TY  - JOUR
AU  - Rogan, Jelena
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Jaglicić, Zvonko
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1922
AB  - A series of novel ternary Co(II), Ni(II) and Cu(II) complexes containing 2,2'-dipyridylamine (dipya), 2,2'-bipyridine (bipy), and 1,10-phenanthroline (phen), as aromatic diamine ligands, and dianion of isophthalic acid (ipht) have been prepared by ligand exchange reactions from diluted H2O/EtOH solutions. The complexes were characterized by elemental analysis, IR spectroscopy, magnetic susceptibility measurements and TG and DSC analysis. Three complexes, Cu(dipya)(ipht)center dot H2O (1), Co(dipya)(ipht)center dot 2H(2)O (2) and Cu(ipht)(phen)center dot 2H(2)O (5) are polymeric with bis-monodentate ipht, while the other two complexes M(bipy)(iPht)center dot 4H(2)O, M=Co(II) (3) and Ni(II) (4), contain ipht as a counter ion. All Co(II) and Ni(II) complexes are (pseudo)octahedral, while Cu(II) complexes have square-pyramidal or distorted octahedral geometry. The variable temperature magnetic susceptibility measurements showed very weak antiferromagnetic behaviour for all complexes. Dehydration processes, decomposition mechanisms and thermal stability of 1-5 are assumed. One complex from the above series, [Ni(bipy)(H2O)(4)](iPht) (4), and one additional complex, [Co(bipy)(iPht)](n) (6), are obtained as single-crystals and their structures are determined from X-ray diffraction data. In both structures M(II) centers are in deformed octahedral environment and they are linked by hemi-ipht ligands (4) and two different bridging ipht ligands (6). Three-dimensional networks in 4 and 6 are governed by strong noncovalent interactions. The cations and ipht anions in 4 are connected by hydrogen bonds building double layers parallel to ab-plane that are further packed by pi-pi interactions. In 6 double chains extending along b-axis are strengthened by interchain pi-pi interactions constructing a three-dimensional framework.
PB  - Elsevier, Amsterdam
T2  - Journal of Molecular Structure
T1  - Synthesis, magnetic, thermal and structural properties of Co(II), Ni(II) and Cu(II) complexes containing isophthalato ligands
EP  - 379
IS  - 2-3
SP  - 371
VL  - 985
DO  - 10.1016/j.molstruc.2010.11.024
ER  - 

@article{
author = "Rogan, Jelena and Poleti, Dejan and Karanović, Ljiljana and Jaglicić, Zvonko",
year = "2011",
abstract = "A series of novel ternary Co(II), Ni(II) and Cu(II) complexes containing 2,2'-dipyridylamine (dipya), 2,2'-bipyridine (bipy), and 1,10-phenanthroline (phen), as aromatic diamine ligands, and dianion of isophthalic acid (ipht) have been prepared by ligand exchange reactions from diluted H2O/EtOH solutions. The complexes were characterized by elemental analysis, IR spectroscopy, magnetic susceptibility measurements and TG and DSC analysis. Three complexes, Cu(dipya)(ipht)center dot H2O (1), Co(dipya)(ipht)center dot 2H(2)O (2) and Cu(ipht)(phen)center dot 2H(2)O (5) are polymeric with bis-monodentate ipht, while the other two complexes M(bipy)(iPht)center dot 4H(2)O, M=Co(II) (3) and Ni(II) (4), contain ipht as a counter ion. All Co(II) and Ni(II) complexes are (pseudo)octahedral, while Cu(II) complexes have square-pyramidal or distorted octahedral geometry. The variable temperature magnetic susceptibility measurements showed very weak antiferromagnetic behaviour for all complexes. Dehydration processes, decomposition mechanisms and thermal stability of 1-5 are assumed. One complex from the above series, [Ni(bipy)(H2O)(4)](iPht) (4), and one additional complex, [Co(bipy)(iPht)](n) (6), are obtained as single-crystals and their structures are determined from X-ray diffraction data. In both structures M(II) centers are in deformed octahedral environment and they are linked by hemi-ipht ligands (4) and two different bridging ipht ligands (6). Three-dimensional networks in 4 and 6 are governed by strong noncovalent interactions. The cations and ipht anions in 4 are connected by hydrogen bonds building double layers parallel to ab-plane that are further packed by pi-pi interactions. In 6 double chains extending along b-axis are strengthened by interchain pi-pi interactions constructing a three-dimensional framework.",
publisher = "Elsevier, Amsterdam",
journal = "Journal of Molecular Structure",
title = "Synthesis, magnetic, thermal and structural properties of Co(II), Ni(II) and Cu(II) complexes containing isophthalato ligands",
pages = "379-371",
number = "2-3",
volume = "985",
doi = "10.1016/j.molstruc.2010.11.024"
}

Rogan, J., Poleti, D., Karanović, L.,& Jaglicić, Z.. (2011). Synthesis, magnetic, thermal and structural properties of Co(II), Ni(II) and Cu(II) complexes containing isophthalato ligands. in Journal of Molecular Structure
Elsevier, Amsterdam., 985(2-3), 371-379.
https://doi.org/10.1016/j.molstruc.2010.11.024

Rogan J, Poleti D, Karanović L, Jaglicić Z. Synthesis, magnetic, thermal and structural properties of Co(II), Ni(II) and Cu(II) complexes containing isophthalato ligands. in Journal of Molecular Structure. 2011;985(2-3):371-379.
doi:10.1016/j.molstruc.2010.11.024 .

Rogan, Jelena, Poleti, Dejan, Karanović, Ljiljana, Jaglicić, Zvonko, "Synthesis, magnetic, thermal and structural properties of Co(II), Ni(II) and Cu(II) complexes containing isophthalato ligands" in Journal of Molecular Structure, 985, no. 2-3 (2011):371-379,
https://doi.org/10.1016/j.molstruc.2010.11.024 . .

TY  - JOUR
AU  - Popov-Pergal, Katarina M.
AU  - Poleti, Dejan
AU  - Rancic, Milica P.
AU  - Meden, Antun
AU  - Pergal, Marija
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5616
AB  - The derivatives of 5-substituted-2,4-thiazolidinedione have a broad spectrum of biological activities. In this article, new 5-(arylidene)-3-(4-methylbenzoyl)thiayolidine-2,4-diones 3a-k, with arylidene groups such as 4-phenylbenzylidene 3a, 3,4-dimethoxybenzylidene 3b, 2-hydroxybenzylidene 3c, 4-ethoxybenzylidene 3d, 5-methyl-2-furfurylidene 3e, 4-dimethylaminobenzylidene 3f, 1-naphthylidene 3g, 3,4-methylenedioxybenzylidene 3h, 4-benzyloxybenzylidene 3i, benzylidene 3j, and 4-methoxybenzylidene 3k, were synthesized by direct acylation of alkali metal salts of 5-arylidene-2,4-thiazolidinediones with 4-methylbenzoylchloride. Their structures were confirmed by elemental analysis, IR, (1)H NMR and MS spectroscopy. In addition, crystal structure of the compound 3d was determined using single-crystal X-ray diffraction data.
PB  - Wiley-Blackwell Publishing, Inc, Malden
T2  - Journal of Heterocyclic Chemistry
T1  - Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones
EP  - 228
IS  - 1
SP  - 224
VL  - 47
DO  - 10.1002/jhet.288
ER  - 

