Tautomerism in Salicylidene Benzylamine
- 1 June 1992
- journal article
- research article
- Published by Taylor & Francis in Spectroscopy Letters
- Vol. 25 (4) , 513-519
- https://doi.org/10.1080/00387019208021526
Abstract
The UV spectra of substituted salicylidene benzylamine schiff bases were studied in four solvents. It was found that substituents which increase the electronic effect and not the steric compression effect in these compounds increase the percentage of the keto form. The intensity (i.e. % keto) of the keto band which occurs at > 400 nm in the UV spectra increases in polar solvents.Keywords
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