## Abstract 3‐Amino‐2‐cyano‐4,6‐disubstituted‐thieno{2,3‐b}pyridines and 3‐aminopyridine were diazotized and coupled with 2‐phenylindole, 2‐methylindole, and 1‐methyl‐2‐phenylindole, respectively. These dyes were characterized by UV‐Visible, FT‐IR, ^1^H NMR, and mass spectroscopic techniques. Solve
1H NMR spectra of a series of disperse azo dyes
✍ Scribed by L. A. Fedorov; P. Savarino; V. I. Dostovalova; G. Viscardi; R. Carpignano; E. Barni
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 134 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^1^H NMR spectra of a series of disperse monoazo dyes in solution are reported and analysed in terms of electronic effects of the substituents, rotational isomerism and hydrogen bonding.
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