TY  - JOUR
AU  - Medaković, Vesna
AU  - Bogdanović, Goran A.
AU  - Milčić, Miloš K.
AU  - Janjić, Goran V.
AU  - Zarić, Snežana D.
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1556
AB  - CH/pi interactions in metal porphyrinato complexes were studied by analyzing data in crystal structures from the Cambridge Structural Database (CSD) and by quantum chemical calculations. The analysis of the data in the CSD shows that both five-membered pyrrole and six-membered chelate rings form CH/pi interactions. The interactions occur more frequently with five-membered rings. The analysis of distances in crystal structures and calculated energies show stronger interactions with six-membered chelate rings, indicating that a larger number of interactions with five-membered rings are not the consequence of stronger interactions, but better accessibility of five-membered pyrrole rings. The calculated energies of the interactions with positions in six-membered rings are -2.09 to -2.83 kcal/mol, while the energies with five-membered rings are -2.05 to -2.26 kcal/mol. The results reveal that stronger interactions of six-membered rings are the consequence of stronger electrostatic interactions. Substituents on the porphyrin ring significantly strengthen the interactions. Substituents on the six-membered ring strengthen the interaction energy by about 20%. The results show that CH/pi interactions play an important role in molecular recognition of metalloporphyrins. The significant influence of the substituents on interaction energies can be very important for the design of model systems in bioinorganic chemistry. (C) 2012 Elsevier Inc. All rights reserved.
PB  - Elsevier Science Inc, New York
T2  - Journal of Inorganic Biochemistry
T1  - CH/pi interactions in metal-porphyrin complexes with pyrrole and chelate rings as hydrogen acceptors
VL  - 117
SP  - 157
EP  - 163
DO  - 10.1016/j.jinorgbio.2012.09.002
ER  - 

@article{
author = "Medaković, Vesna and Bogdanović, Goran A. and Milčić, Miloš K. and Janjić, Goran V. and Zarić, Snežana D.",
year = "2012",
abstract = "CH/pi interactions in metal porphyrinato complexes were studied by analyzing data in crystal structures from the Cambridge Structural Database (CSD) and by quantum chemical calculations. The analysis of the data in the CSD shows that both five-membered pyrrole and six-membered chelate rings form CH/pi interactions. The interactions occur more frequently with five-membered rings. The analysis of distances in crystal structures and calculated energies show stronger interactions with six-membered chelate rings, indicating that a larger number of interactions with five-membered rings are not the consequence of stronger interactions, but better accessibility of five-membered pyrrole rings. The calculated energies of the interactions with positions in six-membered rings are -2.09 to -2.83 kcal/mol, while the energies with five-membered rings are -2.05 to -2.26 kcal/mol. The results reveal that stronger interactions of six-membered rings are the consequence of stronger electrostatic interactions. Substituents on the porphyrin ring significantly strengthen the interactions. Substituents on the six-membered ring strengthen the interaction energy by about 20%. The results show that CH/pi interactions play an important role in molecular recognition of metalloporphyrins. The significant influence of the substituents on interaction energies can be very important for the design of model systems in bioinorganic chemistry. (C) 2012 Elsevier Inc. All rights reserved.",
publisher = "Elsevier Science Inc, New York",
journal = "Journal of Inorganic Biochemistry",
title = "CH/pi interactions in metal-porphyrin complexes with pyrrole and chelate rings as hydrogen acceptors",
volume = "117",
pages = "157-163",
doi = "10.1016/j.jinorgbio.2012.09.002"
}

Medaković, V., Bogdanović, G. A., Milčić, M. K., Janjić, G. V.,& Zarić, S. D.. (2012). CH/pi interactions in metal-porphyrin complexes with pyrrole and chelate rings as hydrogen acceptors. in Journal of Inorganic Biochemistry
Elsevier Science Inc, New York., 117, 157-163.
https://doi.org/10.1016/j.jinorgbio.2012.09.002

Medaković V, Bogdanović GA, Milčić MK, Janjić GV, Zarić SD. CH/pi interactions in metal-porphyrin complexes with pyrrole and chelate rings as hydrogen acceptors. in Journal of Inorganic Biochemistry. 2012;117:157-163.
doi:10.1016/j.jinorgbio.2012.09.002 .

Medaković, Vesna, Bogdanović, Goran A., Milčić, Miloš K., Janjić, Goran V., Zarić, Snežana D., "CH/pi interactions in metal-porphyrin complexes with pyrrole and chelate rings as hydrogen acceptors" in Journal of Inorganic Biochemistry, 117 (2012):157-163,
https://doi.org/10.1016/j.jinorgbio.2012.09.002 . .

TY  - JOUR
AU  - Miodragović Đenana U.
AU  - Jovanović, Dragoljub
AU  - Bogdanović, Goran A.
AU  - Mitić, Dragana
AU  - Anđelković, Katarina K.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1127
AB  - In the reaction of ZnCl(2) with tacrine hydrochloride in water novel tetracoordinated (C(13)H(15)N(2))(2)[ZnCl(4)]-H(2)O complex was obtained and characterized by elemental analysis, molar conductivity and X-ray analysis. The complex crystallizes in the space group P-1 of the triclinic crystal system. The structure contains two crystallographically different molecules of protonated tacrine present as counter cations, the [ZnCl(4)](2-) complex anion and one water solvent molecule. The counter cations slightly differ in the puckering of the cyclohexene ring. The molecules of protonated tacrine are involved in different intermolecular hydrogen bonds. In the crystal, the hydrogen bonding generates a 3D assembly. In the crystal, pi center dot center dot center dot pi stacking interactions between the rings of protonated tacrine were evidenced. The [ZnCl(4)](2-) complex anion has a distorted tetrahedral geometry. Three out of the four Cl atoms are involved in intermolecular hydrogen bonding. The intermolecular H-bond interactions involving the Cl atoms affect the Zn-CI bond lengths.
AB  - U reakciji ZnCl2 sa takrin-hidrohloridom u vodi, dobijen je novi tetrakoordinovani (C13H15N2)2[ZnCl4]?H2O kompleks koji je okarakterisan pomoću elementalne analize, molarne provodljivosti i rendgenske strukturne analize. Kompleks kristališe u prostornoj grupi P?1 trikliničnog kristalnog sistema. Struktura sadrži dva kristalografski različita molekula protonovanog takrina koji su prisutni kao kontra-katjoni, [ZnCl4]2 kompleksni anjon i molekul kristalne vode. Molekuli katjona se neznatno razlikuju u stepenu nabiranja cikloheksenovog prstena. Molekuli protonovanog takrina su uključeni u različite intermolekulske vodonične veze. Intermolekulsko vodonično vezivanje u kristalu generiše 3D molekulski skup pi...pi interakcije između prstenova protonovanog takrina su primećene u kristalu. [ZnCl4]2- ima distorgovanu tetraedarsku geometriju. Tri od četiri Cl atoma su uključena u intermolekulske vodonične veze. Intermolekulske vodonične interakcije koje uključuju Cl atome utiču na dužinu Zn-Cl veza.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis and crystal structure of 1,2,3,4-tetrahydro-9-aminoacridine tetrachlorozincate(II) monohydrate
T1  - Sinteza i kristalna struktura 1,2,3,4-tetrahidro-9-aminoakridin-tetrahlorocinkata(II) monohidrata
VL  - 75
IS  - 9
SP  - 1209
EP  - 1218
DO  - 10.2298/JSC100302059M
ER  - 

@article{
author = "Miodragović Đenana U. and Jovanović, Dragoljub and Bogdanović, Goran A. and Mitić, Dragana and Anđelković, Katarina K.",
year = "2010",
abstract = "In the reaction of ZnCl(2) with tacrine hydrochloride in water novel tetracoordinated (C(13)H(15)N(2))(2)[ZnCl(4)]-H(2)O complex was obtained and characterized by elemental analysis, molar conductivity and X-ray analysis. The complex crystallizes in the space group P-1 of the triclinic crystal system. The structure contains two crystallographically different molecules of protonated tacrine present as counter cations, the [ZnCl(4)](2-) complex anion and one water solvent molecule. The counter cations slightly differ in the puckering of the cyclohexene ring. The molecules of protonated tacrine are involved in different intermolecular hydrogen bonds. In the crystal, the hydrogen bonding generates a 3D assembly. In the crystal, pi center dot center dot center dot pi stacking interactions between the rings of protonated tacrine were evidenced. The [ZnCl(4)](2-) complex anion has a distorted tetrahedral geometry. Three out of the four Cl atoms are involved in intermolecular hydrogen bonding. The intermolecular H-bond interactions involving the Cl atoms affect the Zn-CI bond lengths., U reakciji ZnCl2 sa takrin-hidrohloridom u vodi, dobijen je novi tetrakoordinovani (C13H15N2)2[ZnCl4]?H2O kompleks koji je okarakterisan pomoću elementalne analize, molarne provodljivosti i rendgenske strukturne analize. Kompleks kristališe u prostornoj grupi P?1 trikliničnog kristalnog sistema. Struktura sadrži dva kristalografski različita molekula protonovanog takrina koji su prisutni kao kontra-katjoni, [ZnCl4]2 kompleksni anjon i molekul kristalne vode. Molekuli katjona se neznatno razlikuju u stepenu nabiranja cikloheksenovog prstena. Molekuli protonovanog takrina su uključeni u različite intermolekulske vodonične veze. Intermolekulsko vodonično vezivanje u kristalu generiše 3D molekulski skup pi...pi interakcije između prstenova protonovanog takrina su primećene u kristalu. [ZnCl4]2- ima distorgovanu tetraedarsku geometriju. Tri od četiri Cl atoma su uključena u intermolekulske vodonične veze. Intermolekulske vodonične interakcije koje uključuju Cl atome utiču na dužinu Zn-Cl veza.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis and crystal structure of 1,2,3,4-tetrahydro-9-aminoacridine tetrachlorozincate(II) monohydrate, Sinteza i kristalna struktura 1,2,3,4-tetrahidro-9-aminoakridin-tetrahlorocinkata(II) monohidrata",
volume = "75",
number = "9",
pages = "1209-1218",
doi = "10.2298/JSC100302059M"
}

Miodragović Đenana U., Jovanović, D., Bogdanović, G. A., Mitić, D.,& Anđelković, K. K.. (2010). Synthesis and crystal structure of 1,2,3,4-tetrahydro-9-aminoacridine tetrachlorozincate(II) monohydrate. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 75(9), 1209-1218.
https://doi.org/10.2298/JSC100302059M

Miodragović Đenana U., Jovanović D, Bogdanović GA, Mitić D, Anđelković KK. Synthesis and crystal structure of 1,2,3,4-tetrahydro-9-aminoacridine tetrachlorozincate(II) monohydrate. in Journal of the Serbian Chemical Society. 2010;75(9):1209-1218.
doi:10.2298/JSC100302059M .

Miodragović Đenana U., Jovanović, Dragoljub, Bogdanović, Goran A., Mitić, Dragana, Anđelković, Katarina K., "Synthesis and crystal structure of 1,2,3,4-tetrahydro-9-aminoacridine tetrachlorozincate(II) monohydrate" in Journal of the Serbian Chemical Society, 75, no. 9 (2010):1209-1218,
https://doi.org/10.2298/JSC100302059M . .

