electrochemical method for the degradation of two triketone herbicides, mesotrione, and sulcotrione, in a two-electrode undivided electrochemical cell equipped with commercially available, non-modified, electrode materials. The electrochemical parameters studied included five different electrode systems (Zr/Pt, Pd/Pt, C/Pt, Nb/Pt, and Ti/Pt), current densities (27.66, 55.33, ..., 110.66 mA.cm(-2)) and pH values (3, 7, and 9) in 0.05 M sodium sulfate as supporting electrolyte. The electrical energy consumption and chemical oxygen demand were calculated for optimal conditions. The degradation efficiency was determined by high performance liquid chromatography (HPLC) equipped with a diode array detector, while the degradation products for both pesticides were identified and compared by ultra-high performance liquid chromatography (UHPLC)-mass spectrometry. The results could lead to an accurate estimate of their effect on the environment. A real water sample was used to study the influence of organic matter on pesticide degradation. Based on the results obtained the electrochemical treatment could be used for the successful removal of triketone herbicides from contaminated water.
PB  - Wiley-Blackwell, Hoboken
T2  - CLEAN - Soil Air Water
T1  - Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products
VL  - 43
IS  - 7
SP  - 1093
EP  - 1099
DO  - 10.1002/clen.201300951
UR  - Kon_2890
ER  - 
@article{
author = "Jović, Milica and Manojlović, Dragan D. and Stanković, Dalibor and Gašić, Uroš M. and Jeremić, Dejan and Brčeski, Ilija and Roglić, Goran",
year = "2015",
abstract = "The aim of this paper was the development and optimization of an electrochemical method for the degradation of two triketone herbicides, mesotrione, and sulcotrione, in a two-electrode undivided electrochemical cell equipped with commercially available, non-modified, electrode materials. The electrochemical parameters studied included five different electrode systems (Zr/Pt, Pd/Pt, C/Pt, Nb/Pt, and Ti/Pt), current densities (27.66, 55.33, ..., 110.66 mA.cm(-2)) and pH values (3, 7, and 9) in 0.05 M sodium sulfate as supporting electrolyte. The electrical energy consumption and chemical oxygen demand were calculated for optimal conditions. The degradation efficiency was determined by high performance liquid chromatography (HPLC) equipped with a diode array detector, while the degradation products for both pesticides were identified and compared by ultra-high performance liquid chromatography (UHPLC)-mass spectrometry. The results could lead to an accurate estimate of their effect on the environment. A real water sample was used to study the influence of organic matter on pesticide degradation. Based on the results obtained the electrochemical treatment could be used for the successful removal of triketone herbicides from contaminated water.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "CLEAN - Soil Air Water",
title = "Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products",
volume = "43",
number = "7",
pages = "1093-1099",
doi = "10.1002/clen.201300951",
url = "Kon_2890"
}
Jović, M., Manojlović, D. D., Stanković, D., Gašić, U. M., Jeremić, D., Brčeski, I.,& Roglić, G.. (2015). Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products. in CLEAN - Soil Air Water
Wiley-Blackwell, Hoboken., 43(7), 1093-1099.
https://doi.org/10.1002/clen.201300951
Kon_2890
Jović M, Manojlović DD, Stanković D, Gašić UM, Jeremić D, Brčeski I, Roglić G. Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products. in CLEAN - Soil Air Water. 2015;43(7):1093-1099.
doi:10.1002/clen.201300951
Kon_2890 .
Jović, Milica, Manojlović, Dragan D., Stanković, Dalibor, Gašić, Uroš M., Jeremić, Dejan, Brčeski, Ilija, Roglić, Goran, "Electrochemical Degradation of Triketone Herbicides and Identification of Their Main Degradation Products" in CLEAN - Soil Air Water, 43, no. 7 (2015):1093-1099,
https://doi.org/10.1002/clen.201300951 .,
Kon_2890 .
1
2
2
2

Synthesis and spectroscopic properties of large single-crystals of Pb(II), Hg(II) and Sr(II) methanesulfonato 1D coordination polymers

Đorđević, Milena; Jeremić, Dejan; Kaluđerović, Goran N.; Gomez-Ruiz, Santiago; Anđelković, Boban D.; Radanović, Dušanka D.; Brčeski, Ilija

(Pergamon-Elsevier Science Ltd, Oxford, 2014)

TY  - JOUR
AU  - Đorđević, Milena
AU  - Jeremić, Dejan
AU  - Kaluđerović, Goran N.
AU  - Gomez-Ruiz, Santiago
AU  - Anđelković, Boban D.
AU  - Radanović, Dušanka D.
AU  - Brčeski, Ilija
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1841
AB  - Three new 1D coordination polymers, [Pb-2(CH3SO3)(4)(H2O)(2)](n), [Hg(CH3SO3)(2)(H2O)(2)](n) and [Sr(CH3SO3)(2)(H2O)](n), were synthesized as large single crystals. The crystals were analyzed and characterized by the means of X-ray analysis, IR and NMR spectroscopy, elemental analysis and solid state UV-Vis spectroscopy. The formation of 1D polymeric chains in the crystal structures of the title compounds is affected by the various bonding modes of the bridging methanesulfonate groups. The studied compounds showed no decomposition in the air. (C) 2014 Elsevier Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Polyhedron
T1  - Synthesis and spectroscopic properties of large single-crystals of Pb(II), Hg(II) and Sr(II) methanesulfonato 1D coordination polymers
VL  - 80
SP  - 282
EP  - 289
DO  - 10.1016/j.poly.2014.05.056
UR  - Kon_2724
ER  - 
@article{
author = "Đorđević, Milena and Jeremić, Dejan and Kaluđerović, Goran N. and Gomez-Ruiz, Santiago and Anđelković, Boban D. and Radanović, Dušanka D. and Brčeski, Ilija",
year = "2014",
abstract = "Three new 1D coordination polymers, [Pb-2(CH3SO3)(4)(H2O)(2)](n), [Hg(CH3SO3)(2)(H2O)(2)](n) and [Sr(CH3SO3)(2)(H2O)](n), were synthesized as large single crystals. The crystals were analyzed and characterized by the means of X-ray analysis, IR and NMR spectroscopy, elemental analysis and solid state UV-Vis spectroscopy. The formation of 1D polymeric chains in the crystal structures of the title compounds is affected by the various bonding modes of the bridging methanesulfonate groups. The studied compounds showed no decomposition in the air. (C) 2014 Elsevier Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Polyhedron",
title = "Synthesis and spectroscopic properties of large single-crystals of Pb(II), Hg(II) and Sr(II) methanesulfonato 1D coordination polymers",
volume = "80",
pages = "282-289",
doi = "10.1016/j.poly.2014.05.056",
url = "Kon_2724"
}
Đorđević, M., Jeremić, D., Kaluđerović, G. N., Gomez-Ruiz, S., Anđelković, B. D., Radanović, D. D.,& Brčeski, I.. (2014). Synthesis and spectroscopic properties of large single-crystals of Pb(II), Hg(II) and Sr(II) methanesulfonato 1D coordination polymers. in Polyhedron
Pergamon-Elsevier Science Ltd, Oxford., 80, 282-289.
https://doi.org/10.1016/j.poly.2014.05.056
Kon_2724
Đorđević M, Jeremić D, Kaluđerović GN, Gomez-Ruiz S, Anđelković BD, Radanović DD, Brčeski I. Synthesis and spectroscopic properties of large single-crystals of Pb(II), Hg(II) and Sr(II) methanesulfonato 1D coordination polymers. in Polyhedron. 2014;80:282-289.
doi:10.1016/j.poly.2014.05.056
Kon_2724 .
Đorđević, Milena, Jeremić, Dejan, Kaluđerović, Goran N., Gomez-Ruiz, Santiago, Anđelković, Boban D., Radanović, Dušanka D., Brčeski, Ilija, "Synthesis and spectroscopic properties of large single-crystals of Pb(II), Hg(II) and Sr(II) methanesulfonato 1D coordination polymers" in Polyhedron, 80 (2014):282-289,
https://doi.org/10.1016/j.poly.2014.05.056 .,
Kon_2724 .
1
1

Synthesis, structure and biological activities of Pd(II) and Pt(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone

Đorđević, Milena M.; Jeremić, Dejan; Rodić, Marko; Simic, Vera S.; Brčeski, Ilija; Leovac, Vukadin M.

