TY  - JOUR
AU  - Matijević, Borko M.
AU  - Vaštag, Đenđi
AU  - Perišić-Janjić, Nada
AU  - Apostolov, Suzana
AU  - Milčić, Miloš
AU  - Zivanović, Lidija
AU  - Marinković, Aleksandar
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2754
AB  - UV absorption spectra of N-(substituted phenyl)-2-cyanoacetamides have been recorded in the range 200-400 nm in the set of selected solvents. The solute-solvent interactions were analyzed on the basis of linear solvation energy relationships (LSER) concept proposed by Kamlet and Taft. The effects of substituents on the absorption spectra were interpreted by correlation of absorption frequencies with Hammett substituent constant, sigma. It was found that substituents significantly change the extent of conjugation. Furthermore, the experimental findings were interpreted with the aid of ab initio B3LYP/6-311G(d,p) method. Electronic energies was calculated by the use of 6-311++G(3df,3pd) methods with standard polarized continuum model (PCM) for inclusion of the solvent effect.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy
T1  - Solvent and structural effects on the UV absorption spectra of N-(substituted phenyl)-2-cyanoacetamides
EP  - 575
SP  - 568
VL  - 117
DO  - 10.1016/j.saa.2013.08.040
ER  - 

@article{
author = "Matijević, Borko M. and Vaštag, Đenđi and Perišić-Janjić, Nada and Apostolov, Suzana and Milčić, Miloš and Zivanović, Lidija and Marinković, Aleksandar",
year = "2014",
abstract = "UV absorption spectra of N-(substituted phenyl)-2-cyanoacetamides have been recorded in the range 200-400 nm in the set of selected solvents. The solute-solvent interactions were analyzed on the basis of linear solvation energy relationships (LSER) concept proposed by Kamlet and Taft. The effects of substituents on the absorption spectra were interpreted by correlation of absorption frequencies with Hammett substituent constant, sigma. It was found that substituents significantly change the extent of conjugation. Furthermore, the experimental findings were interpreted with the aid of ab initio B3LYP/6-311G(d,p) method. Electronic energies was calculated by the use of 6-311++G(3df,3pd) methods with standard polarized continuum model (PCM) for inclusion of the solvent effect.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy",
title = "Solvent and structural effects on the UV absorption spectra of N-(substituted phenyl)-2-cyanoacetamides",
pages = "575-568",
volume = "117",
doi = "10.1016/j.saa.2013.08.040"
}

Matijević, B. M., Vaštag, Đ., Perišić-Janjić, N., Apostolov, S., Milčić, M., Zivanović, L.,& Marinković, A.. (2014). Solvent and structural effects on the UV absorption spectra of N-(substituted phenyl)-2-cyanoacetamides. in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy
Pergamon-Elsevier Science Ltd, Oxford., 117, 568-575.
https://doi.org/10.1016/j.saa.2013.08.040

Matijević BM, Vaštag Đ, Perišić-Janjić N, Apostolov S, Milčić M, Zivanović L, Marinković A. Solvent and structural effects on the UV absorption spectra of N-(substituted phenyl)-2-cyanoacetamides. in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy. 2014;117:568-575.
doi:10.1016/j.saa.2013.08.040 .

Matijević, Borko M., Vaštag, Đenđi, Perišić-Janjić, Nada, Apostolov, Suzana, Milčić, Miloš, Zivanović, Lidija, Marinković, Aleksandar, "Solvent and structural effects on the UV absorption spectra of N-(substituted phenyl)-2-cyanoacetamides" in Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy, 117 (2014):568-575,
https://doi.org/10.1016/j.saa.2013.08.040 . .

TY  - JOUR
AU  - Vaštag, Đenđi
AU  - Perišić-Janjić, Nada
AU  - Apostolov, Suzana
AU  - Petrović, Slobodan
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1764
AB  - Retention behavior of some N-(4-phenylsubstituted)-2,3-diphenylpropanamides was investigated on reversed phase thin layer chromatography (RP-C18). Retention constants of investigated compounds were determined in the following solvent systems: water-ethanol, watern-propanol and water-i-propanol. Linear relationships were obtained between retention, RM and volume fraction of organic solvent, ϕ. As a measure of lipophilicity of tested propanamides, Hansch`s lipophilicity parameter, π, were calculated. Chromatography retention constants RM0 were correlated with Hansch`s lipophilicity parameter, and good linear relationships were obtained. These results confirm, that retention constants, (RM0 ), determined in reversed phase thin-layer chromatography (RP-TCL) can be used, as criteria of lipophilicity.
PB  - University of East Sarajevo, Faculty of Technology
T2  - Journal of Engineering & Processing Management
T1  - Chromatographic behavior and lipophilicity of n-(4-phenylsubstituted)-2,3-diphenylpropanamides
EP  - 15
IS  - 1
SP  - 7
VL  - 3
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1764
ER  - 

@article{
author = "Vaštag, Đenđi and Perišić-Janjić, Nada and Apostolov, Suzana and Petrović, Slobodan",
year = "2011",
abstract = "Retention behavior of some N-(4-phenylsubstituted)-2,3-diphenylpropanamides was investigated on reversed phase thin layer chromatography (RP-C18). Retention constants of investigated compounds were determined in the following solvent systems: water-ethanol, watern-propanol and water-i-propanol. Linear relationships were obtained between retention, RM and volume fraction of organic solvent, ϕ. As a measure of lipophilicity of tested propanamides, Hansch`s lipophilicity parameter, π, were calculated. Chromatography retention constants RM0 were correlated with Hansch`s lipophilicity parameter, and good linear relationships were obtained. These results confirm, that retention constants, (RM0 ), determined in reversed phase thin-layer chromatography (RP-TCL) can be used, as criteria of lipophilicity.",
publisher = "University of East Sarajevo, Faculty of Technology",
journal = "Journal of Engineering & Processing Management",
title = "Chromatographic behavior and lipophilicity of n-(4-phenylsubstituted)-2,3-diphenylpropanamides",
pages = "15-7",
number = "1",
volume = "3",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1764"
}

Vaštag, Đ., Perišić-Janjić, N., Apostolov, S.,& Petrović, S.. (2011). Chromatographic behavior and lipophilicity of n-(4-phenylsubstituted)-2,3-diphenylpropanamides. in Journal of Engineering & Processing Management
University of East Sarajevo, Faculty of Technology., 3(1), 7-15.
https://hdl.handle.net/21.15107/rcub_technorep_1764

Vaštag Đ, Perišić-Janjić N, Apostolov S, Petrović S. Chromatographic behavior and lipophilicity of n-(4-phenylsubstituted)-2,3-diphenylpropanamides. in Journal of Engineering & Processing Management. 2011;3(1):7-15.
https://hdl.handle.net/21.15107/rcub_technorep_1764 .

