Electron spin resonance (ESR) and electron nuclear double resonance (ENDOR) measurements were performed for the cation radicals obtained from the model compounds of c~-, #-, 3'and 6-tocopherol (vitamin E) by oxidizing the tocopherol precursors in an AICI3-CHaCI a solution. The proton hyperfine coupl
Electron spin resonance studies of chromanoxyl radicals derived from tocopherols
โ Scribed by Kazuo Mukai; Noriko Tsuzuki; Setsuhiro Ouchi; Kenji Fukuzawa
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- English
- Weight
- 395 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0009-3084
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โฆ Synopsis
Electron Spin resonance measurements were performed for the chromanoxyl radicals obtained from tx-, ~-, ~,-, /i-tocopherol, tocol and their model compounds by oxidizing the phenol precursors with PbO2 in toluene. The proton hyperfine coupling constants were determined, and the 'experimental' spin densities were evaluated from the h, yperfine coupling constants. From the results, the methyl-substitution effects on the unpaired spin distribution and molecular structure of the chromanoxyl radicals have been studied.
๐ SIMILAR VOLUMES
Free radicals generated from a-and/3-ionyl bromides gave well resolved ESR spectra, but retinyl bromide and chloride gave only broad signals. Delocalised radicals were also spectrosopically observed on hydrogen abstraction from a-ionane, a-ionyltrimethylsilylether and buten-3-ynyl-2,6,6-trimethyl-2-