TY  - JOUR
AU  - Šuljagić, Marija
AU  - Vulić, Predrag
AU  - Jeremić, Dejan
AU  - Pavlović, Vladimir B.
AU  - Filipović, Suzana
AU  - Kilanski, Lukasz
AU  - Lewinska, Sabina
AU  - Slawska-Waniewska, Anna
AU  - Milenković, Milica
AU  - Nikolić, Aleksandar S.
AU  - Anđelković, Ljubica
PY  - 2021
UR  - https://dais.sanu.ac.rs/123456789/9515
AB  - To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.
PB  - Elsevier
T2  - Materials Research Bulletin
T1  - The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods
SP  - 111117
VL  - 134
DO  - 10.1016/j.materresbull.2020.111117
UR  - https://hdl.handle.net/21.15107/rcub_dais_9515
ER  - 

@article{
author = "Šuljagić, Marija and Vulić, Predrag and Jeremić, Dejan and Pavlović, Vladimir B. and Filipović, Suzana and Kilanski, Lukasz and Lewinska, Sabina and Slawska-Waniewska, Anna and Milenković, Milica and Nikolić, Aleksandar S. and Anđelković, Ljubica",
year = "2021",
abstract = "To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.",
publisher = "Elsevier",
journal = "Materials Research Bulletin",
title = "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods",
pages = "111117",
volume = "134",
doi = "10.1016/j.materresbull.2020.111117",
url = "https://hdl.handle.net/21.15107/rcub_dais_9515"
}

Šuljagić, M., Vulić, P., Jeremić, D., Pavlović, V. B., Filipović, S., Kilanski, L., Lewinska, S., Slawska-Waniewska, A., Milenković, M., Nikolić, A. S.,& Anđelković, L.. (2021). The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin
Elsevier., 134, 111117.
https://doi.org/10.1016/j.materresbull.2020.111117
https://hdl.handle.net/21.15107/rcub_dais_9515

Šuljagić M, Vulić P, Jeremić D, Pavlović VB, Filipović S, Kilanski L, Lewinska S, Slawska-Waniewska A, Milenković M, Nikolić AS, Anđelković L. The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin. 2021;134:111117.
doi:10.1016/j.materresbull.2020.111117
https://hdl.handle.net/21.15107/rcub_dais_9515 .

Šuljagić, Marija, Vulić, Predrag, Jeremić, Dejan, Pavlović, Vladimir B., Filipović, Suzana, Kilanski, Lukasz, Lewinska, Sabina, Slawska-Waniewska, Anna, Milenković, Milica, Nikolić, Aleksandar S., Anđelković, Ljubica, "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods" in Materials Research Bulletin, 134 (2021):111117,
https://doi.org/10.1016/j.materresbull.2020.111117 .,
https://hdl.handle.net/21.15107/rcub_dais_9515 .

TY  - JOUR
AU  - Šuljagić, Marija
AU  - Vulić, Predrag
AU  - Jeremić, Dejan
AU  - Pavlović, Vladimir B.
AU  - Filipović, Suzana
AU  - Kilanski, Lukasz
AU  - Lewinska, Sabina
AU  - Slawska-Waniewska, Anna
AU  - Milenković, Milica
AU  - Nikolić, Aleksandar S.
AU  - Anđelković, Ljubica
PY  - 2021
UR  - https://dais.sanu.ac.rs/123456789/9514
AB  - To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.
PB  - Elsevier
T2  - Materials Research Bulletin
T1  - The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods
SP  - 111117
VL  - 134
DO  - 10.1016/j.materresbull.2020.111117
UR  - https://hdl.handle.net/21.15107/rcub_dais_9514
ER  - 

@article{
author = "Šuljagić, Marija and Vulić, Predrag and Jeremić, Dejan and Pavlović, Vladimir B. and Filipović, Suzana and Kilanski, Lukasz and Lewinska, Sabina and Slawska-Waniewska, Anna and Milenković, Milica and Nikolić, Aleksandar S. and Anđelković, Ljubica",
year = "2021",
abstract = "To investigate the magnetic behavior of starch-coated cobalt ferrites, well-established synthetic methods, i.e., coprecipitation, mechanochemical, ultrasonically assisted coprecipitation, microemulsion, and microwave-assisted hydrothermal syntheses were chosen for their preparation. The obtained materials had pure single-phase spinel structures. Scanning and transmission electron microscopy analyses revealed that the morphology of the samples is not uniform, and particle aggregation is a dominant process. Fourier transform infrared spectra and thermogravimetric analysis confirmed the presence of starch in all–coated samples. The unusually higher saturation magnetization of starch-coated samples than their as-prepared analogs, obtained by coprecipitation, ultrasonically assisted coprecipitation, and microwave-assisted hydrothermal methods, might be explained by the Ostwald ripening mechanism induced by the coating process. A decrease in magnetization was noticed for the starch-functionalized nanomaterials synthesized by mechanochemical and microemulsion methods, in comparison to their as-prepared analogs, i.e., the size distribution of such nanoparticles is narrow, and the average diameter of the grains is near critical for the Ostwald ripening process.",
publisher = "Elsevier",
journal = "Materials Research Bulletin",
title = "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods",
pages = "111117",
volume = "134",
doi = "10.1016/j.materresbull.2020.111117",
url = "https://hdl.handle.net/21.15107/rcub_dais_9514"
}

Šuljagić, M., Vulić, P., Jeremić, D., Pavlović, V. B., Filipović, S., Kilanski, L., Lewinska, S., Slawska-Waniewska, A., Milenković, M., Nikolić, A. S.,& Anđelković, L.. (2021). The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin
Elsevier., 134, 111117.
https://doi.org/10.1016/j.materresbull.2020.111117
https://hdl.handle.net/21.15107/rcub_dais_9514

Šuljagić M, Vulić P, Jeremić D, Pavlović VB, Filipović S, Kilanski L, Lewinska S, Slawska-Waniewska A, Milenković M, Nikolić AS, Anđelković L. The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods. in Materials Research Bulletin. 2021;134:111117.
doi:10.1016/j.materresbull.2020.111117
https://hdl.handle.net/21.15107/rcub_dais_9514 .

Šuljagić, Marija, Vulić, Predrag, Jeremić, Dejan, Pavlović, Vladimir B., Filipović, Suzana, Kilanski, Lukasz, Lewinska, Sabina, Slawska-Waniewska, Anna, Milenković, Milica, Nikolić, Aleksandar S., Anđelković, Ljubica, "The influence of the starch coating on the magnetic properties of nanosized cobalt ferrites obtained by different synthetic methods" in Materials Research Bulletin, 134 (2021):111117,
https://doi.org/10.1016/j.materresbull.2020.111117 .,
https://hdl.handle.net/21.15107/rcub_dais_9514 .

TY  - DATA
AU  - Ristić, Predrag
AU  - Todorović, Tamara
AU  - Blagojević, Vladimir A.
AU  - Klisurić, Olivera
AU  - Marjanović, Ivana
AU  - Holló, Berta Barta
AU  - Vulić, Predrag J.
AU  - Gulea, Mihaela
AU  - Donnard, Morgan
AU  - Monge, Miguel
AU  - Rodríguez-Castillo, María
AU  - López-de-Luzuriaga, José M.
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9452
AB  - Table S1. Crystallographic data and refinement parameters for SQUEEZED 3 with general formula {[Ag2(H2BTEC)(L)2]}∞; Table S2. Pairwise interaction energies in the crystal structure of 1 based on B3LYP/ DGDZVP energy mode; Table S3. Pairwise interaction energies in the crystal structure of 2 based on B3LYP/ DGDZVP energy mode; Table S4. Pairwise interaction energies in the crystal structure of 3 based on B3LYP/ DGDZVP energy model; Table S5. Pairwise interaction energies in the crystal structure of 4 based on B3LYP/ DGDZVP energy model; Powder X-ray diffraction analysis: All  samples  correspond  to  the  single-phase  X-ray  powder  patterns  (Figure  S1)  in  accordance with the structural model obtained by the single-crystal X-ray diffraction. It should be noted that the best overlap of peaks in the powder pattern for 3 was obtained using  SQUEEZED cif single crystal   data.   According   to   the   results   of   powder   X-ray   structural   analysis,   as   well   as thermogravimetric  analysis,  3  readily  loses  solvent  water  molecules  without  change  of  the structure. For 1, 2 and 4, given the absence of any secondary phases, it can be concluded that all of  the  samples  are  stable  in  air  under  conditions  of  manual  pulverization  required  to  create powder samples from single crystals.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287
UR  - https://hdl.handle.net/21.15107/rcub_dais_9452
ER  - 

@misc{
author = "Ristić, Predrag and Todorović, Tamara and Blagojević, Vladimir A. and Klisurić, Olivera and Marjanović, Ivana and Holló, Berta Barta and Vulić, Predrag J. and Gulea, Mihaela and Donnard, Morgan and Monge, Miguel and Rodríguez-Castillo, María and López-de-Luzuriaga, José M. and Filipović, Nenad R.",
year = "2020",
abstract = "Table S1. Crystallographic data and refinement parameters for SQUEEZED 3 with general formula {[Ag2(H2BTEC)(L)2]}∞; Table S2. Pairwise interaction energies in the crystal structure of 1 based on B3LYP/ DGDZVP energy mode; Table S3. Pairwise interaction energies in the crystal structure of 2 based on B3LYP/ DGDZVP energy mode; Table S4. Pairwise interaction energies in the crystal structure of 3 based on B3LYP/ DGDZVP energy model; Table S5. Pairwise interaction energies in the crystal structure of 4 based on B3LYP/ DGDZVP energy model; Powder X-ray diffraction analysis: All  samples  correspond  to  the  single-phase  X-ray  powder  patterns  (Figure  S1)  in  accordance with the structural model obtained by the single-crystal X-ray diffraction. It should be noted that the best overlap of peaks in the powder pattern for 3 was obtained using  SQUEEZED cif single crystal   data.   According   to   the   results   of   powder   X-ray   structural   analysis,   as   well   as thermogravimetric  analysis,  3  readily  loses  solvent  water  molecules  without  change  of  the structure. For 1, 2 and 4, given the absence of any secondary phases, it can be concluded that all of  the  samples  are  stable  in  air  under  conditions  of  manual  pulverization  required  to  create powder samples from single crystals.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287",
url = "https://hdl.handle.net/21.15107/rcub_dais_9452"
}

Ristić, P., Todorović, T., Blagojević, V. A., Klisurić, O., Marjanović, I., Holló, B. B., Vulić, P. J., Gulea, M., Donnard, M., Monge, M., Rodríguez-Castillo, M., López-de-Luzuriaga, J. M.,& Filipović, N. R.. (2020). Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287. in Crystal Growth & Design
American Chemical Society..
https://hdl.handle.net/21.15107/rcub_dais_9452

Ristić P, Todorović T, Blagojević VA, Klisurić O, Marjanović I, Holló BB, Vulić PJ, Gulea M, Donnard M, Monge M, Rodríguez-Castillo M, López-de-Luzuriaga JM, Filipović NR. Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287. in Crystal Growth & Design. 2020;.
https://hdl.handle.net/21.15107/rcub_dais_9452 .

Ristić, Predrag, Todorović, Tamara, Blagojević, Vladimir A., Klisurić, Olivera, Marjanović, Ivana, Holló, Berta Barta, Vulić, Predrag J., Gulea, Mihaela, Donnard, Morgan, Monge, Miguel, Rodríguez-Castillo, María, López-de-Luzuriaga, José M., Filipović, Nenad R., "Supplementary data for the article: Ristić, P.; Todorović, T. R.; Blagojević, V.; Klisurić, O. R.; Marjanović, I.; Holló, B. B.; Vulić, P.; Gulea, M.; Donnard, M.; Monge, M.; Rodríguez-Castillo, M.; López-de-Luzuriaga, J. M.; Filipović, N. R. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-Carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. Crystal Growth & Design 2020, 20 (7), 4461–4478. https://doi.org/10.1021/acs.cgd.0c00287" in Crystal Growth & Design (2020),
https://hdl.handle.net/21.15107/rcub_dais_9452 .

