OH-H2 entrance channel complexes

  • Richard A. Loomis
  • , Marsha I. Lester

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

Abstract

The entrance channel to the OH + H2 → H2O + H hydrogen abstraction reaction has been investigated from several different experimental approaches and complementary theoretical calculations. Weakly bound complexes between the hydroxyl radical and molecular hydrogen have been stabilized within a shallow well in the entrance channel and characterized via electronic spectroscopy on the OH A2Σ+ - X2Π transition. Laser-induced fluorescence and fluorescence depletion experiments have revealed the binding energy of H2/D2 with ground state OH X2Π radicals, the intermolecular energy levels supported by the OH A2Σ+ (v′ = 0,1) + H2/D2 potential, and the OH-H2/D2 excited state dissociation limit. The OH X2Π + H2 potentials have also been examined through inelastic scattering measurements on Λ-doublet state-selected OH with normal or para-H2. Finally, photodetachment of an electron from the H3O- anion enabled the neutral reaction to be probed in conformations sampled by the two isomeric forms of the anion.

Original languageEnglish
Pages (from-to)643-673
Number of pages31
JournalAnnual Review of Physical Chemistry
Volume48
Issue number1
DOIs
StatePublished - 1997

Keywords

  • Electronic spectroscopy
  • Hydroxyl radicals
  • Intermolecular potentials
  • Prereactive complexes
  • Quenching

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