@article{
author = "Popov-Pergal, Katarina M. and Poleti, Dejan and Rancic, Milica P. and Meden, Antun and Pergal, Marija",
year = "2010",
abstract = "The derivatives of 5-substituted-2,4-thiazolidinedione have a broad spectrum of biological activities. In this article, new 5-(arylidene)-3-(4-methylbenzoyl)thiayolidine-2,4-diones 3a-k, with arylidene groups such as 4-phenylbenzylidene 3a, 3,4-dimethoxybenzylidene 3b, 2-hydroxybenzylidene 3c, 4-ethoxybenzylidene 3d, 5-methyl-2-furfurylidene 3e, 4-dimethylaminobenzylidene 3f, 1-naphthylidene 3g, 3,4-methylenedioxybenzylidene 3h, 4-benzyloxybenzylidene 3i, benzylidene 3j, and 4-methoxybenzylidene 3k, were synthesized by direct acylation of alkali metal salts of 5-arylidene-2,4-thiazolidinediones with 4-methylbenzoylchloride. Their structures were confirmed by elemental analysis, IR, (1)H NMR and MS spectroscopy. In addition, crystal structure of the compound 3d was determined using single-crystal X-ray diffraction data.",
publisher = "Wiley-Blackwell Publishing, Inc, Malden",
journal = "Journal of Heterocyclic Chemistry",
title = "Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones",
pages = "228-224",
number = "1",
volume = "47",
doi = "10.1002/jhet.288"
}

Popov-Pergal, K. M., Poleti, D., Rancic, M. P., Meden, A.,& Pergal, M.. (2010). Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones. in Journal of Heterocyclic Chemistry
Wiley-Blackwell Publishing, Inc, Malden., 47(1), 224-228.
https://doi.org/10.1002/jhet.288

Popov-Pergal KM, Poleti D, Rancic MP, Meden A, Pergal M. Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones. in Journal of Heterocyclic Chemistry. 2010;47(1):224-228.
doi:10.1002/jhet.288 .

Popov-Pergal, Katarina M., Poleti, Dejan, Rancic, Milica P., Meden, Antun, Pergal, Marija, "Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones" in Journal of Heterocyclic Chemistry, 47, no. 1 (2010):224-228,
https://doi.org/10.1002/jhet.288 . .

TY  - JOUR
AU  - Šumar-Ristović, Maja
AU  - Minić, Dragica M.
AU  - Poleti, Dejan
AU  - Miodragović, Zoran
AU  - Miodragović Đenana U.
AU  - Anđelković, Katarina K.
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5620
AB  - Thermal behavior of Co(II), Cd(II), and Zn(II) complexes with N-benzyloxycarbonylglycinato ligand was investigated using the results of TG, DSC and DTG analysis obtained at different heating rates (2.5 to 30 A degrees C min(-1)), from room temperature to about 900 A degrees C. Mechanisms of complex degradation, as well as enthalpies of the degradation processes were determined. It is shown that thermal stability of investigated complexes correlates with their crystal structures, especially with the presence of crystallization and coordinated water molecules. The values of dehydration enthalpies are discussed and correlated with composition of the complexes. Kissinger's, Ozawa's, and Friedman's isoconversion methods were used for the determination of kinetic parameters: the pre-exponential factor A and the apparent activation energy E (a). For all three complexes and all steps of degradation, the values of kinetics parameters obtained by Kissinger's and Ozawa's methods are in good agreement. The results obtained by Friedman's method showed that some decomposition steps are simple and some others are complex ones.
PB  - Springer, Dordrecht
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Thermal stability and degradation of Co(II), Cd(II), and Zn(II) complexes with N-benzyloxycarbonylglycinato ligand
EP  - 90
IS  - 1
SP  - 83
VL  - 102
DO  - 10.1007/s10973-010-0748-2
ER  - 

@article{
author = "Šumar-Ristović, Maja and Minić, Dragica M. and Poleti, Dejan and Miodragović, Zoran and Miodragović Đenana U. and Anđelković, Katarina K.",
year = "2010",
abstract = "Thermal behavior of Co(II), Cd(II), and Zn(II) complexes with N-benzyloxycarbonylglycinato ligand was investigated using the results of TG, DSC and DTG analysis obtained at different heating rates (2.5 to 30 A degrees C min(-1)), from room temperature to about 900 A degrees C. Mechanisms of complex degradation, as well as enthalpies of the degradation processes were determined. It is shown that thermal stability of investigated complexes correlates with their crystal structures, especially with the presence of crystallization and coordinated water molecules. The values of dehydration enthalpies are discussed and correlated with composition of the complexes. Kissinger's, Ozawa's, and Friedman's isoconversion methods were used for the determination of kinetic parameters: the pre-exponential factor A and the apparent activation energy E (a). For all three complexes and all steps of degradation, the values of kinetics parameters obtained by Kissinger's and Ozawa's methods are in good agreement. The results obtained by Friedman's method showed that some decomposition steps are simple and some others are complex ones.",
publisher = "Springer, Dordrecht",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Thermal stability and degradation of Co(II), Cd(II), and Zn(II) complexes with N-benzyloxycarbonylglycinato ligand",
pages = "90-83",
number = "1",
volume = "102",
doi = "10.1007/s10973-010-0748-2"
}

Šumar-Ristović, M., Minić, D. M., Poleti, D., Miodragović, Z., Miodragović Đenana U.,& Anđelković, K. K.. (2010). Thermal stability and degradation of Co(II), Cd(II), and Zn(II) complexes with N-benzyloxycarbonylglycinato ligand. in Journal of Thermal Analysis and Calorimetry
Springer, Dordrecht., 102(1), 83-90.
https://doi.org/10.1007/s10973-010-0748-2

Šumar-Ristović M, Minić DM, Poleti D, Miodragović Z, Miodragović Đenana U., Anđelković KK. Thermal stability and degradation of Co(II), Cd(II), and Zn(II) complexes with N-benzyloxycarbonylglycinato ligand. in Journal of Thermal Analysis and Calorimetry. 2010;102(1):83-90.
doi:10.1007/s10973-010-0748-2 .

Šumar-Ristović, Maja, Minić, Dragica M., Poleti, Dejan, Miodragović, Zoran, Miodragović Đenana U., Anđelković, Katarina K., "Thermal stability and degradation of Co(II), Cd(II), and Zn(II) complexes with N-benzyloxycarbonylglycinato ligand" in Journal of Thermal Analysis and Calorimetry, 102, no. 1 (2010):83-90,
https://doi.org/10.1007/s10973-010-0748-2 . .