TY  - JOUR
AU  - Ristić, Predrag
AU  - Todorović, Tamara R.
AU  - Blagojević, Vladimir
AU  - Klisurić, Olivera R.
AU  - Marjanović, Ivana
AU  - Holló, Berta Barta
AU  - Vulić, Predrag
AU  - Gulea, Mihaela
AU  - Donnard, Morgan
AU  - Monge, Miguel
AU  - Rodríguez-Castillo, María
AU  - López-de-Luzuriaga, José M.
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/8960
AB  - Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study
SP  - 4461
EP  - 4478
VL  - 20
IS  - 7
DO  - 10.1021/acs.cgd.0c00287
UR  - https://hdl.handle.net/21.15107/rcub_dais_8960
ER  - 

@article{
author = "Ristić, Predrag and Todorović, Tamara R. and Blagojević, Vladimir and Klisurić, Olivera R. and Marjanović, Ivana and Holló, Berta Barta and Vulić, Predrag and Gulea, Mihaela and Donnard, Morgan and Monge, Miguel and Rodríguez-Castillo, María and López-de-Luzuriaga, José M. and Filipović, Nenad R.",
year = "2020",
abstract = "Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study",
pages = "4461-4478",
volume = "20",
number = "7",
doi = "10.1021/acs.cgd.0c00287",
url = "https://hdl.handle.net/21.15107/rcub_dais_8960"
}

Ristić, P., Todorović, T. R., Blagojević, V., Klisurić, O. R., Marjanović, I., Holló, B. B., Vulić, P., Gulea, M., Donnard, M., Monge, M., Rodríguez-Castillo, M., López-de-Luzuriaga, J. M.,& Filipović, N. R.. (2020). 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design
American Chemical Society., 20(7), 4461-4478.
https://doi.org/10.1021/acs.cgd.0c00287
https://hdl.handle.net/21.15107/rcub_dais_8960

Ristić P, Todorović TR, Blagojević V, Klisurić OR, Marjanović I, Holló BB, Vulić P, Gulea M, Donnard M, Monge M, Rodríguez-Castillo M, López-de-Luzuriaga JM, Filipović NR. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design. 2020;20(7):4461-4478.
doi:10.1021/acs.cgd.0c00287
https://hdl.handle.net/21.15107/rcub_dais_8960 .

Ristić, Predrag, Todorović, Tamara R., Blagojević, Vladimir, Klisurić, Olivera R., Marjanović, Ivana, Holló, Berta Barta, Vulić, Predrag, Gulea, Mihaela, Donnard, Morgan, Monge, Miguel, Rodríguez-Castillo, María, López-de-Luzuriaga, José M., Filipović, Nenad R., "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study" in Crystal Growth & Design, 20, no. 7 (2020):4461-4478,
https://doi.org/10.1021/acs.cgd.0c00287 .,
https://hdl.handle.net/21.15107/rcub_dais_8960 .

TY  - JOUR
AU  - Ristić, Predrag
AU  - Todorović, Tamara R.
AU  - Blagojević, Vladimir
AU  - Klisurić, Olivera R.
AU  - Marjanović, Ivana
AU  - Holló, Berta Barta
AU  - Vulić, Predrag
AU  - Gulea, Mihaela
AU  - Donnard, Morgan
AU  - Monge, Miguel
AU  - Rodríguez-Castillo, María
AU  - López-de-Luzuriaga, José M.
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/8956
AB  - Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study
SP  - 4461
EP  - 4478
VL  - 20
IS  - 7
DO  - 10.1021/acs.cgd.0c00287
UR  - https://hdl.handle.net/21.15107/rcub_dais_8956
ER  - 

@article{
author = "Ristić, Predrag and Todorović, Tamara R. and Blagojević, Vladimir and Klisurić, Olivera R. and Marjanović, Ivana and Holló, Berta Barta and Vulić, Predrag and Gulea, Mihaela and Donnard, Morgan and Monge, Miguel and Rodríguez-Castillo, María and López-de-Luzuriaga, José M. and Filipović, Nenad R.",
year = "2020",
abstract = "Four silver-based coordination polymers, {[Ag(L)2](BF4)}∞ (1), {[Ag(H2BTC)(L)]·(H3BTC)}∞ (2), {[Ag2(H2BTEC)(L)2]·3.33H2O}∞ (3), and [Ag(H25SSA)(L)]∞ (4), were synthesized using thiomorpholine-4-carbonitrile (L) as the primary ligand and three aromatic polyoxoacids as coligands: trimesic (H3BTC), pyromellitic (H4BTEC), and 5-sulfosalicylic acid (H35SSA). Compounds 1 and 3 are two-dimensional, while 2 and 4 are one-dimensional. L acts as a bis-monodentate ligand, while the Ag(I) ion is three-coordinated in 2 and four-coordinated in all of the other compounds. The tetrahedral coordination of Ag(I) in 3 leads to an almost complete absence of intermolecular interactions with the metal center. All compounds show reasonable photocatalytic activity for photocatalytic degradation of mordant blue 9 dye, with reaction rates in the 0.036–0.056 min–1 range. Changes in the reaction rates can be correlated with the type and coordination of the coligand. Complex 3 exhibits photoluminescence at 77 K, while 4 exhibits photoluminescence at both room temperature and 77 K. Luminescence lifetimes indicate electronic transitions of singlet parentage, where transitions are allowed. A TD-DFT study determined the contributions of individual singlet–singlet electronic excitations to the fluorescence, indicating that metal– intraligand transitions are responsible for luminescence in both complexes.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study",
pages = "4461-4478",
volume = "20",
number = "7",
doi = "10.1021/acs.cgd.0c00287",
url = "https://hdl.handle.net/21.15107/rcub_dais_8956"
}

Ristić, P., Todorović, T. R., Blagojević, V., Klisurić, O. R., Marjanović, I., Holló, B. B., Vulić, P., Gulea, M., Donnard, M., Monge, M., Rodríguez-Castillo, M., López-de-Luzuriaga, J. M.,& Filipović, N. R.. (2020). 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design
American Chemical Society., 20(7), 4461-4478.
https://doi.org/10.1021/acs.cgd.0c00287
https://hdl.handle.net/21.15107/rcub_dais_8956

Ristić P, Todorović TR, Blagojević V, Klisurić OR, Marjanović I, Holló BB, Vulić P, Gulea M, Donnard M, Monge M, Rodríguez-Castillo M, López-de-Luzuriaga JM, Filipović NR. 1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study. in Crystal Growth & Design. 2020;20(7):4461-4478.
doi:10.1021/acs.cgd.0c00287
https://hdl.handle.net/21.15107/rcub_dais_8956 .

Ristić, Predrag, Todorović, Tamara R., Blagojević, Vladimir, Klisurić, Olivera R., Marjanović, Ivana, Holló, Berta Barta, Vulić, Predrag, Gulea, Mihaela, Donnard, Morgan, Monge, Miguel, Rodríguez-Castillo, María, López-de-Luzuriaga, José M., Filipović, Nenad R., "1D and 2D Silver-Based Coordination Polymers with Thiomorpholine-4-carbonitrile and Aromatic Polyoxoacids as Coligands: Structure, Photocatalysis, Photoluminescence, and TD-DFT Study" in Crystal Growth & Design, 20, no. 7 (2020):4461-4478,
https://doi.org/10.1021/acs.cgd.0c00287 .,
https://hdl.handle.net/21.15107/rcub_dais_8956 .

TY  - JOUR
AU  - Filipović, Suzana
AU  - Anđelković, Ljubica
AU  - Jeremić, Dejan
AU  - Vulić, Predrag
AU  - Nikolić, Aleksandar
AU  - Marković, Smilja
AU  - Paunović, Vesna
AU  - Lević, Steva
AU  - Pavlović, Vladimir B.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9449
AB  - Barium titanate (BaTiO3) attracts high scientific and technological attention due to good dielectric and electromechanical properties. Although BaTiO3 is one of the most frequently investigated ferroelectric materials, the need for finding new and/or improved synthesis methods of this material still exists. In this paper, a novel, mild synthesis route for producing tetragonal BaTiO3 from barium nitrate and Ti-oxalate precursor is presented. Morphology of the prepared and subsequently sintered BaTiO3 was determined by SEM. Particle size distribution of the as prepared powder was monitored by the laser diffraction. The phase composition, structure and lattice dynamics were investigated by XRD and Raman spectroscopy. Finally, dielectric parameters were determined in the temperature range from 30 to 180 degrees C, and within a variety of frequencies. Curie temperature was detected at 130 degrees C.
PB  - Belgrade : ETRAN
T2  - Science of Sintering
T1  - Structure and Properties of Nanocrystalline Tetragonal BaTiO3 Prepared by Combustion Solid State Synthesis
SP  - 257
EP  - 268
VL  - 52
DO  - 10.2298/SOS2003257F
UR  - https://hdl.handle.net/21.15107/rcub_dais_9449
ER  - 

@article{
author = "Filipović, Suzana and Anđelković, Ljubica and Jeremić, Dejan and Vulić, Predrag and Nikolić, Aleksandar and Marković, Smilja and Paunović, Vesna and Lević, Steva and Pavlović, Vladimir B.",
year = "2020",
abstract = "Barium titanate (BaTiO3) attracts high scientific and technological attention due to good dielectric and electromechanical properties. Although BaTiO3 is one of the most frequently investigated ferroelectric materials, the need for finding new and/or improved synthesis methods of this material still exists. In this paper, a novel, mild synthesis route for producing tetragonal BaTiO3 from barium nitrate and Ti-oxalate precursor is presented. Morphology of the prepared and subsequently sintered BaTiO3 was determined by SEM. Particle size distribution of the as prepared powder was monitored by the laser diffraction. The phase composition, structure and lattice dynamics were investigated by XRD and Raman spectroscopy. Finally, dielectric parameters were determined in the temperature range from 30 to 180 degrees C, and within a variety of frequencies. Curie temperature was detected at 130 degrees C.",
publisher = "Belgrade : ETRAN",
journal = "Science of Sintering",
title = "Structure and Properties of Nanocrystalline Tetragonal BaTiO3 Prepared by Combustion Solid State Synthesis",
pages = "257-268",
volume = "52",
doi = "10.2298/SOS2003257F",
url = "https://hdl.handle.net/21.15107/rcub_dais_9449"
}

Filipović, S., Anđelković, L., Jeremić, D., Vulić, P., Nikolić, A., Marković, S., Paunović, V., Lević, S.,& Pavlović, V. B.. (2020). Structure and Properties of Nanocrystalline Tetragonal BaTiO3 Prepared by Combustion Solid State Synthesis. in Science of Sintering
Belgrade : ETRAN., 52, 257-268.
https://doi.org/10.2298/SOS2003257F
https://hdl.handle.net/21.15107/rcub_dais_9449

Filipović S, Anđelković L, Jeremić D, Vulić P, Nikolić A, Marković S, Paunović V, Lević S, Pavlović VB. Structure and Properties of Nanocrystalline Tetragonal BaTiO3 Prepared by Combustion Solid State Synthesis. in Science of Sintering. 2020;52:257-268.
doi:10.2298/SOS2003257F
https://hdl.handle.net/21.15107/rcub_dais_9449 .

Filipović, Suzana, Anđelković, Ljubica, Jeremić, Dejan, Vulić, Predrag, Nikolić, Aleksandar, Marković, Smilja, Paunović, Vesna, Lević, Steva, Pavlović, Vladimir B., "Structure and Properties of Nanocrystalline Tetragonal BaTiO3 Prepared by Combustion Solid State Synthesis" in Science of Sintering, 52 (2020):257-268,
https://doi.org/10.2298/SOS2003257F .,
https://hdl.handle.net/21.15107/rcub_dais_9449 .

