Efficient synthesis of highly hindered dicyanoethylenephenol radical

An efficient and convenient method for the preparation of conjugated and highly sterically hindered dicyanoethylenephenol derivatives was described. The corresponding blue phenoxyl radicals were generated from the oxidation of the dicyanoethylenephenol precursor with alkaline K 3Fe(CN) 6 in benzene.

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Bibliographic Details
Published inSynthetic metals Vol. 71; no. 1; pp. 1801 - 1802
Main Authors Chiang, L.Y., Wang, Lee Y., Upasani, R.B.
Format Journal Article
LanguageEnglish
Published LAUSANNE Elsevier B.V 01.04.1995
Elsevier
Subjects
Materials Science
Materials Science, Multidisciplinary
Physical Sciences
Physics
Physics, Condensed Matter
Polymer Science
Science & Technology
Technology
FERROMAGNETIC INTERMOLECULAR INTERACTIONS
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Summary:An efficient and convenient method for the preparation of conjugated and highly sterically hindered dicyanoethylenephenol derivatives was described. The corresponding blue phenoxyl radicals were generated from the oxidation of the dicyanoethylenephenol precursor with alkaline K 3Fe(CN) 6 in benzene.
ISSN:0379-6779
1879-3290
DOI:10.1016/0379-6779(94)03057-D