MASS-SPECTRAL STUDY OF SOME PHENYL-MONO AND DINITROPYRIDYL SULFIDE, ETHER, AMINE AND SULFONE DERIVATIVES

Citation
Fem. Elhegazy et al., MASS-SPECTRAL STUDY OF SOME PHENYL-MONO AND DINITROPYRIDYL SULFIDE, ETHER, AMINE AND SULFONE DERIVATIVES, Rapid communications in mass spectrometry, 11(3), 1997, pp. 316-320
Citations number
18
Categorie Soggetti
Spectroscopy,"Chemistry Analytical
ISSN journal
09514198
Volume
11
Issue
3
Year of publication
1997
Pages
316 - 320
Database
ISI
SICI code
0951-4198(1997)11:3<316:MSOSPA>2.0.ZU;2-6
Abstract
The electron impact ionization of some mono- and dinitropyridylphenyls ulfiede, ether, amine and sulfone derivatives were studied at 70 eV en ergy. All the 8 compounds studied underwent ring closure during the fo rmation of a carbazole radical cation as a general feature in their ma ss spectra. The basic differences in the mass spectral behaviour are m ainly attributed to the position of the nitro group in the pyridyl rin g and the fragmentation pathway is directed by the sulfur, oxygen or n itrogen moiety. The base peak in the mass spectra is determined by suc h differences. (C) 1997 by John Wiley & Sons, Ltd.