| Popis: |
The 13 C NMR spectra of a number of 2,3-dihdyro-1,4-diazepinium salts, like 1 H NMR spectra, confirm shape, and charge distribution for these compounds. The ring has a half-chair shape which is inverting rapidly at room temperature. The atoms in the conjugated portion of the ring show alternating polarity, and phenyl groups attached to these positions act, respectively, as electron-donors or electron-acceptors. A methyl substituent in the saturated portion of the ring shows equal preference for quasi-equatorial and quasi-axial conformations. Some comparisons are drawn between present results and similar results obtained with related benzene derivatives. |
