TY  - JOUR
AU  - Lović, Jelena
AU  - Lađarević, Jelena
AU  - Trišović, Nemanja
AU  - Andrić, Filip
AU  - Mladenović, Aleksandar
AU  - Mijin, Dušan
AU  - Vuković, Dragan
AU  - Petrović, Slobodan D.
AU  - Avramov Ivić, Milka
PY  - 2021
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4419
AB  - The electrochemical characterization of sertraline at gold electrode was examined by cyclic voltammetry measurements (CV) in pH 8.4 bicarbonate buffer. Then Au electrode was evaluated for the quantitative determination of sertraline using square wave voltammetry (SWV). To enhance the sensitivity during the drug determination, (2-hydroxypropyl)-β-cyclodextrin (HPβCD) and β-cyclodextrin (βCD) inclusion complexes were employed. Using the proposed SWV technique, the anodic current peak was linear within a concentration range of 0.1–0.5 µM with a limit of detection (LOD) of 2.0 × 10–8 M and a limit of quantification (LOQ) of 6.7 × 10–8 M. In the case of inclusion complex of the sertraline with HPβCD, a good linearity range of 0.1–0.9 µM was obtained with a LOD of 2.6 × 10–8 M and a LOQ of 8.8 × 10–8 M. The gold electrode revealed the same linearity range for inclusion complex of the sertraline with βCD with a LOD and a LOQ being 2.6 × 10–8 and 8.6 × 10–8 M, respectively. Comparing the regression equations, it can be concluded that the sensitivity in the presence of inclusion complex can be up to 5 times higher. The applicability of the developed method was confirmed by the analysis of this drug in pharmaceutical formulation and in human serum spiked with sertraline standard. The comparison to HPLC method was successfully performed.
PB  - Springer International Publishing
T2  - Monatshefte für Chemie - Chemical Monthly
T2  - Monatshefte für Chemie - Chemical MonthlyMonatsh Chem
T1  - Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution
VL  - 152
IS  - 2
SP  - 185
EP  - 192
DO  - 10.1007/s00706-021-02745-3
ER  - 

@article{
author = "Lović, Jelena and Lađarević, Jelena and Trišović, Nemanja and Andrić, Filip and Mladenović, Aleksandar and Mijin, Dušan and Vuković, Dragan and Petrović, Slobodan D. and Avramov Ivić, Milka",
year = "2021",
abstract = "The electrochemical characterization of sertraline at gold electrode was examined by cyclic voltammetry measurements (CV) in pH 8.4 bicarbonate buffer. Then Au electrode was evaluated for the quantitative determination of sertraline using square wave voltammetry (SWV). To enhance the sensitivity during the drug determination, (2-hydroxypropyl)-β-cyclodextrin (HPβCD) and β-cyclodextrin (βCD) inclusion complexes were employed. Using the proposed SWV technique, the anodic current peak was linear within a concentration range of 0.1–0.5 µM with a limit of detection (LOD) of 2.0 × 10–8 M and a limit of quantification (LOQ) of 6.7 × 10–8 M. In the case of inclusion complex of the sertraline with HPβCD, a good linearity range of 0.1–0.9 µM was obtained with a LOD of 2.6 × 10–8 M and a LOQ of 8.8 × 10–8 M. The gold electrode revealed the same linearity range for inclusion complex of the sertraline with βCD with a LOD and a LOQ being 2.6 × 10–8 and 8.6 × 10–8 M, respectively. Comparing the regression equations, it can be concluded that the sensitivity in the presence of inclusion complex can be up to 5 times higher. The applicability of the developed method was confirmed by the analysis of this drug in pharmaceutical formulation and in human serum spiked with sertraline standard. The comparison to HPLC method was successfully performed.",
publisher = "Springer International Publishing",
journal = "Monatshefte für Chemie - Chemical Monthly, Monatshefte für Chemie - Chemical MonthlyMonatsh Chem",
title = "Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution",
volume = "152",
number = "2",
pages = "185-192",
doi = "10.1007/s00706-021-02745-3"
}

Lović, J., Lađarević, J., Trišović, N., Andrić, F., Mladenović, A., Mijin, D., Vuković, D., Petrović, S. D.,& Avramov Ivić, M.. (2021). Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution. in Monatshefte für Chemie - Chemical Monthly
Springer International Publishing., 152(2), 185-192.
https://doi.org/10.1007/s00706-021-02745-3

Lović J, Lađarević J, Trišović N, Andrić F, Mladenović A, Mijin D, Vuković D, Petrović SD, Avramov Ivić M. Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution. in Monatshefte für Chemie - Chemical Monthly. 2021;152(2):185-192.
doi:10.1007/s00706-021-02745-3 .

