The mechanism of addition reactions of radicals formed during thermal decomposition of benzoyl peroxide with various chloro-substituted p-benzoquinones has been studied by the ESR technique in various solvents. The ESR spectra of the intermediate radicals show that addition occurs at the carbonyl ox
✦ LIBER ✦
Addition of radicals to quinones—II. ESR spectra of radicals derived from fluoranil
✍ Scribed by T.L. Simandi; A. Rockenbauer; F. Tüdős
- Book ID
- 107753870
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 316 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0014-3057
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📜 SIMILAR VOLUMES
Addition of radicals to quinones—I. ESR
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Addition of radicals to quinones. ESR st
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## IReactions of 3,3',5,5'-tetra-ferz-butylstilbene-4,4'-quinone with free radicals from the decomposition of azo compounds and peroxides (R') have been studied by ESR spectroscopy. Relatively stable phenoxyl+,pe free radicals are formed via addition of R' across the exo C=C bond. Their coupling c
Nitrogen-centered free radicals. II. Esr
Nitrogen-centered free radicals. II. Esr spectra of the aziridino and azetidino radicals in solution
✍
Wayne C. Danen; Terry T. Kensler
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1971
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⚖ 207 KB