Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||Ring Cleavages of Dimethylphenoxide Anions|
|Citation:||Rapid Communications in Mass Spectrometry, 1997; 11(18):1996-1998|
|Publisher:||JOHN WILEY & SONS LTD|
|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.|
|Appears in Collections:||Aurora harvest 6|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.