Statistical theories for molecular collisions: A maximum entropy derivation
- 1 March 1980
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 72 (5) , 2990-2997
- https://doi.org/10.1063/1.439499
Abstract
Statistical theories are particularly appropriate when one can define a strong interaction regime. We consider the distribution of classical trajectories which enter or exit from this regime. That distribution of trajectories which is of maximal entropy subject only to total conservation of flux is shown to lead to the familiar ’’phase–space’’ expression for the reaction probability. By including more refined conservation conditions as constraints one obtains improved statistical theories. As an example the ’’unified’’ statistical theory of Miller and the Hirschfelder–Wigner expression for the reaction probability are derived by imposing one more conservation constraint. Transition state theory is derived as a special case corresponding to a particular, extreme, numerical value of the constraint. Phase–space theory is obtained when the value of the constraint is at the other extreme (in which case the constraint is not informative). Essentially, exact results for the reaction probability in the collinear H+H2 reactive collision are obtained using two conservation conditions (beside the conservation of total flux). In general, it is shown that the procedure is variational, i.e., that including additional constraints can only improve the results.Keywords
This publication has 13 references indexed in Scilit:
- Classical transition state theory: A lower bound to the reaction probabilityThe Journal of Chemical Physics, 1980
- Collision experiments with partial resolution of final states: Maximum entropy procedure and surprisal analysisPhysical Review C, 1979
- Unified statistical model for ’’complex’’ and ’’direct’’ reaction mechanisms: A test on the collinear H+H2 exchange reactionThe Journal of Chemical Physics, 1979
- Angular entropy: The information content of molecular scattering angular distributionsThe Journal of Chemical Physics, 1977
- Unified statistical model for ’’complex’’ and ’’direct’’ reaction mechanismsThe Journal of Chemical Physics, 1976
- The well-reasoned choice: An information-theoretic approach to branching ratios in molecular rate processesChemical Physics Letters, 1974
- Statistical theories of chemical reactions. Distributions in the transition regionThe Journal of Chemical Physics, 1973
- Opacity Analysis of Inelastic Molecular Collisions. IV. Statistical Aspects of Rotational Excitation TheoryThe Journal of Chemical Physics, 1970
- Information Theory and Statistical MechanicsPhysical Review B, 1957
- Some Quantum-Mechanical Considerations in the Theory of Reactions Involving an Activation EnergyThe Journal of Chemical Physics, 1939