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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~CO^+^ 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.


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Isomerization of [C6H5C3H5O]+˙ ions: The
✍ J. P. Denhez; H. E. Audier 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 440 KB

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