TY  - JOUR
AU  - Ratkovic, Zoran
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Šegan, Dejan M.
AU  - Vukicevic, Rastko D.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1098
AB  - The one-pot synthesis of seven new (2-alkylthiobenzoyl)ferrocenes has been achieved by Friedel-Crafts acylation of ferrocene with acid chlorides generated in situ from the corresponding carboxylic acids and phosphorous trichloride. The obtained compounds were characterized by spectroscopic data (UV, IR, (1)H and (13)C NMR), whereas their electrochemical properties have been investigated by cyclic voltammetry. The single-crystal X-ray structure determinations for three of them are also reported. Each of the three derivatives exhibits the intramolecular C-H center dot center dot center dot O interaction which involves the donor from the cyclopentadienyl (Cp) ring and the carbonyl oxygen as acceptor. This interaction favors the coplanar arrangement of the two moieties. The angles between the vectors coinciding the C-O bonds and the corresponding Cp planes are all below 6.4 degrees. Conventional hydrogen bonds do not exist in any of the three crystal structures but some weak intermolecular interactions of the C-H center dot center dot center dot, C-H center dot center dot center dot S and C-H center dot center dot center dot pi types have been found and analyzed in detail. Different geometrical parameters for these crystal structures as well as for 22 similar ones extracted from Cambridge Structural Database (CSD) have been compared and analyzed. (C) 2010 Elsevier Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Polyhedron
T1  - Synthesis, spectral characterization and electrochemical properties of (2-alkylthiobenzoyl)ferrocenes. Crystal structures of 2-methylthio, 2-ethylthio and 2-isopropylthio derivatives
VL  - 29
IS  - 11
SP  - 2311
EP  - 2317
DO  - 10.1016/j.poly.2010.04.034
ER  - 

@article{
author = "Ratkovic, Zoran and Novaković, Slađana B. and Bogdanović, Goran A. and Šegan, Dejan M. and Vukicevic, Rastko D.",
year = "2010",
abstract = "The one-pot synthesis of seven new (2-alkylthiobenzoyl)ferrocenes has been achieved by Friedel-Crafts acylation of ferrocene with acid chlorides generated in situ from the corresponding carboxylic acids and phosphorous trichloride. The obtained compounds were characterized by spectroscopic data (UV, IR, (1)H and (13)C NMR), whereas their electrochemical properties have been investigated by cyclic voltammetry. The single-crystal X-ray structure determinations for three of them are also reported. Each of the three derivatives exhibits the intramolecular C-H center dot center dot center dot O interaction which involves the donor from the cyclopentadienyl (Cp) ring and the carbonyl oxygen as acceptor. This interaction favors the coplanar arrangement of the two moieties. The angles between the vectors coinciding the C-O bonds and the corresponding Cp planes are all below 6.4 degrees. Conventional hydrogen bonds do not exist in any of the three crystal structures but some weak intermolecular interactions of the C-H center dot center dot center dot, C-H center dot center dot center dot S and C-H center dot center dot center dot pi types have been found and analyzed in detail. Different geometrical parameters for these crystal structures as well as for 22 similar ones extracted from Cambridge Structural Database (CSD) have been compared and analyzed. (C) 2010 Elsevier Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Polyhedron",
title = "Synthesis, spectral characterization and electrochemical properties of (2-alkylthiobenzoyl)ferrocenes. Crystal structures of 2-methylthio, 2-ethylthio and 2-isopropylthio derivatives",
volume = "29",
number = "11",
pages = "2311-2317",
doi = "10.1016/j.poly.2010.04.034"
}

Ratkovic, Z., Novaković, S. B., Bogdanović, G. A., Šegan, D. M.,& Vukicevic, R. D.. (2010). Synthesis, spectral characterization and electrochemical properties of (2-alkylthiobenzoyl)ferrocenes. Crystal structures of 2-methylthio, 2-ethylthio and 2-isopropylthio derivatives. in Polyhedron
Pergamon-Elsevier Science Ltd, Oxford., 29(11), 2311-2317.
https://doi.org/10.1016/j.poly.2010.04.034

Ratkovic Z, Novaković SB, Bogdanović GA, Šegan DM, Vukicevic RD. Synthesis, spectral characterization and electrochemical properties of (2-alkylthiobenzoyl)ferrocenes. Crystal structures of 2-methylthio, 2-ethylthio and 2-isopropylthio derivatives. in Polyhedron. 2010;29(11):2311-2317.
doi:10.1016/j.poly.2010.04.034 .

Ratkovic, Zoran, Novaković, Slađana B., Bogdanović, Goran A., Šegan, Dejan M., Vukicevic, Rastko D., "Synthesis, spectral characterization and electrochemical properties of (2-alkylthiobenzoyl)ferrocenes. Crystal structures of 2-methylthio, 2-ethylthio and 2-isopropylthio derivatives" in Polyhedron, 29, no. 11 (2010):2311-2317,
https://doi.org/10.1016/j.poly.2010.04.034 . .

TY  - JOUR
AU  - Novaković, Sladjana B.
AU  - Bogdanović, Goran A.
AU  - Brčeski, Ilija
AU  - Leovac, Vukadin M.
PY  - 2009
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1000
AB  - The title compound, [Ni(C20H17N3OP)(N-3)], is the first complex with a semicarbazide-based ligand having a P atom as one of the donors. The influence of the P atom on the deformation of the coordination geometry of the Ni-II ion is evident but less expressed than in the cases of complexes with analogous seleno-and thiosemicarbazide ligands. The torsion angles involving the two bonds formed by the P atom within the six-membered chelate ring have the largest values [C-P-Ni-N = 24.3 (2)degrees and C-C-P-Ni = -24.2 (4)degrees], suggesting that the P atom considerably influences the conformation of the ring. Two types of N-H center dot center dot center dot N hydrogen bond connect the complex units into chains.
PB  - Wiley-Blackwell, Malden
T2  - Acta Crystallographica. Section C: Crystal Structure Communications
T1  - Different intermolecular interactions in azido[2-(diphenylphosphino)benzaldehyde semicarbazonato-kappa P-2,N-1,O]nickel(II)
VL  - 65
DO  - 10.1107/S0108270109021970
ER  - 

@article{
author = "Novaković, Sladjana B. and Bogdanović, Goran A. and Brčeski, Ilija and Leovac, Vukadin M.",
year = "2009",
abstract = "The title compound, [Ni(C20H17N3OP)(N-3)], is the first complex with a semicarbazide-based ligand having a P atom as one of the donors. The influence of the P atom on the deformation of the coordination geometry of the Ni-II ion is evident but less expressed than in the cases of complexes with analogous seleno-and thiosemicarbazide ligands. The torsion angles involving the two bonds formed by the P atom within the six-membered chelate ring have the largest values [C-P-Ni-N = 24.3 (2)degrees and C-C-P-Ni = -24.2 (4)degrees], suggesting that the P atom considerably influences the conformation of the ring. Two types of N-H center dot center dot center dot N hydrogen bond connect the complex units into chains.",
publisher = "Wiley-Blackwell, Malden",
journal = "Acta Crystallographica. Section C: Crystal Structure Communications",
title = "Different intermolecular interactions in azido[2-(diphenylphosphino)benzaldehyde semicarbazonato-kappa P-2,N-1,O]nickel(II)",
volume = "65",
doi = "10.1107/S0108270109021970"
}

Novaković, S. B., Bogdanović, G. A., Brčeski, I.,& Leovac, V. M.. (2009). Different intermolecular interactions in azido[2-(diphenylphosphino)benzaldehyde semicarbazonato-kappa P-2,N-1,O]nickel(II). in Acta Crystallographica. Section C: Crystal Structure Communications
Wiley-Blackwell, Malden., 65.
https://doi.org/10.1107/S0108270109021970

Novaković SB, Bogdanović GA, Brčeski I, Leovac VM. Different intermolecular interactions in azido[2-(diphenylphosphino)benzaldehyde semicarbazonato-kappa P-2,N-1,O]nickel(II). in Acta Crystallographica. Section C: Crystal Structure Communications. 2009;65.
doi:10.1107/S0108270109021970 .

Novaković, Sladjana B., Bogdanović, Goran A., Brčeski, Ilija, Leovac, Vukadin M., "Different intermolecular interactions in azido[2-(diphenylphosphino)benzaldehyde semicarbazonato-kappa P-2,N-1,O]nickel(II)" in Acta Crystallographica. Section C: Crystal Structure Communications, 65 (2009),
https://doi.org/10.1107/S0108270109021970 . .

TY  - JOUR
AU  - Miodragović Đenana U.
AU  - Mitić, Dragana
AU  - Miodragović, Zoran
AU  - Bogdanović, Goran A.
AU  - Vitnik, Zeljko J.
AU  - Vitorovic, Maja D.
AU  - Radulovic, Milanka D.
AU  - Nastasijevic, Branislav J.
AU  - Juranić, Ivan O.
AU  - Anđelković, Katarina K.
PY  - 2008
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/914
AB  - For the first time, complexes of Zn(II), Cd(II) and Co(II) (1-3) with N-benzyloxycarbonylglycine have been synthesized and characterized. The complexes adopt tetrahedral, pentagonal-bipyramidal and octahedral geometry, respectively. The structure of the polymeric cadmium complex was resolved by single crystal X-ray analysis. The cadmium ion has a distorted pentagonal-bipyramidal coordination formed by two water molecules and two N-benzyloxycarbonylglycinato ligands (N-Boc) coordinated in different fashions, one as bidentate and the second connecting three cadmium atoms. In a rather complicated 2D supramolecular structure, the phenyl rings interact mutually exclusively by the CH center dot center dot center dot pi interactions. Investigation of the antimicrobial activity of the obtained complexes and N-benzyloxycarbonylglycine revealed that the ligand does not inhibit the growth of Candida albicans, whereas the newly synthesized complexes suppress the growth of this human fungal pathogen. (c) 2007 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Sa, Lausanne
T2  - Inorganica Chimica Acta
T1  - Syntheses, characterization and antimicrobial activity of the first complexes of Zn(II), Cd(II) and Co(II) with N-benzyloxycarbonylglycine - X-ray crystal structure of the polymeric Cd(II) complex
VL  - 361
IS  - 1
SP  - 86
EP  - 94
DO  - 10.1016/j.ica.2007.06.041
ER  - 

@article{
author = "Miodragović Đenana U. and Mitić, Dragana and Miodragović, Zoran and Bogdanović, Goran A. and Vitnik, Zeljko J. and Vitorovic, Maja D. and Radulovic, Milanka D. and Nastasijevic, Branislav J. and Juranić, Ivan O. and Anđelković, Katarina K.",
year = "2008",
abstract = "For the first time, complexes of Zn(II), Cd(II) and Co(II) (1-3) with N-benzyloxycarbonylglycine have been synthesized and characterized. The complexes adopt tetrahedral, pentagonal-bipyramidal and octahedral geometry, respectively. The structure of the polymeric cadmium complex was resolved by single crystal X-ray analysis. The cadmium ion has a distorted pentagonal-bipyramidal coordination formed by two water molecules and two N-benzyloxycarbonylglycinato ligands (N-Boc) coordinated in different fashions, one as bidentate and the second connecting three cadmium atoms. In a rather complicated 2D supramolecular structure, the phenyl rings interact mutually exclusively by the CH center dot center dot center dot pi interactions. Investigation of the antimicrobial activity of the obtained complexes and N-benzyloxycarbonylglycine revealed that the ligand does not inhibit the growth of Candida albicans, whereas the newly synthesized complexes suppress the growth of this human fungal pathogen. (c) 2007 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Inorganica Chimica Acta",
title = "Syntheses, characterization and antimicrobial activity of the first complexes of Zn(II), Cd(II) and Co(II) with N-benzyloxycarbonylglycine - X-ray crystal structure of the polymeric Cd(II) complex",
volume = "361",
number = "1",
pages = "86-94",
doi = "10.1016/j.ica.2007.06.041"
}

Miodragović Đenana U., Mitić, D., Miodragović, Z., Bogdanović, G. A., Vitnik, Z. J., Vitorovic, M. D., Radulovic, M. D., Nastasijevic, B. J., Juranić, I. O.,& Anđelković, K. K.. (2008). Syntheses, characterization and antimicrobial activity of the first complexes of Zn(II), Cd(II) and Co(II) with N-benzyloxycarbonylglycine - X-ray crystal structure of the polymeric Cd(II) complex. in Inorganica Chimica Acta
Elsevier Science Sa, Lausanne., 361(1), 86-94.
https://doi.org/10.1016/j.ica.2007.06.041

Miodragović Đenana U., Mitić D, Miodragović Z, Bogdanović GA, Vitnik ZJ, Vitorovic MD, Radulovic MD, Nastasijevic BJ, Juranić IO, Anđelković KK. Syntheses, characterization and antimicrobial activity of the first complexes of Zn(II), Cd(II) and Co(II) with N-benzyloxycarbonylglycine - X-ray crystal structure of the polymeric Cd(II) complex. in Inorganica Chimica Acta. 2008;361(1):86-94.
doi:10.1016/j.ica.2007.06.041 .

