The Journal of Chemical Physics · 2012 · 35 citations · 59 references
Natural SciencesChemistryPhysicsPhysical ChemistryQuantum ChemistryTheoretical ChemistryAb Initio MethodsPotential Energy SurfacesReaction DynamicsReaction Mechanism ModelingReaction MechanismsStatistical MechanicsDipole InteractionsFragment-based Potential Energy SurfacesGlobal Potential Energy Surface FittingIon-dipole InteractionsPotential Energy Surface AnalysisPotential Energy Surface ConstructionStatistical Reaction DynamicsZero-point Energy
In this work we present a dynamically biased statistical model to describe the evolution of the title reaction from statistical to a more direct mechanism, using quasi-classical trajectories (QCT). The method is based on the one previously proposed by Park and Light [J. Chem. Phys. 126, 044305 (2007)]. A recent global potential energy surface is used here to calculate the capture probabilities, instead of the long-range ion-induced dipole interactions. The dynamical constraints are introduced by considering a scrambling matrix which depends on energy and determine the probability of the identity/hop/exchange mechanisms. These probabilities are calculated using QCT. It is found that the high zero-point energy of the fragments is transferred to the rest of the degrees of freedom, what shortens the lifetime of H(5)(+) complexes and, as a consequence, the exchange mechanism is produced with lower proportion. The zero-point energy (ZPE) is not properly described in quasi-classical trajectory calculations and an approximation is done in which the initial ZPE of the reactants is reduced in QCT calculations to obtain a new ZPE-biased scrambling matrix. This reduction of the ZPE is explained by the need of correcting the pure classical level number of the H(5)(+) complex, as done in classical simulations of unimolecular processes and to get equivalent quantum and classical rate constants using Rice-Ramsperger-Kassel-Marcus theory. This matrix allows to obtain a ratio of hop/exchange mechanisms, α(T), in rather good agreement with recent experimental results by Crabtree et al. [J. Chem. Phys. 134, 194311 (2011)] at room temperature. At lower temperatures, however, the present simulations predict too high ratios because the biased scrambling matrix is not statistical enough. This demonstrates the importance of applying quantum methods to simulate this reaction at the low temperatures of astrophysical interest.
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Deuterium fractionation in dense interstellar clouds
T. J. Millar, Alec Bennett, Eric Herbst · The Astrophysical Journal · 1989 · 413 citations
Detailed symmetry selection rules for reactive collisions
Martin Qüack · Molecular Physics · 1977 · 308 citations
Natural Sciences, Chemistry, Physics +17