Lović, Jelena, Lađarević, Jelena, Trišović, Nemanja, Andrić, Filip, Mladenović, Aleksandar, Mijin, Dušan, Vuković, Dragan, Petrović, Slobodan D., Avramov Ivić, Milka, "Electrochemical determination of sertraline in pharmaceutical formulation and serum using a gold electrode in a pH 8.4 bicarbonate solution" in Monatshefte für Chemie - Chemical Monthly, 152, no. 2 (2021):185-192,
https://doi.org/10.1007/s00706-021-02745-3 . .

TY  - DATA
AU  - Marković, J. M.
AU  - Trišović, Nemanja P.
AU  - Toth-Katona, T.
AU  - Milčić, Miloš K.
AU  - Marinković, Aleksandar
AU  - Zhang, C.
AU  - Jakli, A. J.
AU  - Fodor-Csorba, K.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3668
PB  - Royal Soc Chemistry, Cambridge
T2  - New Journal of Chemistry
T1  - Supplementary data for the article: Marković, J. M.; Trišović, N. P.; Tóth-Katona, T.; Milčić, M. K.; Marinković, A. D.; Zhang, C.; Jákli, A. J.; Fodor-Csorba, K. A Structure-Property Relationship Study of Bent-Core Mesogens with Pyridine as the Central Unit. New Journal of Chemistry 2014, 38 (4), 1751–1760. https://doi.org/10.1039/c3nj01430d
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3668
ER  - 

@misc{
author = "Marković, J. M. and Trišović, Nemanja P. and Toth-Katona, T. and Milčić, Miloš K. and Marinković, Aleksandar and Zhang, C. and Jakli, A. J. and Fodor-Csorba, K.",
year = "2014",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "New Journal of Chemistry",
title = "Supplementary data for the article: Marković, J. M.; Trišović, N. P.; Tóth-Katona, T.; Milčić, M. K.; Marinković, A. D.; Zhang, C.; Jákli, A. J.; Fodor-Csorba, K. A Structure-Property Relationship Study of Bent-Core Mesogens with Pyridine as the Central Unit. New Journal of Chemistry 2014, 38 (4), 1751–1760. https://doi.org/10.1039/c3nj01430d",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3668"
}

Marković, J. M., Trišović, N. P., Toth-Katona, T., Milčić, M. K., Marinković, A., Zhang, C., Jakli, A. J.,& Fodor-Csorba, K.. (2014). Supplementary data for the article: Marković, J. M.; Trišović, N. P.; Tóth-Katona, T.; Milčić, M. K.; Marinković, A. D.; Zhang, C.; Jákli, A. J.; Fodor-Csorba, K. A Structure-Property Relationship Study of Bent-Core Mesogens with Pyridine as the Central Unit. New Journal of Chemistry 2014, 38 (4), 1751–1760. https://doi.org/10.1039/c3nj01430d. in New Journal of Chemistry
Royal Soc Chemistry, Cambridge..
https://hdl.handle.net/21.15107/rcub_cherry_3668

Marković JM, Trišović NP, Toth-Katona T, Milčić MK, Marinković A, Zhang C, Jakli AJ, Fodor-Csorba K. Supplementary data for the article: Marković, J. M.; Trišović, N. P.; Tóth-Katona, T.; Milčić, M. K.; Marinković, A. D.; Zhang, C.; Jákli, A. J.; Fodor-Csorba, K. A Structure-Property Relationship Study of Bent-Core Mesogens with Pyridine as the Central Unit. New Journal of Chemistry 2014, 38 (4), 1751–1760. https://doi.org/10.1039/c3nj01430d. in New Journal of Chemistry. 2014;.
https://hdl.handle.net/21.15107/rcub_cherry_3668 .