Vaštag, Đenđi, Perišić-Janjić, Nada, Apostolov, Suzana, Petrović, Slobodan, "Chromatographic behavior and lipophilicity of n-(4-phenylsubstituted)-2,3-diphenylpropanamides" in Journal of Engineering & Processing Management, 3, no. 1 (2011):7-15,
https://hdl.handle.net/21.15107/rcub_technorep_1764 .

TY  - JOUR
AU  - Vaštag, Đenđi
AU  - Perišić-Janjić, Nada
AU  - Tomić, Jelena
AU  - Petrović, Slobodan
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1858
AB  - The chromatographic behavior of N-cyclohexyl-N-substituted-2-phenylacetamides was investigated using reversed phase thin-layer chromatography (RP-TLC). RP-TLC was performed on a C-18 bonded phase with different aqueous eluents: water-acetone, water-acetonitrile and water dioxane. Linear relationship between retention parameters and organic modifier content in the mobile phase allows the extrapolation procedure. From results, it is evident that retention behavior of investigated compound depended on structures of substituents R. The correlation between the chromatographic lipophilic parameters (R-M(0)) and calculated log P values and several pharmacokinetics parameters such as HIA (human intestinal absorption) predictor, the plasma protein binding (PB) predictor, and partition predictor for predicting the biological activity of the blood-brain barrier (BBB) has been studied. The results show that reversed-phase R-M(0) proved to express lipophilic nature of investigated compounds as well as biological activity.
PB  - Akademiai Kiado Zrt, Budapest
T2  - JPC-Journal of Planar Chromatography-Modern Tlc
T1  - Evaluation of the Lipophilicity and Prediction of Biological Activity of Some N-Cyclohexyl-N-Substituted-2-Phenylacetamide Derivatives Using RP-TLC
EP  - 440
IS  - 5
SP  - 435
VL  - 24
DO  - 10.1556/JPC.24.2011.5.13
ER  - 

@article{
author = "Vaštag, Đenđi and Perišić-Janjić, Nada and Tomić, Jelena and Petrović, Slobodan",
year = "2011",
abstract = "The chromatographic behavior of N-cyclohexyl-N-substituted-2-phenylacetamides was investigated using reversed phase thin-layer chromatography (RP-TLC). RP-TLC was performed on a C-18 bonded phase with different aqueous eluents: water-acetone, water-acetonitrile and water dioxane. Linear relationship between retention parameters and organic modifier content in the mobile phase allows the extrapolation procedure. From results, it is evident that retention behavior of investigated compound depended on structures of substituents R. The correlation between the chromatographic lipophilic parameters (R-M(0)) and calculated log P values and several pharmacokinetics parameters such as HIA (human intestinal absorption) predictor, the plasma protein binding (PB) predictor, and partition predictor for predicting the biological activity of the blood-brain barrier (BBB) has been studied. The results show that reversed-phase R-M(0) proved to express lipophilic nature of investigated compounds as well as biological activity.",
publisher = "Akademiai Kiado Zrt, Budapest",
journal = "JPC-Journal of Planar Chromatography-Modern Tlc",
title = "Evaluation of the Lipophilicity and Prediction of Biological Activity of Some N-Cyclohexyl-N-Substituted-2-Phenylacetamide Derivatives Using RP-TLC",
pages = "440-435",
number = "5",
volume = "24",
doi = "10.1556/JPC.24.2011.5.13"
}

Vaštag, Đ., Perišić-Janjić, N., Tomić, J.,& Petrović, S.. (2011). Evaluation of the Lipophilicity and Prediction of Biological Activity of Some N-Cyclohexyl-N-Substituted-2-Phenylacetamide Derivatives Using RP-TLC. in JPC-Journal of Planar Chromatography-Modern Tlc
Akademiai Kiado Zrt, Budapest., 24(5), 435-440.
https://doi.org/10.1556/JPC.24.2011.5.13

Vaštag Đ, Perišić-Janjić N, Tomić J, Petrović S. Evaluation of the Lipophilicity and Prediction of Biological Activity of Some N-Cyclohexyl-N-Substituted-2-Phenylacetamide Derivatives Using RP-TLC. in JPC-Journal of Planar Chromatography-Modern Tlc. 2011;24(5):435-440.
doi:10.1556/JPC.24.2011.5.13 .

Vaštag, Đenđi, Perišić-Janjić, Nada, Tomić, Jelena, Petrović, Slobodan, "Evaluation of the Lipophilicity and Prediction of Biological Activity of Some N-Cyclohexyl-N-Substituted-2-Phenylacetamide Derivatives Using RP-TLC" in JPC-Journal of Planar Chromatography-Modern Tlc, 24, no. 5 (2011):435-440,
https://doi.org/10.1556/JPC.24.2011.5.13 . .

TY  - JOUR
AU  - Perišić-Janjić, Nada
AU  - Vastag, Gyongyi
AU  - Tomić, Jelena
AU  - Petrović, Slobodan
PY  - 2007
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1148
AB  - The chromatographic behavior of some N,N-disubstituted-2-phenylacetamide derivatives has been studied on the chemically bonded stationary phase RP-C-18 with acetone, acetonitrile, tetrahydrofuran, dioxane, methanol, ethanol, 1-propanol, and 2-propanol as organic modifiers of aqueous mobile phases. The retention observed with different mobile-phase modifiers was correlated. The effects of different physicochemical properties of the compounds on retention behavior when chromatographed with aqueous mobile phases containing protic and aprotic modifiers were also studied. Multiple linear regression analysis was used to correlate chromatographic retention constants of the compounds with physicochemical properties. The chromatographic lipophilicity R-M(0) (determined by linear extrapolation) was correlated with log P values calculated by use of different theoretical methods. Good relationships were obtained for all the systems investigated. Good correlation was obtained between lipophilicity measured chromatographically and biological activity predictors.
PB  - Akademiai Kiado Zrt, Budapest
T2  - JPC-Journal of Planar Chromatography-Modern Tlc
T1  - Effect of the physicochemical properties of N,N-Disubstituted-2-phenylacetamide derivatives on their retention behavior in RP-TLC
EP  - 359
IS  - 5
SP  - 353
VL  - 20
DO  - 10.1556/JPC.20.2007.5.8
ER  - 

