Radical cation/radical reactions: A Fourier transform ion cyclotron resonance study of allyl radical reacting with aromatic radical cations

Amber L. Russell, Henry W. Rohrs, David Read, Daryl E. Giblin, Peter P. Gaspar, Michael L. Gross

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

A method for the study of reactions of open-shell neutrals (radicals) and radical cations is described. Pyrolysis (25-1500 °C) of thermally labile compounds, such as, 1,5-hexadiene via a Chen nozzle yields a seeded beam of reactive species in helium. The pyrolysis products are then analyzed by electron ionization (EI) or reacted with stored ions. Electron ionization of the pyrolysis products of 1,5-hexadiene shows that both the allyl radical and allene are generated. Reactions of benzene radical cations and the pyrolysis products of 1,5-hexadiene result in carbon-carbon bond formation. Those reactions of allyl radical with the benzene radical cation yield the C7H7+ ion of m/z 91, permitting an unusual entry into arenium ions. The reaction of allene with benzene radical cation in contrast yields C9H10+ and C9H9+.

Original languageEnglish
Pages (from-to)8-15
Number of pages8
JournalInternational Journal of Mass Spectrometry
Volume287
Issue number1-3
DOIs
StatePublished - Oct 15 2009

Keywords

  • Allyl radical
  • Aromatic radical cation
  • Chen nozzle
  • Fourier transform ion cyclotron resonance mass spectrometry
  • Radical-radical cation reaction
  • Reaction mechanism

Fingerprint

Dive into the research topics of 'Radical cation/radical reactions: A Fourier transform ion cyclotron resonance study of allyl radical reacting with aromatic radical cations'. Together they form a unique fingerprint.

Cite this