Rotational relaxation of OCS by spherical and nearly spherical perturbers
Abstract
Collision cross sections for the transverse relaxation of OCS by spherical and nearly spherical perturbers have been measured. The observed cross sections vary linearly with β=[I22/(I1+I2)2α22M]1/5, where I1 and I2 are the ionization energies of OCS and the perturber. α2 is the polarizability of the perturber, and M is the reduced mass of the colliding molecules. Calculations based on the Anderson-Tsao-Curnutte theory using a simple dispersion force model for the OCS-perturber interaction are in qualitative agreement with the experimental results. By doubling the strength of the dispersion forces used to model the OCS-perturber interactions, the calculated cross sections are brought into agreement with the measured ones. The observed linear relation between the cross section and β can be used to predict cross sections for other (polar molecule)-(nonpolar nearly spherical perturber) collisions.
- Publication:
-
Journal of Chemical Physics
- Pub Date:
- May 1989
- DOI:
- 10.1063/1.456581
- Bibcode:
- 1989JChPh..90.4875O
- Keywords:
-
- Carbonyl Compounds;
- Molecular Relaxation;
- Molecular Rotation;
- Perturbation;
- Sulfides;
- Computational Chemistry;
- Electron Transitions;
- Ground State;
- Molecular Collisions;
- Transition Probabilities;
- Atomic and Molecular Physics