## 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
Electron spin resonance study of some polycyclic nitrogen heterocyclic radical anions
✍ Scribed by Arjen J. L. Sevenster; Brian J. Tabner
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 468 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
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 phenazine. The ESR spectra of the radical anions of dibenzolf,h]quinoxaline and dibenzo[a,c]phenazine have been interpreted by computer reconstruction and the hyperhe splitting constants assigned with the aid of Hiickel unpaired electron density calculations.
* Author to whom correspondence should be addressed. lyte. Solutions of the radical anions were prepared for ESR study as described in Ref. 17.
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