Kinetic applications of electron paramagnetic resonance spectroscopy. XXIV. Neophyl rearrangements

From National Research Council Canada

DOIResolve DOI: https://doi.org/10.1021/ja00421a028
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Name affiliation
  1. National Research Council Canada
FormatText
TypeArticle
Journal titleJournal of the American Chemical Society
ISSN0002-7863
Volume98
Issue5
Pages1224–1226; # of pages: 3
Abstract
The rate constants for isomerization of 2-aryl-2-methylpropyl-1 to 1-aryl-2-methylpropyl-2 radicals have been measured by EPR spectroscopy over a range of temperatures. The radicals were derived by hydrogen abstraction from the following compounds: tert-butylbenzene, 1,3-di-tert-butylbenzene, 4-tert-butylpyridine, 2,6-di-tert-butylpyridine, and 2-tert-butylnaphthalene. The rates of isomerization of the radicals derived from the two pyridines and the naphthalene are significantly faster than the rates of isomerization of the radicals from the two benzenes.
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LanguageEnglish
Peer reviewedYes
NPARC number21276700
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Record modified2016-05-09
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