Propanoyl ion formation from metastable [C3H6O]+˙ ions
✍ Scribed by Charles E. Hudson; David J. McAdoo
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 271 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Abstract
Collisionally activated spectra demonstrate that CH~3~CH~2~CO^+^ rather than \documentclass{article}\pagestyle{empty}\begin{document}${\rm CH}_{\rm 2} = {\rm CHCH = }\mathop {\rm O}\limits^{\rm + } {\rm H}$\end{document} is formed in the metastable losses of hydrogen from [C~3~H~6~O]^+˙^ ions with the oxygen on the first carbon. This provides another example of formation of an acyl ion following ‘ketonization’ prior to metastable decomposition.
📜 SIMILAR VOLUMES
Appearance energy and kinetic energy release measurements together with isotopic labelling have shown that the metastable molecular ion of 1-phenylpmpenol isomerizes into those of cinnamic alcohol and 3-phenylpropanal prior to loss of ketene. =C! labelling and thennodynamic considerations prove that