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dc.contributor.authorLara, Manuel
dc.contributor.authorGarcía Jambrina, Pablo 
dc.contributor.authorAoíz Moleres, Francisco Javier
dc.date.accessioned2025-07-07T09:14:59Z
dc.date.available2025-07-07T09:14:59Z
dc.date.issued2023
dc.identifier.citationManuel Lara, P. G. Jambrina, F. J. Aoiz; Universal behavior in complex-mediated reactions: Dynamics of S(1D) + o-D2 → D + SD at low collision energies. J. Chem. Phys. 14 May 2023; 158 (18): 184303. https://doi.org/10.1063/5.0147182es_ES
dc.identifier.issn0021-9606
dc.identifier.urihttp://hdl.handle.net/10366/166357
dc.description.abstract[EN]Reactive and elastic cross sections and rate coefficients have been calculated for the S(1D) + D2(v = 0, j = 0) reaction using a modified hyperspherical quantum reactive scattering method. The considered collision energy ranges from the ultracold regime, where only one partial wave is open, up to the Langevin regime, where many of them contribute. This work presents the extension of the quantum calculations, which in a previous study were compared with the experimental results, down to energies in the cold and ultracold domains. Results are analyzed and compared with the universal case of the quantum defect theory by Jachymski et al. [Phys. Rev. Lett. 110, 213202 (2013)]. State-to-state integral and differential cross sections are also shown covering the ranges of low-thermal, cold, and ultracold collision energy regimes. It is found that at E/kB < 1 K, there are substantial departures from the expected statistical behavior and that dynamical features become increasingly important with decreasing collision energy, leading to vibrational excitation.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherAIP Publishinges_ES
dc.subjectStereodynamicses_ES
dc.subjectComputational chemistryes_ES
dc.subjectReaction dynamicses_ES
dc.titleUniversal behavior in complex-mediated reactions: Dynamics of S(1D) + o-D2 → D + SD at low collision energieses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1063/5.0147182es_ES
dc.identifier.doi10.1063/5.0147182
dc.relation.projectIDPID2021-122839NB- I00es_ES
dc.relation.projectIDPGC2018-096444-B-I00es_ES
dc.relation.projectIDPID2020-113147GA-I00es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1089-7690
dc.journal.titleThe Journal of Chemical Physicses_ES
dc.volume.number158es_ES
dc.issue.number18es_ES
dc.type.hasVersioninfo:eu-repo/semantics/submittedVersiones_ES


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