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Abstrakty
A new series of tricarbonyl compounds, in which the keto groups are at tached to olefinic linkages, have been synthesized by the reaction between acetoacetanilide and aromatic aldehydes (2-chlorobenzaldehyde, 4-chlorobenzaldehyde, 4-hydroxybenzaldehyde and vanillin) under specified conditions. Their IR, 1H NMR and mass spectral data revaealed that only one of the carbonyl groups is enolised and engaged in intramolecular hydrogen bonding. Neutral bidentate coordination of these compounds with Ni(II), Cu(II) and Zn(II) has been established on the basis of analytical and spectral data.
Wydawca
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Rocznik
Tom
Strony
963--971
Opis fizyczny
Bibliogr. 25 poz., rys.
Twórcy
autor
autor
- Department of Chemistry, Unity Women's College, Manjeri, Kerala - 676122, India, mbummathur@rediffmail.com
Bibliografia
- 1. Krishnankutty K., Sayudevi P. and Ummathur M.B., J. Indian Chem. Soc., 84, 337 (2007).
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ6-0024-0106