The Journal of Chemical Physics · 1978 · 253 citations · 23 references
Quantum DynamicEngineeringAtom Exchange ReactionComputational ChemistryChemistryElectronic Excited StateTransition StateTransition StatesVibronic InteractionClassical Bound StatesQuantum Mechanical PropertyQuantum TheoryMolecular KineticsClassical Collinear CollisionQuantum SciencePhysicsAtomic PhysicsPhysical ChemistryQuantum ChemistryNatural SciencesApplied PhysicsQuantum SystemQuantum ChaosMany-body Problem
We show that the best choice of transition state, for the atom exchange reaction in a classical collinear collision of an atom with a diatomic, is a classical bound state embedded in the continuum: a periodic vibration of the triatomic system across the interaction region of the potential surface. These unstable bound states also serve as limit sets of the trapped trajectories that form the boundary of reactivity bands in molecular collisions, and we comment on the implications of this result for calculation of product state distributions. Numerical calculations of transition states are presented for the collinear H+H2 and F+H2 reactions.
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<i>Theory of Ordinary Differential Equations</i>
Earl A. Coddington, Norman Levinson, T. Teichmann · Physics Today · 1956 · 6.2K citations
Potential Energy Surface for H3
R. N. Porter, Martin Karplus · The Journal of Chemical Physics · 1964 · 667 citations