@article{
author = "Perišić-Janjić, Nada and Vastag, Gyongyi and Tomić, Jelena and Petrović, Slobodan",
year = "2007",
abstract = "The chromatographic behavior of some N,N-disubstituted-2-phenylacetamide derivatives has been studied on the chemically bonded stationary phase RP-C-18 with acetone, acetonitrile, tetrahydrofuran, dioxane, methanol, ethanol, 1-propanol, and 2-propanol as organic modifiers of aqueous mobile phases. The retention observed with different mobile-phase modifiers was correlated. The effects of different physicochemical properties of the compounds on retention behavior when chromatographed with aqueous mobile phases containing protic and aprotic modifiers were also studied. Multiple linear regression analysis was used to correlate chromatographic retention constants of the compounds with physicochemical properties. The chromatographic lipophilicity R-M(0) (determined by linear extrapolation) was correlated with log P values calculated by use of different theoretical methods. Good relationships were obtained for all the systems investigated. Good correlation was obtained between lipophilicity measured chromatographically and biological activity predictors.",
publisher = "Akademiai Kiado Zrt, Budapest",
journal = "JPC-Journal of Planar Chromatography-Modern Tlc",
title = "Effect of the physicochemical properties of N,N-Disubstituted-2-phenylacetamide derivatives on their retention behavior in RP-TLC",
pages = "359-353",
number = "5",
volume = "20",
doi = "10.1556/JPC.20.2007.5.8"
}

Perišić-Janjić, N., Vastag, G., Tomić, J.,& Petrović, S.. (2007). Effect of the physicochemical properties of N,N-Disubstituted-2-phenylacetamide derivatives on their retention behavior in RP-TLC. in JPC-Journal of Planar Chromatography-Modern Tlc
Akademiai Kiado Zrt, Budapest., 20(5), 353-359.
https://doi.org/10.1556/JPC.20.2007.5.8

Perišić-Janjić N, Vastag G, Tomić J, Petrović S. Effect of the physicochemical properties of N,N-Disubstituted-2-phenylacetamide derivatives on their retention behavior in RP-TLC. in JPC-Journal of Planar Chromatography-Modern Tlc. 2007;20(5):353-359.
doi:10.1556/JPC.20.2007.5.8 .

Perišić-Janjić, Nada, Vastag, Gyongyi, Tomić, Jelena, Petrović, Slobodan, "Effect of the physicochemical properties of N,N-Disubstituted-2-phenylacetamide derivatives on their retention behavior in RP-TLC" in JPC-Journal of Planar Chromatography-Modern Tlc, 20, no. 5 (2007):353-359,
https://doi.org/10.1556/JPC.20.2007.5.8 . .

TY  - JOUR
AU  - Mijin, Dušan
AU  - Ušćumlić, Gordana
AU  - Perišić-Janjić, Nada
AU  - Valentić, Nataša
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1003
AB  - Absorption spectra of seventeen 5-(3- and 4-substituted arylazo)-4,6-dimethyl-3-cyano-2-pyridones have been recorded in 12 protic and aprotic solvents in the range 200-600 nm. The effects of substituents on the absorption spectra of these new azo dyes are interpreted by correlation of absorption frequencies with Hammett equation. The solute-solvent interactions were clarified on the basis of linear solvation energy relationships concept proposed by Kamlet and Taft. The 2-pyridone/2-hydroxypiridine tautomeric equilibration is found to depend upon substituents as well as on solvents.
PB  - Elsevier Science Bv, Amsterdam
T2  - Chemical Physics Letters
T1  - Substituent and solvent effects on the UV/vis absorption spectra of 5-(3-and 4-substituted arylazo)-4,6-dimethyl-3-eyano-2-pyridones
EP  - 229
IS  - 1-3
SP  - 223
VL  - 418
DO  - 10.1016/j.cplett.2005.10.130
ER  - 

@article{
author = "Mijin, Dušan and Ušćumlić, Gordana and Perišić-Janjić, Nada and Valentić, Nataša",
year = "2006",
abstract = "Absorption spectra of seventeen 5-(3- and 4-substituted arylazo)-4,6-dimethyl-3-cyano-2-pyridones have been recorded in 12 protic and aprotic solvents in the range 200-600 nm. The effects of substituents on the absorption spectra of these new azo dyes are interpreted by correlation of absorption frequencies with Hammett equation. The solute-solvent interactions were clarified on the basis of linear solvation energy relationships concept proposed by Kamlet and Taft. The 2-pyridone/2-hydroxypiridine tautomeric equilibration is found to depend upon substituents as well as on solvents.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Chemical Physics Letters",
title = "Substituent and solvent effects on the UV/vis absorption spectra of 5-(3-and 4-substituted arylazo)-4,6-dimethyl-3-eyano-2-pyridones",
pages = "229-223",
number = "1-3",
volume = "418",
doi = "10.1016/j.cplett.2005.10.130"
}

Mijin, D., Ušćumlić, G., Perišić-Janjić, N.,& Valentić, N.. (2006). Substituent and solvent effects on the UV/vis absorption spectra of 5-(3-and 4-substituted arylazo)-4,6-dimethyl-3-eyano-2-pyridones. in Chemical Physics Letters
Elsevier Science Bv, Amsterdam., 418(1-3), 223-229.
https://doi.org/10.1016/j.cplett.2005.10.130

Mijin D, Ušćumlić G, Perišić-Janjić N, Valentić N. Substituent and solvent effects on the UV/vis absorption spectra of 5-(3-and 4-substituted arylazo)-4,6-dimethyl-3-eyano-2-pyridones. in Chemical Physics Letters. 2006;418(1-3):223-229.
doi:10.1016/j.cplett.2005.10.130 .

Mijin, Dušan, Ušćumlić, Gordana, Perišić-Janjić, Nada, Valentić, Nataša, "Substituent and solvent effects on the UV/vis absorption spectra of 5-(3-and 4-substituted arylazo)-4,6-dimethyl-3-eyano-2-pyridones" in Chemical Physics Letters, 418, no. 1-3 (2006):223-229,
https://doi.org/10.1016/j.cplett.2005.10.130 . .

