TY  - JOUR
AU  - Milosavljević, Milutin M.
AU  - Vukicević, Ivan M.
AU  - Serifi, Veis
AU  - Markovski, Jasmina S.
AU  - Stojiljković, Ivana
AU  - Mijin, Dusan Z.
AU  - Marinković, Aleksandar D.
PY  - 2015
UR  - https://omorika.sfb.bg.ac.rs/handle/123456789/666
AB  - The optimized methods for N-alkyl and N,N-dialkyl substituted thioureas synthesis starting from ammonium thiocyanates, waste water constituent from the production of tetramethylthiuram monosulfide (TMTS), and alkyl amine, are presented in this work., Thioureas synthesis was developed in two ways: Method I-reaction of the thiocyanate and alkylamine in the presence of hydrochloric acid; Method II-reaction of the thiocyanate with benzoyl chloride following by amine addition in the first step, and base hydrolysis in the second step. The structure of the synthesized compounds was confirmed by IR, H-1- and C-13-NMR and MS instrumental methods, and purity was determined by high-performance liquid chromatography method. It is shown that the proposed methods offer a high degree of conversion and purity of product, absence of by-products and technological applicability at industrial scale. Considering the importance of the tetramethylthiuram disulfide (TMTD) and TMTS as vulcanization accelerators as well as thiourea as the pharmacologically active compounds, it can be said that application of the optimized methods of thiourea synthesis will provide significant improvement in sustainable development and implementation of eco-friendly production technology. The described environmentally benign process of thioureas synthesis represents a suitable option to existing methods. thioureas, industrial level, thiocyanate.
PB  - Savez hemijskih inženjera, Beograd
T2  - Chemical Industry & Chemical Engineering Quarterly
T1  - Optimization of the synthesis of n -alkyl and n , n -dialkyl thioureas from waste water containing ammonium thiocyanate
EP  - 510
IS  - 4
SP  - 501
VL  - 21
DO  - 10.2298/CICEQ141221006M
UR  - conv_1198
ER  - 

@article{
author = "Milosavljević, Milutin M. and Vukicević, Ivan M. and Serifi, Veis and Markovski, Jasmina S. and Stojiljković, Ivana and Mijin, Dusan Z. and Marinković, Aleksandar D.",
year = "2015",
abstract = "The optimized methods for N-alkyl and N,N-dialkyl substituted thioureas synthesis starting from ammonium thiocyanates, waste water constituent from the production of tetramethylthiuram monosulfide (TMTS), and alkyl amine, are presented in this work., Thioureas synthesis was developed in two ways: Method I-reaction of the thiocyanate and alkylamine in the presence of hydrochloric acid; Method II-reaction of the thiocyanate with benzoyl chloride following by amine addition in the first step, and base hydrolysis in the second step. The structure of the synthesized compounds was confirmed by IR, H-1- and C-13-NMR and MS instrumental methods, and purity was determined by high-performance liquid chromatography method. It is shown that the proposed methods offer a high degree of conversion and purity of product, absence of by-products and technological applicability at industrial scale. Considering the importance of the tetramethylthiuram disulfide (TMTD) and TMTS as vulcanization accelerators as well as thiourea as the pharmacologically active compounds, it can be said that application of the optimized methods of thiourea synthesis will provide significant improvement in sustainable development and implementation of eco-friendly production technology. The described environmentally benign process of thioureas synthesis represents a suitable option to existing methods. thioureas, industrial level, thiocyanate.",
publisher = "Savez hemijskih inženjera, Beograd",
journal = "Chemical Industry & Chemical Engineering Quarterly",
title = "Optimization of the synthesis of n -alkyl and n , n -dialkyl thioureas from waste water containing ammonium thiocyanate",
pages = "510-501",
number = "4",
volume = "21",
doi = "10.2298/CICEQ141221006M",
url = "conv_1198"
}

Milosavljević, M. M., Vukicević, I. M., Serifi, V., Markovski, J. S., Stojiljković, I., Mijin, D. Z.,& Marinković, A. D.. (2015). Optimization of the synthesis of n -alkyl and n , n -dialkyl thioureas from waste water containing ammonium thiocyanate. in Chemical Industry & Chemical Engineering Quarterly
Savez hemijskih inženjera, Beograd., 21(4), 501-510.
https://doi.org/10.2298/CICEQ141221006M
conv_1198

Milosavljević MM, Vukicević IM, Serifi V, Markovski JS, Stojiljković I, Mijin DZ, Marinković AD. Optimization of the synthesis of n -alkyl and n , n -dialkyl thioureas from waste water containing ammonium thiocyanate. in Chemical Industry & Chemical Engineering Quarterly. 2015;21(4):501-510.
doi:10.2298/CICEQ141221006M
conv_1198 .

Milosavljević, Milutin M., Vukicević, Ivan M., Serifi, Veis, Markovski, Jasmina S., Stojiljković, Ivana, Mijin, Dusan Z., Marinković, Aleksandar D., "Optimization of the synthesis of n -alkyl and n , n -dialkyl thioureas from waste water containing ammonium thiocyanate" in Chemical Industry & Chemical Engineering Quarterly, 21, no. 4 (2015):501-510,
https://doi.org/10.2298/CICEQ141221006M .,
conv_1198 .