(Pergamon-Elsevier Science Ltd, Oxford, 2014)

TY  - JOUR
AU  - Đorđević, Milena M.
AU  - Jeremić, Dejan
AU  - Rodić, Marko
AU  - Simic, Vera S.
AU  - Brčeski, Ilija
AU  - Leovac, Vukadin M.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1504
AB  - The reaction of an ethanolic solution of the newly synthesized 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone (HL) with aqueous solutions of K-2[MCl4] (M = Pd(II), Pt(II)) resulted in neutral complexes of the general formulae [M(L)Cl]. These complexes have a square-planar structure that was achieved by tridentate PNO coordination of the monoprotonated Schiff base and a chloride ligand. The ligand and its metal complexes were analyzed for their antimicrobial activity and their in vitro cytotoxicity in human larynx carcinoma cells (Hep-2) and non-cancerous human lung fibroblast cells (MRC-5). The platinum(II) complex shows cytotoxicity towards Hep-2 cells comparable to oxaliplatin and exhibited improved selectivity for cancer cells. The ligand and its complexes were characterized by elemental analysis, NMR and IR spectroscopy, and single crystal X-ray diffraction analysis. (C) 2013 Elsevier Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Polyhedron
T1  - Synthesis, structure and biological activities of Pd(II) and Pt(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone
VL  - 68
SP  - 234
EP  - 240
DO  - 10.1016/j.poly.2013.10.029
UR  - Kon_2624
ER  - 
@article{
author = "Đorđević, Milena M. and Jeremić, Dejan and Rodić, Marko and Simic, Vera S. and Brčeski, Ilija and Leovac, Vukadin M.",
year = "2014",
abstract = "The reaction of an ethanolic solution of the newly synthesized 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone (HL) with aqueous solutions of K-2[MCl4] (M = Pd(II), Pt(II)) resulted in neutral complexes of the general formulae [M(L)Cl]. These complexes have a square-planar structure that was achieved by tridentate PNO coordination of the monoprotonated Schiff base and a chloride ligand. The ligand and its metal complexes were analyzed for their antimicrobial activity and their in vitro cytotoxicity in human larynx carcinoma cells (Hep-2) and non-cancerous human lung fibroblast cells (MRC-5). The platinum(II) complex shows cytotoxicity towards Hep-2 cells comparable to oxaliplatin and exhibited improved selectivity for cancer cells. The ligand and its complexes were characterized by elemental analysis, NMR and IR spectroscopy, and single crystal X-ray diffraction analysis. (C) 2013 Elsevier Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Polyhedron",
title = "Synthesis, structure and biological activities of Pd(II) and Pt(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone",
volume = "68",
pages = "234-240",
doi = "10.1016/j.poly.2013.10.029",
url = "Kon_2624"
}
Đorđević, M. M., Jeremić, D., Rodić, M., Simic, V. S., Brčeski, I.,& Leovac, V. M.. (2014). Synthesis, structure and biological activities of Pd(II) and Pt(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone. in Polyhedron
Pergamon-Elsevier Science Ltd, Oxford., 68, 234-240.
https://doi.org/10.1016/j.poly.2013.10.029
Kon_2624
Đorđević MM, Jeremić D, Rodić M, Simic VS, Brčeski I, Leovac VM. Synthesis, structure and biological activities of Pd(II) and Pt(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone. in Polyhedron. 2014;68:234-240.
doi:10.1016/j.poly.2013.10.029
Kon_2624 .
Đorđević, Milena M., Jeremić, Dejan, Rodić, Marko, Simic, Vera S., Brčeski, Ilija, Leovac, Vukadin M., "Synthesis, structure and biological activities of Pd(II) and Pt(II) complexes with 2-(diphenylphosphino)benzaldehyde 1-adamantoylhydrazone" in Polyhedron, 68 (2014):234-240,
https://doi.org/10.1016/j.poly.2013.10.029 .,
Kon_2624 .
1
18
20
21

Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid

Đorđević, Milena; Jeremić, Dejan; Anđelković, Katarina K.; Gruden-Pavlović, Maja; Divjaković, Vladimir; Šumar-Ristović, Maja; Brčeski, Ilija

(Serbian Chemical Soc, Belgrade, 2012)

TY  - JOUR
AU  - Đorđević, Milena
AU  - Jeremić, Dejan
AU  - Anđelković, Katarina K.
AU  - Gruden-Pavlović, Maja
AU  - Divjaković, Vladimir
AU  - Šumar-Ristović, Maja
AU  - Brčeski, Ilija
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1553
AB  - In this work, the syntheses and characterization of two novel compounds of adamantane-1-sulfonic acid (1-AdSO(3)H) with cobalt(II) and cadmium(II) are reported. The results of single crystal X-ray analysis of the compounds revealed that adamantane-1-sulfonate (1-AdSO(3)(-)) in the monoanionic form plays different roles in the investigated compounds. Namely, while in compound [Co(H2O)(6)](1-AdSO(3))(2), six water molecules are coordinated to the cobalt(II) ion and 1-AdSO(3)(-) serves as a counter ion, in compound [Cd(H2O)(4)(1-AdSO(3))(2)], two molecules of 1-AdSO(3)(-) are trans-coordinated to the cadmium(II) ion as a monodentate (O)-ligand and the other coordination sites are occupied by water molecules. The obtained compounds showed moderate activity against Artemia salina.
AB  - U ovom radu prikazana je sinteza i karakterizacija dva nova jedinjenja adamantan-1-sulfonske kiseline (1-AdSO3H) sa kobaltom(II) i kadmijumom(II). Rezultati rend- genske strukturne analize datih jedinjenja ukazuju da monoanjon adamantan-1-sulfonata (1-AdSO3 pokazuje različit afinitet prema Co(II) i Cd(II) jonima). U kompleksu [Co(H2O)6](1-AdSO3)2, šest molekula vode se koordinuje za Co(II) jon, dok 1-AdSO3 ima ulogu kontrajona. U kompleksu [Cd(H2O)4(1-AdSO3)2] dva jona 1-AdSO3 su koordinovana za Cd(II) jon kao monodentati u trans položaju preko kiseonikovih atoma, dok su ostala koordinaciona mesta zauzeta molekulima vode. Dobijena jedinjenja su pokazala umerenu aktivnost na Artemia salina.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid
T1  - Nova jedinjenja kobalta(II) i kadmijuma(II) sa adamantan-1-sulfonskom kiselinom
VL  - 77
IS  - 10
SP  - 1391
EP  - 1399
DO  - 10.2298/JSC120419051D
UR  - Kon_2384
ER  - 
@article{
author = "Đorđević, Milena and Jeremić, Dejan and Anđelković, Katarina K. and Gruden-Pavlović, Maja and Divjaković, Vladimir and Šumar-Ristović, Maja and Brčeski, Ilija",
year = "2012",
abstract = "In this work, the syntheses and characterization of two novel compounds of adamantane-1-sulfonic acid (1-AdSO(3)H) with cobalt(II) and cadmium(II) are reported. The results of single crystal X-ray analysis of the compounds revealed that adamantane-1-sulfonate (1-AdSO(3)(-)) in the monoanionic form plays different roles in the investigated compounds. Namely, while in compound [Co(H2O)(6)](1-AdSO(3))(2), six water molecules are coordinated to the cobalt(II) ion and 1-AdSO(3)(-) serves as a counter ion, in compound [Cd(H2O)(4)(1-AdSO(3))(2)], two molecules of 1-AdSO(3)(-) are trans-coordinated to the cadmium(II) ion as a monodentate (O)-ligand and the other coordination sites are occupied by water molecules. The obtained compounds showed moderate activity against Artemia salina., U ovom radu prikazana je sinteza i karakterizacija dva nova jedinjenja adamantan-1-sulfonske kiseline (1-AdSO3H) sa kobaltom(II) i kadmijumom(II). Rezultati rend- genske strukturne analize datih jedinjenja ukazuju da monoanjon adamantan-1-sulfonata (1-AdSO3 pokazuje različit afinitet prema Co(II) i Cd(II) jonima). U kompleksu [Co(H2O)6](1-AdSO3)2, šest molekula vode se koordinuje za Co(II) jon, dok 1-AdSO3 ima ulogu kontrajona. U kompleksu [Cd(H2O)4(1-AdSO3)2] dva jona 1-AdSO3 su koordinovana za Cd(II) jon kao monodentati u trans položaju preko kiseonikovih atoma, dok su ostala koordinaciona mesta zauzeta molekulima vode. Dobijena jedinjenja su pokazala umerenu aktivnost na Artemia salina.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid, Nova jedinjenja kobalta(II) i kadmijuma(II) sa adamantan-1-sulfonskom kiselinom",
volume = "77",
number = "10",
pages = "1391-1399",
doi = "10.2298/JSC120419051D",
url = "Kon_2384"
}
Đorđević, M., Jeremić, D., Anđelković, K. K., Gruden-Pavlović, M., Divjaković, V., Šumar-Ristović, M.,& Brčeski, I.. (2012). Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 77(10), 1391-1399.
https://doi.org/10.2298/JSC120419051D
Kon_2384
Đorđević M, Jeremić D, Anđelković KK, Gruden-Pavlović M, Divjaković V, Šumar-Ristović M, Brčeski I. Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid. in Journal of the Serbian Chemical Society. 2012;77(10):1391-1399.
doi:10.2298/JSC120419051D
Kon_2384 .
Đorđević, Milena, Jeremić, Dejan, Anđelković, Katarina K., Gruden-Pavlović, Maja, Divjaković, Vladimir, Šumar-Ristović, Maja, Brčeski, Ilija, "Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid" in Journal of the Serbian Chemical Society, 77, no. 10 (2012):1391-1399,
https://doi.org/10.2298/JSC120419051D .,
Kon_2384 .
2
1
2