TY  - JOUR
AU  - Mijin, Dušan
AU  - Ušćumlić, Gordana
AU  - Perišić-Janjić, Nada
AU  - Trkulja, Ivan
AU  - Radetić, Maja
AU  - Jovančić, Petar
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/998
AB  - A series of 5-(3- and 4-substituted phenylazo)-4,6-dimethyl-3-cyano-2-pyridones were synthesized, starting from acetylacetone and arenediazonium salt, followed by condensation with cyanoacetamide using a modified literature procedure. The experimental investigation included modification of the synthetic procedure in terms of solvent, temperature, isolation techniques as well as purification and identification of the products. The azo dyes were characterized by melting point, IR, UV/Vis, 1H NMR and MS data. HPLC analyses were also performed. The 2-hydroxypyridine/ 2-pyridone tautomeric equilibration was found to depend on the polarity of the applied solvents. A color assessment of the solid dyes and dyed polyester fabrics was also performed and the correlation between the colour and the structure of the dyes is discussed.
AB  - U okviru rada sintetisani su 5-(3- i 4-supstituisani fenilazo)-4,6-dimetil-3-cijano- 2-piridoni, kondenzacijom proizvoda reakcije acetilacetona i odgovarajuće diazonijumove soli sa cijanoacetamidom. Dobijene azo boje su okarakterisane temperaturama topljenja, IR, UV/Vis, 1 HNMRi MS podacima. Čistoća dobijenih boja ispitivana je HPLC metodom. Utvrđeno je da ravnoteža 2-hidroksipiridin/2-piridon zavisi od polarnosti rastvarača. Određeni su parametri obojenja poliestarskih tkanina bojenih sintetisanim azo bojama. Takođe je ispitivana i obojenost azo boja u čvrstom obliku.
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis, properties and color assessment of some new 5-(3- and 4-substituted phenylazo)-4,6-dimethyl-3-cyano-2-pyridones
T1  - Sinteza, svojstva i obojenost nekih novih 5-(3- i 4-supstituisanih fenilazo)-4,6-dimetil-3-cijano-2-piridona
EP  - 444
IS  - 5
SP  - 435
VL  - 71
UR  - https://hdl.handle.net/21.15107/rcub_technorep_998
ER  - 

@article{
author = "Mijin, Dušan and Ušćumlić, Gordana and Perišić-Janjić, Nada and Trkulja, Ivan and Radetić, Maja and Jovančić, Petar",
year = "2006",
abstract = "A series of 5-(3- and 4-substituted phenylazo)-4,6-dimethyl-3-cyano-2-pyridones were synthesized, starting from acetylacetone and arenediazonium salt, followed by condensation with cyanoacetamide using a modified literature procedure. The experimental investigation included modification of the synthetic procedure in terms of solvent, temperature, isolation techniques as well as purification and identification of the products. The azo dyes were characterized by melting point, IR, UV/Vis, 1H NMR and MS data. HPLC analyses were also performed. The 2-hydroxypyridine/ 2-pyridone tautomeric equilibration was found to depend on the polarity of the applied solvents. A color assessment of the solid dyes and dyed polyester fabrics was also performed and the correlation between the colour and the structure of the dyes is discussed., U okviru rada sintetisani su 5-(3- i 4-supstituisani fenilazo)-4,6-dimetil-3-cijano- 2-piridoni, kondenzacijom proizvoda reakcije acetilacetona i odgovarajuće diazonijumove soli sa cijanoacetamidom. Dobijene azo boje su okarakterisane temperaturama topljenja, IR, UV/Vis, 1 HNMRi MS podacima. Čistoća dobijenih boja ispitivana je HPLC metodom. Utvrđeno je da ravnoteža 2-hidroksipiridin/2-piridon zavisi od polarnosti rastvarača. Određeni su parametri obojenja poliestarskih tkanina bojenih sintetisanim azo bojama. Takođe je ispitivana i obojenost azo boja u čvrstom obliku.",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis, properties and color assessment of some new 5-(3- and 4-substituted phenylazo)-4,6-dimethyl-3-cyano-2-pyridones, Sinteza, svojstva i obojenost nekih novih 5-(3- i 4-supstituisanih fenilazo)-4,6-dimetil-3-cijano-2-piridona",
pages = "444-435",
number = "5",
volume = "71",
url = "https://hdl.handle.net/21.15107/rcub_technorep_998"
}

Mijin, D., Ušćumlić, G., Perišić-Janjić, N., Trkulja, I., Radetić, M.,& Jovančić, P.. (2006). Synthesis, properties and color assessment of some new 5-(3- and 4-substituted phenylazo)-4,6-dimethyl-3-cyano-2-pyridones. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 71(5), 435-444.
https://hdl.handle.net/21.15107/rcub_technorep_998

Mijin D, Ušćumlić G, Perišić-Janjić N, Trkulja I, Radetić M, Jovančić P. Synthesis, properties and color assessment of some new 5-(3- and 4-substituted phenylazo)-4,6-dimethyl-3-cyano-2-pyridones. in Journal of the Serbian Chemical Society. 2006;71(5):435-444.
https://hdl.handle.net/21.15107/rcub_technorep_998 .

Mijin, Dušan, Ušćumlić, Gordana, Perišić-Janjić, Nada, Trkulja, Ivan, Radetić, Maja, Jovančić, Petar, "Synthesis, properties and color assessment of some new 5-(3- and 4-substituted phenylazo)-4,6-dimethyl-3-cyano-2-pyridones" in Journal of the Serbian Chemical Society, 71, no. 5 (2006):435-444,
https://hdl.handle.net/21.15107/rcub_technorep_998 .

TY  - JOUR
AU  - Perišić-Janjić, Nada
AU  - Ušćumlić, Gordana
AU  - Mijin, Dušan
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/921
AB  - The chromatographic behavior of series of azo-dye derivatives has been studied by RP C-18 TLC with water-methanol, water-acetone, water-dioxane, and water-acetonitrile mobile phases. The mechanism of retention was investigated and the retention constants, R-M(0), were determined by extrapolation. Correlations between retention constants, R-M(0), and lipophificity, C-0 (C-0 = R-M(0)/m) and log P (ACD log P) were investigated. Better correlations were obtained between C-0 and log P than between R-M(0) and log P. These C-0 values may be use as a measure of the lipophilicity of the compounds investigated. The effect of mobile phase pH on retention of azo-dye derivatives was studied in RP C-18 TLC with diluted acetic acid-methanol, 20 + 30 (v/v) as mobile phase. Different methods were used to measure mobile phase pH. pK(a) values were determined on the basis of the relationships between analyte retention and mobile phase pH. Because the investigated azo dyes are newly synthesized compounds these pK(a) values have been determined for the first time. Correlations between pK(a) and log P are discussed.
PB  - Akademiai Kiado Zrt, Budapest
T2  - JPC-Journal of Planar Chromatography-Modern Tlc
T1  - RP TLC of some newly synthesized azo-dye derivatives
EP  - 103
IS  - 108
SP  - 98
VL  - 19
DO  - 10.1556/JPC.19.2006.2.2
ER  - 