TY  - JOUR
AU  - Zdujić, Miodrag
AU  - Poleti, Dejan
AU  - Jovalekić, Čedomir
AU  - Karanović, Ljiljana
PY  - 2009
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5532
AB  - A powder mixture of α-Bi2O3 and HfO2, in the molar ratio 2:3, was mechanochemically treated in a planetary ball mill under air, using zirconium oxide vials and balls as the milling medium. After 50 h of milling, the mechanochemical reaction led to the formation of a nanocrystalline δ-Bi2O3 phase (fluorite-type solid solution Bi0.78Hf0.59Zr0.63O3.61), with a crystallite size of 20 nm. The mechanochemical reaction started at a very beginning of milling accompanied by an accumulation of ZrO2 arising from the milling tools. The samples prepared after various milling times were characterized by X-ray powder diffraction and DSC analysis. The electrical properties of the as-milled and pressed Bi0.78Hf0.59Zr0.63O3.61 powder were studied using impedance spectroscopy in the temperature range from 100 to 700°C under air. The electrical conductivity was determined to be 9.43×10-6 and 0.080 S cm-1 for the temperatures of 300 and 700°C, respectively.
AB  - Smeša prahova α-Bi2O3 i HfO2 u molarnom odnosu 2:3 mehanohemijski je tretirana u planetarnom mlinu u atmosferi vazduha, koristeći cirkonijumske posude i kuglice kao medijum za mlevenje. Posle 50 h mlevenja, mehanohemijska reakcija dovodi do stvaranja nanokristalne δ-Bi2O3 faze (čvrsti rastvor fluoritske strukture Bi0,78Hf0,59Zr0,63O3,61), veličine kristalita 20 nm. Mehanohemijska reakcija otpočinje u samom početku mlevenja i praćena je akumulacijum ZrO2 koji potiče od medijuma za mlevenje. Uzorci dobijeni posle različitih vremena mlevenja karakterisani su rendgenskom strukturnom i termijskom analizom. Električna svojstva mlevenih i presovanih Bi0,78Hf0,59Zr0,63O3,61 prahova ispitivana su impedansnom spektroskopijom u temperaturnom opsegu od 100 do 700°C. Dobijena električna provodnost je 9,43·10-6 i 0,080 S cm-1 za temperaturu 300 i 700°C, redom.
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2
EP  - 1411
IS  - 12
SP  - 1401
VL  - 74
DO  - 10.2298/JSC0912401Z
UR  - https://hdl.handle.net/21.15107/rcub_dais_174
ER  - 

@article{
author = "Zdujić, Miodrag and Poleti, Dejan and Jovalekić, Čedomir and Karanović, Ljiljana",
year = "2009",
abstract = "A powder mixture of α-Bi2O3 and HfO2, in the molar ratio 2:3, was mechanochemically treated in a planetary ball mill under air, using zirconium oxide vials and balls as the milling medium. After 50 h of milling, the mechanochemical reaction led to the formation of a nanocrystalline δ-Bi2O3 phase (fluorite-type solid solution Bi0.78Hf0.59Zr0.63O3.61), with a crystallite size of 20 nm. The mechanochemical reaction started at a very beginning of milling accompanied by an accumulation of ZrO2 arising from the milling tools. The samples prepared after various milling times were characterized by X-ray powder diffraction and DSC analysis. The electrical properties of the as-milled and pressed Bi0.78Hf0.59Zr0.63O3.61 powder were studied using impedance spectroscopy in the temperature range from 100 to 700°C under air. The electrical conductivity was determined to be 9.43×10-6 and 0.080 S cm-1 for the temperatures of 300 and 700°C, respectively., Smeša prahova α-Bi2O3 i HfO2 u molarnom odnosu 2:3 mehanohemijski je tretirana u planetarnom mlinu u atmosferi vazduha, koristeći cirkonijumske posude i kuglice kao medijum za mlevenje. Posle 50 h mlevenja, mehanohemijska reakcija dovodi do stvaranja nanokristalne δ-Bi2O3 faze (čvrsti rastvor fluoritske strukture Bi0,78Hf0,59Zr0,63O3,61), veličine kristalita 20 nm. Mehanohemijska reakcija otpočinje u samom početku mlevenja i praćena je akumulacijum ZrO2 koji potiče od medijuma za mlevenje. Uzorci dobijeni posle različitih vremena mlevenja karakterisani su rendgenskom strukturnom i termijskom analizom. Električna svojstva mlevenih i presovanih Bi0,78Hf0,59Zr0,63O3,61 prahova ispitivana su impedansnom spektroskopijom u temperaturnom opsegu od 100 do 700°C. Dobijena električna provodnost je 9,43·10-6 i 0,080 S cm-1 za temperaturu 300 i 700°C, redom.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2",
pages = "1411-1401",
number = "12",
volume = "74",
doi = "10.2298/JSC0912401Z",
url = "https://hdl.handle.net/21.15107/rcub_dais_174"
}

Zdujić, M., Poleti, D., Jovalekić, Č.,& Karanović, L.. (2009). Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 74(12), 1401-1411.
https://doi.org/10.2298/JSC0912401Z
https://hdl.handle.net/21.15107/rcub_dais_174

Zdujić M, Poleti D, Jovalekić Č, Karanović L. Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2. in Journal of the Serbian Chemical Society. 2009;74(12):1401-1411.
doi:10.2298/JSC0912401Z
https://hdl.handle.net/21.15107/rcub_dais_174 .

Zdujić, Miodrag, Poleti, Dejan, Jovalekić, Čedomir, Karanović, Ljiljana, "Mechanochemical synthesis and electrical conductivity of nanocrystalline δ-Bi2O3 stabilized by HfO2 and ZrO2" in Journal of the Serbian Chemical Society, 74, no. 12 (2009):1401-1411,
https://doi.org/10.2298/JSC0912401Z .,
https://hdl.handle.net/21.15107/rcub_dais_174 .

TY  - JOUR
AU  - Zdujić, Miodrag
AU  - Jovalekić, Čedomir
AU  - Poleti, Dejan
AU  - Veljković, Ivana
AU  - Karanović, Ljiljana
PY  - 2009
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5533
AB  - Concurrent milling of Bi4Ti3O12 was carried out in a planetary ball mill with hardened-steel 13 or 6 mm diameter balls with a goal to investigate how the system responds to the constrains imposed by milling. Milling intensity for various milling parameters was derived from the electrical power measurement. The reverse amorphous ↔ crystalline phase transition induced by milling is governed by impact energy and frequency. Below a certain threshold value of impact energy crystallization does not occur, whereas a higher impact frequency accelerates amorphization. Mechanochemical reactions are predominantly discrete processes, which occur at the moment of impact. © 2009 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Materials Letters
T1  - Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound
EP  - 2544
IS  - 29
SP  - 2542
VL  - 63
DO  - 10.1016/j.matlet.2009.08.055
UR  - https://hdl.handle.net/21.15107/rcub_dais_3454
ER  - 

@article{
author = "Zdujić, Miodrag and Jovalekić, Čedomir and Poleti, Dejan and Veljković, Ivana and Karanović, Ljiljana",
year = "2009",
abstract = "Concurrent milling of Bi4Ti3O12 was carried out in a planetary ball mill with hardened-steel 13 or 6 mm diameter balls with a goal to investigate how the system responds to the constrains imposed by milling. Milling intensity for various milling parameters was derived from the electrical power measurement. The reverse amorphous ↔ crystalline phase transition induced by milling is governed by impact energy and frequency. Below a certain threshold value of impact energy crystallization does not occur, whereas a higher impact frequency accelerates amorphization. Mechanochemical reactions are predominantly discrete processes, which occur at the moment of impact. © 2009 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Materials Letters",
title = "Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound",
pages = "2544-2542",
number = "29",
volume = "63",
doi = "10.1016/j.matlet.2009.08.055",
url = "https://hdl.handle.net/21.15107/rcub_dais_3454"
}

Zdujić, M., Jovalekić, Č., Poleti, D., Veljković, I.,& Karanović, L.. (2009). Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound. in Materials Letters
Elsevier., 63(29), 2542-2544.
https://doi.org/10.1016/j.matlet.2009.08.055
https://hdl.handle.net/21.15107/rcub_dais_3454

Zdujić M, Jovalekić Č, Poleti D, Veljković I, Karanović L. Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound. in Materials Letters. 2009;63(29):2542-2544.
doi:10.1016/j.matlet.2009.08.055
https://hdl.handle.net/21.15107/rcub_dais_3454 .

