In dimethylformamide the ESR spectra of the radical anions of dibenzoCf,h]quinoxaline and dibenzo[a,c]phenazine both exhibit line broadening due to slow molecular tumbling over a wide temperature range. Similar effects are also observed in the spectra of the radical anions of quinoxaline and phenazi
Electron spin resonance spectrum of the diphenylcyclobutene anion radical
✍ Scribed by Ira B. Goldberg
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 330 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The anion radical of 1,2‐diphenylcyclobutene was studied by electron spin resonance. The hyperfine splittings were found to be 0·47 and 0·74 G for the meta‐positions, 2·23 and 2·69 G for the ortho‐positions and 4·21 G for the para‐positions of the phenyl rings. The methylene proton splittings were 4·27 G, which would imply that the value of Q is 27 G, much lower than that of other cyclobutene anions. It was also estimated that the angle between the axis of the p‐orbitals of the ethylene group and that of the phenyl group is about 30°, in agreement with that found for the tetraphenylethylene anion.
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