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Photoionization and ion cyclotron resonance studies of the ion chemistry of ethylene oxide

Corderman, Reed R. and LeBreton, P. R. and Buttrill, S. E., Jr. and Williamson, A. D. and Beauchamp, J. L. (1976) Photoionization and ion cyclotron resonance studies of the ion chemistry of ethylene oxide. Journal of Chemical Physics, 65 (11). pp. 4929-4939. ISSN 0021-9606. doi:10.1063/1.432969.

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Time-resolved photoionozation mass spectrometry (PIMS), ion cyclotron resonance spectroscopy (ICR), and photoelectron spectroscopy have been employed to study the formation of the ethylene oxide molecular ion and its subsequent ion–molecule reactions which lead to the products C2H5O+ and C3H5O+. Earlier observations that a structurally and energetically modified species (C2H4O+) * is an intermediate in the production of C3H5O+ are confirmed. The PIMS data detail the effects of internal energy on reactivity, with the ratio of C3H5O+ to C2H5O+ increasing by an order of magnitude with a single quantum of vibrational energy. Evidence is presented for the formation of (C2H4O+) * in a collision-induced isomerization which yields a ring-opened structure by C–C bond cleavage. This species contains considerable internal excitation which is relaxed in collisions with ethylene oxide or bath gases such as SF6 prior to reaction. The relaxed ring-opened C2H4O+ ion reacts with neutral ethylene oxide by CH<sub>2</sub><sup> + </sup> transfer to yield an intermediate product ion C3H6O+ which gives C3H5O+ by loss of H. Isotopic product distributions observed in a mixture of ethylene oxide and ethylene oxide-d4 are consistent with this mechanism. The effects of ion kinetic energy on reactivity are explored using ICR techniques. Increased reactant ion kinetic energy leads to collision-induced dissociation of C2H4O+ rather than isomerization to the open form.

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Beauchamp, J. L.0000-0001-8839-4822
Additional Information:© 1976 American Institute of Physics. Received 6 November 1975. This research was supported in part by the United States Energy Research and Development Administration under Grant No. AT (04-3) 767-8 awarded to J.L. Beauchamp and presents one phase of research carried out at the Jet Propulsion Laboratory, California Institute of Technology under Contract No. NAS7-100, sponsored by the National Aeronautics and Space Administration. The PIMS instrumentation was made possible by a grant from the President's Fund of the California Institute of Technology. [P.R.L. was a] NASA-JPL Postdoctoral Research Fellow, 1972-1973. [S.E.B, Jr. was a] Sherman Fairchild Research Fellow, 1973. [J.L.B. was a] Camille and Henry Dreyfus Teacher-Scholar, 1971-1976. Arthur Amos Noyes Laboratory of Chemical Physics, Contribution No. 5196.
Funding AgencyGrant Number
Energy Research and Development Administration (ERDA)AT (04-3) 767-8
Caltech President’s FundUNSPECIFIED
Sherman Fairchild FoundationUNSPECIFIED
Camille and Henry Dreyfus FoundationUNSPECIFIED
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Arthur Amos Noyes Laboratory of Chemical Physics5196
Issue or Number:11
Record Number:CaltechAUTHORS:CORjcp76
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ID Code:11879
Deposited By: Archive Administrator
Deposited On:08 Oct 2008 20:00
Last Modified:08 Nov 2021 22:22

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