Large Single Crystals of Isomorphous Hexaaquametal(II) D-Camphor-10-sulfonates

Jeremić, Dejan; Kaluđerović, Goran N.; Gomez-Ruiz, Santiago; Brčeski, Ilija; Kasalica, Becko; Leovac, Vukadin M.

(Amer Chemical Soc, Washington, 2010)

TY  - JOUR
AU  - Jeremić, Dejan
AU  - Kaluđerović, Goran N.
AU  - Gomez-Ruiz, Santiago
AU  - Brčeski, Ilija
AU  - Kasalica, Becko
AU  - Leovac, Vukadin M.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1049
AB  - Novel hexaaquametal(II) bis(D-camphor-10-sulfonates) with Mn(II), Fe(II), and Co(II) ions were synthesized as large single crystals. During the crystallization process, suitable metal wires were used to induce crystallization. Crystals were analyzed by means of X-ray analysis, IR spectrophotometry, and solid state UV-vis spectroscopy. The obtained substances are stable in air, and their UV-vis spectra imply their potential use as optical filters and optical materials.
PB  - Amer Chemical Soc, Washington
T2  - Crystal Growth and Design
T1  - Large Single Crystals of Isomorphous Hexaaquametal(II) D-Camphor-10-sulfonates
VL  - 10
IS  - 2
SP  - 559
EP  - 563
DO  - 10.1021/cg9009288
UR  - Kon_2049
ER  - 
@article{
author = "Jeremić, Dejan and Kaluđerović, Goran N. and Gomez-Ruiz, Santiago and Brčeski, Ilija and Kasalica, Becko and Leovac, Vukadin M.",
year = "2010",
abstract = "Novel hexaaquametal(II) bis(D-camphor-10-sulfonates) with Mn(II), Fe(II), and Co(II) ions were synthesized as large single crystals. During the crystallization process, suitable metal wires were used to induce crystallization. Crystals were analyzed by means of X-ray analysis, IR spectrophotometry, and solid state UV-vis spectroscopy. The obtained substances are stable in air, and their UV-vis spectra imply their potential use as optical filters and optical materials.",
publisher = "Amer Chemical Soc, Washington",
journal = "Crystal Growth and Design",
title = "Large Single Crystals of Isomorphous Hexaaquametal(II) D-Camphor-10-sulfonates",
volume = "10",
number = "2",
pages = "559-563",
doi = "10.1021/cg9009288",
url = "Kon_2049"
}
Jeremić, D., Kaluđerović, G. N., Gomez-Ruiz, S., Brčeski, I., Kasalica, B.,& Leovac, V. M.. (2010). Large Single Crystals of Isomorphous Hexaaquametal(II) D-Camphor-10-sulfonates. in Crystal Growth and Design
Amer Chemical Soc, Washington., 10(2), 559-563.
https://doi.org/10.1021/cg9009288
Kon_2049
Jeremić D, Kaluđerović GN, Gomez-Ruiz S, Brčeski I, Kasalica B, Leovac VM. Large Single Crystals of Isomorphous Hexaaquametal(II) D-Camphor-10-sulfonates. in Crystal Growth and Design. 2010;10(2):559-563.
doi:10.1021/cg9009288
Kon_2049 .
Jeremić, Dejan, Kaluđerović, Goran N., Gomez-Ruiz, Santiago, Brčeski, Ilija, Kasalica, Becko, Leovac, Vukadin M., "Large Single Crystals of Isomorphous Hexaaquametal(II) D-Camphor-10-sulfonates" in Crystal Growth and Design, 10, no. 2 (2010):559-563,
https://doi.org/10.1021/cg9009288 .,
Kon_2049 .
12
21
21

Synthesis and characterization of new Pt(II) and Pd(II) complexes with 2-quinolinecarboxaldehyde selenosemicarbazone: Cytotoxic activity evaluation of Cd(II), Zn(II), Ni(II), Pt(II) and Pd(II) complexes with heteroaromatic selenosemicarbazones

Gligorijević, Nevenka; Todorović, Tamara; Radulović, Siniša; Sladić, Dušan; Filipović, Nenad R.; Gođevac, Dejan; Jeremić, Dejan; Anđelković, Katarina K.

