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.
Saved in:
Published in | Synthetic metals Vol. 71; no. 1; pp. 1801 - 1802 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
LAUSANNE
Elsevier B.V
01.04.1995
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
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 |