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Jeremić, Dejan
AU  - Milenković, Milica R.
AU  - Radosavljević, Jelena
AU  - Vulić, Predrag
AU  - Pavlović, Vladimir B.
AU  - Manojlović, Dragan D.
AU  - Nikolić, Aleksandar S.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/6901
AB  - A simple organic-phase synthesis process was used to produce bare NiFe2O4 and ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 ferrite nanoparticles. X-ray powder diffractograms for all investigated powders show characteristic peaks of a spinel cubic structure without a secondary phase. Transmission electron microscopy (TEM) indicated the presence of nanoparticles that are smaller than 20 nm. The release of divalent ions (Ni2+ and Zn2+) from synthesized nanoparticles that were dispersed in saline solution, phosphate-buffered saline (PBS) and human serum, as determined by the inductively coupled plasma mass spectrometry (ICP-MS) method, was lower than 2 wt %. These results demonstrate the stability of the investigated nanoparticles in biologically relevant media and exclude the toxicity of Ni2+ and Zn2+ due to metal ion release, thereby opening a broad range of (bio)medical applications.
PB  - Elsevier
T2  - Ceramics International
T1  - Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles
SP  - 3528
EP  - 3533
VL  - 46
IS  - 3
DO  - 10.1016/j.ceramint.2019.10.068
UR  - https://hdl.handle.net/21.15107/rcub_dais_6901
ER  - 

@article{
author = "Anđelković, Ljubica and Jeremić, Dejan and Milenković, Milica R. and Radosavljević, Jelena and Vulić, Predrag and Pavlović, Vladimir B. and Manojlović, Dragan D. and Nikolić, Aleksandar S.",
year = "2020",
abstract = "A simple organic-phase synthesis process was used to produce bare NiFe2O4 and ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 ferrite nanoparticles. X-ray powder diffractograms for all investigated powders show characteristic peaks of a spinel cubic structure without a secondary phase. Transmission electron microscopy (TEM) indicated the presence of nanoparticles that are smaller than 20 nm. The release of divalent ions (Ni2+ and Zn2+) from synthesized nanoparticles that were dispersed in saline solution, phosphate-buffered saline (PBS) and human serum, as determined by the inductively coupled plasma mass spectrometry (ICP-MS) method, was lower than 2 wt %. These results demonstrate the stability of the investigated nanoparticles in biologically relevant media and exclude the toxicity of Ni2+ and Zn2+ due to metal ion release, thereby opening a broad range of (bio)medical applications.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles",
pages = "3528-3533",
volume = "46",
number = "3",
doi = "10.1016/j.ceramint.2019.10.068",
url = "https://hdl.handle.net/21.15107/rcub_dais_6901"
}

Anđelković, L., Jeremić, D., Milenković, M. R., Radosavljević, J., Vulić, P., Pavlović, V. B., Manojlović, D. D.,& Nikolić, A. S.. (2020). Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles. in Ceramics International
Elsevier., 46(3), 3528-3533.
https://doi.org/10.1016/j.ceramint.2019.10.068
https://hdl.handle.net/21.15107/rcub_dais_6901

Anđelković L, Jeremić D, Milenković MR, Radosavljević J, Vulić P, Pavlović VB, Manojlović DD, Nikolić AS. Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles. in Ceramics International. 2020;46(3):3528-3533.
doi:10.1016/j.ceramint.2019.10.068
https://hdl.handle.net/21.15107/rcub_dais_6901 .

Anđelković, Ljubica, Jeremić, Dejan, Milenković, Milica R., Radosavljević, Jelena, Vulić, Predrag, Pavlović, Vladimir B., Manojlović, Dragan D., Nikolić, Aleksandar S., "Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles" in Ceramics International, 46, no. 3 (2020):3528-3533,
https://doi.org/10.1016/j.ceramint.2019.10.068 .,
https://hdl.handle.net/21.15107/rcub_dais_6901 .

TY  - JOUR
AU  - Vuković, Marina
AU  - Mančić, Lidija
AU  - Dinić, Ivana
AU  - Vulić, Predrag
AU  - Nikolić, Marko G.
AU  - Tan, Zhenquan
AU  - Milošević, Olivera
PY  - 2020
UR  - https://ceramics.onlinelibrary.wiley.com/doi/abs/10.1111/ijac.13363
UR  - https://dais.sanu.ac.rs/123456789/6467
AB  - Single phase β-NaY0.8-xGdxYb0.18Er0.02F4 nanoparticles with different concentrations of gadolinium ions were prepared via PVP-assisted solvothermal treating at 200°C (PVP- polyvinylpyrrolidone). With the increase in Gd3+ concentration, size of the nanoparticles decreased. The up-converting spectra recorded upon 980 nm irradiation showed the green (510-560 nm) and red (640-690 nm) emissions, due to 2H11/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions, respectively. The strongest up-conversion luminescence was detected in 15 mol% Gd3+-doped nanoparticles obtained after 20 hours of solvothermal treating. With the rise of Gd3+ content up-conversion emission decreased due to increased defect concentration in the NaYF4 matrix. Fourier transform infrared spectroscopy proved in situ generation of hydrophilic nanoparticles as a result of PVP ligands retention at the particle surface.
PB  - Wiley
T2  - International Journal of Applied Ceramic Technology
T1  - The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase
SP  - 1445
EP  - 1452
VL  - 17
IS  - 3
DO  - 10.1111/ijac.13363
UR  - https://hdl.handle.net/21.15107/rcub_dais_6467
ER  - 

@article{
author = "Vuković, Marina and Mančić, Lidija and Dinić, Ivana and Vulić, Predrag and Nikolić, Marko G. and Tan, Zhenquan and Milošević, Olivera",
year = "2020",
abstract = "Single phase β-NaY0.8-xGdxYb0.18Er0.02F4 nanoparticles with different concentrations of gadolinium ions were prepared via PVP-assisted solvothermal treating at 200°C (PVP- polyvinylpyrrolidone). With the increase in Gd3+ concentration, size of the nanoparticles decreased. The up-converting spectra recorded upon 980 nm irradiation showed the green (510-560 nm) and red (640-690 nm) emissions, due to 2H11/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions, respectively. The strongest up-conversion luminescence was detected in 15 mol% Gd3+-doped nanoparticles obtained after 20 hours of solvothermal treating. With the rise of Gd3+ content up-conversion emission decreased due to increased defect concentration in the NaYF4 matrix. Fourier transform infrared spectroscopy proved in situ generation of hydrophilic nanoparticles as a result of PVP ligands retention at the particle surface.",
publisher = "Wiley",
journal = "International Journal of Applied Ceramic Technology",
title = "The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase",
pages = "1445-1452",
volume = "17",
number = "3",
doi = "10.1111/ijac.13363",
url = "https://hdl.handle.net/21.15107/rcub_dais_6467"
}

Vuković, M., Mančić, L., Dinić, I., Vulić, P., Nikolić, M. G., Tan, Z.,& Milošević, O.. (2020). The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase. in International Journal of Applied Ceramic Technology
Wiley., 17(3), 1445-1452.
https://doi.org/10.1111/ijac.13363
https://hdl.handle.net/21.15107/rcub_dais_6467

Vuković M, Mančić L, Dinić I, Vulić P, Nikolić MG, Tan Z, Milošević O. The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase. in International Journal of Applied Ceramic Technology. 2020;17(3):1445-1452.
doi:10.1111/ijac.13363
https://hdl.handle.net/21.15107/rcub_dais_6467 .

Vuković, Marina, Mančić, Lidija, Dinić, Ivana, Vulić, Predrag, Nikolić, Marko G., Tan, Zhenquan, Milošević, Olivera, "The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase" in International Journal of Applied Ceramic Technology, 17, no. 3 (2020):1445-1452,
https://doi.org/10.1111/ijac.13363 .,
https://hdl.handle.net/21.15107/rcub_dais_6467 .

TY  - JOUR
AU  - Vuković, Marina
AU  - Mančić, Lidija
AU  - Dinić, Ivana
AU  - Vulić, Predrag
AU  - Nikolić, Marko G.
AU  - Tan, Zhenquan
AU  - Milošević, Olivera
PY  - 2020
UR  - https://ceramics.onlinelibrary.wiley.com/doi/abs/10.1111/ijac.13363
UR  - https://dais.sanu.ac.rs/123456789/8947
AB  - Single phase β-NaY0.8-xGdxYb0.18Er0.02F4 nanoparticles with different concentrations of gadolinium ions were prepared via PVP-assisted solvothermal treating at 200°C (PVP- polyvinylpyrrolidone). With the increase in Gd3+ concentration, size of the nanoparticles decreased. The up-converting spectra recorded upon 980 nm irradiation showed the green (510-560 nm) and red (640-690 nm) emissions, due to 2H11/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions, respectively. The strongest up-conversion luminescence was detected in 15 mol% Gd3+-doped nanoparticles obtained after 20 hours of solvothermal treating. With the rise of Gd3+ content up-conversion emission decreased due to increased defect concentration in the NaYF4 matrix. Fourier transform infrared spectroscopy proved in situ generation of hydrophilic nanoparticles as a result of PVP ligands retention at the particle surface.
PB  - Wiley
T2  - International Journal of Applied Ceramic Technology
T1  - The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase
SP  - 1445
EP  - 1452
VL  - 17
IS  - 3
DO  - 10.1111/ijac.13363
UR  - https://hdl.handle.net/21.15107/rcub_dais_8947
ER  - 

@article{
author = "Vuković, Marina and Mančić, Lidija and Dinić, Ivana and Vulić, Predrag and Nikolić, Marko G. and Tan, Zhenquan and Milošević, Olivera",
year = "2020",
abstract = "Single phase β-NaY0.8-xGdxYb0.18Er0.02F4 nanoparticles with different concentrations of gadolinium ions were prepared via PVP-assisted solvothermal treating at 200°C (PVP- polyvinylpyrrolidone). With the increase in Gd3+ concentration, size of the nanoparticles decreased. The up-converting spectra recorded upon 980 nm irradiation showed the green (510-560 nm) and red (640-690 nm) emissions, due to 2H11/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions, respectively. The strongest up-conversion luminescence was detected in 15 mol% Gd3+-doped nanoparticles obtained after 20 hours of solvothermal treating. With the rise of Gd3+ content up-conversion emission decreased due to increased defect concentration in the NaYF4 matrix. Fourier transform infrared spectroscopy proved in situ generation of hydrophilic nanoparticles as a result of PVP ligands retention at the particle surface.",
publisher = "Wiley",
journal = "International Journal of Applied Ceramic Technology",
title = "The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase",
pages = "1445-1452",
volume = "17",
number = "3",
doi = "10.1111/ijac.13363",
url = "https://hdl.handle.net/21.15107/rcub_dais_8947"
}

Vuković, M., Mančić, L., Dinić, I., Vulić, P., Nikolić, M. G., Tan, Z.,& Milošević, O.. (2020). The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase. in International Journal of Applied Ceramic Technology
Wiley., 17(3), 1445-1452.
https://doi.org/10.1111/ijac.13363
https://hdl.handle.net/21.15107/rcub_dais_8947

Vuković M, Mančić L, Dinić I, Vulić P, Nikolić MG, Tan Z, Milošević O. The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase. in International Journal of Applied Ceramic Technology. 2020;17(3):1445-1452.
doi:10.1111/ijac.13363
https://hdl.handle.net/21.15107/rcub_dais_8947 .

Vuković, Marina, Mančić, Lidija, Dinić, Ivana, Vulić, Predrag, Nikolić, Marko G., Tan, Zhenquan, Milošević, Olivera, "The gadolinium effect on crystallization behavior and luminescence of β-NaYF4:Yb,Er phase" in International Journal of Applied Ceramic Technology, 17, no. 3 (2020):1445-1452,
https://doi.org/10.1111/ijac.13363 .,
https://hdl.handle.net/21.15107/rcub_dais_8947 .

