4-Carboxyl-2,6-dinitrophenylazohydroxynaphthalenes tautomerism NMR re-explained and other methods verified
Author:
Funder
Swiss National Science Foundation
Bulgarian National Science Fund
Publisher
Elsevier BV
Subject
Process Chemistry and Technology,General Chemical Engineering
Reference25 articles.
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2. Relative predominance of azo and hydrazone tautomers of 4-carboxyl-2,6-dinitrophenylazohydroxynaphthalenes in binary solvent mixtures;Adegoke;Spectrochim. Acta Part A Mol Biomol Spectrosc,2011
3. 4-Carboxyl-2,6-dinitrophenylazohydroxynaphthalenes tautomerism theoretically re-explained;Manolova;Dyes Pigments,2017
4. On the azo/hydrazo equilibrium in Sudan I azo dye derivatives;Ferreira;J Phys Chem A,2013
5. Carbon-13 NMR and x-ray structure determination of 1-(arylazo)-2-naphthols. Intramolecular proton transfer between nitrogen and oxygen atoms in the solid state;Olivieri;J Am Chem Soc,1989
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