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- W2095336718 startingPage "105" @default.
- W2095336718 abstract "Nine new bis-azo dyes derived from 5-arylidene-2,4-thiazolidinone have been synthesized in two steps using Knoevenagel condensation and diazotization-coupling reaction. The structures of the compounds were confirmed by UV-vis, IR, (1)H NMR and (13)C NMR spectroscopic techniques. The spectral characterizations demonstrate that there is an equilibrium between the azo (T1) and hydrazine (T2 and T3) tautomers for all prepared dyes in solutions. In addition, the solvatochromic behavior of the prepared dyes was evaluated using polarity/polarizability parameter (π(*)) in various solvents. The UV-vis absorption spectra of dyes show a bathochromic shift with increasing polarity and base strength of the solvents. Finally, the effects of acid and base on the UV-vis absorption spectra of the dyes with different substituent in diazo component are reported." @default.
- W2095336718 created "2016-06-24" @default.
- W2095336718 creator A5020012881 @default.
- W2095336718 creator A5040016464 @default.
- W2095336718 date "2014-05-01" @default.
- W2095336718 modified "2023-10-06" @default.
- W2095336718 title "Synthesis, structural characterization and tautomeric properties of some novel bis-azo dyes derived from 5-arylidene-2,4-thiazolidinone" @default.
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- W2095336718 doi "https://doi.org/10.1016/j.saa.2014.02.010" @default.
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