TY  - JOUR
AU  - Jeremić, Dejan
AU  - Anđelković, Ljubica
AU  - Milenković, Milica R.
AU  - Šuljagić, Marija
AU  - Šumar Ristović, Maja
AU  - Ostojić, Sanja
AU  - Nikolić, Aleksandar S.
AU  - Vulić, Predrag
AU  - Brčeski, Ilija
AU  - Pavlović, Vladimir B.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/12085
AB  - This work is the first report of a very simple and fast one-pot synthesis of nickel oxide (NiO) and hematite (α-Fe2O3) nanoparticles by thermal decomposition of transition metal aqua complexes with camphor sulfonate anions. Obtained nanopowders were characterized by X-ray powder diffraction, Fourier transform IR analysis, scanning electron microscopy, and Energy-dispersive X-ray spectroscopy. X-ray powder diffraction confirmed the formation of high purity NiO and α-Fe2O3 crystal phases. In the case of α-Fe2O3, about five times larger average crystallite size was obtained. Fourier transform IR spectra of synthesized materials showed characteristic peaks for NiO and α-Fe2O3 nanostructures. To visualize the morphology and the chemical composition of the final products Scanning electron microscopy and Energy-dispersive X-ray spectroscopy were performed. The thermogravimetric analysis was done for a better understanding of the general thermal behavior of precursor compounds. This easy-to-perform and fast preparation method opens a broad range of obtained materials’ usage, particularly due to its economic viability
T2  - Science of Sintering
T1  - One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles
SP  - 481
EP  - 490
VL  - 52
IS  - 4
DO  - 10.2298/SOS2004481J
UR  - https://hdl.handle.net/21.15107/rcub_dais_12085
ER  - 

@article{
author = "Jeremić, Dejan and Anđelković, Ljubica and Milenković, Milica R. and Šuljagić, Marija and Šumar Ristović, Maja and Ostojić, Sanja and Nikolić, Aleksandar S. and Vulić, Predrag and Brčeski, Ilija and Pavlović, Vladimir B.",
year = "2020",
abstract = "This work is the first report of a very simple and fast one-pot synthesis of nickel oxide (NiO) and hematite (α-Fe2O3) nanoparticles by thermal decomposition of transition metal aqua complexes with camphor sulfonate anions. Obtained nanopowders were characterized by X-ray powder diffraction, Fourier transform IR analysis, scanning electron microscopy, and Energy-dispersive X-ray spectroscopy. X-ray powder diffraction confirmed the formation of high purity NiO and α-Fe2O3 crystal phases. In the case of α-Fe2O3, about five times larger average crystallite size was obtained. Fourier transform IR spectra of synthesized materials showed characteristic peaks for NiO and α-Fe2O3 nanostructures. To visualize the morphology and the chemical composition of the final products Scanning electron microscopy and Energy-dispersive X-ray spectroscopy were performed. The thermogravimetric analysis was done for a better understanding of the general thermal behavior of precursor compounds. This easy-to-perform and fast preparation method opens a broad range of obtained materials’ usage, particularly due to its economic viability",
journal = "Science of Sintering",
title = "One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles",
pages = "481-490",
volume = "52",
number = "4",
doi = "10.2298/SOS2004481J",
url = "https://hdl.handle.net/21.15107/rcub_dais_12085"
}

Jeremić, D., Anđelković, L., Milenković, M. R., Šuljagić, M., Šumar Ristović, M., Ostojić, S., Nikolić, A. S., Vulić, P., Brčeski, I.,& Pavlović, V. B.. (2020). One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles. in Science of Sintering, 52(4), 481-490.
https://doi.org/10.2298/SOS2004481J
https://hdl.handle.net/21.15107/rcub_dais_12085

Jeremić D, Anđelković L, Milenković MR, Šuljagić M, Šumar Ristović M, Ostojić S, Nikolić AS, Vulić P, Brčeski I, Pavlović VB. One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles. in Science of Sintering. 2020;52(4):481-490.
doi:10.2298/SOS2004481J
https://hdl.handle.net/21.15107/rcub_dais_12085 .

Jeremić, Dejan, Anđelković, Ljubica, Milenković, Milica R., Šuljagić, Marija, Šumar Ristović, Maja, Ostojić, Sanja, Nikolić, Aleksandar S., Vulić, Predrag, Brčeski, Ilija, Pavlović, Vladimir B., "One-pot combustion synthesis of nickel oxide and hematite: From simple coordination compounds to high purity metal oxide nanoparticles" in Science of Sintering, 52, no. 4 (2020):481-490,
https://doi.org/10.2298/SOS2004481J .,
https://hdl.handle.net/21.15107/rcub_dais_12085 .

TY  - DATA
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9455
AB  - Figure S1.IR spectra of gaseous decomposition products obtained during TGexperiments with 1(A) and 2(B);Figure S2.The 3D presentation of thermal decompositions versustime together with IR spectra of their gaseous products: (a)1; (b)2; Figure S3. Overlapped experimental (blue) and calculated (red) powder XRD diffractograms of 1 (A) and 2 (B); Figure S4.Comparison between experimental powder XRD patterns of 1(left) and 2(right) with simulated  patterns  of  their  analogues  with  different positionof M‒Sbondwith  respect  to  the TM-CN ring chair conformation; Figure S5. Optical microscope images of Pt-(left) and Pd-complex (right)showing as-obtained single crystals; Figure S6.SEM images of Pt-(left) and Pd-complex (right)after reduction to powder for XRD measurements; Figure S7. 1H NMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S8. 13CNMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S9. 1H (A) and 13CNMR (B) spectra of 1in DMSO-d6; Figure S10. COSY spectrum of 1in DMSO-d6; Figure S11. NOESY spectrum of 1in DMSO-d6; Figure S12. 1H–13CHSQC spectrum of 1in DMSO-d6, Figure S13. 1H (A) and 13CNMR (B) spectra of 1in CD3NO2; Figure S14. 1H (A) and 13CNMR (B) spectra of 2in DMSO-d6; Figure S15. 1H (A) and 13CNMR (B) spectra of 2in CD3NO2; Scheme S1. Labellingof atoms used for NMR signal assignments;
Table  S1.Experimental  vibrational  frequencies  (cm-1)  and  signals  description  of  complexes studied;Table S2.Crystal data and structure refinement for 1and 2; Table S3.Selected bond lengths (Å) and angles (°) for complexes 1 and 2;Table  S4. Results  of  energy  calculations  for  C-H/Cl-M,  C-H/S-M,  C-H/M  and C-H/NCinteractions  (M=  Pd(II)  and  Pt(II))  at wb97xd/6-31+g**  +lanl2dzlevel  of  theory.  Energies  are expressed in kcal/mol; Table  S5.C-H/M  interactions  obtained  from  the  periodic  calculations  of  axial  and  equatorially coordinated Pd and Pt; Table S6.1H NMR spectral data (399.74 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2; Table S7. 13C NMR spectral data (100.53 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661
UR  - https://hdl.handle.net/21.15107/rcub_dais_9455
ER  - 

@misc{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
abstract = "Figure S1.IR spectra of gaseous decomposition products obtained during TGexperiments with 1(A) and 2(B);Figure S2.The 3D presentation of thermal decompositions versustime together with IR spectra of their gaseous products: (a)1; (b)2; Figure S3. Overlapped experimental (blue) and calculated (red) powder XRD diffractograms of 1 (A) and 2 (B); Figure S4.Comparison between experimental powder XRD patterns of 1(left) and 2(right) with simulated  patterns  of  their  analogues  with  different positionof M‒Sbondwith  respect  to  the TM-CN ring chair conformation; Figure S5. Optical microscope images of Pt-(left) and Pd-complex (right)showing as-obtained single crystals; Figure S6.SEM images of Pt-(left) and Pd-complex (right)after reduction to powder for XRD measurements; Figure S7. 1H NMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S8. 13CNMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S9. 1H (A) and 13CNMR (B) spectra of 1in DMSO-d6; Figure S10. COSY spectrum of 1in DMSO-d6; Figure S11. NOESY spectrum of 1in DMSO-d6; Figure S12. 1H–13CHSQC spectrum of 1in DMSO-d6, Figure S13. 1H (A) and 13CNMR (B) spectra of 1in CD3NO2; Figure S14. 1H (A) and 13CNMR (B) spectra of 2in DMSO-d6; Figure S15. 1H (A) and 13CNMR (B) spectra of 2in CD3NO2; Scheme S1. Labellingof atoms used for NMR signal assignments;
Table  S1.Experimental  vibrational  frequencies  (cm-1)  and  signals  description  of  complexes studied;Table S2.Crystal data and structure refinement for 1and 2; Table S3.Selected bond lengths (Å) and angles (°) for complexes 1 and 2;Table  S4. Results  of  energy  calculations  for  C-H/Cl-M,  C-H/S-M,  C-H/M  and C-H/NCinteractions  (M=  Pd(II)  and  Pt(II))  at wb97xd/6-31+g**  +lanl2dzlevel  of  theory.  Energies  are expressed in kcal/mol; Table  S5.C-H/M  interactions  obtained  from  the  periodic  calculations  of  axial  and  equatorially coordinated Pd and Pt; Table S6.1H NMR spectral data (399.74 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2; Table S7. 13C NMR spectral data (100.53 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661",
url = "https://hdl.handle.net/21.15107/rcub_dais_9455"
}

Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661. in Crystal Growth & Design
American Chemical Society..
https://hdl.handle.net/21.15107/rcub_dais_9455

Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661. in Crystal Growth & Design. 2020;.
https://hdl.handle.net/21.15107/rcub_dais_9455 .

Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661" in Crystal Growth & Design (2020),
https://hdl.handle.net/21.15107/rcub_dais_9455 .

TY  - JOUR
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9454
AB  - Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study
SP  - 3018
EP  - 3033
VL  - 20
IS  - 5
DO  - 10.1021/acs.cgd.9b01661
UR  - https://hdl.handle.net/21.15107/rcub_dais_9454
ER  - 

@article{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
abstract = "Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study",
pages = "3018-3033",
volume = "20",
number = "5",
doi = "10.1021/acs.cgd.9b01661",
url = "https://hdl.handle.net/21.15107/rcub_dais_9454"
}

Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design
American Chemical Society., 20(5), 3018-3033.
https://doi.org/10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9454

Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design. 2020;20(5):3018-3033.
doi:10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9454 .

Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study" in Crystal Growth & Design, 20, no. 5 (2020):3018-3033,
https://doi.org/10.1021/acs.cgd.9b01661 .,
https://hdl.handle.net/21.15107/rcub_dais_9454 .

TY  - JOUR
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9453
AB  - Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study
SP  - 3018
EP  - 3033
VL  - 20
IS  - 5
DO  - 10.1021/acs.cgd.9b01661
UR  - https://hdl.handle.net/21.15107/rcub_dais_9453
ER  - 

@article{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
abstract = "Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study",
pages = "3018-3033",
volume = "20",
number = "5",
doi = "10.1021/acs.cgd.9b01661",
url = "https://hdl.handle.net/21.15107/rcub_dais_9453"
}

Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design
American Chemical Society., 20(5), 3018-3033.
https://doi.org/10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9453

Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design. 2020;20(5):3018-3033.
doi:10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9453 .

Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study" in Crystal Growth & Design, 20, no. 5 (2020):3018-3033,
https://doi.org/10.1021/acs.cgd.9b01661 .,
https://hdl.handle.net/21.15107/rcub_dais_9453 .

TY  - CONF
AU  - Vuković, Marina
AU  - Mančić, Lidija
AU  - Dinić, Ivana
AU  - Vulić, Predrag J.
AU  - Nikolić, Marko G.
AU  - Tan, Zhenquan
AU  - Milošević, Olivera
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/7000
AB  - application as lasers, displays, photo-thermal agents and biomarkers. Due to efficient two-phonon excitation and the large anti-Stocks shift UCNPs are able to emit visible or UV photons under excitation by near-infrared (NIR). Over the last decade, decomposition of organometallic compounds has been indicated as one of the most convenient method for the synthesis of monodisperse NaYF4:Yb3+,Er3+ UCNPs with a hexagonal crystal structure. Herein, NaY0.8-xGdxYb0.18Er0.02F4 (x= 0.3 or 0.15) up-conversion nanoparticles crystallized in the hexagonal space group P63/m were successfully synthesized solvothermally utilizing rare earth nitrates, NaF and polyvinylpyrrolidone (PVP) in ethanol-water mixture at 200 °C. Rietveld refinement of the X-ray powder diffraction (XRPD) data and high resolution transmission microscopy (HRTEM) analysis show that all UCNPs are monocrystalline (60-70 nm), have low defect concentration and uniform dopants distribution. Fourier-transform infrared (FTIR) spectroscopy indicate existence of the PVP ligands at the UCNPs surface, while photoluminescence (PL) spectra shows characteristic green (at 520 and 540 nm, due to 2H11/2, 4S3/2→4I15/2 transitions) and red (at 655 nm, due to 4F9/2 → 4I15/2 transition) emission lines under excitation by NIR (λ =980 nm) light.
PB  - Budapest : [s. n.]
C3  - Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest
T1  - Influence of Gd3+ doping on the NaYF4 :YB3+,ER3+ structural and up-conversion properties
SP  - 19
EP  - 20
UR  - https://hdl.handle.net/21.15107/rcub_dais_7000
ER  - 

@conference{
author = "Vuković, Marina and Mančić, Lidija and Dinić, Ivana and Vulić, Predrag J. and Nikolić, Marko G. and Tan, Zhenquan and Milošević, Olivera",
year = "2019",
abstract = "application as lasers, displays, photo-thermal agents and biomarkers. Due to efficient two-phonon excitation and the large anti-Stocks shift UCNPs are able to emit visible or UV photons under excitation by near-infrared (NIR). Over the last decade, decomposition of organometallic compounds has been indicated as one of the most convenient method for the synthesis of monodisperse NaYF4:Yb3+,Er3+ UCNPs with a hexagonal crystal structure. Herein, NaY0.8-xGdxYb0.18Er0.02F4 (x= 0.3 or 0.15) up-conversion nanoparticles crystallized in the hexagonal space group P63/m were successfully synthesized solvothermally utilizing rare earth nitrates, NaF and polyvinylpyrrolidone (PVP) in ethanol-water mixture at 200 °C. Rietveld refinement of the X-ray powder diffraction (XRPD) data and high resolution transmission microscopy (HRTEM) analysis show that all UCNPs are monocrystalline (60-70 nm), have low defect concentration and uniform dopants distribution. Fourier-transform infrared (FTIR) spectroscopy indicate existence of the PVP ligands at the UCNPs surface, while photoluminescence (PL) spectra shows characteristic green (at 520 and 540 nm, due to 2H11/2, 4S3/2→4I15/2 transitions) and red (at 655 nm, due to 4F9/2 → 4I15/2 transition) emission lines under excitation by NIR (λ =980 nm) light.",
publisher = "Budapest : [s. n.]",
journal = "Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest",
title = "Influence of Gd3+ doping on the NaYF4 :YB3+,ER3+ structural and up-conversion properties",
pages = "19-20",
url = "https://hdl.handle.net/21.15107/rcub_dais_7000"
}

Vuković, M., Mančić, L., Dinić, I., Vulić, P. J., Nikolić, M. G., Tan, Z.,& Milošević, O.. (2019). Influence of Gd3+ doping on the NaYF4 :YB3+,ER3+ structural and up-conversion properties. in Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest
Budapest : [s. n.]., 19-20.
https://hdl.handle.net/21.15107/rcub_dais_7000

Vuković M, Mančić L, Dinić I, Vulić PJ, Nikolić MG, Tan Z, Milošević O. Influence of Gd3+ doping on the NaYF4 :YB3+,ER3+ structural and up-conversion properties. in Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest. 2019;:19-20.
https://hdl.handle.net/21.15107/rcub_dais_7000 .

Vuković, Marina, Mančić, Lidija, Dinić, Ivana, Vulić, Predrag J., Nikolić, Marko G., Tan, Zhenquan, Milošević, Olivera, "Influence of Gd3+ doping on the NaYF4 :YB3+,ER3+ structural and up-conversion properties" in Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest (2019):19-20,
https://hdl.handle.net/21.15107/rcub_dais_7000 .

TY  - CONF
AU  - Vuković, Marina
AU  - Dinić, Ivana
AU  - Mančić, Lidija
AU  - Vulić, Predrag J.
AU  - Nikolić, Marko G.
AU  - Milošević, Olivera
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6978
AB  - There is a great interest for the synthesis of rare earth (RE) doped up-converting nanoparticles (UCNPs) which morphological and luminescence properties are well suited for application in optoelectronics, forensics, security and biomedicine. The synthesis of such particles usually comprises decomposition of organometallic compounds in an oxygen-free environment followed with coating of biocompatible layer or ligands exchange. In this work hydroxyl-carboxyl (HO-C) type of chelators (citric acid and sodium citrate) are used for the stabilization of NaYF4:Gd,Yb,Er UCNPs during solvothermal treatment of rare earth nitrate salts with different fluoride sources (NaF, NH4F and NH4HF2). The x-ray powder diffraction (XRPD) showed that all powders contain the mixture of cubic and hexagonal NaYF4:Gd,Yb,Er phase in nano and micro-sized particles respectively. However, the content of later one prevails in samples obtain when Nacitrate is used as chelator, regardless of which fluoride source is used for precipitation. Additionally, variation of the particles size and shape is detected with a variation of fluoride type. All particles have hydrophilic surface due to retention of citrate ligands and emit intense green light emission centered at 519 and 539 nm (2H11/2,4S3/2→4I15/2) when excited with near infrared light.
PB  - Belgrade : Serbian Ceramic Society
C3  - Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019
T1  - The usage of different fluoride sources during solvothermal synthesis of UCNPs in hydroxyl-carboxyl chelated precursor
SP  - 47
EP  - 47
UR  - https://hdl.handle.net/21.15107/rcub_dais_6978
ER  - 

@conference{
author = "Vuković, Marina and Dinić, Ivana and Mančić, Lidija and Vulić, Predrag J. and Nikolić, Marko G. and Milošević, Olivera",
year = "2019",
abstract = "There is a great interest for the synthesis of rare earth (RE) doped up-converting nanoparticles (UCNPs) which morphological and luminescence properties are well suited for application in optoelectronics, forensics, security and biomedicine. The synthesis of such particles usually comprises decomposition of organometallic compounds in an oxygen-free environment followed with coating of biocompatible layer or ligands exchange. In this work hydroxyl-carboxyl (HO-C) type of chelators (citric acid and sodium citrate) are used for the stabilization of NaYF4:Gd,Yb,Er UCNPs during solvothermal treatment of rare earth nitrate salts with different fluoride sources (NaF, NH4F and NH4HF2). The x-ray powder diffraction (XRPD) showed that all powders contain the mixture of cubic and hexagonal NaYF4:Gd,Yb,Er phase in nano and micro-sized particles respectively. However, the content of later one prevails in samples obtain when Nacitrate is used as chelator, regardless of which fluoride source is used for precipitation. Additionally, variation of the particles size and shape is detected with a variation of fluoride type. All particles have hydrophilic surface due to retention of citrate ligands and emit intense green light emission centered at 519 and 539 nm (2H11/2,4S3/2→4I15/2) when excited with near infrared light.",
publisher = "Belgrade : Serbian Ceramic Society",
journal = "Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019",
title = "The usage of different fluoride sources during solvothermal synthesis of UCNPs in hydroxyl-carboxyl chelated precursor",
pages = "47-47",
url = "https://hdl.handle.net/21.15107/rcub_dais_6978"
}

Vuković, M., Dinić, I., Mančić, L., Vulić, P. J., Nikolić, M. G.,& Milošević, O.. (2019). The usage of different fluoride sources during solvothermal synthesis of UCNPs in hydroxyl-carboxyl chelated precursor. in Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019
Belgrade : Serbian Ceramic Society., 47-47.
https://hdl.handle.net/21.15107/rcub_dais_6978

Vuković M, Dinić I, Mančić L, Vulić PJ, Nikolić MG, Milošević O. The usage of different fluoride sources during solvothermal synthesis of UCNPs in hydroxyl-carboxyl chelated precursor. in Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019. 2019;:47-47.
https://hdl.handle.net/21.15107/rcub_dais_6978 .

Vuković, Marina, Dinić, Ivana, Mančić, Lidija, Vulić, Predrag J., Nikolić, Marko G., Milošević, Olivera, "The usage of different fluoride sources during solvothermal synthesis of UCNPs in hydroxyl-carboxyl chelated precursor" in Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019 (2019):47-47,
https://hdl.handle.net/21.15107/rcub_dais_6978 .

TY  - CONF
AU  - Dinić, Ivana
AU  - Vuković, Marina
AU  - Vulić, Predrag
AU  - Nikolić, Marko G.
AU  - Milošević, Olivera
AU  - Mančić, Lidija
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6970
AB  - Monosized up-converting nanoparticles (UCNPs) with a spherical shape and biocompatible surface have a wide application in biomedicine as new cell markers or light-triggered drug delivery agents. The synthesis of the hexagonal β-NaYF4:Yb/Er phase is of a great interest, because of its most efficient up-conversion luminescence. Beside it, synthesis of the UCNPs based on YF3:Yb/Er phase is also attractive due to its orthorhombic phase arrangement and fact that higher concentration of dopants could be introduced in such crystal lattice. In this work the synthesis of pure and Gd-doped YF3:Yb/Er phases were performed through hydro/solvo thermal method using a biocompatible chitosan as a surfactant. The XRD analysis showed that independently of the gadolinium content formation of the orthorhombic phase is achieved, but intensity of the green emission due to the (2H11/2, 4S3/2) → 4I15/2 electronic transitions was highest for un-doped YF3:Yb/Er sample.
PB  - Belgrade : Institute of Technical Sciences of SASA
C3  - Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia
T1  - Effect of Gd3+ introduction on YF3: Yb, Er structural, morphological and optical properties
SP  - 33
EP  - 33
UR  - https://hdl.handle.net/21.15107/rcub_dais_6970
ER  - 

@conference{
author = "Dinić, Ivana and Vuković, Marina and Vulić, Predrag and Nikolić, Marko G. and Milošević, Olivera and Mančić, Lidija",
year = "2019",
abstract = "Monosized up-converting nanoparticles (UCNPs) with a spherical shape and biocompatible surface have a wide application in biomedicine as new cell markers or light-triggered drug delivery agents. The synthesis of the hexagonal β-NaYF4:Yb/Er phase is of a great interest, because of its most efficient up-conversion luminescence. Beside it, synthesis of the UCNPs based on YF3:Yb/Er phase is also attractive due to its orthorhombic phase arrangement and fact that higher concentration of dopants could be introduced in such crystal lattice. In this work the synthesis of pure and Gd-doped YF3:Yb/Er phases were performed through hydro/solvo thermal method using a biocompatible chitosan as a surfactant. The XRD analysis showed that independently of the gadolinium content formation of the orthorhombic phase is achieved, but intensity of the green emission due to the (2H11/2, 4S3/2) → 4I15/2 electronic transitions was highest for un-doped YF3:Yb/Er sample.",
publisher = "Belgrade : Institute of Technical Sciences of SASA",
journal = "Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia",
title = "Effect of Gd3+ introduction on YF3: Yb, Er structural, morphological and optical properties",
pages = "33-33",
url = "https://hdl.handle.net/21.15107/rcub_dais_6970"
}

Dinić, I., Vuković, M., Vulić, P., Nikolić, M. G., Milošević, O.,& Mančić, L.. (2019). Effect of Gd3+ introduction on YF3: Yb, Er structural, morphological and optical properties. in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia
Belgrade : Institute of Technical Sciences of SASA., 33-33.
https://hdl.handle.net/21.15107/rcub_dais_6970

Dinić I, Vuković M, Vulić P, Nikolić MG, Milošević O, Mančić L. Effect of Gd3+ introduction on YF3: Yb, Er structural, morphological and optical properties. in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia. 2019;:33-33.
https://hdl.handle.net/21.15107/rcub_dais_6970 .