(Elsevier France-Editions Scientifiques Medicales Elsevier, Issy-Les-Moulineaux, 2009)

TY  - JOUR
AU  - Gligorijević, Nevenka
AU  - Todorović, Tamara
AU  - Radulović, Siniša
AU  - Sladić, Dušan
AU  - Filipović, Nenad R.
AU  - Gođevac, Dejan
AU  - Jeremić, Dejan
AU  - Anđelković, Katarina K.
PY  - 2009
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/625
AB  - New complexes of Pt(II) and Pd(II) with 2-quinolinecarboxaldehyde selenosemicarbazone were synthesized and characterized by elemental analysis, NMR and IR spectroscopy and molar conductivity measurements. The assumed geometry of Pt(II) and Pd(II) complexes was square planar where the ligand was tridentately coordinated via the quinoline and imine nitrogen atoms and the selenium atom. The cytotoxic activity of the new Pt(II) and Pd(II) compounds, as well as of some previously synthesized Cd(II), Zn(II) and Ni(II) complexes with the same or analogous ligand, was tested against a panel of three human cancer cell lines: human cervix carcinoma cells (HeLa), human melanoma cells (FemX) and breast cancer cells (MDA-361). All investigated compounds, except Pt(II) complex, possess a strong dose-dependent cytotoxic activity of the same order of magnitude as cisplatin (CDDP). The investigation of potential of these compounds to induce HeLa cell cycle perturbations was also evaluated. (c) 2008 Elsevier Masson SAS. All rights reserved.
PB  - Elsevier France-Editions Scientifiques Medicales Elsevier, Issy-Les-Moulineaux
T2  - European Journal of Medicinal Chemistry
T1  - Synthesis and characterization of new Pt(II) and Pd(II) complexes with 2-quinolinecarboxaldehyde selenosemicarbazone: Cytotoxic activity evaluation of Cd(II), Zn(II), Ni(II), Pt(II) and Pd(II) complexes with heteroaromatic selenosemicarbazones
VL  - 44
IS  - 4
SP  - 1623
EP  - 1629
DO  - 10.1016/j.ejmech.2008.07.033
UR  - Kon_1974
ER  - 
@article{
author = "Gligorijević, Nevenka and Todorović, Tamara and Radulović, Siniša and Sladić, Dušan and Filipović, Nenad R. and Gođevac, Dejan and Jeremić, Dejan and Anđelković, Katarina K.",
year = "2009",
abstract = "New complexes of Pt(II) and Pd(II) with 2-quinolinecarboxaldehyde selenosemicarbazone were synthesized and characterized by elemental analysis, NMR and IR spectroscopy and molar conductivity measurements. The assumed geometry of Pt(II) and Pd(II) complexes was square planar where the ligand was tridentately coordinated via the quinoline and imine nitrogen atoms and the selenium atom. The cytotoxic activity of the new Pt(II) and Pd(II) compounds, as well as of some previously synthesized Cd(II), Zn(II) and Ni(II) complexes with the same or analogous ligand, was tested against a panel of three human cancer cell lines: human cervix carcinoma cells (HeLa), human melanoma cells (FemX) and breast cancer cells (MDA-361). All investigated compounds, except Pt(II) complex, possess a strong dose-dependent cytotoxic activity of the same order of magnitude as cisplatin (CDDP). The investigation of potential of these compounds to induce HeLa cell cycle perturbations was also evaluated. (c) 2008 Elsevier Masson SAS. All rights reserved.",
publisher = "Elsevier France-Editions Scientifiques Medicales Elsevier, Issy-Les-Moulineaux",
journal = "European Journal of Medicinal Chemistry",
title = "Synthesis and characterization of new Pt(II) and Pd(II) complexes with 2-quinolinecarboxaldehyde selenosemicarbazone: Cytotoxic activity evaluation of Cd(II), Zn(II), Ni(II), Pt(II) and Pd(II) complexes with heteroaromatic selenosemicarbazones",
volume = "44",
number = "4",
pages = "1623-1629",
doi = "10.1016/j.ejmech.2008.07.033",
url = "Kon_1974"
}
Gligorijević, N., Todorović, T., Radulović, S., Sladić, D., Filipović, N. R., Gođevac, D., Jeremić, D.,& Anđelković, K. K.. (2009). Synthesis and characterization of new Pt(II) and Pd(II) complexes with 2-quinolinecarboxaldehyde selenosemicarbazone: Cytotoxic activity evaluation of Cd(II), Zn(II), Ni(II), Pt(II) and Pd(II) complexes with heteroaromatic selenosemicarbazones. in European Journal of Medicinal Chemistry
Elsevier France-Editions Scientifiques Medicales Elsevier, Issy-Les-Moulineaux., 44(4), 1623-1629.
https://doi.org/10.1016/j.ejmech.2008.07.033
Kon_1974
Gligorijević N, Todorović T, Radulović S, Sladić D, Filipović NR, Gođevac D, Jeremić D, Anđelković KK. Synthesis and characterization of new Pt(II) and Pd(II) complexes with 2-quinolinecarboxaldehyde selenosemicarbazone: Cytotoxic activity evaluation of Cd(II), Zn(II), Ni(II), Pt(II) and Pd(II) complexes with heteroaromatic selenosemicarbazones. in European Journal of Medicinal Chemistry. 2009;44(4):1623-1629.
doi:10.1016/j.ejmech.2008.07.033
Kon_1974 .
Gligorijević, Nevenka, Todorović, Tamara, Radulović, Siniša, Sladić, Dušan, Filipović, Nenad R., Gođevac, Dejan, Jeremić, Dejan, Anđelković, Katarina K., "Synthesis and characterization of new Pt(II) and Pd(II) complexes with 2-quinolinecarboxaldehyde selenosemicarbazone: Cytotoxic activity evaluation of Cd(II), Zn(II), Ni(II), Pt(II) and Pd(II) complexes with heteroaromatic selenosemicarbazones" in European Journal of Medicinal Chemistry, 44, no. 4 (2009):1623-1629,
https://doi.org/10.1016/j.ejmech.2008.07.033 .,
Kon_1974 .
43
48
44

Tetraaquabis(D-camphor-10-sulfonato)calcium(II)

Jeremić, Dejan; Kaluđerović, Goran N.; Gomez-Ruiz, Santiago; Brčeski, Ilija; Anđelković, Katarina K.

(Wiley-Blackwell Publishing, Inc, Malden, 2009)

TY  - JOUR
AU  - Jeremić, Dejan
AU  - Kaluđerović, Goran N.
AU  - Gomez-Ruiz, Santiago
AU  - Brčeski, Ilija
AU  - Anđelković, Katarina K.
PY  - 2009
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/620
AB  - The structure of the title compound, [Ca(C(10)H(15)O(4)S)(2)(H(2)O)(4)], is the first example in which two d-camphor-10-sulfonate anions are coordinated to a metal ion, in this case with direct Ca-O bonding. The molecule has crystallographically imposed twofold symmetry with the Ca atom on the twofold axis. Hydrogen bonds are formed between the coordinated water molecules and the O atoms of the SO(3)(-) groups of adjacent molecules, leading to the formation of a two-dimensional layered network. The compound displays sharp wavelength-selective transparency in the UV-visible spectrum, offering the potential for application as an optical filter.
PB  - Wiley-Blackwell Publishing, Inc, Malden
T2  - Acta Crystallographica. Section C: Crystal Structure Communications
T1  - Tetraaquabis(D-camphor-10-sulfonato)calcium(II)
VL  - 65
DO  - 10.1107/S0108270109004193
UR  - Kon_1969
ER  - 
@article{
author = "Jeremić, Dejan and Kaluđerović, Goran N. and Gomez-Ruiz, Santiago and Brčeski, Ilija and Anđelković, Katarina K.",
year = "2009",
abstract = "The structure of the title compound, [Ca(C(10)H(15)O(4)S)(2)(H(2)O)(4)], is the first example in which two d-camphor-10-sulfonate anions are coordinated to a metal ion, in this case with direct Ca-O bonding. The molecule has crystallographically imposed twofold symmetry with the Ca atom on the twofold axis. Hydrogen bonds are formed between the coordinated water molecules and the O atoms of the SO(3)(-) groups of adjacent molecules, leading to the formation of a two-dimensional layered network. The compound displays sharp wavelength-selective transparency in the UV-visible spectrum, offering the potential for application as an optical filter.",
publisher = "Wiley-Blackwell Publishing, Inc, Malden",
journal = "Acta Crystallographica. Section C: Crystal Structure Communications",
title = "Tetraaquabis(D-camphor-10-sulfonato)calcium(II)",
volume = "65",
doi = "10.1107/S0108270109004193",
url = "Kon_1969"
}
Jeremić, D., Kaluđerović, G. N., Gomez-Ruiz, S., Brčeski, I.,& Anđelković, K. K.. (2009). Tetraaquabis(D-camphor-10-sulfonato)calcium(II). in Acta Crystallographica. Section C: Crystal Structure Communications
Wiley-Blackwell Publishing, Inc, Malden., 65.
https://doi.org/10.1107/S0108270109004193
Kon_1969
Jeremić D, Kaluđerović GN, Gomez-Ruiz S, Brčeski I, Anđelković KK. Tetraaquabis(D-camphor-10-sulfonato)calcium(II). in Acta Crystallographica. Section C: Crystal Structure Communications. 2009;65.
doi:10.1107/S0108270109004193
Kon_1969 .
Jeremić, Dejan, Kaluđerović, Goran N., Gomez-Ruiz, Santiago, Brčeski, Ilija, Anđelković, Katarina K., "Tetraaquabis(D-camphor-10-sulfonato)calcium(II)" in Acta Crystallographica. Section C: Crystal Structure Communications, 65 (2009),
https://doi.org/10.1107/S0108270109004193 .,
Kon_1969 .
2
3
3

