Tautomerism in Chlorinated O-Hydroxyschiff Bases: Effect of Chlorine Atom Substitution |
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Authors: | Salman R. Salman Sawsan H. Shawkat Ghanim M. Al-obaidi |
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Affiliation: | 1. Chemistry Department , College of Science, University of Baghdad Jadiriya , Baghdad, Iraq;2. Chemistry Department , College of Education, University of Baghdad , Adhamiya, Baghdad, Iraq |
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Abstract: | The UV spectra of some chlorinated o-hydroxyschiff bases were studied in different solvents. It was found that schiff bases derived from condensation of 2-hydroxybenzaldehyde or 5-chloro-2-hydroxy benzaldehyde with substituted aniline exist as enol form, whereas schiff bases derived from the condensation of 3,5-dichloro-2-hydroxybenzaldehyde with substituted aniline exist as enol form, whereas schiff bases derived from the condensation of 3,5-dichloro-2-hydroxybenzaldehyde with aniline exist as keto form especially in dimethyl sulfoxide. The ratio of enol/keto isomers were calculated for these schiff bases. |
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Keywords: | Gossypol gossypol-metal cation complexes uv-visible absorption spectroscopy |
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