Marković, J. M., Trišović, Nemanja P., Toth-Katona, T., Milčić, Miloš K., Marinković, Aleksandar, Zhang, C., Jakli, A. J., Fodor-Csorba, K., "Supplementary data for the article: Marković, J. M.; Trišović, N. P.; Tóth-Katona, T.; Milčić, M. K.; Marinković, A. D.; Zhang, C.; Jákli, A. J.; Fodor-Csorba, K. A Structure-Property Relationship Study of Bent-Core Mesogens with Pyridine as the Central Unit. New Journal of Chemistry 2014, 38 (4), 1751–1760. https://doi.org/10.1039/c3nj01430d" in New Journal of Chemistry (2014),
https://hdl.handle.net/21.15107/rcub_cherry_3668 .

TY  - JOUR
AU  - Rančić, Milica
AU  - Trišović, Nemanja P.
AU  - Milčić, Miloš K.
AU  - Jovanović, Maja
AU  - Jovanovic, Bratislav
AU  - Marinković, Aleksandar
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1857
AB  - Two series of 4-substituted N-[1-(pyridine-3- and -4-yl)ethylidene]anilines have been synthesized using different methods of conventional and microwave-assisted synthesis, and linear free-energy relationships have been applied to the C-13 NMR chemical shifts of the carbon atoms of interest. The substituent-induced chemical shifts have been analyzed using single substituent parameter and dual substituent parameter methods. The presented correlations describe satisfactorily the field and resonance substituent effects having similar contributions for C1 and the azomethine carbon, with exception of the carbon atom in para position to the substituent X. In both series, negative values have been found for C1 atom (reverse substituent effect). Quantum chemical calculations of the optimized geometries at MP2/6-31G++(d,p) level, together with C-13 NMR chemical shifts, give a better insight into the influence of the molecular conformation on the transmission of electronic substituent effects. The comparison of correlation results for different series of imines with phenyl, 4-nitrophenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl group attached at the azomethine carbon with the results for 4-substituted N-[1-(pyridine-3- and -4-yl)ethylidene]anilines for the same substituent set (X) indicates that a combination of the influences of electronic effects of the substituent X and the (1)-unit can be described as a sensitive balance of different resonance structures.
PB  - Wiley-Blackwell, Hoboken
T2  - Journal of Heterocyclic Chemistry
T1  - Linear Free-Energy Relationships Applied to the C-13 NMR Chemical Shifts in 4-Substituted N-[1-(Pyridine-3-and-4-yl)ethylidene]anilines
VL  - 51
IS  - 5
SP  - 1442
EP  - 1451
DO  - 10.1002/jhet.1752
ER  - 

@article{
author = "Rančić, Milica and Trišović, Nemanja P. and Milčić, Miloš K. and Jovanović, Maja and Jovanovic, Bratislav and Marinković, Aleksandar",
year = "2014",
abstract = "Two series of 4-substituted N-[1-(pyridine-3- and -4-yl)ethylidene]anilines have been synthesized using different methods of conventional and microwave-assisted synthesis, and linear free-energy relationships have been applied to the C-13 NMR chemical shifts of the carbon atoms of interest. The substituent-induced chemical shifts have been analyzed using single substituent parameter and dual substituent parameter methods. The presented correlations describe satisfactorily the field and resonance substituent effects having similar contributions for C1 and the azomethine carbon, with exception of the carbon atom in para position to the substituent X. In both series, negative values have been found for C1 atom (reverse substituent effect). Quantum chemical calculations of the optimized geometries at MP2/6-31G++(d,p) level, together with C-13 NMR chemical shifts, give a better insight into the influence of the molecular conformation on the transmission of electronic substituent effects. The comparison of correlation results for different series of imines with phenyl, 4-nitrophenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl group attached at the azomethine carbon with the results for 4-substituted N-[1-(pyridine-3- and -4-yl)ethylidene]anilines for the same substituent set (X) indicates that a combination of the influences of electronic effects of the substituent X and the (1)-unit can be described as a sensitive balance of different resonance structures.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Journal of Heterocyclic Chemistry",
title = "Linear Free-Energy Relationships Applied to the C-13 NMR Chemical Shifts in 4-Substituted N-[1-(Pyridine-3-and-4-yl)ethylidene]anilines",
volume = "51",
number = "5",
pages = "1442-1451",
doi = "10.1002/jhet.1752"
}