Hexaaquamagnesium(II) bis(D-camphor-10-sulfonate)

Jeremić, Dejan; Kaluđerović, Goran N.; Brčeski, Ilija; Gomez-Ruiz, Santiago; Anđelković, Katarina K.

(Blackwell Publishing, Oxford, 2008)

TY  - JOUR
AU  - Jeremić, Dejan
AU  - Kaluđerović, Goran N.
AU  - Brčeski, Ilija
AU  - Gomez-Ruiz, Santiago
AU  - Anđelković, Katarina K.
PY  - 2008
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/950
AB  - The structure of the title complex, [Mg(H2O)(6)](C10H15O4S)(2), consists of regular octahedral [Mg(H2O)(6)](2+) cations and D-camphor-10-sulfonate anions. A three-dimensional supra-molecular architecture is formed via hydrogen-bond interactions [O-H center dot center dot center dot O = 2.723 (2)-2.833 (2) angstrom] to give alternating layers of [Mg(H2O)(6)](2+) cations and D-camphor-10-sulfonate anions. The title compound is isomorphous with the zinc, copper, cadmium and nickel analogues.
PB  - Blackwell Publishing, Oxford
T2  - Acta Crystallographica. Section E: Structure Reports Online
T1  - Hexaaquamagnesium(II) bis(D-camphor-10-sulfonate)
VL  - 64
DO  - 10.1107/S1600536808018047
UR  - Kon_1903
ER  - 
@article{
author = "Jeremić, Dejan and Kaluđerović, Goran N. and Brčeski, Ilija and Gomez-Ruiz, Santiago and Anđelković, Katarina K.",
year = "2008",
abstract = "The structure of the title complex, [Mg(H2O)(6)](C10H15O4S)(2), consists of regular octahedral [Mg(H2O)(6)](2+) cations and D-camphor-10-sulfonate anions. A three-dimensional supra-molecular architecture is formed via hydrogen-bond interactions [O-H center dot center dot center dot O = 2.723 (2)-2.833 (2) angstrom] to give alternating layers of [Mg(H2O)(6)](2+) cations and D-camphor-10-sulfonate anions. The title compound is isomorphous with the zinc, copper, cadmium and nickel analogues.",
publisher = "Blackwell Publishing, Oxford",
journal = "Acta Crystallographica. Section E: Structure Reports Online",
title = "Hexaaquamagnesium(II) bis(D-camphor-10-sulfonate)",
volume = "64",
doi = "10.1107/S1600536808018047",
url = "Kon_1903"
}
Jeremić, D., Kaluđerović, G. N., Brčeski, I., Gomez-Ruiz, S.,& Anđelković, K. K.. (2008). Hexaaquamagnesium(II) bis(D-camphor-10-sulfonate). in Acta Crystallographica. Section E: Structure Reports Online
Blackwell Publishing, Oxford., 64.
https://doi.org/10.1107/S1600536808018047
Kon_1903
Jeremić D, Kaluđerović GN, Brčeski I, Gomez-Ruiz S, Anđelković KK. Hexaaquamagnesium(II) bis(D-camphor-10-sulfonate). in Acta Crystallographica. Section E: Structure Reports Online. 2008;64.
doi:10.1107/S1600536808018047
Kon_1903 .
Jeremić, Dejan, Kaluđerović, Goran N., Brčeski, Ilija, Gomez-Ruiz, Santiago, Anđelković, Katarina K., "Hexaaquamagnesium(II) bis(D-camphor-10-sulfonate)" in Acta Crystallographica. Section E: Structure Reports Online, 64 (2008),
https://doi.org/10.1107/S1600536808018047 .,
Kon_1903 .
3
4
4

Synthesis, structural characterization and cytotoxic activity of two new organoruthenium(II) complexes

Grgurić-Šipka, Sanja; Alshtewi, Mohamed Al. Arbi M.; Jeremić, Dejan; Kaluđerović, Goran N.; Gomez-Ruiz, Santiago; Zizak, Zeljko; Juranić, Zorica D.; Sabo, Tibor

(Serbian Chemical Soc, Belgrade, 2008)

