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 language | English |
|---|---|
| Pages (from-to) | 643-673 |
| Number of pages | 31 |
| Journal | Annual Review of Physical Chemistry |
| Volume | 48 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1997 |
Keywords
- Electronic spectroscopy
- Hydroxyl radicals
- Intermolecular potentials
- Prereactive complexes
- Quenching