@article{
author = "Perišić-Janjić, Nada and Ušćumlić, Gordana and Mijin, Dušan",
year = "2006",
abstract = "The chromatographic behavior of series of azo-dye derivatives has been studied by RP C-18 TLC with water-methanol, water-acetone, water-dioxane, and water-acetonitrile mobile phases. The mechanism of retention was investigated and the retention constants, R-M(0), were determined by extrapolation. Correlations between retention constants, R-M(0), and lipophificity, C-0 (C-0 = R-M(0)/m) and log P (ACD log P) were investigated. Better correlations were obtained between C-0 and log P than between R-M(0) and log P. These C-0 values may be use as a measure of the lipophilicity of the compounds investigated. The effect of mobile phase pH on retention of azo-dye derivatives was studied in RP C-18 TLC with diluted acetic acid-methanol, 20 + 30 (v/v) as mobile phase. Different methods were used to measure mobile phase pH. pK(a) values were determined on the basis of the relationships between analyte retention and mobile phase pH. Because the investigated azo dyes are newly synthesized compounds these pK(a) values have been determined for the first time. Correlations between pK(a) and log P are discussed.",
publisher = "Akademiai Kiado Zrt, Budapest",
journal = "JPC-Journal of Planar Chromatography-Modern Tlc",
title = "RP TLC of some newly synthesized azo-dye derivatives",
pages = "103-98",
number = "108",
volume = "19",
doi = "10.1556/JPC.19.2006.2.2"
}

Perišić-Janjić, N., Ušćumlić, G.,& Mijin, D.. (2006). RP TLC of some newly synthesized azo-dye derivatives. in JPC-Journal of Planar Chromatography-Modern Tlc
Akademiai Kiado Zrt, Budapest., 19(108), 98-103.
https://doi.org/10.1556/JPC.19.2006.2.2

Perišić-Janjić N, Ušćumlić G, Mijin D. RP TLC of some newly synthesized azo-dye derivatives. in JPC-Journal of Planar Chromatography-Modern Tlc. 2006;19(108):98-103.
doi:10.1556/JPC.19.2006.2.2 .

Perišić-Janjić, Nada, Ušćumlić, Gordana, Mijin, Dušan, "RP TLC of some newly synthesized azo-dye derivatives" in JPC-Journal of Planar Chromatography-Modern Tlc, 19, no. 108 (2006):98-103,
https://doi.org/10.1556/JPC.19.2006.2.2 . .

TY  - JOUR
AU  - Perišić-Janjić, Nada
AU  - Ušćumlić, Gordana
AU  - Valentić, Nataša
PY  - 2005
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/824
AB  - The chromatographic behavior of newly synthesized uracil derivatives has been studied by normal and reversed-phase thin-layer chromatography. Benzene-methanol, benzene-acetonitrile, and benzene-isopropanol were used as mobile phases in normal-phase chromatography and water-methanol and water-acetonitrile in reversed-phase chromatography. The mechanism of retention on different TLC supports was investigated. The retention constants determined for the uracils are discussed in terms of the physicochemical properties of both the solutes and stationary and mobile phases. R-M(0) values derived by extrapolation from reversed-phase chromatography were correlated with the hydrophobicity log P calculated by use of the commercial program ACD/logP. In normal-phase chromatography values for C-0 (= R-M(0/n)) were correlated with the hydrophobicity log P. Good correlation was obtained for both types of chromatography. Retention constants R-M(0) and C-0 can be used to express the lipophilicity of the compounds investigated.
PB  - Research Inst Medicinal Plants, Budakalasz
T2  - JPC-Journal of Planar Chromatography-Modern Tlc
T1  - The retention behavior of some uracil derivatives in normal and reversed-phase chromatography. Lipophilicity of the compounds
EP  - 97
IS  - 102
SP  - 92
VL  - 18
DO  - 10.1556/JPC.18.2005.2.1
ER  - 

@article{
author = "Perišić-Janjić, Nada and Ušćumlić, Gordana and Valentić, Nataša",
year = "2005",
abstract = "The chromatographic behavior of newly synthesized uracil derivatives has been studied by normal and reversed-phase thin-layer chromatography. Benzene-methanol, benzene-acetonitrile, and benzene-isopropanol were used as mobile phases in normal-phase chromatography and water-methanol and water-acetonitrile in reversed-phase chromatography. The mechanism of retention on different TLC supports was investigated. The retention constants determined for the uracils are discussed in terms of the physicochemical properties of both the solutes and stationary and mobile phases. R-M(0) values derived by extrapolation from reversed-phase chromatography were correlated with the hydrophobicity log P calculated by use of the commercial program ACD/logP. In normal-phase chromatography values for C-0 (= R-M(0/n)) were correlated with the hydrophobicity log P. Good correlation was obtained for both types of chromatography. Retention constants R-M(0) and C-0 can be used to express the lipophilicity of the compounds investigated.",
publisher = "Research Inst Medicinal Plants, Budakalasz",
journal = "JPC-Journal of Planar Chromatography-Modern Tlc",
title = "The retention behavior of some uracil derivatives in normal and reversed-phase chromatography. Lipophilicity of the compounds",
pages = "97-92",
number = "102",
volume = "18",
doi = "10.1556/JPC.18.2005.2.1"
}

Perišić-Janjić, N., Ušćumlić, G.,& Valentić, N.. (2005). The retention behavior of some uracil derivatives in normal and reversed-phase chromatography. Lipophilicity of the compounds. in JPC-Journal of Planar Chromatography-Modern Tlc
Research Inst Medicinal Plants, Budakalasz., 18(102), 92-97.
https://doi.org/10.1556/JPC.18.2005.2.1

Perišić-Janjić N, Ušćumlić G, Valentić N. The retention behavior of some uracil derivatives in normal and reversed-phase chromatography. Lipophilicity of the compounds. in JPC-Journal of Planar Chromatography-Modern Tlc. 2005;18(102):92-97.
doi:10.1556/JPC.18.2005.2.1 .

Perišić-Janjić, Nada, Ušćumlić, Gordana, Valentić, Nataša, "The retention behavior of some uracil derivatives in normal and reversed-phase chromatography. Lipophilicity of the compounds" in JPC-Journal of Planar Chromatography-Modern Tlc, 18, no. 102 (2005):92-97,
https://doi.org/10.1556/JPC.18.2005.2.1 . .

