Vitamin E and related ether-phenols: A low-temperature dielectric relaxation study

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DOIResolve DOI: http://doi.org/10.1016/0301-0104(85)80171-3
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TypeArticle
Journal titleChemical Physics
ISSN0301-0104
Volume95
Issue3
Pages473481; # of pages: 9
AbstractWithin a classs of phenols comprising durenols and methylated chromenols, chromanols and coumaranols, hydrogen-abstraction rate constants, and therefore radical-scavenging and antioxidant effectiveness are closely paralleled by low-temperature relaxation rates, and are apparently influenced in similar proportions by the inductive and resonance effects of para-alkoxy groups. Relaxation rates of 2,3,5,6-tetrachlorophenol and 2,6-di-tertiary-butyl phenol with and without 4-methoxy substituents are also reported and discussed. © 1985.
Publication date
LanguageEnglish
AffiliationNational Research Council Canada (NRC-CNRC)
Peer reviewedYes
NPARC number21276513
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Record identifierd7699fbb-ef19-40f9-84d0-346410b13905
Record created2015-10-13
Record modified2016-05-09
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