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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 |
| Appears in Collections: | Journal Article |
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| 33 Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl.pdf | 746.99 kB | Adobe PDF | Request a copy |
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