TY  - JOUR
AU  - Ajaj, Ismail
AU  - Markovski, Jasmina
AU  - Rančić, Milica
AU  - Mijin, Dusan
AU  - Milcić, Miloš
AU  - Jovanović, Maja
AU  - Marinković, Aleksandar
PY  - 2015
UR  - https://omorika.sfb.bg.ac.rs/handle/123456789/651
AB  - The state of the tautomeric equilibria of 2(6)-hydroxy-4-methyl-6(2)-oxo-1-(substituted phenyl)-1,2(1,6)-dihydropyridine-3-carbonitriles, 2-PY/6-PY, was evaluated using experimental and theoretical methodology. The experimental data were interpreted with the aid of time-dependent density functional (TD-DFT) method. Electron charge density was obtained by the use of Quantum Theory of Atoms in Molecules, i.e. Bader's analysis. Linear solvation energy relationships (LSER) rationalized solvent influence on tautomeric equilibrium. Linear free energy relationships (LFERs) were applied to the substituent-induced NMR chemical shifts (SCS) using SSP (single substituent parameter) and DSP (dual substituent parameter) model. Theoretical calculations and obtained correlations gave insight into the influence of molecular conformation on the transmission of substituent electronic effects, as well as on different solvent solute interactions, and the state of tautomeric equilibrium.
T2  - Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy
T1  - Solvent and structural effects in tautomeric 2(6)-hydroxy-4-methyl-6(2)-oxo-1-(substituted phenyl)-1,2(1,6)-dihydropyridine-3-carbonitriles: UV, NMR and quantum chemical study
EP  - 585
SP  - 575
VL  - 150
DO  - 10.1016/j.saa.2015.05.055
UR  - conv_1172
ER  - 

@article{
author = "Ajaj, Ismail and Markovski, Jasmina and Rančić, Milica and Mijin, Dusan and Milcić, Miloš and Jovanović, Maja and Marinković, Aleksandar",
year = "2015",
abstract = "The state of the tautomeric equilibria of 2(6)-hydroxy-4-methyl-6(2)-oxo-1-(substituted phenyl)-1,2(1,6)-dihydropyridine-3-carbonitriles, 2-PY/6-PY, was evaluated using experimental and theoretical methodology. The experimental data were interpreted with the aid of time-dependent density functional (TD-DFT) method. Electron charge density was obtained by the use of Quantum Theory of Atoms in Molecules, i.e. Bader's analysis. Linear solvation energy relationships (LSER) rationalized solvent influence on tautomeric equilibrium. Linear free energy relationships (LFERs) were applied to the substituent-induced NMR chemical shifts (SCS) using SSP (single substituent parameter) and DSP (dual substituent parameter) model. Theoretical calculations and obtained correlations gave insight into the influence of molecular conformation on the transmission of substituent electronic effects, as well as on different solvent solute interactions, and the state of tautomeric equilibrium.",
journal = "Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy",
title = "Solvent and structural effects in tautomeric 2(6)-hydroxy-4-methyl-6(2)-oxo-1-(substituted phenyl)-1,2(1,6)-dihydropyridine-3-carbonitriles: UV, NMR and quantum chemical study",
pages = "585-575",
volume = "150",
doi = "10.1016/j.saa.2015.05.055",
url = "conv_1172"
}

Ajaj, I., Markovski, J., Rančić, M., Mijin, D., Milcić, M., Jovanović, M.,& Marinković, A.. (2015). Solvent and structural effects in tautomeric 2(6)-hydroxy-4-methyl-6(2)-oxo-1-(substituted phenyl)-1,2(1,6)-dihydropyridine-3-carbonitriles: UV, NMR and quantum chemical study. in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy, 150, 575-585.
https://doi.org/10.1016/j.saa.2015.05.055
conv_1172

Ajaj I, Markovski J, Rančić M, Mijin D, Milcić M, Jovanović M, Marinković A. Solvent and structural effects in tautomeric 2(6)-hydroxy-4-methyl-6(2)-oxo-1-(substituted phenyl)-1,2(1,6)-dihydropyridine-3-carbonitriles: UV, NMR and quantum chemical study. in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy. 2015;150:575-585.
doi:10.1016/j.saa.2015.05.055
conv_1172 .

Ajaj, Ismail, Markovski, Jasmina, Rančić, Milica, Mijin, Dusan, Milcić, Miloš, Jovanović, Maja, Marinković, Aleksandar, "Solvent and structural effects in tautomeric 2(6)-hydroxy-4-methyl-6(2)-oxo-1-(substituted phenyl)-1,2(1,6)-dihydropyridine-3-carbonitriles: UV, NMR and quantum chemical study" in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy, 150 (2015):575-585,
https://doi.org/10.1016/j.saa.2015.05.055 .,
conv_1172 .