TY  - JOUR
AU  - Alimmari, Adel S.
AU  - Mijin, Dušan
AU  - Vukicević, Radovan
AU  - Božić, Bojan
AU  - Valentić, Nataša
AU  - Vitnik, Vesna
AU  - Vitnik, Željko
AU  - Ušćumlić, Gordana
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2152
AB  - Background: A series of some novel arylazo pyridone dyes was synthesized from the corresponding diazonium salt and 6-hydroxy-4-phenyl-3-cyano-2-pyridone using a classical reaction for the synthesis of the azo compounds. Results: The structure of the dyes was confirmed by UV-vis, FT-IR, H-1 NMR and C-13 NMR spectroscopic techniques and elemental analysis. The solvatochromic behavior of the dyes was evaluated with respect to their visible absorption properties in various solvents. Conclusions: The azo-hydrazone tautomeric equilibration was found to depend on the substituents as well as on the solvent. The geometry data of the investigated dyes were obtained using DFT quantum-chemical calculations. The obtained calculational results are in very good agreement with the experimental data.
PB  - Springeropen, London
T2  - Chemistry Central Journal
T1  - Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes
VL  - 6
DO  - 10.1186/1752-153X-6-71
ER  - 

@article{
author = "Alimmari, Adel S. and Mijin, Dušan and Vukicević, Radovan and Božić, Bojan and Valentić, Nataša and Vitnik, Vesna and Vitnik, Željko and Ušćumlić, Gordana",
year = "2012",
abstract = "Background: A series of some novel arylazo pyridone dyes was synthesized from the corresponding diazonium salt and 6-hydroxy-4-phenyl-3-cyano-2-pyridone using a classical reaction for the synthesis of the azo compounds. Results: The structure of the dyes was confirmed by UV-vis, FT-IR, H-1 NMR and C-13 NMR spectroscopic techniques and elemental analysis. The solvatochromic behavior of the dyes was evaluated with respect to their visible absorption properties in various solvents. Conclusions: The azo-hydrazone tautomeric equilibration was found to depend on the substituents as well as on the solvent. The geometry data of the investigated dyes were obtained using DFT quantum-chemical calculations. The obtained calculational results are in very good agreement with the experimental data.",
publisher = "Springeropen, London",
journal = "Chemistry Central Journal",
title = "Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes",
volume = "6",
doi = "10.1186/1752-153X-6-71"
}

Alimmari, A. S., Mijin, D., Vukicević, R., Božić, B., Valentić, N., Vitnik, V., Vitnik, Ž.,& Ušćumlić, G.. (2012). Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes. in Chemistry Central Journal
Springeropen, London., 6.
https://doi.org/10.1186/1752-153X-6-71

Alimmari AS, Mijin D, Vukicević R, Božić B, Valentić N, Vitnik V, Vitnik Ž, Ušćumlić G. Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes. in Chemistry Central Journal. 2012;6.
doi:10.1186/1752-153X-6-71 .

Alimmari, Adel S., Mijin, Dušan, Vukicević, Radovan, Božić, Bojan, Valentić, Nataša, Vitnik, Vesna, Vitnik, Željko, Ušćumlić, Gordana, "Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes" in Chemistry Central Journal, 6 (2012),
https://doi.org/10.1186/1752-153X-6-71 . .