## Abstract Cycloheptatrienyl radicals with donor and acceptor substituents were generated by hydrogen abstraction from the corresponding cycloheptatrienes and studied by EPR spectroscopy. The barrier to rotation about the Cβ1ο£ΏCο£ΎO bond in ethoxycarbonylcycloheptatrienyl radicals was found to be ca.
Substituent effects in cycloheptatrienyl radicals: An ESR spectroscopic study
β Scribed by Reiner Sustmann; Dieter Brandes; Fritz Lange; Hasan I. Tashtoush
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 297 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
ESR spectral parameters of methoxy-, hydroxy-and cyano-substituted cycloheptatrienyl radicals are reported. The radicals were obtained in adamantane matrices by the rearrangement of substituted bicyclo(3.2.0lheptadienyl radicals. The hypefine splitting parameters are interpreted in terms of the effect of donor and acceptor substituents on the degeneracy of the relevant singly occupied Ys or YA ABMO of the cyclobeptatrienyl radical. In addition, an attempt was made to study the deuterium isotope effect on the degenerate MOs at low temperatures in a ['H,,]adamantane matrix.
π SIMILAR VOLUMES
An electron spin resonance (ESR) study of the presence or lack of interference by ionic hardening mechanisms and ionic coreactants on the polyflavonoid tannin radical autocondensation reaction indicated that in certain cases hardening by ionic coreactants can be coupled with the simultaneous hardeni