Abstraction versus insertion in the reaction O(1D2)+H2→OH(υ″ = 2) + H
✍ Scribed by Gregory M. Jursich; John R. Wiesenfeld
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 300 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
The product hydroxyl radical arising from the reaction 0( 1D 2)-t-H 2 ---, OH + H was detected by LIF following excitation of the off-diagonal transition OH(A2E +, v' = 1 6-X 2II, v" = 2) in the region 348-357 nm. The rotational population distribution in v" = 2 appears to be inverted and quite similar to that previously reported for v" = 0 and 1. Because rotationally cool OH was not observed,, there is no evidence for the existence of an abstractive pathway in which the subject reaction occurs without the initial formation, via insertion, of a chemically activated HOH collision complex.
📜 SIMILAR VOLUMES
The rate constant for the reaction between OH and vibrationally excited H2, OH + H 2 (v = 1) ~ H20 + H, has been measured directly at 298 K. kol is found to be (7.5 -+ 3) X 10 -13 cma/molecule s, corresponding to a vibrational rate enhancement ofkol/koo = (1.2 -+ 0.4) X 102.
## Abstract The kinetics of the hydrogen abstraction from H~2~O~2~ by ^•^OH has been modeled with MP2/6‐31G\*//MP2/6‐31G\*, MP2‐SAC//MP2/6‐31G\*, MP2/6‐31+G\*\*//MP2/6‐31+G\*\*, MP2‐SAC// MP2/6‐31+G\*\*, MP4(SDTQ)/6‐311G\*\*//MP2/6‐31G\*, CCSD(T)/6‐31G\*//CCSD(T)/6‐31G\*, CCSD(T)/6‐31G\*\*//CCSD(T)
## Using translationally excited H atoms generated by laser photolysis of H2S at 193 nm, the reaction dynamics of H + H,O+OH + H2 and H + COIdOH + CO was investigated at collision energies of 2.2 and 2.3 eV, respectively. Nascent OH rotational and vibrational quantum-state distributions and OH pro