Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/841
Title: Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes
Authors: Alimmari, Adel
Mijin, Dušan
Vukićević, Radovan
Božić, Bojan 
Valentić, Nataša
Vitnik, Vesna
Vitnik, Željko
Ušćumlić, Gordana
Keywords: Arylazo pyridone dyes;DFT caculation;Solvent effect;Substituent effect;Tautomerism
Issue Date: 23-Jul-2012
Rank: M21
Journal: Chemistry Central Journal
Volume: 6
Start page: 71
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, 1 H NMR and 13 C 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. © 2012 Alimmari et al.; licensee Chemistry Central Ltd.
URI: https://biore.bio.bg.ac.rs/handle/123456789/841
DOI: 10.1186/1752-153X-6-71
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