Zdujić, Miodrag, Jovalekić, Čedomir, Poleti, Dejan, Veljković, Ivana, Karanović, Ljiljana, "Mechanochemically induced amorphous/crystalline phase transition in the Bi4Ti3O12 compound" in Materials Letters, 63, no. 29 (2009):2542-2544,
https://doi.org/10.1016/j.matlet.2009.08.055 .,
https://hdl.handle.net/21.15107/rcub_dais_3454 .

TY  - JOUR
AU  - Veljković, Ivana
AU  - Poleti, Dejan
AU  - Zdujić, Miodrag
AU  - Karanović, Ljiljana
PY  - 2009
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5534
AB  - Mechanochemistry represents an alternative route in synthesis of nanomaterials. Mechanochemical routes are attractive because of their simplicity, flexibility, and ability to prepare materials by solid state reactions at room temperature. The aim of this work is the mechanochemical synthesis of nanostructured titanium oxides of different composition starting from mixtures of Ti and TiO2, TiO and TiO2 or Ti 2O3 and TiO2. Emphasis is on the Magneli phases Ti4O7 and Ti5O9 because their mixture is commercially known as EBONEX material. The materials prepared were characterized by XRPD, TG/DTA analysis, SEM and optical microscopy. Titanium monoxide and several Magneli oxides, Ti4O7, Ti 5O9 and Ti6O11, are successsfully prepared. The results are very interesting because the EBONEX materials were prepared at lower than usual temperature, which would decrease the effective cost of production.
PB  - Belgrade : Association of the Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Mechanochemistry of titanium oxides
EP  - 251
IS  - 3
SP  - 247
VL  - 63
DO  - 10.2298/HEMIND0903247V
UR  - https://hdl.handle.net/21.15107/rcub_dais_3458
ER  - 

@article{
author = "Veljković, Ivana and Poleti, Dejan and Zdujić, Miodrag and Karanović, Ljiljana",
year = "2009",
abstract = "Mechanochemistry represents an alternative route in synthesis of nanomaterials. Mechanochemical routes are attractive because of their simplicity, flexibility, and ability to prepare materials by solid state reactions at room temperature. The aim of this work is the mechanochemical synthesis of nanostructured titanium oxides of different composition starting from mixtures of Ti and TiO2, TiO and TiO2 or Ti 2O3 and TiO2. Emphasis is on the Magneli phases Ti4O7 and Ti5O9 because their mixture is commercially known as EBONEX material. The materials prepared were characterized by XRPD, TG/DTA analysis, SEM and optical microscopy. Titanium monoxide and several Magneli oxides, Ti4O7, Ti 5O9 and Ti6O11, are successsfully prepared. The results are very interesting because the EBONEX materials were prepared at lower than usual temperature, which would decrease the effective cost of production.",
publisher = "Belgrade : Association of the Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Mechanochemistry of titanium oxides",
pages = "251-247",
number = "3",
volume = "63",
doi = "10.2298/HEMIND0903247V",
url = "https://hdl.handle.net/21.15107/rcub_dais_3458"
}

Veljković, I., Poleti, D., Zdujić, M.,& Karanović, L.. (2009). Mechanochemistry of titanium oxides. in Hemijska industrija
Belgrade : Association of the Chemical Engineers of Serbia., 63(3), 247-251.
https://doi.org/10.2298/HEMIND0903247V
https://hdl.handle.net/21.15107/rcub_dais_3458

Veljković I, Poleti D, Zdujić M, Karanović L. Mechanochemistry of titanium oxides. in Hemijska industrija. 2009;63(3):247-251.
doi:10.2298/HEMIND0903247V
https://hdl.handle.net/21.15107/rcub_dais_3458 .

Veljković, Ivana, Poleti, Dejan, Zdujić, Miodrag, Karanović, Ljiljana, "Mechanochemistry of titanium oxides" in Hemijska industrija, 63, no. 3 (2009):247-251,
https://doi.org/10.2298/HEMIND0903247V .,
https://hdl.handle.net/21.15107/rcub_dais_3458 .

TY  - JOUR
AU  - Šutović, Sabina
AU  - Karanović, Ljiljana
AU  - Poleti, Dejan
PY  - 2009
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5547
AB  - During an investigation of the SrO-CuO-P2O5-H 2O system, single crystals of distrontium hexa-hydroxido-cuprate(II), Sr2 [Cu(OH) 6], were obtained by the hydro-thermal method. The blue prismatic crystals of Sr2 [Cu(OH) 6] adopt the same structure type as Ba2 [Cu(OH) 6], Sr 2 [Zn(OH) 6] and Ba2 [Zn(OH) 6]. The Cu atoms, located at (0, 0, 1/2 ) (site symmetry ), form /mutually isolated and highly elongated Cu(OH) 6 octa-hedra, which are inter-connected to slightly distorted Sr(OH) 6 trigonal prisms, forming a layered structure. The location of H atoms from difference Fourier maps and their refinement allowed the precise determination of a three-dimensional hydrogen-bonding network in which all hy-drox-ide O atoms are involved. In addition, the hydrogen-bonding topologies in Sr2 [Cu(OH) 6] and other similar hexa-hydroxido-metallates with the general formulae M1[M2(OH) 6], M12 [M2(OH) 6] and M13 [M2(OH) 6] were analysed in detail.
PB  - International Union of Crystallography
T2  - Acta Crystallographica Section C: Crystal Structure Communications
T1  - Reinvestigation of Sr2 [Cu(OH)6]
EP  - i51
IS  - 8
SP  - i48
VL  - 65
DO  - 10.1107/S0108270109021519
ER  - 

@article{
author = "Šutović, Sabina and Karanović, Ljiljana and Poleti, Dejan",
year = "2009",
abstract = "During an investigation of the SrO-CuO-P2O5-H 2O system, single crystals of distrontium hexa-hydroxido-cuprate(II), Sr2 [Cu(OH) 6], were obtained by the hydro-thermal method. The blue prismatic crystals of Sr2 [Cu(OH) 6] adopt the same structure type as Ba2 [Cu(OH) 6], Sr 2 [Zn(OH) 6] and Ba2 [Zn(OH) 6]. The Cu atoms, located at (0, 0, 1/2 ) (site symmetry ), form /mutually isolated and highly elongated Cu(OH) 6 octa-hedra, which are inter-connected to slightly distorted Sr(OH) 6 trigonal prisms, forming a layered structure. The location of H atoms from difference Fourier maps and their refinement allowed the precise determination of a three-dimensional hydrogen-bonding network in which all hy-drox-ide O atoms are involved. In addition, the hydrogen-bonding topologies in Sr2 [Cu(OH) 6] and other similar hexa-hydroxido-metallates with the general formulae M1[M2(OH) 6], M12 [M2(OH) 6] and M13 [M2(OH) 6] were analysed in detail.",
publisher = "International Union of Crystallography",
journal = "Acta Crystallographica Section C: Crystal Structure Communications",
title = "Reinvestigation of Sr2 [Cu(OH)6]",
pages = "i51-i48",
number = "8",
volume = "65",
doi = "10.1107/S0108270109021519"
}

Šutović, S., Karanović, L.,& Poleti, D.. (2009). Reinvestigation of Sr2 [Cu(OH)6]. in Acta Crystallographica Section C: Crystal Structure Communications
International Union of Crystallography., 65(8), i48-i51.
https://doi.org/10.1107/S0108270109021519

Šutović S, Karanović L, Poleti D. Reinvestigation of Sr2 [Cu(OH)6]. in Acta Crystallographica Section C: Crystal Structure Communications. 2009;65(8):i48-i51.
doi:10.1107/S0108270109021519 .