Rančić, M., Trišović, N. P., Milčić, M. K., Jovanović, M., Jovanovic, B.,& Marinković, A.. (2014). Linear Free-Energy Relationships Applied to the C-13 NMR Chemical Shifts in 4-Substituted N-[1-(Pyridine-3-and-4-yl)ethylidene]anilines. in Journal of Heterocyclic Chemistry
Wiley-Blackwell, Hoboken., 51(5), 1442-1451.
https://doi.org/10.1002/jhet.1752

Rančić M, Trišović NP, Milčić MK, Jovanović M, Jovanovic B, Marinković A. Linear Free-Energy Relationships Applied to the C-13 NMR Chemical Shifts in 4-Substituted N-[1-(Pyridine-3-and-4-yl)ethylidene]anilines. in Journal of Heterocyclic Chemistry. 2014;51(5):1442-1451.
doi:10.1002/jhet.1752 .

Rančić, Milica, Trišović, Nemanja P., Milčić, Miloš K., Jovanović, Maja, Jovanovic, Bratislav, Marinković, Aleksandar, "Linear Free-Energy Relationships Applied to the C-13 NMR Chemical Shifts in 4-Substituted N-[1-(Pyridine-3-and-4-yl)ethylidene]anilines" in Journal of Heterocyclic Chemistry, 51, no. 5 (2014):1442-1451,
https://doi.org/10.1002/jhet.1752 . .

TY  - JOUR
AU  - Marković, J. M.
AU  - Trišović, Nemanja P.
AU  - Toth-Katona, T.
AU  - Milčić, Miloš K.
AU  - Marinković, Aleksandar
AU  - Zhang, C.
AU  - Jakli, A. J.
AU  - Fodor-Csorba, K.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1518
AB  - Three series of bent-core mesogens having pyridine as the central unit have been synthesized and characterized. A series of 2,6-diaminopyridine derivatives capable of forming inter- and intramolecular hydrogen bonds exhibit very high melting points. A decrease in the polarity of the central part of the bent-core obtained by replacing the amide with ester linkages results in derivatives with lower melting points and formation of B2- and B7-like mesophases. The introduction of the olefinic groups, which connect the pyridine ring with the inner aromatic rings, helps to further lower the polarity of the central part in the five ring system and led to the formation of B1 and B7 phases. The phases have been determined by optical microscopy observations and differential scanning calorimetry (DSC) and confirmed by X-ray studies. The bending angles and polarity of the investigated five-ring systems have been calculated by the density functional theory (DFT) method.
PB  - Royal Soc Chemistry, Cambridge
T2  - New Journal of Chemistry
T1  - A structure-property relationship study of bent-core mesogens with pyridine as the central unit
VL  - 38
IS  - 4
SP  - 1751
EP  - 1760
DO  - 10.1039/c3nj01430d
ER  - 

@article{
author = "Marković, J. M. and Trišović, Nemanja P. and Toth-Katona, T. and Milčić, Miloš K. and Marinković, Aleksandar and Zhang, C. and Jakli, A. J. and Fodor-Csorba, K.",
year = "2014",
abstract = "Three series of bent-core mesogens having pyridine as the central unit have been synthesized and characterized. A series of 2,6-diaminopyridine derivatives capable of forming inter- and intramolecular hydrogen bonds exhibit very high melting points. A decrease in the polarity of the central part of the bent-core obtained by replacing the amide with ester linkages results in derivatives with lower melting points and formation of B2- and B7-like mesophases. The introduction of the olefinic groups, which connect the pyridine ring with the inner aromatic rings, helps to further lower the polarity of the central part in the five ring system and led to the formation of B1 and B7 phases. The phases have been determined by optical microscopy observations and differential scanning calorimetry (DSC) and confirmed by X-ray studies. The bending angles and polarity of the investigated five-ring systems have been calculated by the density functional theory (DFT) method.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "New Journal of Chemistry",
title = "A structure-property relationship study of bent-core mesogens with pyridine as the central unit",
volume = "38",
number = "4",
pages = "1751-1760",
doi = "10.1039/c3nj01430d"
}

Marković, J. M., Trišović, N. P., Toth-Katona, T., Milčić, M. K., Marinković, A., Zhang, C., Jakli, A. J.,& Fodor-Csorba, K.. (2014). A structure-property relationship study of bent-core mesogens with pyridine as the central unit. in New Journal of Chemistry
Royal Soc Chemistry, Cambridge., 38(4), 1751-1760.
https://doi.org/10.1039/c3nj01430d

Marković JM, Trišović NP, Toth-Katona T, Milčić MK, Marinković A, Zhang C, Jakli AJ, Fodor-Csorba K. A structure-property relationship study of bent-core mesogens with pyridine as the central unit. in New Journal of Chemistry. 2014;38(4):1751-1760.
doi:10.1039/c3nj01430d .

