The formation of the styryl ion in the mass spectra of cinnamyl compounds
- 1 March 1969
- journal article
- research article
- Published by Wiley in Journal of Mass Spectrometry
- Vol. 2 (3) , 325-330
- https://doi.org/10.1002/oms.1210020311
Abstract
The formation of the styryl ion \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm PhCH = }\mathop {\rm C}\limits^{\rm + } {\rm H} $\end{document} in the mass spectra of some cinnamic compounds is shown to occur via the intermediate formation of the cinnamoyl ion \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm Ph} - {\rm CH} = {\rm CH} - {\rm C} \equiv \mathop {\rm O}\limits^{\rm + } $\end{document} rather than by direct cleavage of the bond α to the double bond.
Keywords
This publication has 3 references indexed in Scilit:
- Studies in Mass Spectrometry. XIX.1 Evidence for the Occurrence of Aromatic Substitution Reactions upon Electron ImpactJournal of the American Chemical Society, 1966
- Organic Ions in the Gas Phase. X. Decomposition of Benzaldehyde under Electron ImpactJournal of the American Chemical Society, 1963
- Mass spectra of some deuterostyrenesJournal of Research of the National Bureau of Standards, 1959