Author:
Alimmari Adel,Mijin Dušan,Vukićević Radovan,Božić Bojan,Valentić Nataša,Vitnik Vesna,Vitnik Željko,Ušćumlić Gordana
Abstract
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, 1H NMR and 13C 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
Springer Science and Business Media LLC
Cited by
28 articles.
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