Relative predominance of azo and hydrazone tautomers of 4-carboxyl-2,6-dinitrophenylazohydroxynaphthalenes in binary solvent mixtures
Author:
Publisher
Elsevier BV
Subject
Spectroscopy,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry
Reference24 articles.
1. 1H, 13C, NH, HH, CH COSY, HH NOESY NMR and UV–vis studies of Solophenyl red 3BL dye azo-hydrazone tautomerism in various solvents
2. Tautomeric structures, electronic spectra, acid–base properties of some 7-aryl-2,5-diamino-3(4-hydroxyphenyazo)pyrazolo[1,5-a]pyrimidine-6-carbonitriles, and effect of their copper(II) complex solutions on some bacteria and fungi
3. Solvatochromic, acid–base features and time effect of some azo dyes derived from 1,3-benzothiazol-2-ylacetonitrile: Experimental and semiempirical investigations
4. Excited state intramolecular proton transfer in some tautomeric azo dyes and schiff bases containing an intramolecular hydrogen bond
5. Investigation of the interaction between a sulfonated azo dye (AO7) and a TiO2 surface
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3. Preferential Solvation of 4-Carboxyl-2,6-Dinitrophenylazohydroxynaphthalenes in Aqueous Dimethylformamide and Dimethylsulfoxide Binary Mixtures by UV-VIS Spectroscopy;Journal of Applied Spectroscopy;2019-09
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