Miodragović Đenana U., Mitić, Dragana, Miodragović, Zoran, Bogdanović, Goran A., Vitnik, Zeljko J., Vitorovic, Maja D., Radulovic, Milanka D., Nastasijevic, Branislav J., Juranić, Ivan O., Anđelković, Katarina K., "Syntheses, characterization and antimicrobial activity of the first complexes of Zn(II), Cd(II) and Co(II) with N-benzyloxycarbonylglycine - X-ray crystal structure of the polymeric Cd(II) complex" in Inorganica Chimica Acta, 361, no. 1 (2008):86-94,
https://doi.org/10.1016/j.ica.2007.06.041 . .

TY  - JOUR
AU  - Sredojević, Dušan N.
AU  - Bogdanović, Goran A.
AU  - Tomić, Zoran D.
AU  - Zarić, Snežana D.
PY  - 2007
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/862
AB  - The crystal structures of square-planar transition-metal complexes from the Cambridge Structural Database (CSD) with close contacts between planar chelate rings and aryl rings containing six carbon atoms (C-6- aryl) were analyzed. Most of the chelate rings in these structures are fused with aromatic or other pi-delocalized chelate rings. The results show that planar chelate rings can be involved in stacking and CH-pi interactions with organic aryl rings. However, the number of stacking interactions is a few times larger than the number of CH-pi interactions. The analysis also shows that in almost all cases CH-pi interactions are formed only when stacking interactions are prevented by voluminous substituents. Hence, between planar chelate rings and C-6- aryl rings stacking interactions are preferred to CH-pi interactions.
PB  - Royal Soc Chemistry, Cambridge
T2  - CrystEngComm
T1  - Stacking vs. CH-pi interactions between chelate and aryl rings in crystal structures of square-planar transition metal complexes
VL  - 9
IS  - 9
SP  - 793
EP  - 798
DO  - 10.1039/b704302c
ER  - 

@article{
author = "Sredojević, Dušan N. and Bogdanović, Goran A. and Tomić, Zoran D. and Zarić, Snežana D.",
year = "2007",
abstract = "The crystal structures of square-planar transition-metal complexes from the Cambridge Structural Database (CSD) with close contacts between planar chelate rings and aryl rings containing six carbon atoms (C-6- aryl) were analyzed. Most of the chelate rings in these structures are fused with aromatic or other pi-delocalized chelate rings. The results show that planar chelate rings can be involved in stacking and CH-pi interactions with organic aryl rings. However, the number of stacking interactions is a few times larger than the number of CH-pi interactions. The analysis also shows that in almost all cases CH-pi interactions are formed only when stacking interactions are prevented by voluminous substituents. Hence, between planar chelate rings and C-6- aryl rings stacking interactions are preferred to CH-pi interactions.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "CrystEngComm",
title = "Stacking vs. CH-pi interactions between chelate and aryl rings in crystal structures of square-planar transition metal complexes",
volume = "9",
number = "9",
pages = "793-798",
doi = "10.1039/b704302c"
}

Sredojević, D. N., Bogdanović, G. A., Tomić, Z. D.,& Zarić, S. D.. (2007). Stacking vs. CH-pi interactions between chelate and aryl rings in crystal structures of square-planar transition metal complexes. in CrystEngComm
Royal Soc Chemistry, Cambridge., 9(9), 793-798.
https://doi.org/10.1039/b704302c

Sredojević DN, Bogdanović GA, Tomić ZD, Zarić SD. Stacking vs. CH-pi interactions between chelate and aryl rings in crystal structures of square-planar transition metal complexes. in CrystEngComm. 2007;9(9):793-798.
doi:10.1039/b704302c .

Sredojević, Dušan N., Bogdanović, Goran A., Tomić, Zoran D., Zarić, Snežana D., "Stacking vs. CH-pi interactions between chelate and aryl rings in crystal structures of square-planar transition metal complexes" in CrystEngComm, 9, no. 9 (2007):793-798,
https://doi.org/10.1039/b704302c . .

TY  - JOUR
AU  - Draskovic, Bojana M.
AU  - Bogdanović, Goran A.
AU  - Leovac, Vukadin M.
AU  - Brčeski, Ilija
AU  - Poleti, Dejan
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/785
AB  - The title compound, [Ni(C28H30N3O2PS)], crystallizes with two independent molecules in the asymmetric unit. The Ni-II atoms are in significantly deformed square-planar environments formed by an ONNP donor set from a thiosemicarbazide-based tetradentate ligand. The Ni-II atom and the ONN donor atoms are nearly coplanar, while the P atom deviates from their mean planes by 0.278 (4) and 0.202 (4) angstrom for the two independent molecules. The P-containing chelate rings are remarkably non-planar, adopting a boat conformation, which is unusual for chelate rings in transition metal complexes with thiosemicarbazide-based tetradentate ligands. The orientation of the ethoxy group bonded to this chelate ring is caused by an intramolecular C-H center dot center dot center dot pi interaction with the opposing phenyl ring. There are no hydrogen bonds; instead, numerous intermolecular C-H center dot center dot center dot pi interactions dominate in the crystal packing.
PB  - Int Union Crystallography, Chester
T2  - ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY
T1  - Transition metal complexes with thiosemicarbazide-based ligands. LIII. [4-(2-diphenylphosphino-alpha-ethoxybenzyl-kappa P)-S-methyl-1-(4-oxidopent-3-en-4-ylidene-kappa O)-thiosemicarbazido-kappa(2) N-1, N-4]nickel (II)
VL  - 62
IS  - 7
DO  - 10.1107/S0108270106018932
ER  - 

@article{
author = "Draskovic, Bojana M. and Bogdanović, Goran A. and Leovac, Vukadin M. and Brčeski, Ilija and Poleti, Dejan",
year = "2006",
abstract = "The title compound, [Ni(C28H30N3O2PS)], crystallizes with two independent molecules in the asymmetric unit. The Ni-II atoms are in significantly deformed square-planar environments formed by an ONNP donor set from a thiosemicarbazide-based tetradentate ligand. The Ni-II atom and the ONN donor atoms are nearly coplanar, while the P atom deviates from their mean planes by 0.278 (4) and 0.202 (4) angstrom for the two independent molecules. The P-containing chelate rings are remarkably non-planar, adopting a boat conformation, which is unusual for chelate rings in transition metal complexes with thiosemicarbazide-based tetradentate ligands. The orientation of the ethoxy group bonded to this chelate ring is caused by an intramolecular C-H center dot center dot center dot pi interaction with the opposing phenyl ring. There are no hydrogen bonds; instead, numerous intermolecular C-H center dot center dot center dot pi interactions dominate in the crystal packing.",
publisher = "Int Union Crystallography, Chester",
journal = "ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY",
title = "Transition metal complexes with thiosemicarbazide-based ligands. LIII. [4-(2-diphenylphosphino-alpha-ethoxybenzyl-kappa P)-S-methyl-1-(4-oxidopent-3-en-4-ylidene-kappa O)-thiosemicarbazido-kappa(2) N-1, N-4]nickel (II)",
volume = "62",
number = "7",
doi = "10.1107/S0108270106018932"
}

Draskovic, B. M., Bogdanović, G. A., Leovac, V. M., Brčeski, I.,& Poleti, D.. (2006). Transition metal complexes with thiosemicarbazide-based ligands. LIII. [4-(2-diphenylphosphino-alpha-ethoxybenzyl-kappa P)-S-methyl-1-(4-oxidopent-3-en-4-ylidene-kappa O)-thiosemicarbazido-kappa(2) N-1, N-4]nickel (II). in ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY
Int Union Crystallography, Chester., 62(7).
https://doi.org/10.1107/S0108270106018932

Draskovic BM, Bogdanović GA, Leovac VM, Brčeski I, Poleti D. Transition metal complexes with thiosemicarbazide-based ligands. LIII. [4-(2-diphenylphosphino-alpha-ethoxybenzyl-kappa P)-S-methyl-1-(4-oxidopent-3-en-4-ylidene-kappa O)-thiosemicarbazido-kappa(2) N-1, N-4]nickel (II). in ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY. 2006;62(7).
doi:10.1107/S0108270106018932 .

Draskovic, Bojana M., Bogdanović, Goran A., Leovac, Vukadin M., Brčeski, Ilija, Poleti, Dejan, "Transition metal complexes with thiosemicarbazide-based ligands. LIII. [4-(2-diphenylphosphino-alpha-ethoxybenzyl-kappa P)-S-methyl-1-(4-oxidopent-3-en-4-ylidene-kappa O)-thiosemicarbazido-kappa(2) N-1, N-4]nickel (II)" in ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 62, no. 7 (2006),
https://doi.org/10.1107/S0108270106018932 . .

TY  - JOUR
AU  - Kaluderovic, G.N.
AU  - Bogdanović, Goran A.
AU  - Sabo, Tibor
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/48
AB  - C8H18ClN2O4Pt, monoclinic, P121/nl (no. 14), a = 8.181(3) Å, b = 10.303(5) Å, c = 9.073(6) Å, ß = 103.2(1)°, V = 744.6 Å3, Z = 2, Rgt(F) = 0.080, wRref(F2) = 0.247, T = 293 K. © 2014 Oldenbourg Wissenschaftsverlag GmbH, Rosenheimer Str. 145, 81671 München. All rights reserved.
T2  - Zeitschrift fur Kristallographie = New Crystal Structures
T1  - Crystal structure of ethylenediammonium-N,N’-di-3-propionic acid tetrachloroplatmate(II), (CH2NH2(CH2)2COOH)2[PtCl4]
VL  - 221
IS  - 1-4
SP  - 345
EP  - 346
DO  - 10.1524/ncrs.2006.221.14.345
ER  - 

@article{
author = "Kaluderovic, G.N. and Bogdanović, Goran A. and Sabo, Tibor",
year = "2006",
abstract = "C8H18ClN2O4Pt, monoclinic, P121/nl (no. 14), a = 8.181(3) Å, b = 10.303(5) Å, c = 9.073(6) Å, ß = 103.2(1)°, V = 744.6 Å3, Z = 2, Rgt(F) = 0.080, wRref(F2) = 0.247, T = 293 K. © 2014 Oldenbourg Wissenschaftsverlag GmbH, Rosenheimer Str. 145, 81671 München. All rights reserved.",
journal = "Zeitschrift fur Kristallographie = New Crystal Structures",
title = "Crystal structure of ethylenediammonium-N,N’-di-3-propionic acid tetrachloroplatmate(II), (CH2NH2(CH2)2COOH)2[PtCl4]",
volume = "221",
number = "1-4",
pages = "345-346",
doi = "10.1524/ncrs.2006.221.14.345"
}

Kaluderovic, G.N., Bogdanović, G. A.,& Sabo, T.. (2006). Crystal structure of ethylenediammonium-N,N’-di-3-propionic acid tetrachloroplatmate(II), (CH2NH2(CH2)2COOH)2[PtCl4]. in Zeitschrift fur Kristallographie = New Crystal Structures, 221(1-4), 345-346.
https://doi.org/10.1524/ncrs.2006.221.14.345

Kaluderovic G, Bogdanović GA, Sabo T. Crystal structure of ethylenediammonium-N,N’-di-3-propionic acid tetrachloroplatmate(II), (CH2NH2(CH2)2COOH)2[PtCl4]. in Zeitschrift fur Kristallographie = New Crystal Structures. 2006;221(1-4):345-346.
doi:10.1524/ncrs.2006.221.14.345 .

