Vulić, Predrag J.

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  • Vulić, Predrag J. (8)

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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

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.

(American Chemical Society, 2020)

TY  - BOOK
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
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  - 
@book{
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.
Crystal Growth & Design
American Chemical Society..
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. Crystal Growth & Design. 2020;.
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" Crystal Growth & Design (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

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.

(American Chemical Society, 2020)

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
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.
Crystal Growth & Design
American Chemical Society., 20(5), 3018-3033.
https://doi.org/10.1021/acs.cgd.9b01661
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. Crystal Growth & Design. 2020;20(5):3018-3033.
doi:10.1021/acs.cgd.9b01661.
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" Crystal Growth & Design, 20, no. 5 (2020):3018-3033,
https://doi.org/10.1021/acs.cgd.9b01661 .
1
3
2
3

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

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.

(American Chemical Society, 2020)

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
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.
Crystal Growth & Design
American Chemical Society., 20(5), 3018-3033.
https://doi.org/10.1021/acs.cgd.9b01661
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. Crystal Growth & Design. 2020;20(5):3018-3033.
doi:10.1021/acs.cgd.9b01661.
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" Crystal Growth & Design, 20, no. 5 (2020):3018-3033,
https://doi.org/10.1021/acs.cgd.9b01661 .
1
3
2
3

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

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.

(American Chemical Society, 2020)

TY  - BOOK
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
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  - 
@book{
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.
Crystal Growth & Design
American Chemical Society..
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. Crystal Growth & Design. 2020;.
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" Crystal Growth & Design (2020)

Characterization of MgAl2O4 sintered ceramics

Obradović, Nina; Fahrenholtz, William G.; Filipović, Suzana; Corlett, Cole; Đorđević, Pavle; Rogan, Jelena; Vulić, Predrag J.; Buljak, Vladimir; Pavlović, Vladimir B.

(ETRAN, 2019)

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
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.
Science of Sintering
ETRAN., 51(4), 363-376.
https://doi.org/10.2298/SOS1904363O
Obradović N, Fahrenholtz WG, Filipović S, Corlett C, Đorđević P, Rogan J, Vulić PJ, Buljak V, Pavlović VB. Characterization of MgAl2O4 sintered ceramics. Science of Sintering. 2019;51(4):363-376.
doi:10.2298/SOS1904363O.
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" Science of Sintering, 51, no. 4 (2019):363-376,
https://doi.org/10.2298/SOS1904363O .
1
2
4

Characterization of MgAl2O4 sintered ceramics

Obradović, Nina; Fahrenholtz, William G.; Filipović, Suzana; Đorđević, Pavle; Marković, Smilja; Rogan, Jelena; Vulić, Predrag J.; Pavlović, Vladimir B.

(Belgrade : Serbian Ceramic Society, 2019)

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
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.
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.
Obradović N, Fahrenholtz WG, Filipović S, Đorđević P, Marković S, Rogan J, Vulić PJ, Pavlović VB. Characterization of MgAl2O4 sintered ceramics. 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.
Obradović Nina, Fahrenholtz William G., Filipović Suzana, Đorđević Pavle, Marković Smilja, Rogan Jelena, Vulić Predrag J., Pavlović Vladimir B., "Characterization of MgAl2O4 sintered ceramics" 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

The usage of different fluoride sources during solvothermal synthesis of UCNPs in hydroxyl-carboxyl chelated precursor

Vuković, Marina; Dinić, Ivana; Mančić, Lidija; Vulić, Predrag J.; Nikolić, Marko G.; Milošević, Olivera

(Belgrade : Serbian Ceramic Society, 2019)

TY  - CONF
AU  - Vuković, Marina
AU  - Dinić, Ivana
AU  - Mančić, Lidija
AU  - Vulić, Predrag J.
AU  - Nikolić, Marko G.
AU  - Milošević, Olivera
PY  - 2019
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
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"
}
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.
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.
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. 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.
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" 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

Influence of Gd3+ doping on the NaYF4 :YB3+,ER3+ structural and up-conversion properties

Vuković, Marina; Mančić, Lidija; Dinić, Ivana; Vulić, Predrag J.; Nikolić, Marko G.; Tan, Zhenquan; Milošević, Olivera

(Budapest : [s. n.], 2019)

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
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
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"
}
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.
Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest
Budapest : [s. n.]., 19-20.
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. Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest. 2019;:19-20.
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" Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest (2019):19-20