Šutović, Sabina, Karanović, Ljiljana, Poleti, Dejan, "Reinvestigation of Sr2 [Cu(OH)6]" in Acta Crystallographica Section C: Crystal Structure Communications, 65, no. 8 (2009):i48-i51,
https://doi.org/10.1107/S0108270109021519 . .

TY  - JOUR
AU  - Balić-Žunić, Tonči
AU  - Karanović, Ljiljana
AU  - Poleti, Dejan
PY  - 2008
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5556
AB  - The crystal structure of the mineral picotpaulite, TlFe2S 3, was solved and refined using single-crystal X-ray diffraction data collected at room temperature. The symmetry is orthorhombic, space group Cmcm, with unit-cell parameters: a = 9.083(6), b = 10.754(6), c = 5.412(4) Å, V = 528.6(6) Å3, Z = 4. The structure was refined to the conventional R factor 0.0532 for 226 independent reflections with I > 2σ(I) and 21 variables. Picotpaulite is isostructural with minerals rasvumite (KFe2S3) and pautovite (CsFe2S 3), as well as with a number of synthetic compounds belonging to the CsCu2Cl3 structure type. The structure consists of double chains of FeS4-tetrahedra running along [001] interconnected by TlS10 coordination polyhedra, which form zig-zag chains along the same direction. The Fe-Fe distances between neighbours along the chain direction and perpendicular to it are 2.706(2) and 2.693(6) Å, respectively, indicating strong Fe-Fe interactions. The average oxidation state of Fe is +2.5, achieved by electron transfer over the close Fe sites. Thallium coordination polyhedron can be described as a combination of a square antiprism adjacent to a trigonal prism. The 6s2 electrons of Tl behave as an inert pair and the atom is situated in the centroid of its coordination.
PB  - Slovenian Chemical Society
T2  - Acta Chimica Slovenica
T1  - Crystal structure of picotpaulite, TlFe2S3, from Allchar, FYR Macedonia
EP  - 809
IS  - 4
SP  - 801
VL  - 55
UR  - https://hdl.handle.net/21.15107/rcub_technorep_5556
ER  - 

@article{
author = "Balić-Žunić, Tonči and Karanović, Ljiljana and Poleti, Dejan",
year = "2008",
abstract = "The crystal structure of the mineral picotpaulite, TlFe2S 3, was solved and refined using single-crystal X-ray diffraction data collected at room temperature. The symmetry is orthorhombic, space group Cmcm, with unit-cell parameters: a = 9.083(6), b = 10.754(6), c = 5.412(4) Å, V = 528.6(6) Å3, Z = 4. The structure was refined to the conventional R factor 0.0532 for 226 independent reflections with I > 2σ(I) and 21 variables. Picotpaulite is isostructural with minerals rasvumite (KFe2S3) and pautovite (CsFe2S 3), as well as with a number of synthetic compounds belonging to the CsCu2Cl3 structure type. The structure consists of double chains of FeS4-tetrahedra running along [001] interconnected by TlS10 coordination polyhedra, which form zig-zag chains along the same direction. The Fe-Fe distances between neighbours along the chain direction and perpendicular to it are 2.706(2) and 2.693(6) Å, respectively, indicating strong Fe-Fe interactions. The average oxidation state of Fe is +2.5, achieved by electron transfer over the close Fe sites. Thallium coordination polyhedron can be described as a combination of a square antiprism adjacent to a trigonal prism. The 6s2 electrons of Tl behave as an inert pair and the atom is situated in the centroid of its coordination.",
publisher = "Slovenian Chemical Society",
journal = "Acta Chimica Slovenica",
title = "Crystal structure of picotpaulite, TlFe2S3, from Allchar, FYR Macedonia",
pages = "809-801",
number = "4",
volume = "55",
url = "https://hdl.handle.net/21.15107/rcub_technorep_5556"
}

Balić-Žunić, T., Karanović, L.,& Poleti, D.. (2008). Crystal structure of picotpaulite, TlFe2S3, from Allchar, FYR Macedonia. in Acta Chimica Slovenica
Slovenian Chemical Society., 55(4), 801-809.
https://hdl.handle.net/21.15107/rcub_technorep_5556

Balić-Žunić T, Karanović L, Poleti D. Crystal structure of picotpaulite, TlFe2S3, from Allchar, FYR Macedonia. in Acta Chimica Slovenica. 2008;55(4):801-809.
https://hdl.handle.net/21.15107/rcub_technorep_5556 .

Balić-Žunić, Tonči, Karanović, Ljiljana, Poleti, Dejan, "Crystal structure of picotpaulite, TlFe2S3, from Allchar, FYR Macedonia" in Acta Chimica Slovenica, 55, no. 4 (2008):801-809,
https://hdl.handle.net/21.15107/rcub_technorep_5556 .

TY  - JOUR
AU  - Jovalekić, Čedomir
AU  - Zdujić, Miodrag
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Mitrić, Miodrag
PY  - 2008
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5578
AB  - Powder mixtures of α-Bi2O3 (bismite) and monoclinic m-ZrO2 (baddeleyite) in the molar ratio 2:3 were mechanochemically and thermally treated with the goal to examine the phases, which may appear during such procedures. The prepared samples were characterized by X-ray powder diffraction, differential scanning calorimetry (DSC), electrical measurements, as well as scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The mechanochemical reaction leads to the gradual formation of a nanocrystalline phase, which resembles δ-Bi2O3, a high-temperature Bi2O3 polymorph. Isothermal sintering in air at a temperature of 820 °C for 24 h followed by quenching to room temperature yielded a mixture of ZrO2-stabilized β-Bi2O3 and m-ZrO2 phases, whereas in slowly cooled products, the complete separation of the initial α-Bi2O3 and m-ZrO2 constituents was observed. The dielectric permittivity of the sintered samples significantly depended on the temperature. The sintered and quenched samples exhibited a hysteresis dependence of the dielectric shift, showing that the ZrO2-doped β-Bi2O3 phase possess ferroelectric properties, which were detected for the first time. This fact, together with Rietveld refinement of the β-Bi2O3/m-ZrO2 mixture based on neutron powder diffraction data showed that ZrO2-doped β-Bi2O3 has a non-centrosymmetric structure with P over(4, -) 21 c as the true space group. The ZrO2 content in the doped β-Bi2O3 and the crystal chemical reasons for the stabilization of the β-Bi2O3 phase by the addition of m-ZrO2 are discussed. © 2008 Elsevier Inc. All rights reserved.
T2  - Journal of Solid State Chemistry
T1  - Structural and electrical properties of the 2Bi2O3·3ZrO2 system
EP  - 1329
IS  - 6
SP  - 1321
VL  - 181
DO  - 10.1016/j.jssc.2008.02.038
UR  - https://hdl.handle.net/21.15107/rcub_dais_3582
ER  - 

