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

DOIResolve DOI: https://doi.org/10.1016/0301-0104(85)80171-3
AuthorSearch for: ; Search for: 1; Search for: 1
Affiliation
  1. National Research Council Canada
FormatText, Article
Abstract
Within 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
In
  • Chemical Physics 95, no. 3 (1985): 473–481.
LanguageEnglish
Peer reviewedYes
NPARC number21276513
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Record identifierd7699fbb-ef19-40f9-84d0-346410b13905
Record created2015-10-13
Record modified2020-03-17

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