## 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
Dynamics of OH and H2O groups in sodalites
✍ Scribed by O. Elsenhans; W. Bührer; I. Anderson; J. Nicol; T. Udovic; F. Rieutord; J. Felsche; P. Sieger; G. Engelhardt
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 321 KB
- Volume
- 180-181
- Category
- Article
- ISSN
- 0921-4526
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract To investigate the extent of nonadiabatic effects in the title reaction, quasi‐classical trajectory and nonadiabatic quantum scattering as well as the nonadiabatic quantum‐classical trajectory calculations were performed on the accurate __ab initio__ benchmark potential energy surfaces
## Abstract The ability to use calculated OH frequencies to assign experimentally observed peaks in hydrogen bonded systems hinges on the accuracy of the calculation. Here we test the ability of several commonly employed model chemistries—HF, MP2, and several density functionals paired with the 6‐3
Pure rotational transitions have been used to probe high rotational states of OH(X 'H, v=O) formed in the reaction H+O+ OH+0 at 2.6 eV collision energy. The infrared diode absorption/gain technique is complementary to laser-induced fluorescence (LIF) and particularly useful for probing those high ro