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Authordc.contributor.authorYepes, Diana 
Authordc.contributor.authorMunarriz, Julen 
Authordc.contributor.authorl'Anson, Daniel 
Authordc.contributor.authorContreras García, Julia 
Authordc.contributor.authorJaque Olmedo, Pablo 
Admission datedc.date.accessioned2020-05-27T13:03:19Z
Available datedc.date.available2020-05-27T13:03:19Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationJ. Phys. Chem. A 2020, 124, 1959−1972es_ES
Identifierdc.identifier.other10.1021/acs.jpca.9b10508
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/174987
Abstractdc.description.abstractIn this article, we present a complementary analysis based on the reaction force F(xi)/reaction force constant kappa(xi) and noncovalent interactions (NCI) index to characterize the energetics (kinetic and thermodynamics) and mechanistic pathways of two sets of multibond chemical reactions, namely, two double-proton transfer and two Diels-Alder cycloaddition reactions. This approach offers a very straightforward and useful way to delve into a deeper understanding of this type of process. While F(xi) allows the partition of the whole pathway into three regions or phases, kappa(xi) describes how orchestrated are the bond-breaking and bondformation events. In turn, NCI indicates how the inter- and intramolecular bonds evolve. The most innovative aspect is the inclusion of the formation of the reactant complex along the pathway, which, by means of NCI, unveils the early molecular recognition and the comprehension of its role in determining the degree of the synchronicity/nonsynchronicity of one-step processes. This approach should be a useful and alternative tool to characterize the energetics and the mechanism of general chemical reactions.es_ES
Patrocinadordc.description.sponsorshipComisión Nacional de Investigación Científica y Tecnológica (CONICYT) CONICYT FONDECYT 1181914 Spanish Ministerio de Ciencia, Innovación y Universidades FPU14/06003 EST17/00161 Universidad de Zaragoza Fundación Bancaria Ibercaja Fundación CAI CB 6/17es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherAmerican Chemical Societyes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceJournal of Physical Chemistry Aes_ES
Keywordsdc.subjectDiels-alder reactionses_ES
Keywordsdc.subjectElectron localization functiones_ES
Keywordsdc.subjectDouble proton-transferes_ES
Keywordsdc.subjectBond formationes_ES
Keywordsdc.subjectMolecular-mechanismes_ES
Keywordsdc.subjectTransition-stateses_ES
Keywordsdc.subjectConstantes_ES
Keywordsdc.subjectDynamicses_ES
Keywordsdc.subjectSynchronicityes_ES
Títulodc.titleReal-space approach to the reaction force: understanding the origin of synchronicity/nonsynchronicity in multibond chemical reactionses_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorctces_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile