Vasić, Milica M.

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  • Vasić, Milica M. (2)
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Author's Bibliography

Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex

Begović, Nebojša; Vasić, Milica M.; Blagojević, Vladimir A.; Filipović, Nenad; Marinković, Aleksandar D.; Malesević, Aleksandar; Minić, Dragica M.

(Springer, Dordrecht, 2017)

TY  - JOUR
AU  - Begović, Nebojša
AU  - Vasić, Milica M.
AU  - Blagojević, Vladimir A.
AU  - Filipović, Nenad
AU  - Marinković, Aleksandar D.
AU  - Malesević, Aleksandar
AU  - Minić, Dragica M.
PY  - 2017
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/4483
AB  - The structure of new cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex was determined using a combination of XRD and IR measurements and DFT calculations. Inherent flexibility of its structure is evident from the complexity of its IR spectrum, which could only be theoretically reproduced as a combination of several closely related structures, involving rotation around C-O bond and changes in hydrogen interactions of its -OH group. Its thermal stability and decomposition were studied non-isothermally, and the thermal decomposition mechanism was proposed using correlation with DFT calculations at the molecular level. It was determined that the initial degradation step consists of the release of Cl free radical, which then reacts with both the initial compound and the degradation products. Besides the endothermic steps, there are exothermic ones, contributing to the complex shape of the DSC curve, consisted of overlapping endothermic and exothermic peaks. Deconvolution of DTG curve allowed identification of primary fragments of the initial degradation process and, in conjunction with DFT calculations, construction of the most likely reaction mechanism.
PB  - Springer, Dordrecht
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex
EP  - 711
IS  - 2
SP  - 701
VL  - 130
DO  - 10.1007/s10973-017-6458-2
ER  - 
@article{
author = "Begović, Nebojša and Vasić, Milica M. and Blagojević, Vladimir A. and Filipović, Nenad and Marinković, Aleksandar D. and Malesević, Aleksandar and Minić, Dragica M.",
year = "2017",
abstract = "The structure of new cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex was determined using a combination of XRD and IR measurements and DFT calculations. Inherent flexibility of its structure is evident from the complexity of its IR spectrum, which could only be theoretically reproduced as a combination of several closely related structures, involving rotation around C-O bond and changes in hydrogen interactions of its -OH group. Its thermal stability and decomposition were studied non-isothermally, and the thermal decomposition mechanism was proposed using correlation with DFT calculations at the molecular level. It was determined that the initial degradation step consists of the release of Cl free radical, which then reacts with both the initial compound and the degradation products. Besides the endothermic steps, there are exothermic ones, contributing to the complex shape of the DSC curve, consisted of overlapping endothermic and exothermic peaks. Deconvolution of DTG curve allowed identification of primary fragments of the initial degradation process and, in conjunction with DFT calculations, construction of the most likely reaction mechanism.",
publisher = "Springer, Dordrecht",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex",
pages = "711-701",
number = "2",
volume = "130",
doi = "10.1007/s10973-017-6458-2"
}
Begović, N., Vasić, M. M., Blagojević, V. A., Filipović, N., Marinković, A. D., Malesević, A.,& Minić, D. M.. (2017). Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex. in Journal of Thermal Analysis and Calorimetry
Springer, Dordrecht., 130(2), 701-711.
https://doi.org/10.1007/s10973-017-6458-2
Begović N, Vasić MM, Blagojević VA, Filipović N, Marinković AD, Malesević A, Minić DM. Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex. in Journal of Thermal Analysis and Calorimetry. 2017;130(2):701-711.
doi:10.1007/s10973-017-6458-2 .
Begović, Nebojša, Vasić, Milica M., Blagojević, Vladimir A., Filipović, Nenad, Marinković, Aleksandar D., Malesević, Aleksandar, Minić, Dragica M., "Synthesis and thermal stability of cis-dichloro[(E)-ethyl-2-(2-((8-hydroxyquinolin-2-il)methylene)hidrazinyl)acetate-kappa(2) N]-palladium(II) complex" in Journal of Thermal Analysis and Calorimetry, 130, no. 2 (2017):701-711,
https://doi.org/10.1007/s10973-017-6458-2 . .
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Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy

Vasić, Milica M.; Blagojević, Vladimir A.; Begović, Nebojša; Zak, Tomas; Pavlović, Vladimir; Minić, Dragica M.

(Elsevier Science Bv, Amsterdam, 2015)

TY  - JOUR
AU  - Vasić, Milica M.
AU  - Blagojević, Vladimir A.
AU  - Begović, Nebojša
AU  - Zak, Tomas
AU  - Pavlović, Vladimir
AU  - Minić, Dragica M.
PY  - 2015
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/3703
AB  - The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate.
PB  - Elsevier Science Bv, Amsterdam
T2  - Thermochimica Acta
T1  - Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy
EP  - 136
SP  - 129
VL  - 614
DO  - 10.1016/j.tca.2015.06.015
ER  - 
@article{
author = "Vasić, Milica M. and Blagojević, Vladimir A. and Begović, Nebojša and Zak, Tomas and Pavlović, Vladimir and Minić, Dragica M.",
year = "2015",
abstract = "The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Thermochimica Acta",
title = "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy",
pages = "136-129",
volume = "614",
doi = "10.1016/j.tca.2015.06.015"
}
Vasić, M. M., Blagojević, V. A., Begović, N., Zak, T., Pavlović, V.,& Minić, D. M.. (2015). Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy. in Thermochimica Acta
Elsevier Science Bv, Amsterdam., 614, 129-136.
https://doi.org/10.1016/j.tca.2015.06.015
Vasić MM, Blagojević VA, Begović N, Zak T, Pavlović V, Minić DM. Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy. in Thermochimica Acta. 2015;614:129-136.
doi:10.1016/j.tca.2015.06.015 .
Vasić, Milica M., Blagojević, Vladimir A., Begović, Nebojša, Zak, Tomas, Pavlović, Vladimir, Minić, Dragica M., "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy" in Thermochimica Acta, 614 (2015):129-136,
https://doi.org/10.1016/j.tca.2015.06.015 . .
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