Synthesis and spectroscopic properties of new azo dyes derived from 3-Ethylthio-5-cyanomethyl-4-phenyl-1,2,4-triazole

22Citations
Citations of this article
42Readers
Mendeley users who have this article in their library.

Abstract

New 1,2,4-triazole colorants were obtained, in high yields, by coupling 3-ethylthio-5-cyanomethyl-4-phenyl-1,2,4-triazole (1) with diazotized aniline derivatives 2, 4 and 6. The azo dyes prepared in this work may exist in three tautomeric forms. We found that the tautomerism is influenced mainly by the nature of substituent at the para position of the aniline coupling component. This tautomerisation was observed in the NMR spectra of the dyes. The dyes were characterized by IR, 1H-NMR, 13C-NMR and MS spectroscopic techniques.© 2014 by the authors; licensee MDPI, Basel, Switzerland.

Cite

CITATION STYLE

APA

Al-Sheikh, M., Medrasi, H. Y., Sadek, K. U., & Mekheimer, R. A. (2014). Synthesis and spectroscopic properties of new azo dyes derived from 3-Ethylthio-5-cyanomethyl-4-phenyl-1,2,4-triazole. Molecules, 19(3), 2993–3003. https://doi.org/10.3390/molecules19032993

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free