TY  - JOUR
AU  - Grgurić-Šipka, Sanja
AU  - Alshtewi, Mohamed Al. Arbi M.
AU  - Jeremić, Dejan
AU  - Kaluđerović, Goran N.
AU  - Gomez-Ruiz, Santiago
AU  - Zizak, Zeljko
AU  - Juranić, Zorica D.
AU  - Sabo, Tibor
PY  - 2008
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/966
AB  - Two new p-cymene ruthenium(II) complexes containing as additional ligands N-methylpiperazine ([(eta(6)-p-cymene)RuCl2(CH3NH(CH2)(4)NH)]PF6, complex 1) or vitamin K-3-thiosemicarbazone ([(eta(6)-p-cymene)RuCl2(K(3)tsc)], complex 2) were synthesized starting from [(eta(6)-p-cymene)(2)RuCl2](2) and the corresponding ligand. The complexes were characterized by elemental analysis, IR, electronic absorption and NMR spectroscopy. The X-ray crystal structure determination of complex 1 revealed "piano-stool" geometry. The differences in the cytotoxic activity of the two complexes are discussed in terms of the ligand present.
AB  - Sintetisana su dva nova p-cimen-rutenijum(II) kompleksa koji sadrže kao dodatne ligande N-metilpiperazin ([(h6-p-cimen)RuCl2(CH3NH(CH2)4NH)]PF6, kompleks 1) i vitamin K3-tiosemikarbazon ([(h6-p-cimen)RuCl2(K3tsc)], kompleks 2). Oba nova kompleksa dobijena su polazeći od [(h6-p-cimen)2RuCl2]2 kompleksa i odgovarajućeg liganda. Kompleksi su okarakterisani elementalnom analizom, IC, elektronsko-apsorpcionom i NMR spektroskopijom. Rendgeno-strukturna analiza kompleksa 1 pokazala je “piano-stool” geometriju. U zavisnosti od prisutnog liganda diskutovana je razlika u citotoksičnoj aktivnosti ova dva dobijena kompleksa.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis, structural characterization and cytotoxic activity of two new organoruthenium(II) complexes
T1  - Sinteza, strukturna karakterizacija i citotoksična aktivnost dva nova organorutenijum(II) kompleksa
VL  - 73
IS  - 6
SP  - 619
EP  - 630
DO  - 10.2298/JSC0806619G
UR  - Kon_1919
ER  - 
@article{
author = "Grgurić-Šipka, Sanja and Alshtewi, Mohamed Al. Arbi M. and Jeremić, Dejan and Kaluđerović, Goran N. and Gomez-Ruiz, Santiago and Zizak, Zeljko and Juranić, Zorica D. and Sabo, Tibor",
year = "2008",
abstract = "Two new p-cymene ruthenium(II) complexes containing as additional ligands N-methylpiperazine ([(eta(6)-p-cymene)RuCl2(CH3NH(CH2)(4)NH)]PF6, complex 1) or vitamin K-3-thiosemicarbazone ([(eta(6)-p-cymene)RuCl2(K(3)tsc)], complex 2) were synthesized starting from [(eta(6)-p-cymene)(2)RuCl2](2) and the corresponding ligand. The complexes were characterized by elemental analysis, IR, electronic absorption and NMR spectroscopy. The X-ray crystal structure determination of complex 1 revealed "piano-stool" geometry. The differences in the cytotoxic activity of the two complexes are discussed in terms of the ligand present., Sintetisana su dva nova p-cimen-rutenijum(II) kompleksa koji sadrže kao dodatne ligande N-metilpiperazin ([(h6-p-cimen)RuCl2(CH3NH(CH2)4NH)]PF6, kompleks 1) i vitamin K3-tiosemikarbazon ([(h6-p-cimen)RuCl2(K3tsc)], kompleks 2). Oba nova kompleksa dobijena su polazeći od [(h6-p-cimen)2RuCl2]2 kompleksa i odgovarajućeg liganda. Kompleksi su okarakterisani elementalnom analizom, IC, elektronsko-apsorpcionom i NMR spektroskopijom. Rendgeno-strukturna analiza kompleksa 1 pokazala je “piano-stool” geometriju. U zavisnosti od prisutnog liganda diskutovana je razlika u citotoksičnoj aktivnosti ova dva dobijena kompleksa.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis, structural characterization and cytotoxic activity of two new organoruthenium(II) complexes, Sinteza, strukturna karakterizacija i citotoksična aktivnost dva nova organorutenijum(II) kompleksa",
volume = "73",
number = "6",
pages = "619-630",
doi = "10.2298/JSC0806619G",
url = "Kon_1919"
}
Grgurić-Šipka, S., Alshtewi, M. Al. A. M., Jeremić, D., Kaluđerović, G. N., Gomez-Ruiz, S., Zizak, Z., Juranić, Z. D.,& Sabo, T.. (2008). Synthesis, structural characterization and cytotoxic activity of two new organoruthenium(II) complexes. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 73(6), 619-630.
https://doi.org/10.2298/JSC0806619G
Kon_1919
Grgurić-Šipka S, Alshtewi MAAM, Jeremić D, Kaluđerović GN, Gomez-Ruiz S, Zizak Z, Juranić ZD, Sabo T. Synthesis, structural characterization and cytotoxic activity of two new organoruthenium(II) complexes. in Journal of the Serbian Chemical Society. 2008;73(6):619-630.
doi:10.2298/JSC0806619G
Kon_1919 .
Grgurić-Šipka, Sanja, Alshtewi, Mohamed Al. Arbi M., Jeremić, Dejan, Kaluđerović, Goran N., Gomez-Ruiz, Santiago, Zizak, Zeljko, Juranić, Zorica D., Sabo, Tibor, "Synthesis, structural characterization and cytotoxic activity of two new organoruthenium(II) complexes" in Journal of the Serbian Chemical Society, 73, no. 6 (2008):619-630,
https://doi.org/10.2298/JSC0806619G .,
Kon_1919 .
10
9
14

Synthesis, characterization and biological activity evaluation of novel Pd(II) and Pt(II) complexes with heterocyclic hydrazone ligands

Filipović, Nenad R.; Todorović, Tamara; Sladić, Dušan; Novaković, Irena T.; Jeremić, Dejan; Anđelković, Katarina K.

(Trans Tech Publications Ltd, Durnten-Zurich, 2007)

TY  - CONF
AU  - Filipović, Nenad R.
AU  - Todorović, Tamara
AU  - Sladić, Dušan
AU  - Novaković, Irena T.
AU  - Jeremić, Dejan
AU  - Anđelković, Katarina K.
PY  - 2007
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/866
AB  - New complexes of Pt(II) with condensation derivatives of ethyl hydrazino acetate and either 2-acetylpyridine or 2-quinolinecarboxaldehyde, and of Pd(II) with the condensation derivative of ethyl hydrazinoacetate and 2-quinolinecarboxaldehyde were synthesized and characterized by elemental analysis, IR, H-1- and C-13-NMR spectroscopy, and molar conductivity measurements. The complexes have a square planar geometry, ligands binding as bidentates in the neutral form, and the remaining two coordination sites being occupied by chloride ions. Biological activity of new complexes, and of previously synthesized Pd(II), Cd(II), Co(III) and Zn(II) complexes with this ligand type was evaluated by the brine shrimp test. All the complexes showed a moderate activity.
PB  - Trans Tech Publications Ltd, Durnten-Zurich
C3  - Materials Science Forum
T1  - Synthesis, characterization and biological activity evaluation of novel Pd(II) and Pt(II) complexes with heterocyclic hydrazone ligands
VL  - 555
SP  - 423
EP  - 427
DO  - 10.4028/www.scientific.net/MSF.555.423
UR  - Kon_1819
ER  - 
@conference{
author = "Filipović, Nenad R. and Todorović, Tamara and Sladić, Dušan and Novaković, Irena T. and Jeremić, Dejan and Anđelković, Katarina K.",
year = "2007",
abstract = "New complexes of Pt(II) with condensation derivatives of ethyl hydrazino acetate and either 2-acetylpyridine or 2-quinolinecarboxaldehyde, and of Pd(II) with the condensation derivative of ethyl hydrazinoacetate and 2-quinolinecarboxaldehyde were synthesized and characterized by elemental analysis, IR, H-1- and C-13-NMR spectroscopy, and molar conductivity measurements. The complexes have a square planar geometry, ligands binding as bidentates in the neutral form, and the remaining two coordination sites being occupied by chloride ions. Biological activity of new complexes, and of previously synthesized Pd(II), Cd(II), Co(III) and Zn(II) complexes with this ligand type was evaluated by the brine shrimp test. All the complexes showed a moderate activity.",
publisher = "Trans Tech Publications Ltd, Durnten-Zurich",
journal = "Materials Science Forum",
title = "Synthesis, characterization and biological activity evaluation of novel Pd(II) and Pt(II) complexes with heterocyclic hydrazone ligands",
volume = "555",
pages = "423-427",
doi = "10.4028/www.scientific.net/MSF.555.423",
url = "Kon_1819"
}
Filipović, N. R., Todorović, T., Sladić, D., Novaković, I. T., Jeremić, D.,& Anđelković, K. K.. (2007). Synthesis, characterization and biological activity evaluation of novel Pd(II) and Pt(II) complexes with heterocyclic hydrazone ligands. in Materials Science Forum
Trans Tech Publications Ltd, Durnten-Zurich., 555, 423-427.
https://doi.org/10.4028/www.scientific.net/MSF.555.423
Kon_1819
Filipović NR, Todorović T, Sladić D, Novaković IT, Jeremić D, Anđelković KK. Synthesis, characterization and biological activity evaluation of novel Pd(II) and Pt(II) complexes with heterocyclic hydrazone ligands. in Materials Science Forum. 2007;555:423-427.
doi:10.4028/www.scientific.net/MSF.555.423
Kon_1819 .
Filipović, Nenad R., Todorović, Tamara, Sladić, Dušan, Novaković, Irena T., Jeremić, Dejan, Anđelković, Katarina K., "Synthesis, characterization and biological activity evaluation of novel Pd(II) and Pt(II) complexes with heterocyclic hydrazone ligands" in Materials Science Forum, 555 (2007):423-427,
https://doi.org/10.4028/www.scientific.net/MSF.555.423 .,
Kon_1819 .
8
9
9

Investigation of thermal stability of Zn(II), Pt(II) and Pd(II) complexes with (E)-2-oxo-2-(N-[1-(pyridin-2-yl)ethylidene]hydrazino}acetamide

Todorović, Tamara; Anđelković, Katarina K.; Sladić, Dušan; Jeremić, Dejan; Minić, Dragica M.

