Kremenović, Aleksandar

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  • Kremenović, Aleksandar (5)

Author's Bibliography

Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites

Nikolić, Aleksandar S.; Jović, Nataša G.; Rogan, Jelena; Kremenović, Aleksandar; Ristić, Mira; Meden, A.; Antić, Bratislav

(Elsevier Sci Ltd, Oxford, 2013)

TY  - JOUR
AU  - Nikolić, Aleksandar S.
AU  - Jović, Nataša G.
AU  - Rogan, Jelena
AU  - Kremenović, Aleksandar
AU  - Ristić, Mira
AU  - Meden, A.
AU  - Antić, Bratislav
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2403
AB  - Different synthesis methods for the preparation of nanocrystalline nickel ferrites are reported: the thermal decomposition of precursors, made of: (i) metal-nitrate salts with carboxylic acids (citric, malonic and tartaric), and (ii) metal-nitrate salts and polyethylene glycol (PEG), in the presence of potassium chloride as a capping agent. The as-prepared gel precursors were characterized by TGA/DTA, while the samples obtained after annealing at 450 degrees C were investigated by FTIR, FESEM, XRD and Mossbauer spectroscopy. Regardless of the type of carboxylic acid used, nanocrystallites prepared by (i) method are similar in size (11-16 nm), while the method (ii) gives crystallites similar to 33 nm in size with negligible microstrain. The differences in the lattice parameter, ranging from 8.3369(2) to 8.3574(2) angstrom, result from cation distribution, nonstoichiometry and structural imperfections in the nickel ferrite nanoparticles. The Mossbauer spectra analysis indicates existence of large distortions of tetrahedral and octahedral sites in these spinel compounds.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites
EP  - 6688
IS  - 6
SP  - 6681
VL  - 39
DO  - 10.1016/j.ceramint.2013.01.106
ER  - 
@article{
author = "Nikolić, Aleksandar S. and Jović, Nataša G. and Rogan, Jelena and Kremenović, Aleksandar and Ristić, Mira and Meden, A. and Antić, Bratislav",
year = "2013",
abstract = "Different synthesis methods for the preparation of nanocrystalline nickel ferrites are reported: the thermal decomposition of precursors, made of: (i) metal-nitrate salts with carboxylic acids (citric, malonic and tartaric), and (ii) metal-nitrate salts and polyethylene glycol (PEG), in the presence of potassium chloride as a capping agent. The as-prepared gel precursors were characterized by TGA/DTA, while the samples obtained after annealing at 450 degrees C were investigated by FTIR, FESEM, XRD and Mossbauer spectroscopy. Regardless of the type of carboxylic acid used, nanocrystallites prepared by (i) method are similar in size (11-16 nm), while the method (ii) gives crystallites similar to 33 nm in size with negligible microstrain. The differences in the lattice parameter, ranging from 8.3369(2) to 8.3574(2) angstrom, result from cation distribution, nonstoichiometry and structural imperfections in the nickel ferrite nanoparticles. The Mossbauer spectra analysis indicates existence of large distortions of tetrahedral and octahedral sites in these spinel compounds.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites",
pages = "6688-6681",
number = "6",
volume = "39",
doi = "10.1016/j.ceramint.2013.01.106"
}
Nikolić, A. S., Jović, N. G., Rogan, J., Kremenović, A., Ristić, M., Meden, A.,& Antić, B.. (2013). Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites. in Ceramics International
Elsevier Sci Ltd, Oxford., 39(6), 6681-6688.
https://doi.org/10.1016/j.ceramint.2013.01.106
Nikolić AS, Jović NG, Rogan J, Kremenović A, Ristić M, Meden A, Antić B. Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites. in Ceramics International. 2013;39(6):6681-6688.
doi:10.1016/j.ceramint.2013.01.106 .
Nikolić, Aleksandar S., Jović, Nataša G., Rogan, Jelena, Kremenović, Aleksandar, Ristić, Mira, Meden, A., Antić, Bratislav, "Carboxylic acids and polyethylene glycol assisted synthesis of nanocrystalline nickel ferrites" in Ceramics International, 39, no. 6 (2013):6681-6688,
https://doi.org/10.1016/j.ceramint.2013.01.106 . .
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Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction

