Tautomerism in salicylidenebenzylamine

Fadhil S. Kamounah, Sawsan H. Shawkat, Salman R. Salman

Research output: Contribution to journalJournal articleResearchpeer-review

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.
Original languageEnglish
Article number44
JournalSpectroscopy Letters
Volume25
Issue number4
Pages (from-to)513-519
Number of pages7
ISSN0038-7010
DOIs
Publication statusPublished - 1992
Externally publishedYes

Cite this