Kaluderovic, G.N., Bogdanović, Goran A., Sabo, Tibor, "Crystal structure of ethylenediammonium-N,N’-di-3-propionic acid tetrachloroplatmate(II), (CH2NH2(CH2)2COOH)2[PtCl4]" in Zeitschrift fur Kristallographie = New Crystal Structures, 221, no. 1-4 (2006):345-346,
https://doi.org/10.1524/ncrs.2006.221.14.345 . .

TY  - JOUR
AU  - Kaluderovic, G. N.
AU  - Bogdanović, Goran A.
AU  - Sabo, Tibor
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/814
AB  - C8H18Cl4N2O4Pt, monoclinic, P12(1)/n1 (no. 14), a = 8.181(3) angstrom, b = 10.303(5) angstrom, c = 9.073(6) angstrom, beta = 103.2(1)degrees, V = 744.6 angstrom(3), Z = 2, R-gt(F) = 0.080, wR(ref)(F-2) = 0.247, T = 293 K.
PB  - Oldenbourg Verlag, Munich
T2  - Zeitschrift fur Kristallographie = New Crystal Structures
T1  - Crystal structure of ethylenediammonium-N,N '-di-3-propionic acid tetrachloroplatinate(II), (CH2NH2(CH2)(2)COOH)(2)[PtCl4]
VL  - 221
IS  - 3
SP  - 345
EP  - 346
DO  - 10.1524/ncrs.2006.0103
ER  - 

@article{
author = "Kaluderovic, G. N. and Bogdanović, Goran A. and Sabo, Tibor",
year = "2006",
abstract = "C8H18Cl4N2O4Pt, monoclinic, P12(1)/n1 (no. 14), a = 8.181(3) angstrom, b = 10.303(5) angstrom, c = 9.073(6) angstrom, beta = 103.2(1)degrees, V = 744.6 angstrom(3), Z = 2, R-gt(F) = 0.080, wR(ref)(F-2) = 0.247, T = 293 K.",
publisher = "Oldenbourg Verlag, Munich",
journal = "Zeitschrift fur Kristallographie = New Crystal Structures",
title = "Crystal structure of ethylenediammonium-N,N '-di-3-propionic acid tetrachloroplatinate(II), (CH2NH2(CH2)(2)COOH)(2)[PtCl4]",
volume = "221",
number = "3",
pages = "345-346",
doi = "10.1524/ncrs.2006.0103"
}

Kaluderovic, G. N., Bogdanović, G. A.,& Sabo, T.. (2006). Crystal structure of ethylenediammonium-N,N '-di-3-propionic acid tetrachloroplatinate(II), (CH2NH2(CH2)(2)COOH)(2)[PtCl4]. in Zeitschrift fur Kristallographie = New Crystal Structures
Oldenbourg Verlag, Munich., 221(3), 345-346.
https://doi.org/10.1524/ncrs.2006.0103

Kaluderovic GN, Bogdanović GA, Sabo T. Crystal structure of ethylenediammonium-N,N '-di-3-propionic acid tetrachloroplatinate(II), (CH2NH2(CH2)(2)COOH)(2)[PtCl4]. in Zeitschrift fur Kristallographie = New Crystal Structures. 2006;221(3):345-346.
doi:10.1524/ncrs.2006.0103 .

Kaluderovic, G. N., Bogdanović, Goran A., Sabo, Tibor, "Crystal structure of ethylenediammonium-N,N '-di-3-propionic acid tetrachloroplatinate(II), (CH2NH2(CH2)(2)COOH)(2)[PtCl4]" in Zeitschrift fur Kristallographie = New Crystal Structures, 221, no. 3 (2006):345-346,
https://doi.org/10.1524/ncrs.2006.0103 . .

TY  - JOUR
AU  - Djinovic, VM
AU  - Mančić, Lidija
AU  - Bogdanović, Goran A.
AU  - Vulić, Predrag J.
AU  - del Rosario, G
AU  - Sabo, Tibor
AU  - Milošević, Olivera
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/703
AB  - Pure and Pt-doped ZnO nanophase particles were synthesized by ultrasonic spray pyrolysis. The particles were obtained through the decomposition of zinc nitrate and with a newly developed Pt(IV) complex with 1,3 -propylenediamine-NN'-diacetate tetradentate class ligand (pdda). The complex was characterized by elemental analysis, electronic absorption and infrared spectroscopy. The form of the determined complex structure {trans-[Pt(pdda)Br-2]center dot H2O} implies that Pt(IV) ion has a distorted octahedral coordination due to intramolecular N-H center dot center dot center dot Br interaction. The results of structural refinement (cell parameters, bond lengths, and ion occupancy) of ultrasonically derived pure and Pt-doped ZnO particles suggest either the formation of Zn-i interstitials or platinum ion incorporation into the ZnO lattice in octahedral interstitial positions, respectively. A well-crystallized hexagonal wurtzite structure of ZnO was pronounced in all investigated samples [JCPDS card 36-1415, Joint Committee on Powder Diffraction Standards, defined by International Centre for Diffraction Data (www.icdd.com)]. Phase determination also indicated the presence of a nitrate hydroxide hydrate phase (JCPDS card 24-1460), as a result of incomplete precursor decomposition and a spinel Zn2PtO4 phase (below 1.0 wt%) located in the boundary region for a Pt-doped ZnO sample. Based on x-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy analyses, it was shown that the different particle growing morphologies, which were either spheroidally or pyramidally shaped, were influenced by the precursor chemistry, processing parameters and the presence of platinum ions. The composite internal particle structure revealed by transmission electron microscopy and selected area electron diffraction analyses, implied that the secondary particles represent an assembly of primary particles sized under 60 nm aroused during the processes of nucleation, growth and aggregation. Both hexagonal and spheroidal shape of primary particles was evident. The particle morphology, primarily particle size and the mechanism of Pt4+ ion introduction into the ZnO cell was discussed based on the structural refinement and selected area electron diffraction analysis.
PB  - Cambridge Univ Press, New York
T2  - Journal of Materials Research
T1  - Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions
VL  - 20
IS  - 1
SP  - 102
EP  - 113
DO  - 10.1557/JMR.2005.0006
ER  - 

@article{
author = "Djinovic, VM and Mančić, Lidija and Bogdanović, Goran A. and Vulić, Predrag J. and del Rosario, G and Sabo, Tibor and Milošević, Olivera",
year = "2005",
abstract = "Pure and Pt-doped ZnO nanophase particles were synthesized by ultrasonic spray pyrolysis. The particles were obtained through the decomposition of zinc nitrate and with a newly developed Pt(IV) complex with 1,3 -propylenediamine-NN'-diacetate tetradentate class ligand (pdda). The complex was characterized by elemental analysis, electronic absorption and infrared spectroscopy. The form of the determined complex structure {trans-[Pt(pdda)Br-2]center dot H2O} implies that Pt(IV) ion has a distorted octahedral coordination due to intramolecular N-H center dot center dot center dot Br interaction. The results of structural refinement (cell parameters, bond lengths, and ion occupancy) of ultrasonically derived pure and Pt-doped ZnO particles suggest either the formation of Zn-i interstitials or platinum ion incorporation into the ZnO lattice in octahedral interstitial positions, respectively. A well-crystallized hexagonal wurtzite structure of ZnO was pronounced in all investigated samples [JCPDS card 36-1415, Joint Committee on Powder Diffraction Standards, defined by International Centre for Diffraction Data (www.icdd.com)]. Phase determination also indicated the presence of a nitrate hydroxide hydrate phase (JCPDS card 24-1460), as a result of incomplete precursor decomposition and a spinel Zn2PtO4 phase (below 1.0 wt%) located in the boundary region for a Pt-doped ZnO sample. Based on x-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy analyses, it was shown that the different particle growing morphologies, which were either spheroidally or pyramidally shaped, were influenced by the precursor chemistry, processing parameters and the presence of platinum ions. The composite internal particle structure revealed by transmission electron microscopy and selected area electron diffraction analyses, implied that the secondary particles represent an assembly of primary particles sized under 60 nm aroused during the processes of nucleation, growth and aggregation. Both hexagonal and spheroidal shape of primary particles was evident. The particle morphology, primarily particle size and the mechanism of Pt4+ ion introduction into the ZnO cell was discussed based on the structural refinement and selected area electron diffraction analysis.",
publisher = "Cambridge Univ Press, New York",
journal = "Journal of Materials Research",
title = "Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions",
volume = "20",
number = "1",
pages = "102-113",
doi = "10.1557/JMR.2005.0006"
}

Djinovic, V., Mančić, L., Bogdanović, G. A., Vulić, P. J., del Rosario, G., Sabo, T.,& Milošević, O.. (2005). Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions. in Journal of Materials Research
Cambridge Univ Press, New York., 20(1), 102-113.
https://doi.org/10.1557/JMR.2005.0006

Djinovic V, Mančić L, Bogdanović GA, Vulić PJ, del Rosario G, Sabo T, Milošević O. Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions. in Journal of Materials Research. 2005;20(1):102-113.
doi:10.1557/JMR.2005.0006 .

Djinovic, VM, Mančić, Lidija, Bogdanović, Goran A., Vulić, Predrag J., del Rosario, G, Sabo, Tibor, Milošević, Olivera, "Aerosol synthesis of pure and Pt-doped ZnO particles using nitrate and pdda-Pt(IV) complex solutions" in Journal of Materials Research, 20, no. 1 (2005):102-113,
https://doi.org/10.1557/JMR.2005.0006 . .

