Classical analysis of collinear light atom transfer reactions
- 1 February 1983
- journal article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 78 (3), 1228-1236
- https://doi.org/10.1063/1.444834
Abstract
A classical direct reaction theory is formulated and shown to account for the recently observed quantal oscillations in the reaction probability of light atom transfer reactions. Quasiperiodic orbits and irregular orbits are found for the systems although the potential energy surfaces used have only saddle points in the interaction region. These orbits imply the existence of a new type of bound species—an adiabatic molecule.Keywords
This publication has 28 references indexed in Scilit:
- A quasiclassical model for resonance widths in quantal collinear reactive scatteringThe Journal of Chemical Physics, 1982
- A simple classical prediction of quantal resonances in collinear reactive scatteringChemical Physics, 1981
- On the collinear I + HI and I + muI reactionsChemical Physics Letters, 1981
- Quantum mechanical coupled-channel collision-induced dissociation calculations with hyperspherical coordinatesChemical Physics Letters, 1981
- Intramolecular Dynamics of Van Der Waals MoleculesAdvances in Chemical Physics, 1981
- Van Der Waals MoleculesAdvances in Chemical Physics, 1981
- Hyperspherical coordinates in quantum mechanical collinear reactive scatteringChemical Physics Letters, 1980
- Semiclassical calculation of compound state resonancesChemical Physics Letters, 1980
- Statistical theories for molecular collisions: A maximum entropy derivationThe Journal of Chemical Physics, 1980
- Potential Energy Surface for H3The Journal of Chemical Physics, 1964