Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
February 1, 1982The Journal of Chemical Physics

Polyatomic canonical variational theory for chemical reaction rates. Separable-mode formalism with application to OH+H2→H2O+H

View Full Paper
Ask AI
Bookmark
Share

Authors

AIAlan D. IsaacsonUniversity of Minnesota
Donald G. Truhlar
Donald G. TruhlarButler University

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Isaacson et al. (1982) studied this question.

synapsesocial.com/papers/6a6f2caefebe604dd7082f88https://doi.org/10.1063/1.443130
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Comparison of variational transition state theory and the unified statistical model with vibrationally adiabatic transmission coefficients to accurate collinear rate constants for T+HD→TH+D1980 · 38 citations
  2. 2Variational transition state theory, vibrationally adiabatic transmission coefficients, and the unified statistical model tested against accurate quantal rate constants for collinear F+H2, H+F2, and isotopic analogs1980 · 38 citations
  3. 3Variational transition state theory. Primary kinetic isotope effects for atom transfer reactions1980 · 69 citations
  4. 4A theoretical study of the potential energy surface for OH+H21980 · 219 citations
  5. 5Generalized transition state theory. Classical mechanical theory and applications to collinear reactions of hydrogen molecules1979 · 486 citations