Multichannel scattering calculations are used to evaluate the role of nonadiabatic interactions and interference effect on the predissociation linewidths of several vibrational levels of the A 2 Z + state of OH due to coupling to three different repulsive electronic states. Oxygen atom fme structure
A quantum mechanical analysis on the selective production of the oxygen atom fine-structure states along asymmetric resonances in OH predissociation
โ Scribed by Sungyul Lee
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 549 KB
- Volume
- 240
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
Predissociation of the A *Z+ state is treated by an exact theory employing two frame transformation matrices, each of which connects the atomic term limits (q3P) and O('D)) to the correlating adiabatic Born-Oppenheimer states. Resonances corresponding to the higher (v > 7) rovibrational levels of the A '2+ state are predicted to have asymmetric (Fano-type) profiles. The branching ratios of Oc3Pj, j = 0, 1, 2) are shown to be influenced by nonadiabatic interactions in the Franck-Condon region between the A *2+ and dissociative 48-, *8-and 411 st ates. The branching ratios show a strong variation along asymmetric resonances, while remaining energy independent along Lorentzian resonances.
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