Some structural problems and the vibration spectra of a series of N-substituted ethylenimines |
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Authors: | R. R. Shagidullin and N. P. Grechkin |
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Affiliation: | (1) Arbuzov Chemical Institute, AS USSR, Kazan |
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Abstract: | On a basis of comparison of Raman and IR absorption spectra, as well as measurements of intensities and degrees of depolarization of Raman lines, pulsation (breathing) vibrations of the ethylenimine ring -sNin a series of N-substituted ethylenimines are identified. Alkyl substituents increasesNas compared with ethylenimine, probably because of change in the hydridization of the electron clouds of the nitrogen due to steric causes. The high values ofsNfor substituents capable of conjugation effects, is in accord with the hypothesis that the lone electron pair of the nitrogen participates in conjugation. Furthermore, when N enters into the composition of a 3-membered ring, the lone pair exhibits diminished capacity for delocalization. The intensity of the Raman linesN of N-phenylethylenimine is anomalously high, and the cause of this requires explaining. UV spectra are given. |
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