Theoretical calculations of the low-energy CH+ photodissociation spectrum display extremely complicated structure due to strong non-adiabatic couplings which are present when molecules dissociate to open-shell atoms. An analysis of the spectrum, using methods which will be explained elsewhere, leads
Low-energy resonances in photodissociation of CH+
โ Scribed by Sherwin J. Singer; Karl F. Freed; Yehuda B. Band
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 453 KB
- Volume
- 105
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
Close coupling ~lculakms for the photodissociation cross sections of CH++ hv* C?(*P) + H(*S) exhibit near threshold peaks not ascribable only to quasi-bound 1eveLF in the A 'It potential. Our ckulations demonstrate the importance of non-adiabatic transitions and thereby suggest the necewty to revise earlier predictions of the rate of radiative association of C+wth H.
๐ SIMILAR VOLUMES
The application is described of our recently developed current density analysis of photodissociation to the methyl nitrite (CHaONO) system. The spectrum exhibits a series of vibrational resonances, or predissociating states, arising from a local minimum in the excited state potential surface. The de
The molecular methane ion C\*q was observed to dissociate to the methyl cation and a hydrogen atom upon irradiation with white li&t from a 2.5 K'T' xenon arc lamp. The maximum photodissociation CIOSS section was estimated as 3 X LO-l9 cm' at 3350 A and a spectrum was obtained.