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Dehydrodimers of arylaldoxime—‐a convenient source of iminoxy radicals
Author(s) -
Wei XuDong,
Hu HongWen,
Hu YueFei,
Jin YongShu,
Jin TongZheng,
Han ShiYing,
Xu YunXia
Publication year - 1992
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.19920100409
Subject(s) - chemistry , radical , chloroform , x ray photoelectron spectroscopy , photochemistry , combinatorial chemistry , organic chemistry , chemical engineering , engineering
Arylaldoxime dehydrodimers 3a—1 have been prepared from the corresponding oximes 1a—1 by using (HCrO 4 ) 2 (Py) 4 Co as oxidant. Their structures were assigned to be bisnitrone by XPS studies. ESR studies of 3a—1 in hot chloroform show that iminoxy radicals 2a—1 are formed. Therefore the dehydrodimers can provide a convenient source of these radicals.
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