Zur Kurzanzeige

dc.contributor.authorGómez Carrasco, Susana Raquel 
dc.contributor.authorGonzález Sánchez, Lola 
dc.contributor.authorAguado, Alfredo
dc.contributor.authorSanz-Sanz, Cristina
dc.contributor.authorZanchet, Alexandre
dc.contributor.authorRoncero, Octavio
dc.date.accessioned2026-02-05T11:09:28Z
dc.date.available2026-02-05T11:09:28Z
dc.date.issued2012
dc.identifier.citationGómez-Carrasco S, González-Sánchez L, Aguado A, Sanz-Sanz C, Zanchet A, Roncero O. Dynamically biased statistical model for the ortho/para conversion in the H2 + H3+ → H3+ + H2 reaction. J Chem Phys. 2012 Sep 7;137(9):094303. doi: 10.1063/1.4747548. PMID: 22957565.es_ES
dc.identifier.issn0021-9606
dc.identifier.urihttp://hdl.handle.net/10366/169538
dc.description.abstract[EN]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, alpha(7), 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.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherAIP Publishinges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectZero point energyes_ES
dc.subjectSelection ruleses_ES
dc.subjectAB-initioes_ES
dc.subjectDeuterium Fractionationes_ES
dc.subjectCross sectionses_ES
dc.subjectH5+es_ES
dc.titleDynamically biased statistical model for the ortho/para conversion in the ${\rm H}_2 + {\rm H}_3^+$H2+H3+ → ${\rm H}_3^{+} +$H3++ H2 reactiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1063/1.4747548es_ES
dc.identifier.doi10.1063/1.4747548
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1089-7690
dc.journal.titleThe Journal of Chemical Physicses_ES
dc.volume.number137es_ES
dc.issue.number9es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


Dateien zu dieser Ressource

Thumbnail

Das Dokument erscheint in:

Zur Kurzanzeige

Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Solange nicht anders angezeigt, wird die Lizenz wie folgt beschrieben: Attribution-NonCommercial-NoDerivatives 4.0 Internacional