Journal of the American Chemical Society · 2005 · 95 citations · 10 references
EngineeringComputational ChemistryChemistryIndirect Reactive TrajectoriesKinetics (Physics)Internal EnergyReaction IntermediateMolecular KineticsBiophysicsMinimum Energy PathPhysicsAtomic PhysicsPhysical ChemistryReactivity (Chemistry)Quantum ChemistryNon-equilibrium ProcessReactive TrajectoriesNatural SciencesTrajectories FarHydrogen BondReaction ProcessChemical Kinetics
The importance of reactive trajectories straying far from the minimum energy path is demonstrated for the bimolecular reaction H + HBr --> H2(v', j') + Br at 53 kcal/mol collision energy. Product quantum state distributions are measured and calculated using the quasi-classical trajectory technique, and the calculations indicate that highly internally excited H2 products result from indirect reactive trajectories with bent transition states. A general argument is made suggesting that reaction products with internal energy exceeding a kinematic constraint can, in general, be attributed to reactive collisions straying far from the minimum energy path.
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