@article{
author = "Jovalekić, Čedomir and Zdujić, Miodrag and Poleti, Dejan and Karanović, Ljiljana and Mitrić, Miodrag",
year = "2008",
abstract = "Powder mixtures of α-Bi2O3 (bismite) and monoclinic m-ZrO2 (baddeleyite) in the molar ratio 2:3 were mechanochemically and thermally treated with the goal to examine the phases, which may appear during such procedures. The prepared samples were characterized by X-ray powder diffraction, differential scanning calorimetry (DSC), electrical measurements, as well as scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The mechanochemical reaction leads to the gradual formation of a nanocrystalline phase, which resembles δ-Bi2O3, a high-temperature Bi2O3 polymorph. Isothermal sintering in air at a temperature of 820 °C for 24 h followed by quenching to room temperature yielded a mixture of ZrO2-stabilized β-Bi2O3 and m-ZrO2 phases, whereas in slowly cooled products, the complete separation of the initial α-Bi2O3 and m-ZrO2 constituents was observed. The dielectric permittivity of the sintered samples significantly depended on the temperature. The sintered and quenched samples exhibited a hysteresis dependence of the dielectric shift, showing that the ZrO2-doped β-Bi2O3 phase possess ferroelectric properties, which were detected for the first time. This fact, together with Rietveld refinement of the β-Bi2O3/m-ZrO2 mixture based on neutron powder diffraction data showed that ZrO2-doped β-Bi2O3 has a non-centrosymmetric structure with P over(4, -) 21 c as the true space group. The ZrO2 content in the doped β-Bi2O3 and the crystal chemical reasons for the stabilization of the β-Bi2O3 phase by the addition of m-ZrO2 are discussed. © 2008 Elsevier Inc. All rights reserved.",
journal = "Journal of Solid State Chemistry",
title = "Structural and electrical properties of the 2Bi2O3·3ZrO2 system",
pages = "1329-1321",
number = "6",
volume = "181",
doi = "10.1016/j.jssc.2008.02.038",
url = "https://hdl.handle.net/21.15107/rcub_dais_3582"
}

Jovalekić, Č., Zdujić, M., Poleti, D., Karanović, L.,& Mitrić, M.. (2008). Structural and electrical properties of the 2Bi2O3·3ZrO2 system. in Journal of Solid State Chemistry, 181(6), 1321-1329.
https://doi.org/10.1016/j.jssc.2008.02.038
https://hdl.handle.net/21.15107/rcub_dais_3582

Jovalekić Č, Zdujić M, Poleti D, Karanović L, Mitrić M. Structural and electrical properties of the 2Bi2O3·3ZrO2 system. in Journal of Solid State Chemistry. 2008;181(6):1321-1329.
doi:10.1016/j.jssc.2008.02.038
https://hdl.handle.net/21.15107/rcub_dais_3582 .

Jovalekić, Čedomir, Zdujić, Miodrag, Poleti, Dejan, Karanović, Ljiljana, Mitrić, Miodrag, "Structural and electrical properties of the 2Bi2O3·3ZrO2 system" in Journal of Solid State Chemistry, 181, no. 6 (2008):1321-1329,
https://doi.org/10.1016/j.jssc.2008.02.038 .,
https://hdl.handle.net/21.15107/rcub_dais_3582 .

TY  - JOUR
AU  - Karanovic, Ljiljana
AU  - Poleti, Dejan
AU  - Balic-Zunic, Tonci
AU  - Makovicky, Emil
AU  - Gržetić, Ivan
PY  - 2008
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5586
AB  - Two new sulphosalts Tl(3)Ag(3)Sb(2)S(6), (1) and Tl(3)Ag(3)AS(2)S(6), (2) were prepared in reaction of synthetic binary sulfides: argentite (Ag(2)S), carlinite (Tl(2)S) and orpiment (As(2)O(3)) or stibnite (Sb(2)S(3)), and their crystal structures have been determined using single-crystal data. The compounds are isostructural and crystallize in the space group P2(1)/C (Z = 4), with a = 11.6854(17) angstrom, b = 11.8602(17) angstrom, c = 12.1294(18) angstrom, beta = 123.356(2)degrees, V = 1404.1(4) angstrom(3) for 1, and a = 11.4415(14) angstrom, b = 11.7530(15) angstrom, c = 11.9880(16) angstrom, beta = 123.516(3)degrees, V= 1344.0(3) angstrom(3) for2. Refinements involving anisotropic displacement parameters for all atoms converged to the conventional R-factors: R(1) = 0.0496 for 1 and R(1) = 0.0372 for 2. The structures consist of two kinds of slabs alternately situated along [1 0 0] direction and sharing S atoms located between them. The first slab is built up of Tl1S(8), Tl(2)S(6), Tl(3)S(5)Ag(3) coordination polyhedra and Ag(3)S(3)n(3) distorted trigonal pyramid (the average  lt  Ag(3)-S  gt  distance is 2.542 for 1 and 2.539 angstrom for 2) combined with trigonal Sb1S(3) or As1S(3) coordination pyramids ( lt  Sb1-S  gt  and  lt  As1-S  gt  are 2.438 and 2.259 angstrom, respectively). The thallium atom Tl1 is surrounded by eight S atoms forming a square anti-prism ( lt  Tl1-S  gt : 3.393 for 1 and 3.356 angstrom for 2), while the coordination polyhedron of Tl2 can be described as a significantly distorted trigonal prism or as an extremely distorted octahedron ( lt  Tl2-S  gt : 3.236 angstrom for 1 and 3.238 angstrom for 2). Thallium Tl3 is surrounded by six atoms (one Ag, four S at shorter and one S at longer distance), which form a distorted trigonal prism ( lt  Tl3-S  gt : 3.165 angstrom in 1 and 3.155 angstrom in 2). The second slab consists of trigonal Sb(2)S(3) or As(2)S(3) coordination pyramids combined with Ag1S(4) and Ag(2)S(4) coordination tetrahedra ( lt  Sb2-S  gt  and  lt  As2-S  gt  are 2.433 and 2.251 angstrom, respectively;  lt  Ag1-S  gt : 2.623 angstrom for 1 and 2.612 A for 2;  lt  Ag2-S  gt : 2.623 angstrom for 1 and 2.630 angstrom for 2). The most interesting feature of both structures is the existence of short Tl3-Ag(3) contacts of 2.959(2) angstrom in 1 and 2.922(1) angstrom in 2. These contacts are the shortest found so far and indicate very strong Tl-Ag interactions. They are discussed in terms of metallophilicity principle and relativistic effects. It is also pointed out that if only valence shell electrons are considered (Tl-Ag)(2+) group is isoelectronic with the (Hg-Hg)(2+) ion, therefore new examples of short Tl-Ag contacts could be expected. (C) 2007 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Alloys and Compounds
T1  - Two new examples of very short thallium-transition metal contacts: Tl(3)Ag(3)Sb(2)S(6) and Tl(3)Ag(3)As(2)S(6)
EP  - 74
IS  - 1-2
SP  - 66
VL  - 457
DO  - 10.1016/j.jallcom.2007.03.014
ER  - 