TY  - JOUR
AU  - Sabo, Tibor
AU  - Dinovic, VA
AU  - Kaluđerović, Goran N.
AU  - Stanojković, Tatjana
AU  - Bogdanović, Goran A.
AU  - Juranic, ZD
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/693
AB  - Four platinum(IV) complexes, trans,trans-dichlorobis(N,N-dimethylglycinato)platinum(IV), trans,trans-[Pt(dmgly)(2)Cl-2] (1) and trans.trans-dibromobis(N,N'-dimethylglycinato)platinum(IV), trans,trans-[Pt(dmgly)(2)Br-2] (2), as well as, trans,trans-dichlorobis(N-methylglycinato)platinum(IV), trans,trans-[Pt(sar)(2)Cl-2] (3) and trans,trans-dibromobis(N-methylglycinato)platinum(IV), trans,trans-[Pt(sar)(2)Br-2] (4) (with configuration index for all complexes OC-6-14), were synthesized and characterized by elemental analysis, infrared and H-1 NMR spectroscopy. In the aim to assess the selectivity in the antitumor action of these complexes, the antiproliferative action of these compounds was determined to human adenocarcinoma HeLa cells; to human myelogenous leukemia K562 cells and to normal immunocompetent cells; i.e., on human PBMC. The details of the crystal structure synthesized trans,trans-[Pt(sar)(2)Br-2] complex were also reported here. In the crystal structure of trans, trans-[Pt(sar)(2)Br-2] the Pt(IV) ion had a deformed octahedral coordination with both N-methylglycinates and bromides bonded trans to one another and with the NPt-Br bond angles of 84.1(4) and 95.9(4)degrees. The trans, trans-[Pt(sar)(2)Br-2] complex molecules form 2D-layers with multiple N-H (...) O and C-H (...) O hydrogen bonds. (c) 2005 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Sa, Lausanne
T2  - Inorganica Chimica Acta
T1  - Syntheses and activity of some platinum(IV) complexes with N-methyl derivate of glycine and halogeno ligands against HeLa, K562 cell lines and human PBMC
VL  - 358
IS  - 7
SP  - 2239
EP  - 2245
DO  - 10.1016/j.ica.2005.01.007
ER  - 

@article{
author = "Sabo, Tibor and Dinovic, VA and Kaluđerović, Goran N. and Stanojković, Tatjana and Bogdanović, Goran A. and Juranic, ZD",
year = "2005",
abstract = "Four platinum(IV) complexes, trans,trans-dichlorobis(N,N-dimethylglycinato)platinum(IV), trans,trans-[Pt(dmgly)(2)Cl-2] (1) and trans.trans-dibromobis(N,N'-dimethylglycinato)platinum(IV), trans,trans-[Pt(dmgly)(2)Br-2] (2), as well as, trans,trans-dichlorobis(N-methylglycinato)platinum(IV), trans,trans-[Pt(sar)(2)Cl-2] (3) and trans,trans-dibromobis(N-methylglycinato)platinum(IV), trans,trans-[Pt(sar)(2)Br-2] (4) (with configuration index for all complexes OC-6-14), were synthesized and characterized by elemental analysis, infrared and H-1 NMR spectroscopy. In the aim to assess the selectivity in the antitumor action of these complexes, the antiproliferative action of these compounds was determined to human adenocarcinoma HeLa cells; to human myelogenous leukemia K562 cells and to normal immunocompetent cells; i.e., on human PBMC. The details of the crystal structure synthesized trans,trans-[Pt(sar)(2)Br-2] complex were also reported here. In the crystal structure of trans, trans-[Pt(sar)(2)Br-2] the Pt(IV) ion had a deformed octahedral coordination with both N-methylglycinates and bromides bonded trans to one another and with the NPt-Br bond angles of 84.1(4) and 95.9(4)degrees. The trans, trans-[Pt(sar)(2)Br-2] complex molecules form 2D-layers with multiple N-H (...) O and C-H (...) O hydrogen bonds. (c) 2005 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Inorganica Chimica Acta",
title = "Syntheses and activity of some platinum(IV) complexes with N-methyl derivate of glycine and halogeno ligands against HeLa, K562 cell lines and human PBMC",
volume = "358",
number = "7",
pages = "2239-2245",
doi = "10.1016/j.ica.2005.01.007"
}

Sabo, T., Dinovic, V., Kaluđerović, G. N., Stanojković, T., Bogdanović, G. A.,& Juranic, Z.. (2005). Syntheses and activity of some platinum(IV) complexes with N-methyl derivate of glycine and halogeno ligands against HeLa, K562 cell lines and human PBMC. in Inorganica Chimica Acta
Elsevier Science Sa, Lausanne., 358(7), 2239-2245.
https://doi.org/10.1016/j.ica.2005.01.007

Sabo T, Dinovic V, Kaluđerović GN, Stanojković T, Bogdanović GA, Juranic Z. Syntheses and activity of some platinum(IV) complexes with N-methyl derivate of glycine and halogeno ligands against HeLa, K562 cell lines and human PBMC. in Inorganica Chimica Acta. 2005;358(7):2239-2245.
doi:10.1016/j.ica.2005.01.007 .

Sabo, Tibor, Dinovic, VA, Kaluđerović, Goran N., Stanojković, Tatjana, Bogdanović, Goran A., Juranic, ZD, "Syntheses and activity of some platinum(IV) complexes with N-methyl derivate of glycine and halogeno ligands against HeLa, K562 cell lines and human PBMC" in Inorganica Chimica Acta, 358, no. 7 (2005):2239-2245,
https://doi.org/10.1016/j.ica.2005.01.007 . .

TY  - JOUR
AU  - Bogdanović, Goran A.
AU  - Medaković, Vesna
AU  - Milčić, Miloš K.
AU  - Zarić, Snežana D.
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/644
AB  - Cambridge Structural Database (CSD) was screened in order to find intramolecular C-H...pi interactions with a chelate ring of coordinated porphyrin. It was found 154 crystal structures with 244 intramolecular C-H...pi interactions in transition metal complexes with derivatives of porphyrin. Comparison of interacting distances indicates that interactions of hydrogen atoms in positions 2 and 6 of axially coordinated pyridine are more favorable with ruffled than with planar porphyrin.
PB  - Mdpi Ag, Basel
T2  - International Journal of Molecular Sciences
T1  - Intramolecular C-H center dot center dot center dot pi interactions in metal-porphyrin complexes
VL  - 5
IS  - 4-7
SP  - 174
EP  - 185
DO  - 10.3390/i5040174
ER  - 

@article{
author = "Bogdanović, Goran A. and Medaković, Vesna and Milčić, Miloš K. and Zarić, Snežana D.",
year = "2004",
abstract = "Cambridge Structural Database (CSD) was screened in order to find intramolecular C-H...pi interactions with a chelate ring of coordinated porphyrin. It was found 154 crystal structures with 244 intramolecular C-H...pi interactions in transition metal complexes with derivatives of porphyrin. Comparison of interacting distances indicates that interactions of hydrogen atoms in positions 2 and 6 of axially coordinated pyridine are more favorable with ruffled than with planar porphyrin.",
publisher = "Mdpi Ag, Basel",
journal = "International Journal of Molecular Sciences",
title = "Intramolecular C-H center dot center dot center dot pi interactions in metal-porphyrin complexes",
volume = "5",
number = "4-7",
pages = "174-185",
doi = "10.3390/i5040174"
}

Bogdanović, G. A., Medaković, V., Milčić, M. K.,& Zarić, S. D.. (2004). Intramolecular C-H center dot center dot center dot pi interactions in metal-porphyrin complexes. in International Journal of Molecular Sciences
Mdpi Ag, Basel., 5(4-7), 174-185.
https://doi.org/10.3390/i5040174

Bogdanović GA, Medaković V, Milčić MK, Zarić SD. Intramolecular C-H center dot center dot center dot pi interactions in metal-porphyrin complexes. in International Journal of Molecular Sciences. 2004;5(4-7):174-185.
doi:10.3390/i5040174 .

Bogdanović, Goran A., Medaković, Vesna, Milčić, Miloš K., Zarić, Snežana D., "Intramolecular C-H center dot center dot center dot pi interactions in metal-porphyrin complexes" in International Journal of Molecular Sciences, 5, no. 4-7 (2004):174-185,
https://doi.org/10.3390/i5040174 . .

TY  - JOUR
AU  - Medaković, Vesna
AU  - Milčić, Miloš K.
AU  - Bogdanović, Goran A.
AU  - Zarić, Snežana D.
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/667
AB  - Specific C-H(...)pi interactions with the pi-system of porphyrinato chelate ring were found in crystal structures of transition metal complexes from the Cambridge Structural Database and statistical analysis of geometrical parameters for intramolecular and intermolecular interactions was done. By density functional theory calculations on a model system it was evaluated that an interaction energy is above 1.5 kcal/mol and that the strongest interaction occurs when the distance between hydrogen atom and the center of the chelate ring is 2.6 Angstrom. This prediction is in good agreement with the distances for intermolecular interactions found in the crystal structures. In many cases the intramolecular interaction distances are much shorter than 2.6 Angstrom, and these short distances are caused by geometrical constrains. The C-H(...)pi interactions with chelate ring of porphyrinato ligand can influence the structure, contribute to its stability, and play some role in the function of biomolecules with metalo porphyrins. (C) 2004 Elsevier Inc. All rights reserved.
PB  - Elsevier Science Inc, New York
T2  - Journal of Inorganic Biochemistry
T1  - C-H center dot center dot center dot pi interactions in the metal-porphyrin complexes with chelate ring as the H acceptor
VL  - 98
IS  - 11
SP  - 1867
EP  - 1873
DO  - 10.1016/j.jinorgbio.2004.08.012
ER  - 

@article{
author = "Medaković, Vesna and Milčić, Miloš K. and Bogdanović, Goran A. and Zarić, Snežana D.",
year = "2004",
abstract = "Specific C-H(...)pi interactions with the pi-system of porphyrinato chelate ring were found in crystal structures of transition metal complexes from the Cambridge Structural Database and statistical analysis of geometrical parameters for intramolecular and intermolecular interactions was done. By density functional theory calculations on a model system it was evaluated that an interaction energy is above 1.5 kcal/mol and that the strongest interaction occurs when the distance between hydrogen atom and the center of the chelate ring is 2.6 Angstrom. This prediction is in good agreement with the distances for intermolecular interactions found in the crystal structures. In many cases the intramolecular interaction distances are much shorter than 2.6 Angstrom, and these short distances are caused by geometrical constrains. The C-H(...)pi interactions with chelate ring of porphyrinato ligand can influence the structure, contribute to its stability, and play some role in the function of biomolecules with metalo porphyrins. (C) 2004 Elsevier Inc. All rights reserved.",
publisher = "Elsevier Science Inc, New York",
journal = "Journal of Inorganic Biochemistry",
title = "C-H center dot center dot center dot pi interactions in the metal-porphyrin complexes with chelate ring as the H acceptor",
volume = "98",
number = "11",
pages = "1867-1873",
doi = "10.1016/j.jinorgbio.2004.08.012"
}

Medaković, V., Milčić, M. K., Bogdanović, G. A.,& Zarić, S. D.. (2004). C-H center dot center dot center dot pi interactions in the metal-porphyrin complexes with chelate ring as the H acceptor. in Journal of Inorganic Biochemistry
Elsevier Science Inc, New York., 98(11), 1867-1873.
https://doi.org/10.1016/j.jinorgbio.2004.08.012

Medaković V, Milčić MK, Bogdanović GA, Zarić SD. C-H center dot center dot center dot pi interactions in the metal-porphyrin complexes with chelate ring as the H acceptor. in Journal of Inorganic Biochemistry. 2004;98(11):1867-1873.
doi:10.1016/j.jinorgbio.2004.08.012 .

Medaković, Vesna, Milčić, Miloš K., Bogdanović, Goran A., Zarić, Snežana D., "C-H center dot center dot center dot pi interactions in the metal-porphyrin complexes with chelate ring as the H acceptor" in Journal of Inorganic Biochemistry, 98, no. 11 (2004):1867-1873,
https://doi.org/10.1016/j.jinorgbio.2004.08.012 . .

