The modes of fragmentation of perchlorylbenzene (C6H6C10s) and its perdeutero derivative under electron impact are reported and discussed. The occurrence of the [C,H,O]and [C,H,O]+ ions is accounted for in terms of a novel phenyl migration from chlorine to oxygen.
The electron-impact-induced fragmentation of acridine
β Scribed by R. M. Acheson; R. T. Aplin; R. G. Bolton
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 393 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
Abstract
Studies of both high and low resolution spectra, and of metastable decompositions occurring in both the first and second fieldβfree regions of the mass spectrometer have led to a postulated scheme for the fragmentation of acridine under electronβimpact. There is no specific loss of label from either [9β^2^H~1~]acridine or [4,5β^2^H~2~]acridine in any fragmentation, nor is there any total scrambling of label in either molecular ion prior to loss of HCN. There is certainly some degree of scrambling preceding HCN loss from [M]^+^Λ at 70 eV, but this does not involve the 9βH to any detectable extent. There is no strong evidence for the acridine molecular ion having the same structure as that of four other C~13~H~9~N isomers.
π SIMILAR VOLUMES
The fragmentation behaviour of 18 vicinally substituted aminonitropyridines was studied under electron impact conditions. The decomposition patterns were found to be strongly dependent on the position of substituents The formation of the am analogue of carbazole seems phenylamioopyridine.