TY  - JOUR
AU  - Đaković-Sekulić, Tatjana
AU  - Perišić-Janjić, Nada
AU  - Petrović, Slobodan
PY  - 2003
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/524
AB  - The chromatographic behavior of Para-substituted amides of alpha-phenylacetic, benzoic, propanoic, and 2,2-dimethylpropanoic acid has been studied in reversed-phase thin-layer chromatography on silica gel impregnated with paraffin oil. Mobile phases used were acetone-water, methanol-water, and dioxane-water. R-M(0) values were calculated by linear extrapolation of retention to 0% organic modifier for each mobile phase. The relationships between R-M(0) Values obtained with different organic modifiers in the mobile phases are discussed. C-0 values were obtained from the slopes and intercepts of linear relationships between retention and volume fraction of modifier. Correlation between partition coefficient, log P, and R-M(0) and between log P and C-0 was examined. Results show that C-0 is a better measure of the lipophilicity of the amides than R-M(0).
PB  - Springer Heidelberg, Heidelberg
T2  - JPC-Journal of Planar Chromatography-Modern Tlc
T1  - Influence of the mobile-phase modifier on the retention of some para-substituted amides; Correlation with compound lipophilicity
EP  - 153
IS  - 2
SP  - 147
VL  - 16
DO  - 10.1556/JPC.16.2003.2.12
ER  - 

@article{
author = "Đaković-Sekulić, Tatjana and Perišić-Janjić, Nada and Petrović, Slobodan",
year = "2003",
abstract = "The chromatographic behavior of Para-substituted amides of alpha-phenylacetic, benzoic, propanoic, and 2,2-dimethylpropanoic acid has been studied in reversed-phase thin-layer chromatography on silica gel impregnated with paraffin oil. Mobile phases used were acetone-water, methanol-water, and dioxane-water. R-M(0) values were calculated by linear extrapolation of retention to 0% organic modifier for each mobile phase. The relationships between R-M(0) Values obtained with different organic modifiers in the mobile phases are discussed. C-0 values were obtained from the slopes and intercepts of linear relationships between retention and volume fraction of modifier. Correlation between partition coefficient, log P, and R-M(0) and between log P and C-0 was examined. Results show that C-0 is a better measure of the lipophilicity of the amides than R-M(0).",
publisher = "Springer Heidelberg, Heidelberg",
journal = "JPC-Journal of Planar Chromatography-Modern Tlc",
title = "Influence of the mobile-phase modifier on the retention of some para-substituted amides; Correlation with compound lipophilicity",
pages = "153-147",
number = "2",
volume = "16",
doi = "10.1556/JPC.16.2003.2.12"
}

Đaković-Sekulić, T., Perišić-Janjić, N.,& Petrović, S.. (2003). Influence of the mobile-phase modifier on the retention of some para-substituted amides; Correlation with compound lipophilicity. in JPC-Journal of Planar Chromatography-Modern Tlc
Springer Heidelberg, Heidelberg., 16(2), 147-153.
https://doi.org/10.1556/JPC.16.2003.2.12

Đaković-Sekulić T, Perišić-Janjić N, Petrović S. Influence of the mobile-phase modifier on the retention of some para-substituted amides; Correlation with compound lipophilicity. in JPC-Journal of Planar Chromatography-Modern Tlc. 2003;16(2):147-153.
doi:10.1556/JPC.16.2003.2.12 .

Đaković-Sekulić, Tatjana, Perišić-Janjić, Nada, Petrović, Slobodan, "Influence of the mobile-phase modifier on the retention of some para-substituted amides; Correlation with compound lipophilicity" in JPC-Journal of Planar Chromatography-Modern Tlc, 16, no. 2 (2003):147-153,
https://doi.org/10.1556/JPC.16.2003.2.12 . .

TY  - JOUR
AU  - Đaković-Sekulić, Tatjana
AU  - Perišić-Janjić, Nada
AU  - Petrović, Slobodan
PY  - 2002
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/425
AB  - The chromatographic behavior of newly synthesized para-substituted propanoic acid amides has been studied in normal- and reversed-phase thin-layer chromatography. The retention mechanism on different TLC supports was investigated. The retention constants determined for the amides are discussed in terms of the physicochernical properties of the solute and the stationary and mobile phases. R-M,R-w, derived by extrapolation from retention in reversed-phase chromatography, was correlated with hydrophobic parameters pi and log P, calculated by the Rekker fragmental method and by use of the commercial program ACD/log P.
PB  - Springer Heidelberg, Heidelberg
T2  - JPC-Journal of Planar Chromatography-Modern Tlc
T1  - Normal- and reversed-phase chromatography of para-substituted propanoic acid Amides
EP  - 279
IS  - 4
SP  - 274
VL  - 15
DO  - 10.1556/JPC.15.2002.4.6
ER  - 

@article{
author = "Đaković-Sekulić, Tatjana and Perišić-Janjić, Nada and Petrović, Slobodan",
year = "2002",
abstract = "The chromatographic behavior of newly synthesized para-substituted propanoic acid amides has been studied in normal- and reversed-phase thin-layer chromatography. The retention mechanism on different TLC supports was investigated. The retention constants determined for the amides are discussed in terms of the physicochernical properties of the solute and the stationary and mobile phases. R-M,R-w, derived by extrapolation from retention in reversed-phase chromatography, was correlated with hydrophobic parameters pi and log P, calculated by the Rekker fragmental method and by use of the commercial program ACD/log P.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "JPC-Journal of Planar Chromatography-Modern Tlc",
title = "Normal- and reversed-phase chromatography of para-substituted propanoic acid Amides",
pages = "279-274",
number = "4",
volume = "15",
doi = "10.1556/JPC.15.2002.4.6"
}

Đaković-Sekulić, T., Perišić-Janjić, N.,& Petrović, S.. (2002). Normal- and reversed-phase chromatography of para-substituted propanoic acid Amides. in JPC-Journal of Planar Chromatography-Modern Tlc
Springer Heidelberg, Heidelberg., 15(4), 274-279.
https://doi.org/10.1556/JPC.15.2002.4.6

Đaković-Sekulić T, Perišić-Janjić N, Petrović S. Normal- and reversed-phase chromatography of para-substituted propanoic acid Amides. in JPC-Journal of Planar Chromatography-Modern Tlc. 2002;15(4):274-279.
doi:10.1556/JPC.15.2002.4.6 .