TY  - CONF
AU  - Bogdanović, Goran A.
AU  - Medaković, Vesna
AU  - Milčić, Miloš K.
AU  - Zarić, Snežana D.
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/66
AB  - Cambridge Structural Database (CSD) was screened in order to find intramolecular C-H⋯π interactions with a chelate ring of coordinated porphyrin. It was found 154 crystal structures with 244 intramolecular C-H⋯π interactions in transition metal complexes with derivatives of porphyrin. Comparison of interacting distances indicates that interactions of hydrogen atoms in positions 2 and 6 of axially coordinated pyridine are more favorable with ruffled than with planar porphyrin.
C3  - International Journal of Molecular Sciences
T1  - Intramolecular C-H⋯π interactions in metal-porphyrin complexes
VL  - 5
IS  - SPEC ISS
SP  - 174
EP  - 185
UR  - https://hdl.handle.net/21.15107/rcub_cherry_66
ER  - 

@conference{
author = "Bogdanović, Goran A. and Medaković, Vesna and Milčić, Miloš K. and Zarić, Snežana D.",
year = "2004",
abstract = "Cambridge Structural Database (CSD) was screened in order to find intramolecular C-H⋯π interactions with a chelate ring of coordinated porphyrin. It was found 154 crystal structures with 244 intramolecular C-H⋯π interactions in transition metal complexes with derivatives of porphyrin. Comparison of interacting distances indicates that interactions of hydrogen atoms in positions 2 and 6 of axially coordinated pyridine are more favorable with ruffled than with planar porphyrin.",
journal = "International Journal of Molecular Sciences",
title = "Intramolecular C-H⋯π interactions in metal-porphyrin complexes",
volume = "5",
number = "SPEC ISS",
pages = "174-185",
url = "https://hdl.handle.net/21.15107/rcub_cherry_66"
}

Bogdanović, G. A., Medaković, V., Milčić, M. K.,& Zarić, S. D.. (2004). Intramolecular C-H⋯π interactions in metal-porphyrin complexes. in International Journal of Molecular Sciences, 5(SPEC ISS), 174-185.
https://hdl.handle.net/21.15107/rcub_cherry_66

Bogdanović GA, Medaković V, Milčić MK, Zarić SD. Intramolecular C-H⋯π interactions in metal-porphyrin complexes. in International Journal of Molecular Sciences. 2004;5(SPEC ISS):174-185.
https://hdl.handle.net/21.15107/rcub_cherry_66 .

Bogdanović, Goran A., Medaković, Vesna, Milčić, Miloš K., Zarić, Snežana D., "Intramolecular C-H⋯π interactions in metal-porphyrin complexes" in International Journal of Molecular Sciences, 5, no. SPEC ISS (2004):174-185,
https://hdl.handle.net/21.15107/rcub_cherry_66 .

TY  - JOUR
AU  - Brčeski, Ilija
AU  - Leovac, Vukadin M.
AU  - Bogdanović, Goran A.
AU  - Sovilj, Sofija P.
AU  - Revenco, M
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/569
AB  - The syntheses of a new ligand 2-(diphenylphosphino)benzaldehyde selenosemicarbazone (HL) and the corresponding complex with Ni(II) of the formula [Ni(L)(NCS)] are reported. The complex was characterized by single crystal X-ray analysis. The compound complex is diamagnetic and has a markedly deformed square-planar structure with PNSe set of donor atoms of the ligand, the Schiff base monoanion, and the N atom of the coordinated NCS group. The phosphorus atom deviates even by 0.494(3) Angstrom from the mean plane defined by the other coordination atoms (NSeN) and the metal atom. (C) 2003 Published by Elsevier B.V.
PB  - Elsevier Science Bv, Amsterdam
T2  - Inorganic Chemistry Communications
T1  - Synthesis, physicochemical properties and crystal structure of isothiocianato [2-(diphenylphosphino)benzaldehyde selenosemicarbazonato(1(-))] nickel(II)
VL  - 7
IS  - 2
SP  - 253
EP  - 256
DO  - 10.1016/j.inoche.2003.11.013
ER  - 

@article{
author = "Brčeski, Ilija and Leovac, Vukadin M. and Bogdanović, Goran A. and Sovilj, Sofija P. and Revenco, M",
year = "2004",
abstract = "The syntheses of a new ligand 2-(diphenylphosphino)benzaldehyde selenosemicarbazone (HL) and the corresponding complex with Ni(II) of the formula [Ni(L)(NCS)] are reported. The complex was characterized by single crystal X-ray analysis. The compound complex is diamagnetic and has a markedly deformed square-planar structure with PNSe set of donor atoms of the ligand, the Schiff base monoanion, and the N atom of the coordinated NCS group. The phosphorus atom deviates even by 0.494(3) Angstrom from the mean plane defined by the other coordination atoms (NSeN) and the metal atom. (C) 2003 Published by Elsevier B.V.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Inorganic Chemistry Communications",
title = "Synthesis, physicochemical properties and crystal structure of isothiocianato [2-(diphenylphosphino)benzaldehyde selenosemicarbazonato(1(-))] nickel(II)",
volume = "7",
number = "2",
pages = "253-256",
doi = "10.1016/j.inoche.2003.11.013"
}

Brčeski, I., Leovac, V. M., Bogdanović, G. A., Sovilj, S. P.,& Revenco, M.. (2004). Synthesis, physicochemical properties and crystal structure of isothiocianato [2-(diphenylphosphino)benzaldehyde selenosemicarbazonato(1(-))] nickel(II). in Inorganic Chemistry Communications
Elsevier Science Bv, Amsterdam., 7(2), 253-256.
https://doi.org/10.1016/j.inoche.2003.11.013

Brčeski I, Leovac VM, Bogdanović GA, Sovilj SP, Revenco M. Synthesis, physicochemical properties and crystal structure of isothiocianato [2-(diphenylphosphino)benzaldehyde selenosemicarbazonato(1(-))] nickel(II). in Inorganic Chemistry Communications. 2004;7(2):253-256.
doi:10.1016/j.inoche.2003.11.013 .

Brčeski, Ilija, Leovac, Vukadin M., Bogdanović, Goran A., Sovilj, Sofija P., Revenco, M, "Synthesis, physicochemical properties and crystal structure of isothiocianato [2-(diphenylphosphino)benzaldehyde selenosemicarbazonato(1(-))] nickel(II)" in Inorganic Chemistry Communications, 7, no. 2 (2004):253-256,
https://doi.org/10.1016/j.inoche.2003.11.013 . .

TY  - JOUR
AU  - Dinovic, VM
AU  - Bogdanović, Goran A.
AU  - Novaković, Slađana B.
AU  - Sabo, Tibor
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/649
AB  - The trans-geometrical isomer of the first Pt(IV) complex with the tetradentate ligand 1,3-propylenediamine-N,N'-diacetate ion (pdda) was prepared by a direct synthesis from potassium hexachloroplatinate(IV) and pdda in the presence of lithium hydroxide. The crystal structure of trans-[Pt(pdda)Cl-2] (.) H2O complex has been determined. The Pt(IV) ion has a distorted octahedral coordination due to intramolecular N-(HCl)-Cl-... interactions.
PB  - Taylor & Francis Ltd, Abingdon
T2  - Journal of Coordination Chemistry
T1  - Synthesis and crystal structure of trans-dichloro(1,3-propylenediamine-N,N '-diacetato)platinum(IV) monohydrate
VL  - 57
IS  - 7
SP  - 535
EP  - 541
DO  - 10.1080/00958970410001671110
ER  - 

@article{
author = "Dinovic, VM and Bogdanović, Goran A. and Novaković, Slađana B. and Sabo, Tibor",
year = "2004",
abstract = "The trans-geometrical isomer of the first Pt(IV) complex with the tetradentate ligand 1,3-propylenediamine-N,N'-diacetate ion (pdda) was prepared by a direct synthesis from potassium hexachloroplatinate(IV) and pdda in the presence of lithium hydroxide. The crystal structure of trans-[Pt(pdda)Cl-2] (.) H2O complex has been determined. The Pt(IV) ion has a distorted octahedral coordination due to intramolecular N-(HCl)-Cl-... interactions.",
publisher = "Taylor & Francis Ltd, Abingdon",
journal = "Journal of Coordination Chemistry",
title = "Synthesis and crystal structure of trans-dichloro(1,3-propylenediamine-N,N '-diacetato)platinum(IV) monohydrate",
volume = "57",
number = "7",
pages = "535-541",
doi = "10.1080/00958970410001671110"
}

Dinovic, V., Bogdanović, G. A., Novaković, S. B.,& Sabo, T.. (2004). Synthesis and crystal structure of trans-dichloro(1,3-propylenediamine-N,N '-diacetato)platinum(IV) monohydrate. in Journal of Coordination Chemistry
Taylor & Francis Ltd, Abingdon., 57(7), 535-541.
https://doi.org/10.1080/00958970410001671110

Dinovic V, Bogdanović GA, Novaković SB, Sabo T. Synthesis and crystal structure of trans-dichloro(1,3-propylenediamine-N,N '-diacetato)platinum(IV) monohydrate. in Journal of Coordination Chemistry. 2004;57(7):535-541.
doi:10.1080/00958970410001671110 .

Dinovic, VM, Bogdanović, Goran A., Novaković, Slađana B., Sabo, Tibor, "Synthesis and crystal structure of trans-dichloro(1,3-propylenediamine-N,N '-diacetato)platinum(IV) monohydrate" in Journal of Coordination Chemistry, 57, no. 7 (2004):535-541,
https://doi.org/10.1080/00958970410001671110 . .

TY  - JOUR
AU  - Bogdanović, Goran A.
AU  - Bire, ASD
AU  - Zarić, Snežana D.
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/497
AB  - Structural and computational evidence is given for a special type of C-H(...)pi interaction where the C-H group interacts with the pi-system of a six-membered chelate ring. An investigation of crystal structures shows that these interactions take place in quite a number of metal complexes, including organometallic compounds; in the CSD we found over 1200 structures with these interactions, These interactions exist in complexes of different metals and various chelate rings, DFT calculations on three model systems show that the energy of these interactions is about 1 kcal/mol. ((C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002).
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Inorganic Chemistry
T1  - Evidence based on crystal structures and calculations of a C-H-...pi interaction between an organic moiety and a chelate ring in transition metal complexes
IS  - 7
SP  - 1599
EP  - 1602
UR  - https://hdl.handle.net/21.15107/rcub_cherry_497
ER  - 

@article{
author = "Bogdanović, Goran A. and Bire, ASD and Zarić, Snežana D.",
year = "2002",
abstract = "Structural and computational evidence is given for a special type of C-H(...)pi interaction where the C-H group interacts with the pi-system of a six-membered chelate ring. An investigation of crystal structures shows that these interactions take place in quite a number of metal complexes, including organometallic compounds; in the CSD we found over 1200 structures with these interactions, These interactions exist in complexes of different metals and various chelate rings, DFT calculations on three model systems show that the energy of these interactions is about 1 kcal/mol. ((C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002).",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Inorganic Chemistry",
title = "Evidence based on crystal structures and calculations of a C-H-...pi interaction between an organic moiety and a chelate ring in transition metal complexes",
number = "7",
pages = "1599-1602",
url = "https://hdl.handle.net/21.15107/rcub_cherry_497"
}

Bogdanović, G. A., Bire, A.,& Zarić, S. D.. (2002). Evidence based on crystal structures and calculations of a C-H-...pi interaction between an organic moiety and a chelate ring in transition metal complexes. in European Journal of Inorganic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim.(7), 1599-1602.
https://hdl.handle.net/21.15107/rcub_cherry_497

Bogdanović GA, Bire A, Zarić SD. Evidence based on crystal structures and calculations of a C-H-...pi interaction between an organic moiety and a chelate ring in transition metal complexes. in European Journal of Inorganic Chemistry. 2002;(7):1599-1602.
https://hdl.handle.net/21.15107/rcub_cherry_497 .

