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Cytotoxicity of reactive metabolites resulting from the pheraoxy radicals of 2,6-di-tert-butyl-4-methylphenol (BHT) and related alkylphenols

✍ Scribed by J.A. Thompson; J.L. Bolton; K.M. Schullek; D. Ross


Book ID
115886421
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
216 KB
Volume
183
Category
Article
ISSN
0014-2999

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Radical pairs are formed by photolysis of single crystals of 2,6-di-tert-butyl-4-methylphenol (ionol) (1) or 2,6-di-tert-butylphenol (2 ), doped by several different molecules, and investigated by the EPR method. A possible two-hydrogen-atom transfer is discussed as the photochemical act.