Dinić, Ivana, Vuković, Marina, Vulić, Predrag, Nikolić, Marko G., Milošević, Olivera, Mančić, Lidija, "Effect of Gd3+ introduction on YF3: Yb, Er structural, morphological and optical properties" in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia (2019):33-33,
https://hdl.handle.net/21.15107/rcub_dais_6970 .

TY  - CONF
AU  - Dinić, Ivana
AU  - Vuković, Marina
AU  - Vulić, Predrag
AU  - Nikolić, Marko G.
AU  - Milošević, Olivera
AU  - Mančić, Lidija
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6672
AB  - Thanks to the unique optical properties, up-converting nanoparticles (UCNPs) have a wide application in optoelectronics, forensics, security and biomedicine. The synthesis of the most efficient hexagonal β-NaYF4: Yb/Er phase is usually performed through thermal decomposition of organic precursors which could cause the UCNP cytotoxicity. Since cubic polymorph is kinetically more stable than hexagonal, we used citric acid and Na-citrate for the nucleation of hexagonal NaYF4: Yb, Er phase in nanosized particles. Additionally, effect of different precipitation agents (NaF, NH4F and NH4HF2) used during solvothermal synthesis is explored. The XRPD analysis showed that using of citric acid led to a product composed from mixture of cubic and hexagonal NaYF4: Yb/Er phase, while the presence of Na-citrate influences the nucleation of well crystallized hexagonal β-NaYF4: Yb/Er phase, regardless of precipitation agents used. All samples are composed of polycrystalline spherical particles which size is influenced by the precursor chemistry. UCNPs emit intense green emission due to the (2H11/2, 4S3/2) → 4I15/2 electronic transitions, after been excited with infrared light (λ=978 nm).
PB  - Belgrade : Materials Research Society of Serbia
C3  - Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019
T1  - Citrate assisted solvothermal synthesis of beta-NaYF4: Yb, Er up-converting nanoparticles
SP  - 128
EP  - 128
UR  - https://hdl.handle.net/21.15107/rcub_dais_6672
ER  - 

@conference{
author = "Dinić, Ivana and Vuković, Marina and Vulić, Predrag and Nikolić, Marko G. and Milošević, Olivera and Mančić, Lidija",
year = "2019",
abstract = "Thanks to the unique optical properties, up-converting nanoparticles (UCNPs) have a wide application in optoelectronics, forensics, security and biomedicine. The synthesis of the most efficient hexagonal β-NaYF4: Yb/Er phase is usually performed through thermal decomposition of organic precursors which could cause the UCNP cytotoxicity. Since cubic polymorph is kinetically more stable than hexagonal, we used citric acid and Na-citrate for the nucleation of hexagonal NaYF4: Yb, Er phase in nanosized particles. Additionally, effect of different precipitation agents (NaF, NH4F and NH4HF2) used during solvothermal synthesis is explored. The XRPD analysis showed that using of citric acid led to a product composed from mixture of cubic and hexagonal NaYF4: Yb/Er phase, while the presence of Na-citrate influences the nucleation of well crystallized hexagonal β-NaYF4: Yb/Er phase, regardless of precipitation agents used. All samples are composed of polycrystalline spherical particles which size is influenced by the precursor chemistry. UCNPs emit intense green emission due to the (2H11/2, 4S3/2) → 4I15/2 electronic transitions, after been excited with infrared light (λ=978 nm).",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019",
title = "Citrate assisted solvothermal synthesis of beta-NaYF4: Yb, Er up-converting nanoparticles",
pages = "128-128",
url = "https://hdl.handle.net/21.15107/rcub_dais_6672"
}

Dinić, I., Vuković, M., Vulić, P., Nikolić, M. G., Milošević, O.,& Mančić, L.. (2019). Citrate assisted solvothermal synthesis of beta-NaYF4: Yb, Er up-converting nanoparticles. in Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019
Belgrade : Materials Research Society of Serbia., 128-128.
https://hdl.handle.net/21.15107/rcub_dais_6672

Dinić I, Vuković M, Vulić P, Nikolić MG, Milošević O, Mančić L. Citrate assisted solvothermal synthesis of beta-NaYF4: Yb, Er up-converting nanoparticles. in Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019. 2019;:128-128.
https://hdl.handle.net/21.15107/rcub_dais_6672 .

Dinić, Ivana, Vuković, Marina, Vulić, Predrag, Nikolić, Marko G., Milošević, Olivera, Mančić, Lidija, "Citrate assisted solvothermal synthesis of beta-NaYF4: Yb, Er up-converting nanoparticles" in Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019 (2019):128-128,
https://hdl.handle.net/21.15107/rcub_dais_6672 .

TY  - CONF
AU  - Obradović, Nina
AU  - Fahrenholtz, William G.
AU  - Filipović, Suzana
AU  - Đorđević, Pavle
AU  - Marković, Smilja
AU  - Rogan, Jelena
AU  - Vulić, Predrag J.
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6980
AB  - Single crystalline phase MgAl2O4 is made from the predetermined composition of MgO-Al2O3 powder mixture by using ball-milling. Mixtures of MgO and Al2O3 are treated in planetary ball mill for 30, 60, 90 and 120 minutes, in air. The aim of this experiment was to examine phase composition, microstructure, and densification behavior of all sintered samples and to find out which sample has the best features for further use. After sintering in dilatometer at 1500 °C, XRD patterns and SEM images were recorded. The results show that mechanical activation is an efficient method to improve the densification behavior of MgAl2O4 sintered specimens. With the prolonged milling time, densities increased, reaching the maximum value of 2.8 g/cm3 for sample activated 120 minutes.
PB  - Belgrade : Serbian Ceramic Society
C3  - Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019
T1  - Characterization of MgAl2O4 sintered ceramics
SP  - 54
EP  - 54
UR  - https://hdl.handle.net/21.15107/rcub_dais_6980
ER  - 

@conference{
author = "Obradović, Nina and Fahrenholtz, William G. and Filipović, Suzana and Đorđević, Pavle and Marković, Smilja and Rogan, Jelena and Vulić, Predrag J. and Pavlović, Vladimir B.",
year = "2019",
abstract = "Single crystalline phase MgAl2O4 is made from the predetermined composition of MgO-Al2O3 powder mixture by using ball-milling. Mixtures of MgO and Al2O3 are treated in planetary ball mill for 30, 60, 90 and 120 minutes, in air. The aim of this experiment was to examine phase composition, microstructure, and densification behavior of all sintered samples and to find out which sample has the best features for further use. After sintering in dilatometer at 1500 °C, XRD patterns and SEM images were recorded. The results show that mechanical activation is an efficient method to improve the densification behavior of MgAl2O4 sintered specimens. With the prolonged milling time, densities increased, reaching the maximum value of 2.8 g/cm3 for sample activated 120 minutes.",
publisher = "Belgrade : Serbian Ceramic Society",
journal = "Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019",
title = "Characterization of MgAl2O4 sintered ceramics",
pages = "54-54",
url = "https://hdl.handle.net/21.15107/rcub_dais_6980"
}

Obradović, N., Fahrenholtz, W. G., Filipović, S., Đorđević, P., Marković, S., Rogan, J., Vulić, P. J.,& Pavlović, V. B.. (2019). Characterization of MgAl2O4 sintered ceramics. in Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019
Belgrade : Serbian Ceramic Society., 54-54.
https://hdl.handle.net/21.15107/rcub_dais_6980

Obradović N, Fahrenholtz WG, Filipović S, Đorđević P, Marković S, Rogan J, Vulić PJ, Pavlović VB. Characterization of MgAl2O4 sintered ceramics. in Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019. 2019;:54-54.
https://hdl.handle.net/21.15107/rcub_dais_6980 .

Obradović, Nina, Fahrenholtz, William G., Filipović, Suzana, Đorđević, Pavle, Marković, Smilja, Rogan, Jelena, Vulić, Predrag J., Pavlović, Vladimir B., "Characterization of MgAl2O4 sintered ceramics" in Program and the Book of abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VIII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 23-25. September 2019 (2019):54-54,
https://hdl.handle.net/21.15107/rcub_dais_6980 .

TY  - JOUR
AU  - Obradović, Nina
AU  - Fahrenholtz, William G.
AU  - Filipović, Suzana
AU  - Corlett, Cole
AU  - Đorđević, Pavle
AU  - Rogan, Jelena
AU  - Vulić, Predrag J.
AU  - Buljak, Vladimir
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6949
AB  - Single phase MgAl2O4 was made from a one-to-one molar ratio of MgO and Al2O3 powders mixed using ball-milling. Mixtures of MgO and Al2O3 were subsequently treated in planetary ball mill for 30, 60, 90 and 120 minutes in air. The aim of this study was to examine phase composition, microstructure, and densification behavior of sintered specimens. After sintering in dilatometer at 1500 °C, the powder was converted to single phase MgAl2O4. The results show that mechanical activation improved the densification behavior of MgAl2O4 sintered specimens, and it reduced the onset temperature for sintering by approx. 100 oC. Based on dilatometer data, powders were subsequently densified at 1450 oC by hot pressing. Almost аll specimens exhibited full density, while sample activated for 30 minutes showed the fastest densification rate.
PB  - ETRAN
T2  - Science of Sintering
T1  - Characterization of MgAl2O4 sintered ceramics
SP  - 363
EP  - 376
VL  - 51
IS  - 4
DO  - 10.2298/SOS1904363O
UR  - https://hdl.handle.net/21.15107/rcub_dais_6949
ER  - 

@article{
author = "Obradović, Nina and Fahrenholtz, William G. and Filipović, Suzana and Corlett, Cole and Đorđević, Pavle and Rogan, Jelena and Vulić, Predrag J. and Buljak, Vladimir and Pavlović, Vladimir B.",
year = "2019",
abstract = "Single phase MgAl2O4 was made from a one-to-one molar ratio of MgO and Al2O3 powders mixed using ball-milling. Mixtures of MgO and Al2O3 were subsequently treated in planetary ball mill for 30, 60, 90 and 120 minutes in air. The aim of this study was to examine phase composition, microstructure, and densification behavior of sintered specimens. After sintering in dilatometer at 1500 °C, the powder was converted to single phase MgAl2O4. The results show that mechanical activation improved the densification behavior of MgAl2O4 sintered specimens, and it reduced the onset temperature for sintering by approx. 100 oC. Based on dilatometer data, powders were subsequently densified at 1450 oC by hot pressing. Almost аll specimens exhibited full density, while sample activated for 30 minutes showed the fastest densification rate.",
publisher = "ETRAN",
journal = "Science of Sintering",
title = "Characterization of MgAl2O4 sintered ceramics",
pages = "363-376",
volume = "51",
number = "4",
doi = "10.2298/SOS1904363O",
url = "https://hdl.handle.net/21.15107/rcub_dais_6949"
}

Obradović, N., Fahrenholtz, W. G., Filipović, S., Corlett, C., Đorđević, P., Rogan, J., Vulić, P. J., Buljak, V.,& Pavlović, V. B.. (2019). Characterization of MgAl2O4 sintered ceramics. in Science of Sintering
ETRAN., 51(4), 363-376.
https://doi.org/10.2298/SOS1904363O
https://hdl.handle.net/21.15107/rcub_dais_6949

Obradović N, Fahrenholtz WG, Filipović S, Corlett C, Đorđević P, Rogan J, Vulić PJ, Buljak V, Pavlović VB. Characterization of MgAl2O4 sintered ceramics. in Science of Sintering. 2019;51(4):363-376.
doi:10.2298/SOS1904363O
https://hdl.handle.net/21.15107/rcub_dais_6949 .

Obradović, Nina, Fahrenholtz, William G., Filipović, Suzana, Corlett, Cole, Đorđević, Pavle, Rogan, Jelena, Vulić, Predrag J., Buljak, Vladimir, Pavlović, Vladimir B., "Characterization of MgAl2O4 sintered ceramics" in Science of Sintering, 51, no. 4 (2019):363-376,
https://doi.org/10.2298/SOS1904363O .,
https://hdl.handle.net/21.15107/rcub_dais_6949 .

