Dissociative charge exchange of C3F6

Sohrab Habibi‐Goudarzi*, Tapio Kotiaho, R. G. Cooks, T. Ast

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Charge exchange of neutral C3F6 by a variety of atomic and molecular ions in the 1 to 25 eV range of collision energies is used to characterize the energies associated with formation of [C3F6]+˙. The internal energy of the nascent [C3F6]+˙ ion, assessed by observing the degree to which it fragments, increases with the recombination energy of the charge‐exchange reagent. The existence of excited states of the reagent ions is identified from the fragmentation behaviour of [C3F6]+˙ in the cases of [CS2]+˙, NO+, O2+˙, [NH3]+˙ and possibly [CH4]+˙. In addition, the data confirm that the [C3F6]+˙ parent ion fragments from both the ground state and a long‐lived isolated electronic state. The latter is populated by near‐resonant charge transfer. Translational excitation contributes relatively little to internal excitation of the charge‐exchanged product ion and even less in the case of the isolated state.

Original languageEnglish (US)
Pages (from-to)1008-1016
Number of pages9
JournalOrganic Mass Spectrometry
Volume26
Issue number11
DOIs
StatePublished - Nov 1991

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Instrumentation

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