Angular distributions from photodissociations. V. The bent triatomic molecule

Michael D. Morse, Yehuda B. Band, Karl F. Freed

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

The generalized Franck-Condon theory of bent triatomic molecule dissociations is extended to permit the calculation of state-to-state photofragment angular distributions. The axial recoil limiting forms of Zare and Bersohn are obtained for the state-averaged angular anisotropies β̄ with corrections for the effects of bending vibrations. For certain orientations of the transition dipole within the molecule, βfi is found to be nearly independent of fragment rotational angular momentum j, while for other orientations, it is found to be a strongly oscillatory function of j. In some cases, calculated photofragment rotational distributions at fixed detection angles are strong functions of the detection angle, suggesting the possibility of partial state selection by spatial resolution. Approximate analytical expressions for βfi are presented for initially bound molecular states that are either nonrotating or are well described by a prolate symmetric top wave function with k=0. The distributions are linear combinations of parallel and perpendicular-type distributions. Numerical applications are provided for direct photodissociations from the bent X̃ HOCl and C̃ HCN states.

Original languageEnglish
Pages (from-to)6066-6078
Number of pages13
JournalJournal of Chemical Physics
Volume78
Issue number10
DOIs
StatePublished - 1 Jan 1982

Fingerprint

Dive into the research topics of 'Angular distributions from photodissociations. V. The bent triatomic molecule'. Together they form a unique fingerprint.

Cite this