TY  - CONF
AU  - Vuković, Marina
AU  - Dinić, Ivana
AU  - Mančić, Lidija
AU  - Vulić, Predrag
PY  - 2018
UR  - https://dais.sanu.ac.rs/123456789/4117
AB  - NaYF4 doped with Rare Earth elements such as Yb and Er is well known as a compound with the remarkable up-conversion photoluminesce and wide application. In this work, the influence of additional co-doping of NaYF4:Yb,Er with gadolinium (0, 15 and 30 mol%) was explored. The syntheses were performed solvothermally using the mixture of water/ethanol as medium and polyvinylpyrrolidone (PVP) as capping ligand. The obtained powders were subjected to X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy and photoluminesce (PL) analyses. Structural refinement shown that NaYF4:Yb,Er particles generally crystallized in a cubic form (Fm-3m), while the additional presence of Gd3+ in the crystal lattice lead to the pure hexagonal phase crystallization (P63/m). Morphological analyses revealed that all powders are composed from nanodimensional particles with the size in the range of 50-70 nm, while FTIR spectra confirmed the presence of PVP functional groups on the particles surfaces. The strongest effect of Gd3+ doping was notices in the PL spectra, where the up-conversion response increases with the mol% of this dopant.
PB  - Belgrade : Serbian Ceramic Society
C3  - Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018
T1  - Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure
SP  - 72
EP  - 72
UR  - https://hdl.handle.net/21.15107/rcub_dais_4117
ER  - 

@conference{
author = "Vuković, Marina and Dinić, Ivana and Mančić, Lidija and Vulić, Predrag",
year = "2018",
abstract = "NaYF4 doped with Rare Earth elements such as Yb and Er is well known as a compound with the remarkable up-conversion photoluminesce and wide application. In this work, the influence of additional co-doping of NaYF4:Yb,Er with gadolinium (0, 15 and 30 mol%) was explored. The syntheses were performed solvothermally using the mixture of water/ethanol as medium and polyvinylpyrrolidone (PVP) as capping ligand. The obtained powders were subjected to X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy and photoluminesce (PL) analyses. Structural refinement shown that NaYF4:Yb,Er particles generally crystallized in a cubic form (Fm-3m), while the additional presence of Gd3+ in the crystal lattice lead to the pure hexagonal phase crystallization (P63/m). Morphological analyses revealed that all powders are composed from nanodimensional particles with the size in the range of 50-70 nm, while FTIR spectra confirmed the presence of PVP functional groups on the particles surfaces. The strongest effect of Gd3+ doping was notices in the PL spectra, where the up-conversion response increases with the mol% of this dopant.",
publisher = "Belgrade : Serbian Ceramic Society",
journal = "Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018",
title = "Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure",
pages = "72-72",
url = "https://hdl.handle.net/21.15107/rcub_dais_4117"
}

Vuković, M., Dinić, I., Mančić, L.,& Vulić, P.. (2018). Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure. in Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018
Belgrade : Serbian Ceramic Society., 72-72.
https://hdl.handle.net/21.15107/rcub_dais_4117

Vuković M, Dinić I, Mančić L, Vulić P. Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure. in Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018. 2018;:72-72.
https://hdl.handle.net/21.15107/rcub_dais_4117 .

Vuković, Marina, Dinić, Ivana, Mančić, Lidija, Vulić, Predrag, "Effects of Gd3+ co-doping on NaYF4:Yb,Er nanoparticles structure" in Program and the Book of Abstracts / Serbian Ceramic Society Conference Advanced Ceramics and Application VII : New Frontiers in Multifunctional Material Science and Processing, Serbia, Belgrade, 17-19 September 2018 (2018):72-72,
https://hdl.handle.net/21.15107/rcub_dais_4117 .

TY  - JOUR
AU  - Lojpur, Vesna
AU  - Mančić, Lidija
AU  - Vulić, Predrag
AU  - Dramićanin, Miroslav
AU  - Rabanal, Maria Eugenia
AU  - Milošević, Olivera
PY  - 2014
UR  - https://dais.sanu.ac.rs/123456789/545
AB  - Sub-micronic, spherical Y2O3:Yb/Er particles comprising clustered nano-units (70 nm) were prepared via ultrasonic spray pyrolysis from pure nitrate precursor solutions with different Yb/Er dopant ratios. The particles were additionally thermally treated at 1100 °C for 12, 24 and 48 h. The structural and morphological characteristics of particles were studied by X-ray powder diffraction, Fourier transform infrared spectroscopy, field-emission scanning electron microscopy, energy dispersive X-ray analysis and specific surface area (BET) and were further correlated with their advanced optical properties. For the recorded up-conversion emissions, originating from the following Er3+ transitions: [2H9/2→4I15/2] in blue (407–420 nm); [2H11/2, 4S3/2→4I15/2] green: 510–590 nm; and [4F9/2→4I15/2] in red (640–720 nm) spectral region, the corresponding lifetimes were acquired in the wide temperature range (10–300 K). The most intense green up-conversion emission with the long decay of 550 ms is recorded for Y1.97Yb0.02Er0.01O3 particles thermally treated at 1100 °C for 24 h.
T2  - Ceramics International
T1  - Structural, morphological and up-converting luminescence characteristics of nanocrystalline Y2O3:Yb/Er powders obtained via spray pyrolysis
SP  - 3089
EP  - 3095
VL  - 40
IS  - 2
DO  - 10.1016/j.ceramint.2013.10.002
UR  - https://hdl.handle.net/21.15107/rcub_dais_545
ER  - 

@article{
author = "Lojpur, Vesna and Mančić, Lidija and Vulić, Predrag and Dramićanin, Miroslav and Rabanal, Maria Eugenia and Milošević, Olivera",
year = "2014",
abstract = "Sub-micronic, spherical Y2O3:Yb/Er particles comprising clustered nano-units (70 nm) were prepared via ultrasonic spray pyrolysis from pure nitrate precursor solutions with different Yb/Er dopant ratios. The particles were additionally thermally treated at 1100 °C for 12, 24 and 48 h. The structural and morphological characteristics of particles were studied by X-ray powder diffraction, Fourier transform infrared spectroscopy, field-emission scanning electron microscopy, energy dispersive X-ray analysis and specific surface area (BET) and were further correlated with their advanced optical properties. For the recorded up-conversion emissions, originating from the following Er3+ transitions: [2H9/2→4I15/2] in blue (407–420 nm); [2H11/2, 4S3/2→4I15/2] green: 510–590 nm; and [4F9/2→4I15/2] in red (640–720 nm) spectral region, the corresponding lifetimes were acquired in the wide temperature range (10–300 K). The most intense green up-conversion emission with the long decay of 550 ms is recorded for Y1.97Yb0.02Er0.01O3 particles thermally treated at 1100 °C for 24 h.",
journal = "Ceramics International",
title = "Structural, morphological and up-converting luminescence characteristics of nanocrystalline Y2O3:Yb/Er powders obtained via spray pyrolysis",
pages = "3089-3095",
volume = "40",
number = "2",
doi = "10.1016/j.ceramint.2013.10.002",
url = "https://hdl.handle.net/21.15107/rcub_dais_545"
}

Lojpur, V., Mančić, L., Vulić, P., Dramićanin, M., Rabanal, M. E.,& Milošević, O.. (2014). Structural, morphological and up-converting luminescence characteristics of nanocrystalline Y2O3:Yb/Er powders obtained via spray pyrolysis. in Ceramics International, 40(2), 3089-3095.
https://doi.org/10.1016/j.ceramint.2013.10.002
https://hdl.handle.net/21.15107/rcub_dais_545

Lojpur V, Mančić L, Vulić P, Dramićanin M, Rabanal ME, Milošević O. Structural, morphological and up-converting luminescence characteristics of nanocrystalline Y2O3:Yb/Er powders obtained via spray pyrolysis. in Ceramics International. 2014;40(2):3089-3095.
doi:10.1016/j.ceramint.2013.10.002
https://hdl.handle.net/21.15107/rcub_dais_545 .

Lojpur, Vesna, Mančić, Lidija, Vulić, Predrag, Dramićanin, Miroslav, Rabanal, Maria Eugenia, Milošević, Olivera, "Structural, morphological and up-converting luminescence characteristics of nanocrystalline Y2O3:Yb/Er powders obtained via spray pyrolysis" in Ceramics International, 40, no. 2 (2014):3089-3095,
https://doi.org/10.1016/j.ceramint.2013.10.002 .,
https://hdl.handle.net/21.15107/rcub_dais_545 .

TY  - JOUR
AU  - Đinović, Vesna M.
AU  - Mančić, Lidija
AU  - Bogdanović, Goran A.
AU  - Vulić, Predrag
AU  - Del Rosario, Gilberte
AU  - Sabo, Tibor
AU  - Milošević, Olivera
PY  - 2005
UR  - https://dais.sanu.ac.rs/123456789/15207
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
SP  - 102
EP  - 113
VL  - 20
IS  - 1
DO  - 10.1557/JMR.2005.0006
UR  - https://hdl.handle.net/21.15107/rcub_dais_15207
ER  - 

@article{
author = "Đinović, Vesna M. and Mančić, Lidija and Bogdanović, Goran A. and Vulić, Predrag and Del Rosario, Gilberte 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",
pages = "102-113",
volume = "20",
number = "1",
doi = "10.1557/JMR.2005.0006",
url = "https://hdl.handle.net/21.15107/rcub_dais_15207"
}

Đinović, V. M., Mančić, L., Bogdanović, G. A., Vulić, P., 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
https://hdl.handle.net/21.15107/rcub_dais_15207

Đinović VM, Mančić L, Bogdanović GA, Vulić P, 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
https://hdl.handle.net/21.15107/rcub_dais_15207 .

Đinović, Vesna M., Mančić, Lidija, Bogdanović, Goran A., Vulić, Predrag, Del Rosario, Gilberte, 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 .,
https://hdl.handle.net/21.15107/rcub_dais_15207 .

TY  - CHAP
AU  - Milošević, Olivera
AU  - Mančić, Lidija
AU  - Del Rosario, Gilberte
AU  - Ohara, Satoshi
AU  - Vulić, Predrag
PY  - 2005
UR  - https://dais.sanu.ac.rs/123456789/14756
AB  - Nanophase phosphor particles in the complex Y3Al5O12Ce system were synthesized from aerosols of 0.06 mol/dm3 nitrate solution ultrasonically generated with frequency of 8105 s-1 and thermally treated at 1273 to 1473 K. The secondary particles obtained are spherical, and range in size from 300- 800 nm. TEM reveals a composite secondary particle structure comprised of clusters of < 60 nm primary particles. XRD of the as-synthesized powders indicates the presence of poorly crystallized phases. The phase development and structural changes, followed using a Koalariet-Xfit program, identifies the target cubic YAG - Y3AI5O12 being prevalent after annealing at 1073 K, with The YAG content increases with temperature. Both CeÛ2 and monoclinic Y4AI2O9 are present in lower concentration. EDX analysis verifies a uniform distribution of the constitutive elements inside the secondary particles. Photoluminescence measurements show an emission spectrum peak maximum at 537 nm for the thermally treated particles, which is attributed to the phase content of the powder.
PB  - John Wiley & Sons, Ltd.
T2  - Characterization & Control of Interfaces for High Quality Advanced Materials
T1  - Aerosol Synthesis and Phase Development in Ce-Doped Nanophased Yttrium-Aluminum Garnet (Y3Al50I2:Ce)
SP  - 435
EP  - 441
DO  - 10.1002/9781118406038.ch53
UR  - https://hdl.handle.net/21.15107/rcub_dais_14756
ER  - 

