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Tautomerism in Chlorinated O-Hydroxyschiff Bases: Effect of Chlorine Atom Substitution
Authors:Salman R. Salman  Sawsan H. Shawkat  Ghanim M. Al-obaidi
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
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.
Keywords:Gossypol  gossypol-metal cation complexes  uv-visible absorption spectroscopy
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