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Type: Journal article
Title: Ring Cleavages of Dimethylphenoxide Anions
Author: Dua, S.
Bowie, J.
Citation: Rapid Communications in Mass Spectrometry, 1997; 11(18):1996-1998
Issue Date: 1997
ISSN: 0951-4198
Abstract: The major fragmentations of isomeric dimethylphenoxide anions upon collisional activation are losses of H· and Me·. Two minor processes involve the formation of m/z 79 (C6H7-) (-C2H2O) and m/z 77 (C6H5-) [- (Me· + CHO·)]. The former is only observed when (at least) one of the ortho carbons bears a hydrogen substituent, the latter only when there is a 4-methyl substituent.
DOI: 10.1002/(sici)1097-0231(199712)11:18<1996::aid-rcm103>;2-a
Published version:;2-a
Appears in Collections:Aurora harvest 6
Chemistry publications

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