@inbook{
author = "Milošević, Olivera and Mančić, Lidija and Del Rosario, Gilberte and Ohara, Satoshi and Vulić, Predrag",
year = "2005",
abstract = "Nanophase phosphor particles in the complex Y3Al5O12Ce system were synthesized from aerosols of 0.06 mol/dm3 nitrate solution ultrasonically generated with frequency of 8105 s-1 and thermally treated at 1273 to 1473 K. The secondary particles obtained are spherical, and range in size from 300- 800 nm. TEM reveals a composite secondary particle structure comprised of clusters of < 60 nm primary particles. XRD of the as-synthesized powders indicates the presence of poorly crystallized phases. The phase development and structural changes, followed using a Koalariet-Xfit program, identifies the target cubic YAG - Y3AI5O12 being prevalent after annealing at 1073 K, with The YAG content increases with temperature. Both CeÛ2 and monoclinic Y4AI2O9 are present in lower concentration. EDX analysis verifies a uniform distribution of the constitutive elements inside the secondary particles. Photoluminescence measurements show an emission spectrum peak maximum at 537 nm for the thermally treated particles, which is attributed to the phase content of the powder.",
publisher = "John Wiley & Sons, Ltd.",
journal = "Characterization & Control of Interfaces for High Quality Advanced Materials",
booktitle = "Aerosol Synthesis and Phase Development in Ce-Doped Nanophased Yttrium-Aluminum Garnet (Y3Al50I2:Ce)",
pages = "435-441",
doi = "10.1002/9781118406038.ch53",
url = "https://hdl.handle.net/21.15107/rcub_dais_14756"
}

Milošević, O., Mančić, L., Del Rosario, G., Ohara, S.,& Vulić, P.. (2005). Aerosol Synthesis and Phase Development in Ce-Doped Nanophased Yttrium-Aluminum Garnet (Y3Al50I2:Ce). in Characterization & Control of Interfaces for High Quality Advanced Materials
John Wiley & Sons, Ltd.., 435-441.
https://doi.org/10.1002/9781118406038.ch53
https://hdl.handle.net/21.15107/rcub_dais_14756

Milošević O, Mančić L, Del Rosario G, Ohara S, Vulić P. Aerosol Synthesis and Phase Development in Ce-Doped Nanophased Yttrium-Aluminum Garnet (Y3Al50I2:Ce). in Characterization & Control of Interfaces for High Quality Advanced Materials. 2005;:435-441.
doi:10.1002/9781118406038.ch53
https://hdl.handle.net/21.15107/rcub_dais_14756 .

Milošević, Olivera, Mančić, Lidija, Del Rosario, Gilberte, Ohara, Satoshi, Vulić, Predrag, "Aerosol Synthesis and Phase Development in Ce-Doped Nanophased Yttrium-Aluminum Garnet (Y3Al50I2:Ce)" in Characterization & Control of Interfaces for High Quality Advanced Materials (2005):435-441,
https://doi.org/10.1002/9781118406038.ch53 .,
https://hdl.handle.net/21.15107/rcub_dais_14756 .

TY  - JOUR
AU  - Marinković, Zorica
AU  - Mančić, Lidija
AU  - Vulić, Predrag J.
AU  - Milošević, Olivera
PY  - 2005
UR  - https://dais.sanu.ac.rs/123456789/12882
AB  - An equimolar mixtures of starting ZnO and Cr2O3 powders were mechanically activated by grinding using a planetary ball mill for various periods of time (40-320min). Formation of nanocrystalline ZnCr2O4 as normal spine] structure at room temperature is detected in all samples-after ball-milling. A detailed XRD structural analysis (the relative phase abundances of different phases, lattice parameter changes, site occupancy, the average primary crystallite sizes, crystal lattice microstrains) is realized by the pattern decomposition technique, performed in accordance with the procedure based on Rietveld software KOALARIET-XFIT. Due to the importance of cation distribution on the chemical and physical properties of spinels, a study of site occupation factors of ZnCr2O4 spinels has been undertaken. The calculation based on the atomistic methods for the description of the perfect and defect spinel ZnCr2O4 crystal lattice is applied and the presence of the individual structural defects is determined.
PB  - Oxford : Elsevier Sci
T2  - Journal of the European Ceramic Society
T1  - Microstructural characterization of mechanically activated ZnO-Cr2O3 system
SP  - 2081
EP  - 2084
VL  - 25
IS  - 12
DO  - 10.1016/j.jeurceramsoc.2005.03.085
UR  - https://hdl.handle.net/21.15107/rcub_dais_12882
ER  - 

@article{
author = "Marinković, Zorica and Mančić, Lidija and Vulić, Predrag J. and Milošević, Olivera",
year = "2005",
abstract = "An equimolar mixtures of starting ZnO and Cr2O3 powders were mechanically activated by grinding using a planetary ball mill for various periods of time (40-320min). Formation of nanocrystalline ZnCr2O4 as normal spine] structure at room temperature is detected in all samples-after ball-milling. A detailed XRD structural analysis (the relative phase abundances of different phases, lattice parameter changes, site occupancy, the average primary crystallite sizes, crystal lattice microstrains) is realized by the pattern decomposition technique, performed in accordance with the procedure based on Rietveld software KOALARIET-XFIT. Due to the importance of cation distribution on the chemical and physical properties of spinels, a study of site occupation factors of ZnCr2O4 spinels has been undertaken. The calculation based on the atomistic methods for the description of the perfect and defect spinel ZnCr2O4 crystal lattice is applied and the presence of the individual structural defects is determined.",
publisher = "Oxford : Elsevier Sci",
journal = "Journal of the European Ceramic Society",
title = "Microstructural characterization of mechanically activated ZnO-Cr2O3 system",
pages = "2081-2084",
volume = "25",
number = "12",
doi = "10.1016/j.jeurceramsoc.2005.03.085",
url = "https://hdl.handle.net/21.15107/rcub_dais_12882"
}

Marinković, Z., Mančić, L., Vulić, P. J.,& Milošević, O.. (2005). Microstructural characterization of mechanically activated ZnO-Cr2O3 system. in Journal of the European Ceramic Society
Oxford : Elsevier Sci., 25(12), 2081-2084.
https://doi.org/10.1016/j.jeurceramsoc.2005.03.085
https://hdl.handle.net/21.15107/rcub_dais_12882

Marinković Z, Mančić L, Vulić PJ, Milošević O. Microstructural characterization of mechanically activated ZnO-Cr2O3 system. in Journal of the European Ceramic Society. 2005;25(12):2081-2084.
doi:10.1016/j.jeurceramsoc.2005.03.085
https://hdl.handle.net/21.15107/rcub_dais_12882 .

Marinković, Zorica, Mančić, Lidija, Vulić, Predrag J., Milošević, Olivera, "Microstructural characterization of mechanically activated ZnO-Cr2O3 system" in Journal of the European Ceramic Society, 25, no. 12 (2005):2081-2084,
https://doi.org/10.1016/j.jeurceramsoc.2005.03.085 .,
https://hdl.handle.net/21.15107/rcub_dais_12882 .

TY  - JOUR
AU  - Dimitrijević, Radovan
AU  - Dondur, Vera
AU  - Vulić, Predrag
AU  - Marković, Smilja
AU  - Macura, Slobodan
PY  - 2004
UR  - https://dais.sanu.ac.rs/123456789/16226
AB  - Using the zeolite thermally induced transformation route and starting from Na-LTA, Na-FAU and Na-GIS zeolites as precursors, we synthesized pure sodium nephelines (ps-Ne) with Si/Al ratios between 1.0 and 1.5 (ps-NeLTA, ps-NeFAU, ps-NeGIS). By X-ray diffraction analysis of intermediaries, we found that ps-NeLTA and ps-NeFAU were obtained as polymorphous transformation products from carnegieite phases and ps-NeGIS was synthesized directly from amorphous zeolite precursor. Stoichiometric ps-NeLTA {Na8[Al8Si8]16O32} and nonstoichiometric ps-NeFAU {(Na7.20A0.80)8[Al7.20Si8.80]16O32} and ps-NeGIS {(Na6.41A1.59)8[Al6.41Si9.59]16O32} were obtained at temperatures 900– 1200 8C. The crystal structures of these ps-Ne-s were refined in the P63 space group, from X-ray powder data using the Rietveld method. Mean T – O bond lengths decreases almost linearly with increasing the Si/Al ratio. These changes are induced by short-range order–disorder of Si, Al cations through the TG and TS sites. The increase of short-range disorder over T-sites, is followed and confirmed by 29Si MAS NMR and IR spectroscopy. Comparison of the Si/Al ordering of synthesized ps-Ne structures with the published data shows inverse segregation of framework cations (Si; T1 ¼ T4 and Al; T2 ¼ T3). That is probably a consequence of applied synthesis route.
T2  - Journal of Physics and Chemistry of Solids
T1  - Structural characterization of pure Na-nephelines synthesized by zeolite conversion route
SP  - 1623
EP  - 1633
VL  - 65
IS  - 10
DO  - 10.1016/j.jpcs.2004.03.005
UR  - https://hdl.handle.net/21.15107/rcub_dais_16226
ER  - 

@article{
author = "Dimitrijević, Radovan and Dondur, Vera and Vulić, Predrag and Marković, Smilja and Macura, Slobodan",
year = "2004",
abstract = "Using the zeolite thermally induced transformation route and starting from Na-LTA, Na-FAU and Na-GIS zeolites as precursors, we synthesized pure sodium nephelines (ps-Ne) with Si/Al ratios between 1.0 and 1.5 (ps-NeLTA, ps-NeFAU, ps-NeGIS). By X-ray diffraction analysis of intermediaries, we found that ps-NeLTA and ps-NeFAU were obtained as polymorphous transformation products from carnegieite phases and ps-NeGIS was synthesized directly from amorphous zeolite precursor. Stoichiometric ps-NeLTA {Na8[Al8Si8]16O32} and nonstoichiometric ps-NeFAU {(Na7.20A0.80)8[Al7.20Si8.80]16O32} and ps-NeGIS {(Na6.41A1.59)8[Al6.41Si9.59]16O32} were obtained at temperatures 900– 1200 8C. The crystal structures of these ps-Ne-s were refined in the P63 space group, from X-ray powder data using the Rietveld method. Mean T – O bond lengths decreases almost linearly with increasing the Si/Al ratio. These changes are induced by short-range order–disorder of Si, Al cations through the TG and TS sites. The increase of short-range disorder over T-sites, is followed and confirmed by 29Si MAS NMR and IR spectroscopy. Comparison of the Si/Al ordering of synthesized ps-Ne structures with the published data shows inverse segregation of framework cations (Si; T1 ¼ T4 and Al; T2 ¼ T3). That is probably a consequence of applied synthesis route.",
journal = "Journal of Physics and Chemistry of Solids",
title = "Structural characterization of pure Na-nephelines synthesized by zeolite conversion route",
pages = "1623-1633",
volume = "65",
number = "10",
doi = "10.1016/j.jpcs.2004.03.005",
url = "https://hdl.handle.net/21.15107/rcub_dais_16226"
}

Dimitrijević, R., Dondur, V., Vulić, P., Marković, S.,& Macura, S.. (2004). Structural characterization of pure Na-nephelines synthesized by zeolite conversion route. in Journal of Physics and Chemistry of Solids, 65(10), 1623-1633.
https://doi.org/10.1016/j.jpcs.2004.03.005
https://hdl.handle.net/21.15107/rcub_dais_16226

Dimitrijević R, Dondur V, Vulić P, Marković S, Macura S. Structural characterization of pure Na-nephelines synthesized by zeolite conversion route. in Journal of Physics and Chemistry of Solids. 2004;65(10):1623-1633.
doi:10.1016/j.jpcs.2004.03.005
https://hdl.handle.net/21.15107/rcub_dais_16226 .

Dimitrijević, Radovan, Dondur, Vera, Vulić, Predrag, Marković, Smilja, Macura, Slobodan, "Structural characterization of pure Na-nephelines synthesized by zeolite conversion route" in Journal of Physics and Chemistry of Solids, 65, no. 10 (2004):1623-1633,
https://doi.org/10.1016/j.jpcs.2004.03.005 .,
https://hdl.handle.net/21.15107/rcub_dais_16226 .