Marković, J. M., Trišović, Nemanja P., Toth-Katona, T., Milčić, Miloš K., Marinković, Aleksandar, Zhang, C., Jakli, A. J., Fodor-Csorba, K., "A structure-property relationship study of bent-core mesogens with pyridine as the central unit" in New Journal of Chemistry, 38, no. 4 (2014):1751-1760,
https://doi.org/10.1039/c3nj01430d . .

TY  - JOUR
AU  - Rančić, Milica
AU  - Trišović, Nemanja P.
AU  - Milčić, Miloš K.
AU  - Ajaj, Ismail A.
AU  - Marinković, Aleksandar
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1404
AB  - The electronic structure of 5-arylidene-2,4-thiazolidinediones has been studied by using experimental and theoretical methodology. The theoretical calculations of the investigated 5-arylidene-2,4-thiazolidinediones have been performed by the use of quantum chemical methods. The calculated C-13 NMR chemical shifts and NBO atomic charges provide an insight into the influence of such a structure on the transmission of electronic substituent effects. Linear free energy relationships (LFERs) have been further applied to their C-13 NMR chemical shifts. The correlation analyses for the substituent-induced chemical shifts (SCS) have been performed with sigma using SSP (single substituent parameter), field (sigma(F)) and resonance (sigma(R)) parameters using DSP (dual substituent parameter), as well as the Yukawa-Tsuno model. The presented correlations account satisfactorily for the polar and resonance substituent effects operative at C-beta. and C-7 carbons, while reverse substituent effect was found for C-alpha. The comparison of correlation results for the investigated molecules with those obtained for seven structurally related styrene series has indicated that specific cross-interaction of phenyl substituent and groups attached at C-alpha carbon causes increased sensitivity of SCS C-beta to the resonance effect with increasing of electron-accepting capabilities of the group present at C-beta.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Molecular Structure
T1  - Experimental and theoretical study of substituent effect on C-13 NMR chemical shifts of 5-arylidene-2,4-thiazolidinediones
VL  - 1049
SP  - 59
EP  - 68
DO  - 10.1016/j.molstruc.2013.06.027
ER  - 

@article{
author = "Rančić, Milica and Trišović, Nemanja P. and Milčić, Miloš K. and Ajaj, Ismail A. and Marinković, Aleksandar",
year = "2013",
abstract = "The electronic structure of 5-arylidene-2,4-thiazolidinediones has been studied by using experimental and theoretical methodology. The theoretical calculations of the investigated 5-arylidene-2,4-thiazolidinediones have been performed by the use of quantum chemical methods. The calculated C-13 NMR chemical shifts and NBO atomic charges provide an insight into the influence of such a structure on the transmission of electronic substituent effects. Linear free energy relationships (LFERs) have been further applied to their C-13 NMR chemical shifts. The correlation analyses for the substituent-induced chemical shifts (SCS) have been performed with sigma using SSP (single substituent parameter), field (sigma(F)) and resonance (sigma(R)) parameters using DSP (dual substituent parameter), as well as the Yukawa-Tsuno model. The presented correlations account satisfactorily for the polar and resonance substituent effects operative at C-beta. and C-7 carbons, while reverse substituent effect was found for C-alpha. The comparison of correlation results for the investigated molecules with those obtained for seven structurally related styrene series has indicated that specific cross-interaction of phenyl substituent and groups attached at C-alpha carbon causes increased sensitivity of SCS C-beta to the resonance effect with increasing of electron-accepting capabilities of the group present at C-beta.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Molecular Structure",
title = "Experimental and theoretical study of substituent effect on C-13 NMR chemical shifts of 5-arylidene-2,4-thiazolidinediones",
volume = "1049",
pages = "59-68",
doi = "10.1016/j.molstruc.2013.06.027"
}

Rančić, M., Trišović, N. P., Milčić, M. K., Ajaj, I. A.,& Marinković, A.. (2013). Experimental and theoretical study of substituent effect on C-13 NMR chemical shifts of 5-arylidene-2,4-thiazolidinediones. in Journal of Molecular Structure
Elsevier Science Bv, Amsterdam., 1049, 59-68.
https://doi.org/10.1016/j.molstruc.2013.06.027

Rančić M, Trišović NP, Milčić MK, Ajaj IA, Marinković A. Experimental and theoretical study of substituent effect on C-13 NMR chemical shifts of 5-arylidene-2,4-thiazolidinediones. in Journal of Molecular Structure. 2013;1049:59-68.
doi:10.1016/j.molstruc.2013.06.027 .