Kremenović, Aleksandar; Jančar, Boštjan; Ristić, Mira; Vucinić-Vasić, Milica; Rogan, Jelena; Pacevski, Aleksandar; Antić, Bratislav

(Amer Chemical Soc, Washington, 2012)

TY  - JOUR
AU  - Kremenović, Aleksandar
AU  - Jančar, Boštjan
AU  - Ristić, Mira
AU  - Vucinić-Vasić, Milica
AU  - Rogan, Jelena
AU  - Pacevski, Aleksandar
AU  - Antić, Bratislav
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2223
AB  - Transition-metal-oxide/transition-metal nanocomposites, such as NiO/Ni, FeO/Fe, and CoO/Co, have been the subject of much recent investigation (i) because of their potential applications and (ii) because they are good model systems for studies of some effects on the nanoscale. They are used, for example, as catalysts, fuel-cell electrodes, magnetic memories, etc. When a nanocomposite is composed of both ferromagnetic (FM) and antiferromagnetic (AFM) nanoparticles, interesting physical properties can occur, such as the phenomenon of exchange bias (EB). A Ni/NiO nanocomposite obtained by the thermal decomposition of nickel(II) acetate tetrahydrate, Ni(CH3COO)(2)center dot 4H(2)O, at 300 degrees C, is composed of NiO (62%) and Ni (38%) with crystallite sizes of 11 and 278 nm, respectively. We observed an increase in the crystallite size for NiO and decrease of crystallite size for Ni, a decrease in the microstrain for both and an increase in the NiO phase content with thermal annealing in air, while high-energy ball milling leads to a decrease of the crystallite size, an increase in the size of the agglomerates, and microstrain as well as reduction, NiO - gt  Ni. The lattice parameters of the nanosized NiO and Ni show a deviation from the value for the bulk counterparts as a consequence of crystallite size reduction and the grain-surface relaxation effect. The exchange bias found in a milled sample with particles of 10 nm (NiO) and 11 nm (Ni) disappears for larger particles as a consequence of a coupling-area decrease between the antiferromagnetic and ferromagnetic particles. Due to reduction/oxidation (NiO  lt - gt  Ni) and size as well as surface-relaxation effects the saturation magnetization value increases/decreases with milling/annealing, respectively. Having in mind the effect of size on the exchange bias, coercivity, and magnetization values, it is possible, by annealing/milling, to tailor the composition and particle size and then control the exchange bias and improve the other magnetic properties of the Ni/NiO.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Physical Chemistry C
T1  - Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction
EP  - 4364
IS  - 7
SP  - 4356
VL  - 116
DO  - 10.1021/jp206658v
ER  - 
@article{
author = "Kremenović, Aleksandar and Jančar, Boštjan and Ristić, Mira and Vucinić-Vasić, Milica and Rogan, Jelena and Pacevski, Aleksandar and Antić, Bratislav",
year = "2012",
abstract = "Transition-metal-oxide/transition-metal nanocomposites, such as NiO/Ni, FeO/Fe, and CoO/Co, have been the subject of much recent investigation (i) because of their potential applications and (ii) because they are good model systems for studies of some effects on the nanoscale. They are used, for example, as catalysts, fuel-cell electrodes, magnetic memories, etc. When a nanocomposite is composed of both ferromagnetic (FM) and antiferromagnetic (AFM) nanoparticles, interesting physical properties can occur, such as the phenomenon of exchange bias (EB). A Ni/NiO nanocomposite obtained by the thermal decomposition of nickel(II) acetate tetrahydrate, Ni(CH3COO)(2)center dot 4H(2)O, at 300 degrees C, is composed of NiO (62%) and Ni (38%) with crystallite sizes of 11 and 278 nm, respectively. We observed an increase in the crystallite size for NiO and decrease of crystallite size for Ni, a decrease in the microstrain for both and an increase in the NiO phase content with thermal annealing in air, while high-energy ball milling leads to a decrease of the crystallite size, an increase in the size of the agglomerates, and microstrain as well as reduction, NiO - gt  Ni. The lattice parameters of the nanosized NiO and Ni show a deviation from the value for the bulk counterparts as a consequence of crystallite size reduction and the grain-surface relaxation effect. The exchange bias found in a milled sample with particles of 10 nm (NiO) and 11 nm (Ni) disappears for larger particles as a consequence of a coupling-area decrease between the antiferromagnetic and ferromagnetic particles. Due to reduction/oxidation (NiO  lt - gt  Ni) and size as well as surface-relaxation effects the saturation magnetization value increases/decreases with milling/annealing, respectively. Having in mind the effect of size on the exchange bias, coercivity, and magnetization values, it is possible, by annealing/milling, to tailor the composition and particle size and then control the exchange bias and improve the other magnetic properties of the Ni/NiO.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Physical Chemistry C",
title = "Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction",
pages = "4364-4356",
number = "7",
volume = "116",
doi = "10.1021/jp206658v"
}
Kremenović, A., Jančar, B., Ristić, M., Vucinić-Vasić, M., Rogan, J., Pacevski, A.,& Antić, B.. (2012). Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction. in Journal of Physical Chemistry C
Amer Chemical Soc, Washington., 116(7), 4356-4364.
https://doi.org/10.1021/jp206658v
Kremenović A, Jančar B, Ristić M, Vucinić-Vasić M, Rogan J, Pacevski A, Antić B. Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction. in Journal of Physical Chemistry C. 2012;116(7):4356-4364.
doi:10.1021/jp206658v .
Kremenović, Aleksandar, Jančar, Boštjan, Ristić, Mira, Vucinić-Vasić, Milica, Rogan, Jelena, Pacevski, Aleksandar, Antić, Bratislav, "Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction" in Journal of Physical Chemistry C, 116, no. 7 (2012):4356-4364,
https://doi.org/10.1021/jp206658v . .
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Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes

