Phase-Space Theory of Chemical Kinetics
- 1 June 1964
- journal article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 40 (11) , 3221-3229
- https://doi.org/10.1063/1.1724989
Abstract
A theory of the cross sections of three‐body gas‐phase reactions which proceed without activation energy is presented. It is based on the hypothesis that the decomposition of a collision complex is governed by the phase space available to each product under conservation of angular momentum and energy. Calculations on model ion—molecule systems show that the cross section is enhanced if the reaction is exothermic, the final reduced mass is large, and the final long‐range attractive forces are large. The theory gives a consistent explanation for the cross sections of the reactions between He+ and H2, and He and H2+ which is in satisfactory agreement with experiment.Keywords
This publication has 23 references indexed in Scilit:
- Reactive collisions in crossed molecular beamsDiscussions of the Faraday Society, 1962
- Energy distribution among reaction products. Part 1.—The reaction atomic hydrogen plus molecular chlorineDiscussions of the Faraday Society, 1962
- Atomic oxygen and nitrogen density measurements with e.p.r.Discussions of the Faraday Society, 1962
- Multiple Ionization in Argon and Krypton by Electron ImpactThe Journal of Chemical Physics, 1960
- Threshold Law for Multiple IonizationPhysical Review B, 1955
- Properties of the Hydrogen Molecular Ion I: Quadrupole Transitions in the Ground Electronic State and Dipole Transitions of the Isotopic IonsProceedings of the Physical Society. Section A, 1953
- The Threshold Law for Single Ionization of Atoms or Ions by ElectronsPhysical Review B, 1953
- New Developments in Molecular Orbital TheoryReviews of Modern Physics, 1951
- On the Behavior of Cross Sections Near ThresholdsPhysical Review B, 1948
- The Theoretical Treatment of Chemical Reactions Produced by Ionization Processes Part I. The Ortho-Para Hydrogen Conversion by Alpha-ParticlesThe Journal of Chemical Physics, 1936