Rančić, Milica, Trišović, Nemanja P., Milčić, Miloš K., Ajaj, Ismail A., Marinković, Aleksandar, "Experimental and theoretical study of substituent effect on C-13 NMR chemical shifts of 5-arylidene-2,4-thiazolidinediones" in Journal of Molecular Structure, 1049 (2013):59-68,
https://doi.org/10.1016/j.molstruc.2013.06.027 . .

TY  - JOUR
AU  - Rančić, Milica
AU  - Trišović, Nemanja P.
AU  - Milčić, Miloš K.
AU  - Uscumlic, Gordana
AU  - Marinković, Aleksandar
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1252
AB  - The absorption spectra of twelve 5-arylidene-2,4-thiazolidinediones were recorded in twenty one solvents in the range from 300 to 600 nm. The effect of specific and non-specific solvent-solute interactions on the absorption maxima shifts were evaluated by using the Catalan solvent parameter set. Furthermore, the experimental findings were interpreted with the aid of ab initio MP2 and time-dependent density functional (TD-DFT) methods. It was found that different substituents significantly change the extent of conjugation in the molecules and further affect their intramolecular charge transfer character. (C) 2011 Elsevier B.V. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Spectrochimica Acta. Part A: Molecular and Biomolecular Spectroscopy
T1  - Substituent and solvent effects on intramolecular charge transfer of 5-arylidene-2,4-thiazolidinediones
VL  - 86
SP  - 500
EP  - 507
DO  - 10.1016/j.saa.2011.10.074
ER  - 

@article{
author = "Rančić, Milica and Trišović, Nemanja P. and Milčić, Miloš K. and Uscumlic, Gordana and Marinković, Aleksandar",
year = "2012",
abstract = "The absorption spectra of twelve 5-arylidene-2,4-thiazolidinediones were recorded in twenty one solvents in the range from 300 to 600 nm. The effect of specific and non-specific solvent-solute interactions on the absorption maxima shifts were evaluated by using the Catalan solvent parameter set. Furthermore, the experimental findings were interpreted with the aid of ab initio MP2 and time-dependent density functional (TD-DFT) methods. It was found that different substituents significantly change the extent of conjugation in the molecules and further affect their intramolecular charge transfer character. (C) 2011 Elsevier B.V. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Spectrochimica Acta. Part A: Molecular and Biomolecular Spectroscopy",
title = "Substituent and solvent effects on intramolecular charge transfer of 5-arylidene-2,4-thiazolidinediones",
volume = "86",
pages = "500-507",
doi = "10.1016/j.saa.2011.10.074"
}

Rančić, M., Trišović, N. P., Milčić, M. K., Uscumlic, G.,& Marinković, A.. (2012). Substituent and solvent effects on intramolecular charge transfer of 5-arylidene-2,4-thiazolidinediones. in Spectrochimica Acta. Part A: Molecular and Biomolecular Spectroscopy
Pergamon-Elsevier Science Ltd, Oxford., 86, 500-507.
https://doi.org/10.1016/j.saa.2011.10.074

Rančić M, Trišović NP, Milčić MK, Uscumlic G, Marinković A. Substituent and solvent effects on intramolecular charge transfer of 5-arylidene-2,4-thiazolidinediones. in Spectrochimica Acta. Part A: Molecular and Biomolecular Spectroscopy. 2012;86:500-507.
doi:10.1016/j.saa.2011.10.074 .

Rančić, Milica, Trišović, Nemanja P., Milčić, Miloš K., Uscumlic, Gordana, Marinković, Aleksandar, "Substituent and solvent effects on intramolecular charge transfer of 5-arylidene-2,4-thiazolidinediones" in Spectrochimica Acta. Part A: Molecular and Biomolecular Spectroscopy, 86 (2012):500-507,
https://doi.org/10.1016/j.saa.2011.10.074 . .