| Autor: |
Bogdanov, V. S., Krylov, S. S., Shvedova, S. N., Tartakoyskii, V. A. |
| Zdroj: |
Russian Chemical Bulletin; September 1987, Vol. 36 Issue: 9 p1829-1834, 6p |
| Abstrakt: |
1.13C and1H NMR has been used in investigating the structure of azacations. It has been found that the cations exist in the form of Immonium salts, and the contribution of the limiting structure, which is an aminocarbonium ion, is small. The cations of the protonated imines have mainly the trans configuration.2.The presence of aryl substituents leads to partial delocalization of plus charge from the N=C bond onto the aromatic rings bonded to the N atom and/or to the methylene C atom.3.A determination has been made of ß-Isotope effects on $$\delta ^{13} C\mathop N\limits^ + = C$$ and $$---C---\mathop N\limits^ + = $$ carbons: the deuterium isotope shift of carbon resonance corresponds to an increase in screening of the carbon nuclei. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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