English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/65118
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

DC FieldValueLanguage
dc.contributor.authorGómez Carrasco, Susana-
dc.contributor.authorGonzález-Sánchez, Lola-
dc.contributor.authorAguado, Alfredo-
dc.contributor.authorSanz-Sanz, Cristina-
dc.contributor.authorZanchet, Alexandre-
dc.contributor.authorRoncero, Octavio-
dc.identifierdoi: dx.doi.org/10.1063/1.4747548-
dc.identifierissn: 0021-9606-
dc.identifier.citationJournal of Chemical Physics 137: 094303 (2012)-
dc.description.abstractIn 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 quasiclassical 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, ¿(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.-
dc.description.sponsorshipThis work has been supported by the program CONSOLIDER-INGENIO 2010 of Ministerio de Ciencia e Innovación under Grant No. CSD2009-00038, entitled “Molecular Astrophysics: the Herschel and Alma era,” and by Grant Nos. FIS2011-29596-C02 and QCQ2008- 02578, and by Comunidad Autónoma de Madrid (CAM) under Grant No. S-2009/MAT/1467.-
dc.publisherAmerican Institute of Physics-
dc.titleDynamically biased statistical model for the ortho/para conversion in the H 2+H 3 + → H 3 + + H 2 reaction-
dc.description.versionPeer Reviewed-
Appears in Collections:(CFMAC-IFF) Artículos
Files in This Item:
File Description SizeFormat 
380495.pdf1,55 MBUnknownView/Open
Show simple item record

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.