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Electron ionization and chemical ionization mass spectra of pyridinium and isoquinolinium ylides
Author(s) -
Bowen D. V.,
Skett P. W.,
Thorpe J.,
Plunkett A. O.
Publication year - 1984
Publication title -
organic mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 0030-493X
DOI - 10.1002/oms.1210190605
Subject(s) - chemical ionization , electron ionization , chemistry , mass spectrum , ionization , fragmentation (computing) , pyridinium , ion , spectral line , electron transfer , molecule , mass spectrometry , polyatomic ion , photochemistry , organic chemistry , physics , chromatography , astronomy , computer science , operating system
Abstract Electron ionization (EI) spectra and both positive and negative chemical ionization (CI) spectra have been obtained for four isoquinolinium ylides and two pyridinium ylides. Electron transfer reactions dominate the CI mass specra. The base peak in negative chemical ionization is the [M] −· ion, formed by electron capture. In the positive methane CI spectra the molecular ion, [M] +· , is relatively more intense than [MH] + showing electron transfer to be the main positive ionization process. In the positive ammonia CI spectra, proton transfer to give [MH] + is the main ionization process, but electron transfer is also observed. The EI spectra show fragmentations in which the aromatic nitrogen moiety retains the charge and fragmentation is by loss of radicals or small neutral molecules from the side‐chains. Radical driven reactions are proposed to explain these spectra.