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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4855
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dc.contributor.authorDua, S.-
dc.contributor.authorBowie, J.-
dc.date.issued1997-
dc.identifier.citationRapid Communications in Mass Spectrometry, 1997; 11(18):1996-1998-
dc.identifier.issn0951-4198-
dc.identifier.urihttp://hdl.handle.net/2440/4855-
dc.description.abstractThe 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.-
dc.language.isoen-
dc.publisherJOHN WILEY & SONS LTD-
dc.titleRing Cleavages of Dimethylphenoxide Anions-
dc.typeJournal article-
dc.identifier.doi10.1002/(sici)1097-0231(199712)11:18<1996::aid-rcm103>3.3.co;2-a-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 6
Chemistry publications

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