Đaković-Sekulić, Tatjana, Perišić-Janjić, Nada, Petrović, Slobodan, "Normal- and reversed-phase chromatography of para-substituted propanoic acid Amides" in JPC-Journal of Planar Chromatography-Modern Tlc, 15, no. 4 (2002):274-279,
https://doi.org/10.1556/JPC.15.2002.4.6 . .

TY  - JOUR
AU  - Đaković-Sekulić, Tatjana
AU  - Petrović, SM
AU  - Perišić-Janjić, Nada
AU  - Petrović, Slobodan
PY  - 2001
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/382
AB  - The chromatographic behavior of para substituted anilides of 2,2-dimethylpropanoic, benzoic and alpha -phenyl acetic acid has been studied by reversed-phase high performance liquid chromatography HPLC was performed on a C-18 column with various aqueous methanol mobile phases. The Influence on the retention of anilide type and additional substituents in the molecule is discussed. Several chromatographic hydrophobicity parameters (CHP) have been calculated by linear correlation between log k of the investigated compounds and the concentration of methanol in the mobile phase. The chromatographic hydrophobicity parameters were compared with the log P values calculated by Rekker's fragmental method. The results show moderate correlations of CHIP with log Mus, multiple linear regressions have been applied. It was found that besides log P even the electronic effects of individual polar groups capable of hydrogen bonding proved to be very important in hydrophobic characterization of the molecule.
PB  - Springer Heidelberg, Heidelberg
T2  - Chromatographia
T1  - HPLC behavior and hydrophobic parameters of some anilides
EP  - 64
IS  - 1-2
SP  - 60
VL  - 54
DO  - 10.1007/BF02491834
ER  - 

@article{
author = "Đaković-Sekulić, Tatjana and Petrović, SM and Perišić-Janjić, Nada and Petrović, Slobodan",
year = "2001",
abstract = "The chromatographic behavior of para substituted anilides of 2,2-dimethylpropanoic, benzoic and alpha -phenyl acetic acid has been studied by reversed-phase high performance liquid chromatography HPLC was performed on a C-18 column with various aqueous methanol mobile phases. The Influence on the retention of anilide type and additional substituents in the molecule is discussed. Several chromatographic hydrophobicity parameters (CHP) have been calculated by linear correlation between log k of the investigated compounds and the concentration of methanol in the mobile phase. The chromatographic hydrophobicity parameters were compared with the log P values calculated by Rekker's fragmental method. The results show moderate correlations of CHIP with log Mus, multiple linear regressions have been applied. It was found that besides log P even the electronic effects of individual polar groups capable of hydrogen bonding proved to be very important in hydrophobic characterization of the molecule.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Chromatographia",
title = "HPLC behavior and hydrophobic parameters of some anilides",
pages = "64-60",
number = "1-2",
volume = "54",
doi = "10.1007/BF02491834"
}

Đaković-Sekulić, T., Petrović, S., Perišić-Janjić, N.,& Petrović, S.. (2001). HPLC behavior and hydrophobic parameters of some anilides. in Chromatographia
Springer Heidelberg, Heidelberg., 54(1-2), 60-64.
https://doi.org/10.1007/BF02491834

Đaković-Sekulić T, Petrović S, Perišić-Janjić N, Petrović S. HPLC behavior and hydrophobic parameters of some anilides. in Chromatographia. 2001;54(1-2):60-64.
doi:10.1007/BF02491834 .

Đaković-Sekulić, Tatjana, Petrović, SM, Perišić-Janjić, Nada, Petrović, Slobodan, "HPLC behavior and hydrophobic parameters of some anilides" in Chromatographia, 54, no. 1-2 (2001):60-64,
https://doi.org/10.1007/BF02491834 . .

TY  - JOUR
AU  - Podunavac-Kuzmanović, Sanja O.
AU  - Leovac, VM
AU  - Perišić-Janjić, Nada
AU  - Rogan, Jelena
AU  - Balaz, J
PY  - 1999
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/230
AB  - The preparation and properties of some complexes of cobalt(II), zinc(II) and copper(II) with several newly synthesized benzimidazole derivatives (L) are reported, The complexes, of the general formula [MCl2(L)over dot(2)] (M=CO(II), Zn(II)) and [CuCl2L(H2O]), have a tetrahedral structure. The complexes were characterized by elemental analysis, molar conductivity, magnetic susceptibility measurements, IR and absorption electronic spectra. The antibacterial activity of the benzimidazoles and their complexes was evaluated against Erwinia carotovora subsp. carotovora and Erwinia amylovora. The complexes were found to be more toxic than the ligands.
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Complexes cobalt(II), zinc(II) and copper(II) with some newly synthesized benzimidazole derivatives and their antibacterial activity
EP  - 388
IS  - 5-6
SP  - 381
VL  - 64
DO  - 10.2298/jsc9906381p
ER  - 

@article{
author = "Podunavac-Kuzmanović, Sanja O. and Leovac, VM and Perišić-Janjić, Nada and Rogan, Jelena and Balaz, J",
year = "1999",
abstract = "The preparation and properties of some complexes of cobalt(II), zinc(II) and copper(II) with several newly synthesized benzimidazole derivatives (L) are reported, The complexes, of the general formula [MCl2(L)over dot(2)] (M=CO(II), Zn(II)) and [CuCl2L(H2O]), have a tetrahedral structure. The complexes were characterized by elemental analysis, molar conductivity, magnetic susceptibility measurements, IR and absorption electronic spectra. The antibacterial activity of the benzimidazoles and their complexes was evaluated against Erwinia carotovora subsp. carotovora and Erwinia amylovora. The complexes were found to be more toxic than the ligands.",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Complexes cobalt(II), zinc(II) and copper(II) with some newly synthesized benzimidazole derivatives and their antibacterial activity",
pages = "388-381",
number = "5-6",
volume = "64",
doi = "10.2298/jsc9906381p"
}

Podunavac-Kuzmanović, S. O., Leovac, V., Perišić-Janjić, N., Rogan, J.,& Balaz, J.. (1999). Complexes cobalt(II), zinc(II) and copper(II) with some newly synthesized benzimidazole derivatives and their antibacterial activity. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 64(5-6), 381-388.
https://doi.org/10.2298/jsc9906381p

Podunavac-Kuzmanović SO, Leovac V, Perišić-Janjić N, Rogan J, Balaz J. Complexes cobalt(II), zinc(II) and copper(II) with some newly synthesized benzimidazole derivatives and their antibacterial activity. in Journal of the Serbian Chemical Society. 1999;64(5-6):381-388.
doi:10.2298/jsc9906381p .