Bogdanović, Goran A., Bire, ASD, Zarić, Snežana D., "Evidence based on crystal structures and calculations of a C-H-...pi interaction between an organic moiety and a chelate ring in transition metal complexes" in European Journal of Inorganic Chemistry, no. 7 (2002):1599-1602,
https://hdl.handle.net/21.15107/rcub_cherry_497 .

TY  - JOUR
AU  - Kaluđerović, Goran N.
AU  - Bogdanović, Goran A.
AU  - Sabo, Tibor
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/503
AB  - This paper reports the first synthesized Pt(IV) complex with ethylenediamine-N,N'-di-3-propionato ligand (eddp). The crystal structure of trans-[Pt(eddp)Cl-2] . H2O complex has been determined. Pt(IV) has a distorted octahedral coordination due to an intramolecular N-H...Cl interaction.
PB  - Taylor & Francis Ltd, Abingdon
T2  - Journal of Coordination Chemistry
T1  - Synthesis and crystal structure of trans-dichloro(ethylenediamine-N,N '-di-3-propionato)platinum(IV) monohydrate
VL  - 55
IS  - 7
SP  - 817
EP  - 822
DO  - 10.1080/0095897022000001566
ER  - 

@article{
author = "Kaluđerović, Goran N. and Bogdanović, Goran A. and Sabo, Tibor",
year = "2002",
abstract = "This paper reports the first synthesized Pt(IV) complex with ethylenediamine-N,N'-di-3-propionato ligand (eddp). The crystal structure of trans-[Pt(eddp)Cl-2] . H2O complex has been determined. Pt(IV) has a distorted octahedral coordination due to an intramolecular N-H...Cl interaction.",
publisher = "Taylor & Francis Ltd, Abingdon",
journal = "Journal of Coordination Chemistry",
title = "Synthesis and crystal structure of trans-dichloro(ethylenediamine-N,N '-di-3-propionato)platinum(IV) monohydrate",
volume = "55",
number = "7",
pages = "817-822",
doi = "10.1080/0095897022000001566"
}

Kaluđerović, G. N., Bogdanović, G. A.,& Sabo, T.. (2002). Synthesis and crystal structure of trans-dichloro(ethylenediamine-N,N '-di-3-propionato)platinum(IV) monohydrate. in Journal of Coordination Chemistry
Taylor & Francis Ltd, Abingdon., 55(7), 817-822.
https://doi.org/10.1080/0095897022000001566

Kaluđerović GN, Bogdanović GA, Sabo T. Synthesis and crystal structure of trans-dichloro(ethylenediamine-N,N '-di-3-propionato)platinum(IV) monohydrate. in Journal of Coordination Chemistry. 2002;55(7):817-822.
doi:10.1080/0095897022000001566 .

Kaluđerović, Goran N., Bogdanović, Goran A., Sabo, Tibor, "Synthesis and crystal structure of trans-dichloro(ethylenediamine-N,N '-di-3-propionato)platinum(IV) monohydrate" in Journal of Coordination Chemistry, 55, no. 7 (2002):817-822,
https://doi.org/10.1080/0095897022000001566 . .

TY  - JOUR
AU  - Dinovic, VM
AU  - Bogdanović, Goran A.
AU  - Novaković, S
AU  - Sabo, Tibor
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/505
AB  - The s-cis-geometrical isomer of the cobalt(III) complex with N,N-dimethylglycine (dmgly) and the tetradentate ligand ethylenediamine-N,N'-diacetate ion (edda) was prepared by a direct synthesis from cobalt(II) chloride hexahydrate, N,N-dimethylglycine and edda in the presence of lead(IV) oxide. The complex has been isolated chromatographically and characterized by elemental analyses, electron absorption spectra, infrared spectra and X-ray diffraction analysis.
PB  - Marcel Dekker Inc, New York
T2  - Synthesis and Reactivity in Inorganic and Metal-organic Chemistry
T1  - Synthesis and crystal structure of s-cis-(ethylenediamine-N,N '-diacetato)cobalt(III) complex with N,N-dimethylglycine
VL  - 32
IS  - 6
SP  - 1085
EP  - 1097
DO  - 10.1081/SIM-120013022
ER  - 

@article{
author = "Dinovic, VM and Bogdanović, Goran A. and Novaković, S and Sabo, Tibor",
year = "2002",
abstract = "The s-cis-geometrical isomer of the cobalt(III) complex with N,N-dimethylglycine (dmgly) and the tetradentate ligand ethylenediamine-N,N'-diacetate ion (edda) was prepared by a direct synthesis from cobalt(II) chloride hexahydrate, N,N-dimethylglycine and edda in the presence of lead(IV) oxide. The complex has been isolated chromatographically and characterized by elemental analyses, electron absorption spectra, infrared spectra and X-ray diffraction analysis.",
publisher = "Marcel Dekker Inc, New York",
journal = "Synthesis and Reactivity in Inorganic and Metal-organic Chemistry",
title = "Synthesis and crystal structure of s-cis-(ethylenediamine-N,N '-diacetato)cobalt(III) complex with N,N-dimethylglycine",
volume = "32",
number = "6",
pages = "1085-1097",
doi = "10.1081/SIM-120013022"
}

Dinovic, V., Bogdanović, G. A., Novaković, S.,& Sabo, T.. (2002). Synthesis and crystal structure of s-cis-(ethylenediamine-N,N '-diacetato)cobalt(III) complex with N,N-dimethylglycine. in Synthesis and Reactivity in Inorganic and Metal-organic Chemistry
Marcel Dekker Inc, New York., 32(6), 1085-1097.
https://doi.org/10.1081/SIM-120013022

Dinovic V, Bogdanović GA, Novaković S, Sabo T. Synthesis and crystal structure of s-cis-(ethylenediamine-N,N '-diacetato)cobalt(III) complex with N,N-dimethylglycine. in Synthesis and Reactivity in Inorganic and Metal-organic Chemistry. 2002;32(6):1085-1097.
doi:10.1081/SIM-120013022 .

Dinovic, VM, Bogdanović, Goran A., Novaković, S, Sabo, Tibor, "Synthesis and crystal structure of s-cis-(ethylenediamine-N,N '-diacetato)cobalt(III) complex with N,N-dimethylglycine" in Synthesis and Reactivity in Inorganic and Metal-organic Chemistry, 32, no. 6 (2002):1085-1097,
https://doi.org/10.1081/SIM-120013022 . .

TY  - JOUR
AU  - Bogdanović, Goran A.
AU  - Medaković, Vesna
AU  - Vojinovic, LS
AU  - Cesljevic, VI
AU  - Leovac, Vukadin M.
AU  - Spasojevic-de Bire, A
AU  - Zarić, Snežana D.
PY  - 2001
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/466
AB  - Two compounds, [Co-III(L)(py)(3)][Co-II(PY)Cl-3]. EtOH and [Co-III(L)(PY)(3)]I-3 (H2L = salicylaldehyde S-methylisothiosemicarbazone, py = pyridine), were synthesized and the crystal structures deter-mined by single-crystal X-ray diffraction. In both structures the geometries of the cation are very similar to a thiosemicarbazide-based ligand coordinated in the mer configuration. The axial pyridines are in mutual perpendicular orientation. the angles between the planes being 85.3(2) and 82.5(2)degrees. The plane of the equatorial pyridine is tilted with respect to the equatorial plane by about 40 degrees. The orientations of the pyridines were studied in model systems by quantum chemistry calculations. It was shown that the interactions between axial and equatorial pyridines are responsible for the orientation of pyridines in the complex cation: consequently, there are very similar geometries of the complex cation in both crystal structures. The compounds were also characterized by elemental analysis, molar conductivity, magnetic susceptibility and electronic absorption spectra. (C) 2001 Elsevier Science Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Polyhedron
T1  - Transition metal complexes with thiosemicarbazide-based ligands. Part XLI. Two crystal structures of cobalt(III) complexes with salicylaldehyde S-methylisothiosemicarbazone and theoretical study on orientations of coordinated pyridines
VL  - 20
IS  - 17
SP  - 2231
EP  - 2240
DO  - 10.1016/S0277-5387(01)00819-1
ER  - 

@article{
author = "Bogdanović, Goran A. and Medaković, Vesna and Vojinovic, LS and Cesljevic, VI and Leovac, Vukadin M. and Spasojevic-de Bire, A and Zarić, Snežana D.",
year = "2001",
abstract = "Two compounds, [Co-III(L)(py)(3)][Co-II(PY)Cl-3]. EtOH and [Co-III(L)(PY)(3)]I-3 (H2L = salicylaldehyde S-methylisothiosemicarbazone, py = pyridine), were synthesized and the crystal structures deter-mined by single-crystal X-ray diffraction. In both structures the geometries of the cation are very similar to a thiosemicarbazide-based ligand coordinated in the mer configuration. The axial pyridines are in mutual perpendicular orientation. the angles between the planes being 85.3(2) and 82.5(2)degrees. The plane of the equatorial pyridine is tilted with respect to the equatorial plane by about 40 degrees. The orientations of the pyridines were studied in model systems by quantum chemistry calculations. It was shown that the interactions between axial and equatorial pyridines are responsible for the orientation of pyridines in the complex cation: consequently, there are very similar geometries of the complex cation in both crystal structures. The compounds were also characterized by elemental analysis, molar conductivity, magnetic susceptibility and electronic absorption spectra. (C) 2001 Elsevier Science Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Polyhedron",
title = "Transition metal complexes with thiosemicarbazide-based ligands. Part XLI. Two crystal structures of cobalt(III) complexes with salicylaldehyde S-methylisothiosemicarbazone and theoretical study on orientations of coordinated pyridines",
volume = "20",
number = "17",
pages = "2231-2240",
doi = "10.1016/S0277-5387(01)00819-1"
}

Bogdanović, G. A., Medaković, V., Vojinovic, L., Cesljevic, V., Leovac, V. M., Spasojevic-de Bire, A.,& Zarić, S. D.. (2001). Transition metal complexes with thiosemicarbazide-based ligands. Part XLI. Two crystal structures of cobalt(III) complexes with salicylaldehyde S-methylisothiosemicarbazone and theoretical study on orientations of coordinated pyridines. in Polyhedron
Pergamon-Elsevier Science Ltd, Oxford., 20(17), 2231-2240.
https://doi.org/10.1016/S0277-5387(01)00819-1

Bogdanović GA, Medaković V, Vojinovic L, Cesljevic V, Leovac VM, Spasojevic-de Bire A, Zarić SD. Transition metal complexes with thiosemicarbazide-based ligands. Part XLI. Two crystal structures of cobalt(III) complexes with salicylaldehyde S-methylisothiosemicarbazone and theoretical study on orientations of coordinated pyridines. in Polyhedron. 2001;20(17):2231-2240.
doi:10.1016/S0277-5387(01)00819-1 .

Bogdanović, Goran A., Medaković, Vesna, Vojinovic, LS, Cesljevic, VI, Leovac, Vukadin M., Spasojevic-de Bire, A, Zarić, Snežana D., "Transition metal complexes with thiosemicarbazide-based ligands. Part XLI. Two crystal structures of cobalt(III) complexes with salicylaldehyde S-methylisothiosemicarbazone and theoretical study on orientations of coordinated pyridines" in Polyhedron, 20, no. 17 (2001):2231-2240,
https://doi.org/10.1016/S0277-5387(01)00819-1 . .