@article{
author = "Karanovic, Ljiljana and Poleti, Dejan and Balic-Zunic, Tonci and Makovicky, Emil and Gržetić, Ivan",
year = "2008",
abstract = "Two new sulphosalts Tl(3)Ag(3)Sb(2)S(6), (1) and Tl(3)Ag(3)AS(2)S(6), (2) were prepared in reaction of synthetic binary sulfides: argentite (Ag(2)S), carlinite (Tl(2)S) and orpiment (As(2)O(3)) or stibnite (Sb(2)S(3)), and their crystal structures have been determined using single-crystal data. The compounds are isostructural and crystallize in the space group P2(1)/C (Z = 4), with a = 11.6854(17) angstrom, b = 11.8602(17) angstrom, c = 12.1294(18) angstrom, beta = 123.356(2)degrees, V = 1404.1(4) angstrom(3) for 1, and a = 11.4415(14) angstrom, b = 11.7530(15) angstrom, c = 11.9880(16) angstrom, beta = 123.516(3)degrees, V= 1344.0(3) angstrom(3) for2. Refinements involving anisotropic displacement parameters for all atoms converged to the conventional R-factors: R(1) = 0.0496 for 1 and R(1) = 0.0372 for 2. The structures consist of two kinds of slabs alternately situated along [1 0 0] direction and sharing S atoms located between them. The first slab is built up of Tl1S(8), Tl(2)S(6), Tl(3)S(5)Ag(3) coordination polyhedra and Ag(3)S(3)n(3) distorted trigonal pyramid (the average  lt  Ag(3)-S  gt  distance is 2.542 for 1 and 2.539 angstrom for 2) combined with trigonal Sb1S(3) or As1S(3) coordination pyramids ( lt  Sb1-S  gt  and  lt  As1-S  gt  are 2.438 and 2.259 angstrom, respectively). The thallium atom Tl1 is surrounded by eight S atoms forming a square anti-prism ( lt  Tl1-S  gt : 3.393 for 1 and 3.356 angstrom for 2), while the coordination polyhedron of Tl2 can be described as a significantly distorted trigonal prism or as an extremely distorted octahedron ( lt  Tl2-S  gt : 3.236 angstrom for 1 and 3.238 angstrom for 2). Thallium Tl3 is surrounded by six atoms (one Ag, four S at shorter and one S at longer distance), which form a distorted trigonal prism ( lt  Tl3-S  gt : 3.165 angstrom in 1 and 3.155 angstrom in 2). The second slab consists of trigonal Sb(2)S(3) or As(2)S(3) coordination pyramids combined with Ag1S(4) and Ag(2)S(4) coordination tetrahedra ( lt  Sb2-S  gt  and  lt  As2-S  gt  are 2.433 and 2.251 angstrom, respectively;  lt  Ag1-S  gt : 2.623 angstrom for 1 and 2.612 A for 2;  lt  Ag2-S  gt : 2.623 angstrom for 1 and 2.630 angstrom for 2). The most interesting feature of both structures is the existence of short Tl3-Ag(3) contacts of 2.959(2) angstrom in 1 and 2.922(1) angstrom in 2. These contacts are the shortest found so far and indicate very strong Tl-Ag interactions. They are discussed in terms of metallophilicity principle and relativistic effects. It is also pointed out that if only valence shell electrons are considered (Tl-Ag)(2+) group is isoelectronic with the (Hg-Hg)(2+) ion, therefore new examples of short Tl-Ag contacts could be expected. (C) 2007 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Alloys and Compounds",
title = "Two new examples of very short thallium-transition metal contacts: Tl(3)Ag(3)Sb(2)S(6) and Tl(3)Ag(3)As(2)S(6)",
pages = "74-66",
number = "1-2",
volume = "457",
doi = "10.1016/j.jallcom.2007.03.014"
}

Karanovic, L., Poleti, D., Balic-Zunic, T., Makovicky, E.,& Gržetić, I.. (2008). Two new examples of very short thallium-transition metal contacts: Tl(3)Ag(3)Sb(2)S(6) and Tl(3)Ag(3)As(2)S(6). in Journal of Alloys and Compounds
Elsevier Science Sa, Lausanne., 457(1-2), 66-74.
https://doi.org/10.1016/j.jallcom.2007.03.014

Karanovic L, Poleti D, Balic-Zunic T, Makovicky E, Gržetić I. Two new examples of very short thallium-transition metal contacts: Tl(3)Ag(3)Sb(2)S(6) and Tl(3)Ag(3)As(2)S(6). in Journal of Alloys and Compounds. 2008;457(1-2):66-74.
doi:10.1016/j.jallcom.2007.03.014 .

Karanovic, Ljiljana, Poleti, Dejan, Balic-Zunic, Tonci, Makovicky, Emil, Gržetić, Ivan, "Two new examples of very short thallium-transition metal contacts: Tl(3)Ag(3)Sb(2)S(6) and Tl(3)Ag(3)As(2)S(6)" in Journal of Alloys and Compounds, 457, no. 1-2 (2008):66-74,
https://doi.org/10.1016/j.jallcom.2007.03.014 . .

TY  - JOUR
AU  - Poleti, Dejan
AU  - Karanović, Ljiljana
AU  - Dapčević, Aleksandra
PY  - 2007
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1113
AB  - A series of microcrystalline products containing the gamma-Bi2O3 phase doped with Co, Fe, Mn, Pb, Sb, Si, Ti, V and Zn has been prepared by solid state reaction. Based on the heating temperature and heating time, the following order of increasing relative stability of the doped gamma-Bi2O3 phases was established: Sb 51  lt  Co2+ Mn4+  lt  Fe3+ approximate to Si4+  lt  Ti4+  lt  V5+  lt  Zn2+  lt  Ph2+. The unit cell parameters of the prepared samples were compared with available structural data, which were also further analyzed concerning the geometrical parameters and overall reliability. The analysis confirmed the socalled Radaev's model for the doped gamma-Bi2O3 structure, which assumes the presence of Bi2(3+) ions slightly displaced from the tetrahedral M site and corresponding vacancies (resulting from a lone pair on Bi2(3+)) in the coordinating oxygen positions. In addition, the analysis suggested that this model can be further improved. The existence of an approximate linear relationship between the unit cell parameters of the doped gamma-Bi2O3 phases and the ionic radii of the M cations was found.
PB  - Walter de Gruyter Gmbh, Berlin
T2  - Zeitschrift Fur Kristallographie
T1  - Doped gamma-Bi2O3: synthesis of microcrystalline samples and crystal chemical analysis of structural data
EP  - 72
IS  - 2
SP  - 59
VL  - 222
DO  - 10.1524/zkri.2007.222.2.59
ER  - 