(Trans Tech Publications Ltd, Zurich-Uetikon, 2005)

TY  - JOUR
AU  - Todorović, Tamara
AU  - Anđelković, Katarina K.
AU  - Sladić, Dušan
AU  - Jeremić, Dejan
AU  - Minić, Dragica M.
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/724
AB  - Thermal stability of neutral Zn(II), Pd(II) and Pt(II) complexes of formulae [Zn(apsox)(2)](.)3H(2)O and [M(apsox)Cl] (M=Pd(II), Pt(II), HL=(E)-2-oxo-2-{N -[1-(pyridin-2yl)ethylidene]hydrazino)acetamide) were studied. The results of DSC and TG analyses within the temperature range from 20 to 600 degrees C in nitrogen atmosphere showed that the loss of crystal water represents the first step during decomposition of the octahedral Zn(II) complex followed by structural rearrangement of its anhydrous form. After that the complex remained stable to about 330 degrees C. Different from neutral square-planar Pd(II) and Pt(II) complexes, a satisfactory resolution of the peaks in DSC of the Zn(II) complex enabled determination of the activation energies of its structural transformation and thermal degradation.
PB  - Trans Tech Publications Ltd, Zurich-Uetikon
T2  - Materials Science Forum
T1  - Investigation of thermal stability of Zn(II), Pt(II) and Pd(II) complexes with (E)-2-oxo-2-(N-[1-(pyridin-2-yl)ethylidene]hydrazino}acetamide
VL  - 494
SP  - 375
EP  - 379
DO  - 10.4028/0-87849-971-7.375
UR  - Kon_1677
ER  - 
@article{
author = "Todorović, Tamara and Anđelković, Katarina K. and Sladić, Dušan and Jeremić, Dejan and Minić, Dragica M.",
year = "2005",
abstract = "Thermal stability of neutral Zn(II), Pd(II) and Pt(II) complexes of formulae [Zn(apsox)(2)](.)3H(2)O and [M(apsox)Cl] (M=Pd(II), Pt(II), HL=(E)-2-oxo-2-{N -[1-(pyridin-2yl)ethylidene]hydrazino)acetamide) were studied. The results of DSC and TG analyses within the temperature range from 20 to 600 degrees C in nitrogen atmosphere showed that the loss of crystal water represents the first step during decomposition of the octahedral Zn(II) complex followed by structural rearrangement of its anhydrous form. After that the complex remained stable to about 330 degrees C. Different from neutral square-planar Pd(II) and Pt(II) complexes, a satisfactory resolution of the peaks in DSC of the Zn(II) complex enabled determination of the activation energies of its structural transformation and thermal degradation.",
publisher = "Trans Tech Publications Ltd, Zurich-Uetikon",
journal = "Materials Science Forum",
title = "Investigation of thermal stability of Zn(II), Pt(II) and Pd(II) complexes with (E)-2-oxo-2-(N-[1-(pyridin-2-yl)ethylidene]hydrazino}acetamide",
volume = "494",
pages = "375-379",
doi = "10.4028/0-87849-971-7.375",
url = "Kon_1677"
}
Todorović, T., Anđelković, K. K., Sladić, D., Jeremić, D.,& Minić, D. M.. (2005). Investigation of thermal stability of Zn(II), Pt(II) and Pd(II) complexes with (E)-2-oxo-2-(N-[1-(pyridin-2-yl)ethylidene]hydrazino}acetamide. in Materials Science Forum
Trans Tech Publications Ltd, Zurich-Uetikon., 494, 375-379.
https://doi.org/10.4028/0-87849-971-7.375
Kon_1677
Todorović T, Anđelković KK, Sladić D, Jeremić D, Minić DM. Investigation of thermal stability of Zn(II), Pt(II) and Pd(II) complexes with (E)-2-oxo-2-(N-[1-(pyridin-2-yl)ethylidene]hydrazino}acetamide. in Materials Science Forum. 2005;494:375-379.
doi:10.4028/0-87849-971-7.375
Kon_1677 .
Todorović, Tamara, Anđelković, Katarina K., Sladić, Dušan, Jeremić, Dejan, Minić, Dragica M., "Investigation of thermal stability of Zn(II), Pt(II) and Pd(II) complexes with (E)-2-oxo-2-(N-[1-(pyridin-2-yl)ethylidene]hydrazino}acetamide" in Materials Science Forum, 494 (2005):375-379,
https://doi.org/10.4028/0-87849-971-7.375 .,
Kon_1677 .

Synthesis and structural characterization of the Co(III) complex with 2 '-[1-(2-pyridinyl)-ethylidene]oxamohydrazide (Hapsox): The crystal structure of bis-{2 '-[1-(2-pyridinyl)-ethylidene]-oxamohydrazido} cobalt(III) perchlorate, [Co(apsox)(2)]ClO4

Anđelković, Katarina K.; Howing, J; Tellgren, R; Jeremić, Dejan; Ivanović-Burmazović, Ivana; Sladić, Dušan

(Taylor & Francis Ltd, Abingdon, 2003)