Kremenović, Aleksandar; Antić, Bratislav; Vucinić-Vasić, Milica; Ristić, Mira; Jančar, Boštjan; Rogan, Jelena

(Int Union Crystallography, Chester, 2011)

TY  - JOUR
AU  - Kremenović, Aleksandar
AU  - Antić, Bratislav
AU  - Vucinić-Vasić, Milica
AU  - Ristić, Mira
AU  - Jančar, Boštjan
AU  - Rogan, Jelena
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1771
PB  - Int Union Crystallography, Chester
T2  - Acta Crystallographica A-Foundation and Advances
T1  - Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes
EP  - C324
SP  - C324
VL  - 67
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1771
ER  - 
@article{
author = "Kremenović, Aleksandar and Antić, Bratislav and Vucinić-Vasić, Milica and Ristić, Mira and Jančar, Boštjan and Rogan, Jelena",
year = "2011",
publisher = "Int Union Crystallography, Chester",
journal = "Acta Crystallographica A-Foundation and Advances",
title = "Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes",
pages = "C324-C324",
volume = "67",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1771"
}
Kremenović, A., Antić, B., Vucinić-Vasić, M., Ristić, M., Jančar, B.,& Rogan, J.. (2011). Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes. in Acta Crystallographica A-Foundation and Advances
Int Union Crystallography, Chester., 67, C324-C324.
https://hdl.handle.net/21.15107/rcub_technorep_1771
Kremenović A, Antić B, Vucinić-Vasić M, Ristić M, Jančar B, Rogan J. Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes. in Acta Crystallographica A-Foundation and Advances. 2011;67:C324-C324.
https://hdl.handle.net/21.15107/rcub_technorep_1771 .
Kremenović, Aleksandar, Antić, Bratislav, Vucinić-Vasić, Milica, Ristić, Mira, Jančar, Boštjan, Rogan, Jelena, "Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes" in Acta Crystallographica A-Foundation and Advances, 67 (2011):C324-C324,
https://hdl.handle.net/21.15107/rcub_technorep_1771 .

Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes

Antić, Bratislav; Rogan, Jelena; Kremenović, Aleksandar; Nikolić, Aleksandar S.; Vucinić-Vasić, Milica; Božanić, Dušan K.; Goya, G. F.; Colomban, Ph

(IOP Publishing Ltd, Bristol, 2010)

TY  - JOUR
AU  - Antić, Bratislav
AU  - Rogan, Jelena
AU  - Kremenović, Aleksandar
AU  - Nikolić, Aleksandar S.
AU  - Vucinić-Vasić, Milica
AU  - Božanić, Dušan K.
AU  - Goya, G. F.
AU  - Colomban, Ph
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1693
AB  - Spherical shaped nanoparticles of series Y2-xEuxO3 (x = 0.06, 0.10, 0.20, and 2) and Gd2-xEuxO3 (x = 0.06, 0.10) were prepared by thermolysis of 2,4-pentanedione complexes of Y, Gd, and Eu. The bixbyite phase of Gd2-xEuxO3 samples was formed at 500 degrees C, whereas the thermal decomposition of Y and Eu complexes' mixtures occurred at higher temperatures. Linearity in the concentration dependence on lattice parameter confirmed the formation of solid solutions. The distribution of Eu3+ in Gd2-xEuxO3 was changed with thermal annealing: in the as-prepared sample (x = 0.10) the distribution was preferential at C-3i sites while in the annealed samples, Eu3+ were distributed at both C-2 and C-3i sites. Rietveld refinement of site occupancies as well as emission spectra showed a random distribution of cations in Y2-xEuxO3. The photoluminescence (PL) measurements of the sample showed red emission with the main peak at 614 nm (D-5(0)-F-7(2)). The PL intensity increased with increasing concentration of Eu3+ in both series. Infrared excitation was required to obtain good Raman spectra. The linear dependence of the main Raman peak wavenumber offers a non-destructive method for monitoring the substitution level and its homogeneity at the micron scale.
PB  - IOP Publishing Ltd, Bristol
T2  - Nanotechnology
T1  - Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes
IS  - 24
VL  - 21
DO  - 10.1088/0957-4484/21/24/245702
ER  - 
@article{
author = "Antić, Bratislav and Rogan, Jelena and Kremenović, Aleksandar and Nikolić, Aleksandar S. and Vucinić-Vasić, Milica and Božanić, Dušan K. and Goya, G. F. and Colomban, Ph",
year = "2010",
abstract = "Spherical shaped nanoparticles of series Y2-xEuxO3 (x = 0.06, 0.10, 0.20, and 2) and Gd2-xEuxO3 (x = 0.06, 0.10) were prepared by thermolysis of 2,4-pentanedione complexes of Y, Gd, and Eu. The bixbyite phase of Gd2-xEuxO3 samples was formed at 500 degrees C, whereas the thermal decomposition of Y and Eu complexes' mixtures occurred at higher temperatures. Linearity in the concentration dependence on lattice parameter confirmed the formation of solid solutions. The distribution of Eu3+ in Gd2-xEuxO3 was changed with thermal annealing: in the as-prepared sample (x = 0.10) the distribution was preferential at C-3i sites while in the annealed samples, Eu3+ were distributed at both C-2 and C-3i sites. Rietveld refinement of site occupancies as well as emission spectra showed a random distribution of cations in Y2-xEuxO3. The photoluminescence (PL) measurements of the sample showed red emission with the main peak at 614 nm (D-5(0)-F-7(2)). The PL intensity increased with increasing concentration of Eu3+ in both series. Infrared excitation was required to obtain good Raman spectra. The linear dependence of the main Raman peak wavenumber offers a non-destructive method for monitoring the substitution level and its homogeneity at the micron scale.",
publisher = "IOP Publishing Ltd, Bristol",
journal = "Nanotechnology",
title = "Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes",
number = "24",
volume = "21",
doi = "10.1088/0957-4484/21/24/245702"
}
Antić, B., Rogan, J., Kremenović, A., Nikolić, A. S., Vucinić-Vasić, M., Božanić, D. K., Goya, G. F.,& Colomban, P.. (2010). Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes. in Nanotechnology
IOP Publishing Ltd, Bristol., 21(24).
https://doi.org/10.1088/0957-4484/21/24/245702
Antić B, Rogan J, Kremenović A, Nikolić AS, Vucinić-Vasić M, Božanić DK, Goya GF, Colomban P. Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes. in Nanotechnology. 2010;21(24).
doi:10.1088/0957-4484/21/24/245702 .
Antić, Bratislav, Rogan, Jelena, Kremenović, Aleksandar, Nikolić, Aleksandar S., Vucinić-Vasić, Milica, Božanić, Dušan K., Goya, G. F., Colomban, Ph, "Optimization of photoluminescence of Y2O3:Eu and Gd2O3:Eu phosphors synthesized by thermolysis of 2,4-pentanedione complexes" in Nanotechnology, 21, no. 24 (2010),
https://doi.org/10.1088/0957-4484/21/24/245702 . .
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Disorder of lattice solvent molecules in the structure of hexaaqua(μ2-1,2,4,5-benzenetetracarboxylato)-bis(2,2’-dipyridylamine)dinickel(II) hexahydrate DMSO solvate