@article{
author = "Poleti, Dejan and Karanović, Ljiljana and Dapčević, Aleksandra",
year = "2007",
abstract = "A series of microcrystalline products containing the gamma-Bi2O3 phase doped with Co, Fe, Mn, Pb, Sb, Si, Ti, V and Zn has been prepared by solid state reaction. Based on the heating temperature and heating time, the following order of increasing relative stability of the doped gamma-Bi2O3 phases was established: Sb 51  lt  Co2+ Mn4+  lt  Fe3+ approximate to Si4+  lt  Ti4+  lt  V5+  lt  Zn2+  lt  Ph2+. The unit cell parameters of the prepared samples were compared with available structural data, which were also further analyzed concerning the geometrical parameters and overall reliability. The analysis confirmed the socalled Radaev's model for the doped gamma-Bi2O3 structure, which assumes the presence of Bi2(3+) ions slightly displaced from the tetrahedral M site and corresponding vacancies (resulting from a lone pair on Bi2(3+)) in the coordinating oxygen positions. In addition, the analysis suggested that this model can be further improved. The existence of an approximate linear relationship between the unit cell parameters of the doped gamma-Bi2O3 phases and the ionic radii of the M cations was found.",
publisher = "Walter de Gruyter Gmbh, Berlin",
journal = "Zeitschrift Fur Kristallographie",
title = "Doped gamma-Bi2O3: synthesis of microcrystalline samples and crystal chemical analysis of structural data",
pages = "72-59",
number = "2",
volume = "222",
doi = "10.1524/zkri.2007.222.2.59"
}

Poleti, D., Karanović, L.,& Dapčević, A.. (2007). Doped gamma-Bi2O3: synthesis of microcrystalline samples and crystal chemical analysis of structural data. in Zeitschrift Fur Kristallographie
Walter de Gruyter Gmbh, Berlin., 222(2), 59-72.
https://doi.org/10.1524/zkri.2007.222.2.59

Poleti D, Karanović L, Dapčević A. Doped gamma-Bi2O3: synthesis of microcrystalline samples and crystal chemical analysis of structural data. in Zeitschrift Fur Kristallographie. 2007;222(2):59-72.
doi:10.1524/zkri.2007.222.2.59 .

Poleti, Dejan, Karanović, Ljiljana, Dapčević, Aleksandra, "Doped gamma-Bi2O3: synthesis of microcrystalline samples and crystal chemical analysis of structural data" in Zeitschrift Fur Kristallographie, 222, no. 2 (2007):59-72,
https://doi.org/10.1524/zkri.2007.222.2.59 . .

TY  - JOUR
AU  - Zdujić, Miodrag
AU  - Poleti, Dejan
AU  - Jovalekić, Čedomir
AU  - Karanović, Ljiljana
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5466
AB  - Concurrent mechanochemical treatment of either a stoichiometric 2Bi 2 O 3 · 3TiO 2 powder mixture or (pulverized) Bi 4 Ti 3 O 12 compound was performed in a planetary ball mill. Relevant structural parameters: crystallite size, amount of amorphous phase and the transformed fraction (as a result of chemical reaction between Bi 2 O 3 and TiO 2 ) of the powders milled for various milling times and intensities were derived from X-ray powder diffraction data. The obtained structural parameters were used to follow the kinetics of the reduction of crystallite size, amorphous phase formation and chemical reaction. In the powder mixture, during the early stage of mechanochemical treatment the Bi 2 (CO 3 )O 2 phase was found as an intermediate product which transformed into the highly amorphized Bi 4 Ti 3 O 12 phase as the milling progressed. On the other hand, mechanochemical treatment of Bi 4 Ti 3 O 12 powder induced a gradual deformation of the crystal lattice and destruction of the perovskite-type structure. However, in both cases, after a certain milling time, a very disordered, amorphous/nanocrystalline structure was obtained. It was demonstrated that in the steady state, the amorphous/nanocrystalline phase ratio depends on the milling conditions. Higher milling intensities induce 'nanocrystallization' of the amorphous phase, i.e., precipitation of crystallites with an average size below 20 nm. A kinetic model involving a nanocrystalline ↔ amorphous reaction, in which the forward and reverse reaction were first-order was postulated and used to analyze the formation of an amorphous phase.
PB  - Elsevier
T2  - Journal of Non-Crystalline Solids
T1  - The evolution of structure induced by intensive milling in the system 2Bi 2 O 3 · 3TiO 2
EP  - 3068
IS  - 28-29
SP  - 3058
VL  - 352
DO  - 10.1016/j.jnoncrysol.2006.03.072
ER  - 

@article{
author = "Zdujić, Miodrag and Poleti, Dejan and Jovalekić, Čedomir and Karanović, Ljiljana",
year = "2006",
abstract = "Concurrent mechanochemical treatment of either a stoichiometric 2Bi 2 O 3 · 3TiO 2 powder mixture or (pulverized) Bi 4 Ti 3 O 12 compound was performed in a planetary ball mill. Relevant structural parameters: crystallite size, amount of amorphous phase and the transformed fraction (as a result of chemical reaction between Bi 2 O 3 and TiO 2 ) of the powders milled for various milling times and intensities were derived from X-ray powder diffraction data. The obtained structural parameters were used to follow the kinetics of the reduction of crystallite size, amorphous phase formation and chemical reaction. In the powder mixture, during the early stage of mechanochemical treatment the Bi 2 (CO 3 )O 2 phase was found as an intermediate product which transformed into the highly amorphized Bi 4 Ti 3 O 12 phase as the milling progressed. On the other hand, mechanochemical treatment of Bi 4 Ti 3 O 12 powder induced a gradual deformation of the crystal lattice and destruction of the perovskite-type structure. However, in both cases, after a certain milling time, a very disordered, amorphous/nanocrystalline structure was obtained. It was demonstrated that in the steady state, the amorphous/nanocrystalline phase ratio depends on the milling conditions. Higher milling intensities induce 'nanocrystallization' of the amorphous phase, i.e., precipitation of crystallites with an average size below 20 nm. A kinetic model involving a nanocrystalline ↔ amorphous reaction, in which the forward and reverse reaction were first-order was postulated and used to analyze the formation of an amorphous phase.",
publisher = "Elsevier",
journal = "Journal of Non-Crystalline Solids",
title = "The evolution of structure induced by intensive milling in the system 2Bi 2 O 3 · 3TiO 2",
pages = "3068-3058",
number = "28-29",
volume = "352",
doi = "10.1016/j.jnoncrysol.2006.03.072"
}

Zdujić, M., Poleti, D., Jovalekić, Č.,& Karanović, L.. (2006). The evolution of structure induced by intensive milling in the system 2Bi 2 O 3 · 3TiO 2. in Journal of Non-Crystalline Solids
Elsevier., 352(28-29), 3058-3068.
https://doi.org/10.1016/j.jnoncrysol.2006.03.072

Zdujić M, Poleti D, Jovalekić Č, Karanović L. The evolution of structure induced by intensive milling in the system 2Bi 2 O 3 · 3TiO 2. in Journal of Non-Crystalline Solids. 2006;352(28-29):3058-3068.
doi:10.1016/j.jnoncrysol.2006.03.072 .

Zdujić, Miodrag, Poleti, Dejan, Jovalekić, Čedomir, Karanović, Ljiljana, "The evolution of structure induced by intensive milling in the system 2Bi 2 O 3 · 3TiO 2" in Journal of Non-Crystalline Solids, 352, no. 28-29 (2006):3058-3068,
https://doi.org/10.1016/j.jnoncrysol.2006.03.072 . .