Podunavac-Kuzmanović, Sanja O., Leovac, VM, Perišić-Janjić, Nada, Rogan, Jelena, Balaz, J, "Complexes cobalt(II), zinc(II) and copper(II) with some newly synthesized benzimidazole derivatives and their antibacterial activity" in Journal of the Serbian Chemical Society, 64, no. 5-6 (1999):381-388,
https://doi.org/10.2298/jsc9906381p . .

TY  - JOUR
AU  - Đaković-Sekulić, Tatjana
AU  - Perišić-Janjić, Nada
AU  - Petrović, Slobodan
PY  - 1997
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/132
AB  - The TLC retention behavior of formanilide and I substituted acetanilides on starch and cellulose layers has been studied using aqueous mobile phases with methanol, acetonitrile, acetone, and 1-propanol as modifiers, R-Mw values derived by linear extrapolation of the plot of R-M against volume fraction of organic modifier to 100% water are not dependent on the nature of the organic modifier, Correlation was observed between R-Mw values on starch and cellulose layers, Because R-M values are related to the partitioning of the solute molecules in the given system, they can be regarded as a measure of a solute's hydrophobicity, We correlated R-Mw values with the lipophilicity parameters, pi and logP; the quadratic equation fit the data well, Multiple regression analyses was, furthermore, successfully applied with pi, sigma, and HD as independent variables? suggesting that the electronic properties and hydrogen bonding of the substituent participate in the retention mechanism.
PB  - Akademiai Kiado Zrt, Budapest
T2  - JPC-Journal of Planar Chromatography-Modern Tlc
T1  - The retention behavior of some anilides on unconventional TLC supports
EP  - 302
IS  - 4
SP  - 298
VL  - 10
UR  - https://hdl.handle.net/21.15107/rcub_technorep_132
ER  - 

@article{
author = "Đaković-Sekulić, Tatjana and Perišić-Janjić, Nada and Petrović, Slobodan",
year = "1997",
abstract = "The TLC retention behavior of formanilide and I substituted acetanilides on starch and cellulose layers has been studied using aqueous mobile phases with methanol, acetonitrile, acetone, and 1-propanol as modifiers, R-Mw values derived by linear extrapolation of the plot of R-M against volume fraction of organic modifier to 100% water are not dependent on the nature of the organic modifier, Correlation was observed between R-Mw values on starch and cellulose layers, Because R-M values are related to the partitioning of the solute molecules in the given system, they can be regarded as a measure of a solute's hydrophobicity, We correlated R-Mw values with the lipophilicity parameters, pi and logP; the quadratic equation fit the data well, Multiple regression analyses was, furthermore, successfully applied with pi, sigma, and HD as independent variables? suggesting that the electronic properties and hydrogen bonding of the substituent participate in the retention mechanism.",
publisher = "Akademiai Kiado Zrt, Budapest",
journal = "JPC-Journal of Planar Chromatography-Modern Tlc",
title = "The retention behavior of some anilides on unconventional TLC supports",
pages = "302-298",
number = "4",
volume = "10",
url = "https://hdl.handle.net/21.15107/rcub_technorep_132"
}

Đaković-Sekulić, T., Perišić-Janjić, N.,& Petrović, S.. (1997). The retention behavior of some anilides on unconventional TLC supports. in JPC-Journal of Planar Chromatography-Modern Tlc
Akademiai Kiado Zrt, Budapest., 10(4), 298-302.
https://hdl.handle.net/21.15107/rcub_technorep_132

Đaković-Sekulić T, Perišić-Janjić N, Petrović S. The retention behavior of some anilides on unconventional TLC supports. in JPC-Journal of Planar Chromatography-Modern Tlc. 1997;10(4):298-302.
https://hdl.handle.net/21.15107/rcub_technorep_132 .

Đaković-Sekulić, Tatjana, Perišić-Janjić, Nada, Petrović, Slobodan, "The retention behavior of some anilides on unconventional TLC supports" in JPC-Journal of Planar Chromatography-Modern Tlc, 10, no. 4 (1997):298-302,
https://hdl.handle.net/21.15107/rcub_technorep_132 .

TY  - JOUR
AU  - Perišić-Janjić, Nada
AU  - Petrović, S.M.
AU  - Đaković, T.
AU  - Nikolić, A.D.
AU  - Petrović, Slobodan
PY  - 1992
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/41
AB  - The retention behavior and separation ability of reversed- and normal-phase TLC with, polar and nonpolar mobile phases, has been studied by measuring the retentions of a series of amides. The retention behavior and separation ability are discussed in terms of the nature of the solute, stationary phase and eluent.
PB  - Springer Heidelberg, Heidelberg
T2  - Chromatographia
T1  - Retention behavior of some amides in reversed- and normal-phase thin-layer chromatography
EP  - 539
IS  - 9-10
SP  - 537
VL  - 34
DO  - 10.1007/BF02290249
ER  - 

@article{
author = "Perišić-Janjić, Nada and Petrović, S.M. and Đaković, T. and Nikolić, A.D. and Petrović, Slobodan",
year = "1992",
abstract = "The retention behavior and separation ability of reversed- and normal-phase TLC with, polar and nonpolar mobile phases, has been studied by measuring the retentions of a series of amides. The retention behavior and separation ability are discussed in terms of the nature of the solute, stationary phase and eluent.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Chromatographia",
title = "Retention behavior of some amides in reversed- and normal-phase thin-layer chromatography",
pages = "539-537",
number = "9-10",
volume = "34",
doi = "10.1007/BF02290249"
}

Perišić-Janjić, N., Petrović, S.M., Đaković, T., Nikolić, A.D.,& Petrović, S.. (1992). Retention behavior of some amides in reversed- and normal-phase thin-layer chromatography. in Chromatographia
Springer Heidelberg, Heidelberg., 34(9-10), 537-539.
https://doi.org/10.1007/BF02290249

Perišić-Janjić N, Petrović S, Đaković T, Nikolić A, Petrović S. Retention behavior of some amides in reversed- and normal-phase thin-layer chromatography. in Chromatographia. 1992;34(9-10):537-539.
doi:10.1007/BF02290249 .

Perišić-Janjić, Nada, Petrović, S.M., Đaković, T., Nikolić, A.D., Petrović, Slobodan, "Retention behavior of some amides in reversed- and normal-phase thin-layer chromatography" in Chromatographia, 34, no. 9-10 (1992):537-539,
https://doi.org/10.1007/BF02290249 . .