Azo Dye Tautomeric Structures Determined by Laser-Raman Spectroscopy

Author:

Trotter P. J.1

Affiliation:

1. Research Laboratories, Eastman Kodak Company, Rochester, New York 14650

Abstract

Raman spectra of a number of azo dye structures have been analyzed. In azonaphthol and azopyrazol dyes, hydroxyazo to keto-hydrazone tautomerizations, [Formula: see text] were observed in aqueous basic and acidic media. Observations of azo and ring vibrations, as well as hydrazone (C=N plus C=0) bands, were made. It was noted that the azo-anions (examined at pH 12) convert to the protonated neutral hydrazone (keto) form in aqueous acid (run at pH 2). Infrared spectra were used to confirm the presence of the C=0 group in keto-tautomeric forms.

Publisher

SAGE Publications

Subject

Spectroscopy,Instrumentation

Reference24 articles.

1. (a) Herzberg G., Infrared and Raman Spectra of Polymeric Molecules (Van Nostrand Reinhold, New York, 1945), p. 256;

2. The Infra-red Spectra of Complex Molecules

3. Infrared and Raman spectra of solid and matrix isolated diimide, HNNH

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