TY  - JOUR
AU  - Anđelković, Katarina K.
AU  - Howing, J
AU  - Tellgren, R
AU  - Jeremić, Dejan
AU  - Ivanović-Burmazović, Ivana
AU  - Sladić, Dušan
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/145
AB  - The synthesis of a novel ligand 2'-[1-(2-pyridinyl)-ethylidene]-oxamohydrazide (Hapsox), from a series of 2-acetylpyridine acylhydrazones, and its complex with Co(III), which is the first in this series of complexes are described. Both the ligand and the complex were characterized by elemental analysis, IR, H-1-NMR, and C-13-NMR spectra, and the structure of the complex [Co(apsox)(2)]ClO4 was determined by X-ray structural analysis. It was established that [Co(apsox)(2)]ClO4 has an octahedral geometry with two tridentate apsox ligands in monoanionic form. Structural characteristics, lengths of the bonds, and angles between the bonds were typical for Co(III) complexes of distorted octahedral geometry. Both direct and template synthesis afforded the same geometrical isomer of the complex with two apsox ligands meridionally bound to the central metal ion, even in the case when equimolar quantities of Co(ClO4)(2) and Hapsox were applied.
PB  - Taylor & Francis Ltd, Abingdon
T2  - Journal of Coordination Chemistry
T1  - Synthesis and structural characterization of the Co(III) complex with 2 '-[1-(2-pyridinyl)-ethylidene]oxamohydrazide (Hapsox): The crystal structure of bis-{2 '-[1-(2-pyridinyl)-ethylidene]-oxamohydrazido} cobalt(III) perchlorate, [Co(apsox)(2)]ClO4
VL  - 56
IS  - 7
SP  - 611
EP  - 622
DO  - 10.1080/0095897031000113986
UR  - Kon_1540
ER  - 
@article{
author = "Anđelković, Katarina K. and Howing, J and Tellgren, R and Jeremić, Dejan and Ivanović-Burmazović, Ivana and Sladić, Dušan",
year = "2003",
abstract = "The synthesis of a novel ligand 2'-[1-(2-pyridinyl)-ethylidene]-oxamohydrazide (Hapsox), from a series of 2-acetylpyridine acylhydrazones, and its complex with Co(III), which is the first in this series of complexes are described. Both the ligand and the complex were characterized by elemental analysis, IR, H-1-NMR, and C-13-NMR spectra, and the structure of the complex [Co(apsox)(2)]ClO4 was determined by X-ray structural analysis. It was established that [Co(apsox)(2)]ClO4 has an octahedral geometry with two tridentate apsox ligands in monoanionic form. Structural characteristics, lengths of the bonds, and angles between the bonds were typical for Co(III) complexes of distorted octahedral geometry. Both direct and template synthesis afforded the same geometrical isomer of the complex with two apsox ligands meridionally bound to the central metal ion, even in the case when equimolar quantities of Co(ClO4)(2) and Hapsox were applied.",
publisher = "Taylor & Francis Ltd, Abingdon",
journal = "Journal of Coordination Chemistry",
title = "Synthesis and structural characterization of the Co(III) complex with 2 '-[1-(2-pyridinyl)-ethylidene]oxamohydrazide (Hapsox): The crystal structure of bis-{2 '-[1-(2-pyridinyl)-ethylidene]-oxamohydrazido} cobalt(III) perchlorate, [Co(apsox)(2)]ClO4",
volume = "56",
number = "7",
pages = "611-622",
doi = "10.1080/0095897031000113986",
url = "Kon_1540"
}
Anđelković, K. K., Howing, J., Tellgren, R., Jeremić, D., Ivanović-Burmazović, I.,& Sladić, D.. (2003). Synthesis and structural characterization of the Co(III) complex with 2 '-[1-(2-pyridinyl)-ethylidene]oxamohydrazide (Hapsox): The crystal structure of bis-{2 '-[1-(2-pyridinyl)-ethylidene]-oxamohydrazido} cobalt(III) perchlorate, [Co(apsox)(2)]ClO4. in Journal of Coordination Chemistry
Taylor & Francis Ltd, Abingdon., 56(7), 611-622.
https://doi.org/10.1080/0095897031000113986
Kon_1540
Anđelković KK, Howing J, Tellgren R, Jeremić D, Ivanović-Burmazović I, Sladić D. Synthesis and structural characterization of the Co(III) complex with 2 '-[1-(2-pyridinyl)-ethylidene]oxamohydrazide (Hapsox): The crystal structure of bis-{2 '-[1-(2-pyridinyl)-ethylidene]-oxamohydrazido} cobalt(III) perchlorate, [Co(apsox)(2)]ClO4. in Journal of Coordination Chemistry. 2003;56(7):611-622.
doi:10.1080/0095897031000113986
Kon_1540 .
Anđelković, Katarina K., Howing, J, Tellgren, R, Jeremić, Dejan, Ivanović-Burmazović, Ivana, Sladić, Dušan, "Synthesis and structural characterization of the Co(III) complex with 2 '-[1-(2-pyridinyl)-ethylidene]oxamohydrazide (Hapsox): The crystal structure of bis-{2 '-[1-(2-pyridinyl)-ethylidene]-oxamohydrazido} cobalt(III) perchlorate, [Co(apsox)(2)]ClO4" in Journal of Coordination Chemistry, 56, no. 7 (2003):611-622,
https://doi.org/10.1080/0095897031000113986 .,
Kon_1540 .
15
8
16

Synthesis and structural characterization of copper(II) complexes with the 2 '-[1-(2-pyridinyl)ethylidene]oxalohydrazide ligand

Bacchi, A; Pelizzi, G; Jeremić, Dejan; Sladić, Dušan; Gruden-Pavlović, Maja; Anđelković, Katarina K.

(Kluwer Academic Publ, Dordrecht, 2003)

TY  - JOUR
AU  - Bacchi, A
AU  - Pelizzi, G
AU  - Jeremić, Dejan
AU  - Sladić, Dušan
AU  - Gruden-Pavlović, Maja
AU  - Anđelković, Katarina K.
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/159
AB  - The octahedral copper(II) complex with two 2'-[1-(2-pyridinyl) ethylidene] oxalohydrazide molecules was synthesized from bis(acetylacetonato) copper(II) and 2'-[1-(2-pyridinyl) ethylidene] oxamohydrazide (Hapsox). The complex is unstable when not in solution. X-ray analysis confirmed the tridentate coordination of the ligands in the monoanionic form. In addition, the stable tetrahedral copper(II) complex with one ligand molecule coordinated as a tridentate in the dianionic form was prepared by direct synthesis from Cu(NO3)(2) . 3H(2)O and Hapsox, and characterized by elemental analysis, magnetic measurements and by i.r. and u.v./vis. spectrophotometry.
PB  - Kluwer Academic Publ, Dordrecht
T2  - Transition Metal Chemistry
T1  - Synthesis and structural characterization of copper(II) complexes with the 2 '-[1-(2-pyridinyl)ethylidene]oxalohydrazide ligand
VL  - 28
IS  - 8
SP  - 935
EP  - 938
DO  - 10.1023/A:1026316611296
UR  - Kon_1554
ER  - 
@article{
author = "Bacchi, A and Pelizzi, G and Jeremić, Dejan and Sladić, Dušan and Gruden-Pavlović, Maja and Anđelković, Katarina K.",
year = "2003",
abstract = "The octahedral copper(II) complex with two 2'-[1-(2-pyridinyl) ethylidene] oxalohydrazide molecules was synthesized from bis(acetylacetonato) copper(II) and 2'-[1-(2-pyridinyl) ethylidene] oxamohydrazide (Hapsox). The complex is unstable when not in solution. X-ray analysis confirmed the tridentate coordination of the ligands in the monoanionic form. In addition, the stable tetrahedral copper(II) complex with one ligand molecule coordinated as a tridentate in the dianionic form was prepared by direct synthesis from Cu(NO3)(2) . 3H(2)O and Hapsox, and characterized by elemental analysis, magnetic measurements and by i.r. and u.v./vis. spectrophotometry.",
publisher = "Kluwer Academic Publ, Dordrecht",
journal = "Transition Metal Chemistry",
title = "Synthesis and structural characterization of copper(II) complexes with the 2 '-[1-(2-pyridinyl)ethylidene]oxalohydrazide ligand",
volume = "28",
number = "8",
pages = "935-938",
doi = "10.1023/A:1026316611296",
url = "Kon_1554"
}
Bacchi, A., Pelizzi, G., Jeremić, D., Sladić, D., Gruden-Pavlović, M.,& Anđelković, K. K.. (2003). Synthesis and structural characterization of copper(II) complexes with the 2 '-[1-(2-pyridinyl)ethylidene]oxalohydrazide ligand. in Transition Metal Chemistry
Kluwer Academic Publ, Dordrecht., 28(8), 935-938.
https://doi.org/10.1023/A:1026316611296
Kon_1554
Bacchi A, Pelizzi G, Jeremić D, Sladić D, Gruden-Pavlović M, Anđelković KK. Synthesis and structural characterization of copper(II) complexes with the 2 '-[1-(2-pyridinyl)ethylidene]oxalohydrazide ligand. in Transition Metal Chemistry. 2003;28(8):935-938.
doi:10.1023/A:1026316611296
Kon_1554 .
Bacchi, A, Pelizzi, G, Jeremić, Dejan, Sladić, Dušan, Gruden-Pavlović, Maja, Anđelković, Katarina K., "Synthesis and structural characterization of copper(II) complexes with the 2 '-[1-(2-pyridinyl)ethylidene]oxalohydrazide ligand" in Transition Metal Chemistry, 28, no. 8 (2003):935-938,
https://doi.org/10.1023/A:1026316611296 .,
Kon_1554 .
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