TY  - JOUR
AU  - Miodragović Đenana U.
AU  - Bogdanović, Goran A.
AU  - Milosavljević, Slobodan M.
AU  - Malinar, M.J.
AU  - Celap, MB
AU  - Spasojevic-de Bire, A
AU  - Macura, S.
AU  - Juranić, N.
PY  - 2001
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/476
AB  - In the reaction of trans-[CoCl2(en)(2)](+) with L-tyrosine all six theoretically possible diastereomers of the (1,2-diaminoethane)bis(L-tyrosinato)cobalt(III) complex were formed. The following five were isolated: Delta -trans(O); and Lambda- and Delta -C-2-cis(O) and Lambda- and Delta -C-1-cis(O) diastereomers, while the Delta -trans(O) diastereomer was only detected in the corresponding eluate. Separation of the obtained diastereomers was performed by chromatography on a Dowex 1 x 4 column. Characterization of the isolated diastereomers was carried out by means of elemental analysis, electronic absorption, circular dichroic, H-1 and C-13 NMR spectra, and by x-ray crystal structure analysis in the case of the Delta -C-1-cis(O) diastereomer. We established the general rule of preference of diasteromers formation in complexes of [Co(L-aa)(2)diamine](+) (L-aa = L-amino acid anion; diamine = 1,2-diaminoethane or 1,3-diaminopropane) type.
PB  - Gordon Breach Publishing, Taylor & Francis Group, Philadelphia
T2  - Enantiomer
T1  - Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part II. Synthesis and configuration of (1,2-diaminoethane)bis(L-tyrosinato)-cobalt(III)complex diastereomers. The crystal structure of the Delta-C-1-cis(O) diastereomer
VL  - 6
IS  - 5
SP  - 299
EP  - 308
UR  - https://hdl.handle.net/21.15107/rcub_cherry_476
ER  - 

@article{
author = "Miodragović Đenana U. and Bogdanović, Goran A. and Milosavljević, Slobodan M. and Malinar, M.J. and Celap, MB and Spasojevic-de Bire, A and Macura, S. and Juranić, N.",
year = "2001",
abstract = "In the reaction of trans-[CoCl2(en)(2)](+) with L-tyrosine all six theoretically possible diastereomers of the (1,2-diaminoethane)bis(L-tyrosinato)cobalt(III) complex were formed. The following five were isolated: Delta -trans(O); and Lambda- and Delta -C-2-cis(O) and Lambda- and Delta -C-1-cis(O) diastereomers, while the Delta -trans(O) diastereomer was only detected in the corresponding eluate. Separation of the obtained diastereomers was performed by chromatography on a Dowex 1 x 4 column. Characterization of the isolated diastereomers was carried out by means of elemental analysis, electronic absorption, circular dichroic, H-1 and C-13 NMR spectra, and by x-ray crystal structure analysis in the case of the Delta -C-1-cis(O) diastereomer. We established the general rule of preference of diasteromers formation in complexes of [Co(L-aa)(2)diamine](+) (L-aa = L-amino acid anion; diamine = 1,2-diaminoethane or 1,3-diaminopropane) type.",
publisher = "Gordon Breach Publishing, Taylor & Francis Group, Philadelphia",
journal = "Enantiomer",
title = "Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part II. Synthesis and configuration of (1,2-diaminoethane)bis(L-tyrosinato)-cobalt(III)complex diastereomers. The crystal structure of the Delta-C-1-cis(O) diastereomer",
volume = "6",
number = "5",
pages = "299-308",
url = "https://hdl.handle.net/21.15107/rcub_cherry_476"
}

Miodragović Đenana U., Bogdanović, G. A., Milosavljević, S. M., Malinar, M.J., Celap, M., Spasojevic-de Bire, A., Macura, S.,& Juranić, N.. (2001). Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part II. Synthesis and configuration of (1,2-diaminoethane)bis(L-tyrosinato)-cobalt(III)complex diastereomers. The crystal structure of the Delta-C-1-cis(O) diastereomer. in Enantiomer
Gordon Breach Publishing, Taylor & Francis Group, Philadelphia., 6(5), 299-308.
https://hdl.handle.net/21.15107/rcub_cherry_476

Miodragović Đenana U., Bogdanović GA, Milosavljević SM, Malinar M, Celap M, Spasojevic-de Bire A, Macura S, Juranić N. Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part II. Synthesis and configuration of (1,2-diaminoethane)bis(L-tyrosinato)-cobalt(III)complex diastereomers. The crystal structure of the Delta-C-1-cis(O) diastereomer. in Enantiomer. 2001;6(5):299-308.
https://hdl.handle.net/21.15107/rcub_cherry_476 .

Miodragović Đenana U., Bogdanović, Goran A., Milosavljević, Slobodan M., Malinar, M.J., Celap, MB, Spasojevic-de Bire, A, Macura, S., Juranić, N., "Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part II. Synthesis and configuration of (1,2-diaminoethane)bis(L-tyrosinato)-cobalt(III)complex diastereomers. The crystal structure of the Delta-C-1-cis(O) diastereomer" in Enantiomer, 6, no. 5 (2001):299-308,
https://hdl.handle.net/21.15107/rcub_cherry_476 .

TY  - JOUR
AU  - Marković, Z.B.
AU  - Bogdanović, Goran A.
AU  - Spasojević-de Biré, A.
AU  - Sabo, Tibor
AU  - Trifunović, Srećko R.
PY  - 2000
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/70
AB  - C4H10N2O4, orthorhombic, Pccn (No. 56), a = 7.782(2) Å, b = 8.642(2) Å, c = 10.230(3) Å, V = 688.0 Å3, Z = 4, Rgt(F) = 0.071, wRref(F2) = 0.215, T = 293 K. © by Oldenbourg Wissenschaftsverlag,.
T2  - Zeitschrift fur Kristallographie = New Crystal Structures
T1  - Crystal structure of ammonium iminodiacetate, NH4C4H6NO4
VL  - 215
IS  - 3
SP  - 363
EP  - 364
DO  - 10.1515/ncrs-2000-0328
ER  - 

@article{
author = "Marković, Z.B. and Bogdanović, Goran A. and Spasojević-de Biré, A. and Sabo, Tibor and Trifunović, Srećko R.",
year = "2000",
abstract = "C4H10N2O4, orthorhombic, Pccn (No. 56), a = 7.782(2) Å, b = 8.642(2) Å, c = 10.230(3) Å, V = 688.0 Å3, Z = 4, Rgt(F) = 0.071, wRref(F2) = 0.215, T = 293 K. © by Oldenbourg Wissenschaftsverlag,.",
journal = "Zeitschrift fur Kristallographie = New Crystal Structures",
title = "Crystal structure of ammonium iminodiacetate, NH4C4H6NO4",
volume = "215",
number = "3",
pages = "363-364",
doi = "10.1515/ncrs-2000-0328"
}

Marković, Z.B., Bogdanović, G. A., Spasojević-de Biré, A., Sabo, T.,& Trifunović, S. R.. (2000). Crystal structure of ammonium iminodiacetate, NH4C4H6NO4. in Zeitschrift fur Kristallographie = New Crystal Structures, 215(3), 363-364.
https://doi.org/10.1515/ncrs-2000-0328

Marković Z, Bogdanović GA, Spasojević-de Biré A, Sabo T, Trifunović SR. Crystal structure of ammonium iminodiacetate, NH4C4H6NO4. in Zeitschrift fur Kristallographie = New Crystal Structures. 2000;215(3):363-364.
doi:10.1515/ncrs-2000-0328 .

Marković, Z.B., Bogdanović, Goran A., Spasojević-de Biré, A., Sabo, Tibor, Trifunović, Srećko R., "Crystal structure of ammonium iminodiacetate, NH4C4H6NO4" in Zeitschrift fur Kristallographie = New Crystal Structures, 215, no. 3 (2000):363-364,
https://doi.org/10.1515/ncrs-2000-0328 . .

TY  - JOUR
AU  - Sladić, Dušan
AU  - Beljanski, V
AU  - Prelesnik, B
AU  - Bogdanović, Goran A.
AU  - Ivanović, I.
AU  - Anđelković, Katarina K.
PY  - 1998
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/373
AB  - Three condensation products of usnic acid with the hydrazides of alpha-naphthoic, caprylic, and oxamic acids, respectively, have been prepared and characterized by spectrometric methods. A reassignment of the C-13-NMR spectral data of usnic acid has been done. The crystal structure of usnic acid 11-[(1-naphthoyl)hydrazone] ethanol solvate (1:1) has been determined. This substance crystallizes in the monoclinic crystal system, the space group P2(1), with the unit cell dimensiones a=7.7365(7) Angstrom, b = 19.632(2) Angstrom, c = 9.4150(15) Angstrom, beta = 108.830(11)degrees, V = 1405.0(4) Angstrom(3), and Z=2. At the end of the structure analysis R = 0.055, R-w = 0.052 and S = 0.89. The antibacterial activities of the compounds have been evaluated. The greatest activity against Staphylococcus aureus was found for usnic acid, somewhat lower for the derivatives with hydrazides of alpha-naphthoic and caprylic acid, and much lower for the derivative with semioxamazide. The activities of these compounds probably depend on their lipophilicity.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Preparation, crystal structure and antibacterial activity of condensation products of usnic acid and acyl hydrazides
VL  - 63
IS  - 3
SP  - 171
EP  - 182
UR  - https://hdl.handle.net/21.15107/rcub_cherry_373
ER  - 

@article{
author = "Sladić, Dušan and Beljanski, V and Prelesnik, B and Bogdanović, Goran A. and Ivanović, I. and Anđelković, Katarina K.",
year = "1998",
abstract = "Three condensation products of usnic acid with the hydrazides of alpha-naphthoic, caprylic, and oxamic acids, respectively, have been prepared and characterized by spectrometric methods. A reassignment of the C-13-NMR spectral data of usnic acid has been done. The crystal structure of usnic acid 11-[(1-naphthoyl)hydrazone] ethanol solvate (1:1) has been determined. This substance crystallizes in the monoclinic crystal system, the space group P2(1), with the unit cell dimensiones a=7.7365(7) Angstrom, b = 19.632(2) Angstrom, c = 9.4150(15) Angstrom, beta = 108.830(11)degrees, V = 1405.0(4) Angstrom(3), and Z=2. At the end of the structure analysis R = 0.055, R-w = 0.052 and S = 0.89. The antibacterial activities of the compounds have been evaluated. The greatest activity against Staphylococcus aureus was found for usnic acid, somewhat lower for the derivatives with hydrazides of alpha-naphthoic and caprylic acid, and much lower for the derivative with semioxamazide. The activities of these compounds probably depend on their lipophilicity.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Preparation, crystal structure and antibacterial activity of condensation products of usnic acid and acyl hydrazides",
volume = "63",
number = "3",
pages = "171-182",
url = "https://hdl.handle.net/21.15107/rcub_cherry_373"
}

Sladić, D., Beljanski, V., Prelesnik, B., Bogdanović, G. A., Ivanović, I.,& Anđelković, K. K.. (1998). Preparation, crystal structure and antibacterial activity of condensation products of usnic acid and acyl hydrazides. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 63(3), 171-182.
https://hdl.handle.net/21.15107/rcub_cherry_373

Sladić D, Beljanski V, Prelesnik B, Bogdanović GA, Ivanović I, Anđelković KK. Preparation, crystal structure and antibacterial activity of condensation products of usnic acid and acyl hydrazides. in Journal of the Serbian Chemical Society. 1998;63(3):171-182.
https://hdl.handle.net/21.15107/rcub_cherry_373 .

Sladić, Dušan, Beljanski, V, Prelesnik, B, Bogdanović, Goran A., Ivanović, I., Anđelković, Katarina K., "Preparation, crystal structure and antibacterial activity of condensation products of usnic acid and acyl hydrazides" in Journal of the Serbian Chemical Society, 63, no. 3 (1998):171-182,
https://hdl.handle.net/21.15107/rcub_cherry_373 .