K-scrambling in a near-symmetric top molecule containing an excited noncoaxial internal rotor

Journal Article · Thu Jun 15 04:00:00 EDT 2000 · Journal of Chemical Physics

DOI:https://doi.org/10.1063/1.481663· OSTI ID:20216743

Ortigoso, Juan ^[1]; Hougen, Jon T ^[2]

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1. Instituto de Estructura de la Materia, Consejo Superior de Investigaciones Cientificas, Serrano 121, 28006 Madrid, (Spain)
2. Optical Technology Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8441 (United States)

Classical trajectories on rotational energy surfaces and coherent-state quantum projections have been used to study an asymmetric-top molecule containing a freely rotating internal symmetric top whose symmetry axis is not coincident with a principal axis of the molecule. Stationary points on the rotational energy surface, which strongly influence the trajectories, increase in number from two to four to six as J/n increases from zero to infinity (where J is the total and n is the free-internal-rotor angular momentum). For some J/n values trajectories can arise that sample a large fraction of K values (where K is the z-axis projection of J), corresponding in quantum wave functions to extensive K mixing in the symmetric-top basis set |J,K>. When such mixing cannot be made small for any choice of z axis, we call it K scrambling. For typical values of the torsion-rotation coupling parameter {rho}, rotational eigenfunctions for a given J and torsional state turn out to be quite different from eigenfunctions for the same J in some other torsional state. Nonzero rotational overlap integrals are then distributed among many rotational functions for each (n,n{sup '}) pair, which may, in turn, contribute to internal rotation enhancement of intramolecular vibrational energy redistribution. We have also examined near-free-rotor levels of our test molecule acetaldehyde, which arise for excitation of ten or more quanta of methyl group torsion, and find that barrier effects do not change the qualitative picture obtained from the free-rotor treatment. (c) 2000 American Institute of Physics.

• OSTI ID: 20216743
• Journal Information: Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 23 Vol. 112; ISSN JCPSA6; ISSN 0021-9606
• Country of Publication: United States
• Language: English

Related Subjects

74 ATOMIC AND MOLECULAR PHYSICS
EIGENFUNCTIONS
ENERGY TRANSFER
MOLECULES
ROTATIONAL STATES
THEORETICAL DATA
TORSION
WAVE FUNCTIONS