Poleti, Dejan; Karanović, Ljiljana; Kremenović, Aleksandar; Rogan, Jelena

(Serbian Chemical Society, Belgrade, 2007)

TY  - JOUR
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Kremenović, Aleksandar
AU  - Rogan, Jelena
PY  - 2007
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1166
AB  - The crystal structure of the complex [Ni2(btc)(dipya)2(H2O)6]⋅6H2O·DMSO (btc = tetra-anion of 1,2,4,5-benzenetetracarboxylic acid, dipya = 2,2’-dipyridylamine) was refined in the triclinic system, space group P1, using low temperature (170 K) X-ray diffraction data. The compound consists of binuclear complex entities and lattice solvent molecules making pseudo-layers parallel to the 101 plane and channels parallel to the b-axis. The observed structural features were compared with the previously reported results and formula [Ni2(btc)(dipya)2(H2O)6]⋅4H2O based on room temperature X-ray diffraction data. A possible arrangement of the disordered lattice solvent molecules located in the structural channels is described and discussed. It is concluded that the layout of these molecules is non-centrosymmetric, although the remaining and main part of the structure is centrosymmetric. .
AB  - Kristalna struktura kompleksa [Ni2(btc)(dipya)2(H2O)6]⋅6H2O·DMSO (btc = tetraanjon 1,2,4,5-benzentetrakarboksilne kiseline, dipya = 2,2’-dipiridilamin) utačnjena je u trikliničnom sistemu, prostorna grupa P1, na osnovu podataka dobijenih rendgenskom difrakcijom na niskoj temperaturi (170K). Jedinjenje se sastoji od binuklearnih kompleksnih jedinki i nekoordiniranih molekula rastvarača, koji formiraju pseudo-slojeve paralelne ravni 101 i kanale paralelne b-osi. Strukturne karakteristike kompleksa upoređene su sa ranije objavljenim rezultatima i formulom [Ni2(btc)(dipya)2(H2O)6]⋅4H2O, koji su bili zasnovani na podacima prikupljenim na sobnoj temperaturi. U radu je opisan i diskutovan mogući raspored neuređenih molekula rastvarača koji se nalaze u ranije pomenutim kanalima. Zaključeno je da raspored tih molekula mora biti necentrosimetričan, iako je preostali i najveći deo strukture centrosimetričan. .
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Disorder of lattice solvent molecules in the structure of hexaaqua(μ2-1,2,4,5-benzenetetracarboxylato)-bis(2,2’-dipyridylamine)dinickel(II) hexahydrate DMSO solvate
T1  - Neuređenost molekula rastvarača u strukturi heksaakva(μ2-1,2,4,5-benzentetrakarboksilato)-bis(2,2’-dipiridilamin)dinikal(II)-heksahidrata-DMSO solvata
EP  - 771
IS  - 8-9
SP  - 767
VL  - 72
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1166
ER  - 
@article{
author = "Poleti, Dejan and Karanović, Ljiljana and Kremenović, Aleksandar and Rogan, Jelena",
year = "2007",
abstract = "The crystal structure of the complex [Ni2(btc)(dipya)2(H2O)6]⋅6H2O·DMSO (btc = tetra-anion of 1,2,4,5-benzenetetracarboxylic acid, dipya = 2,2’-dipyridylamine) was refined in the triclinic system, space group P1, using low temperature (170 K) X-ray diffraction data. The compound consists of binuclear complex entities and lattice solvent molecules making pseudo-layers parallel to the 101 plane and channels parallel to the b-axis. The observed structural features were compared with the previously reported results and formula [Ni2(btc)(dipya)2(H2O)6]⋅4H2O based on room temperature X-ray diffraction data. A possible arrangement of the disordered lattice solvent molecules located in the structural channels is described and discussed. It is concluded that the layout of these molecules is non-centrosymmetric, although the remaining and main part of the structure is centrosymmetric. ., Kristalna struktura kompleksa [Ni2(btc)(dipya)2(H2O)6]⋅6H2O·DMSO (btc = tetraanjon 1,2,4,5-benzentetrakarboksilne kiseline, dipya = 2,2’-dipiridilamin) utačnjena je u trikliničnom sistemu, prostorna grupa P1, na osnovu podataka dobijenih rendgenskom difrakcijom na niskoj temperaturi (170K). Jedinjenje se sastoji od binuklearnih kompleksnih jedinki i nekoordiniranih molekula rastvarača, koji formiraju pseudo-slojeve paralelne ravni 101 i kanale paralelne b-osi. Strukturne karakteristike kompleksa upoređene su sa ranije objavljenim rezultatima i formulom [Ni2(btc)(dipya)2(H2O)6]⋅4H2O, koji su bili zasnovani na podacima prikupljenim na sobnoj temperaturi. U radu je opisan i diskutovan mogući raspored neuređenih molekula rastvarača koji se nalaze u ranije pomenutim kanalima. Zaključeno je da raspored tih molekula mora biti necentrosimetričan, iako je preostali i najveći deo strukture centrosimetričan. .",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Disorder of lattice solvent molecules in the structure of hexaaqua(μ2-1,2,4,5-benzenetetracarboxylato)-bis(2,2’-dipyridylamine)dinickel(II) hexahydrate DMSO solvate, Neuređenost molekula rastvarača u strukturi heksaakva(μ2-1,2,4,5-benzentetrakarboksilato)-bis(2,2’-dipiridilamin)dinikal(II)-heksahidrata-DMSO solvata",
pages = "771-767",
number = "8-9",
volume = "72",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1166"
}
Poleti, D., Karanović, L., Kremenović, A.,& Rogan, J.. (2007). Disorder of lattice solvent molecules in the structure of hexaaqua(μ2-1,2,4,5-benzenetetracarboxylato)-bis(2,2’-dipyridylamine)dinickel(II) hexahydrate DMSO solvate. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 72(8-9), 767-771.
https://hdl.handle.net/21.15107/rcub_technorep_1166
Poleti D, Karanović L, Kremenović A, Rogan J. Disorder of lattice solvent molecules in the structure of hexaaqua(μ2-1,2,4,5-benzenetetracarboxylato)-bis(2,2’-dipyridylamine)dinickel(II) hexahydrate DMSO solvate. in Journal of the Serbian Chemical Society. 2007;72(8-9):767-771.
https://hdl.handle.net/21.15107/rcub_technorep_1166 .
Poleti, Dejan, Karanović, Ljiljana, Kremenović, Aleksandar, Rogan, Jelena, "Disorder of lattice solvent molecules in the structure of hexaaqua(μ2-1,2,4,5-benzenetetracarboxylato)-bis(2,2’-dipyridylamine)dinickel(II) hexahydrate DMSO solvate" in Journal of the Serbian Chemical Society, 72, no. 8-9 (2007):767-771,
https://hdl.handle.net/21.15107/rcub_technorep_1166 .
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