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dc.creatorFernando Cortes-Guzman-
dc.date.accessioned2020-02-18T15:39:15Z-
dc.date.available2020-02-18T15:39:15Z-
dc.date.issued2020-
dc.identifier.urihttp://rdu.iquimica.unam.mx/handle/20.500.12214/1216-
dc.description.abstractThe kinetic energy is the center of a controversy between two opposite points of view about its role in the formation of a chemical bond. One school states that a lowering of the kinetic energy associated with electron delocalization is the key stabilization mechanism of covalent bonding. In contrast, the opposite school holds that a chemical bond is formed by a decrease in the potential energy due to a concentration of electron density within the binding region. In this work, a topographic analysis of the Hamiltonian Kinetic Energy Density (KED) and its Laplacian is presented to gain more insight into the role of the kinetic energy within chemical interactions. This study is focused on atoms, diatomic and organic molecules, along with their dimers.es_MX
dc.language.isoenges_MX
dc.rightsinfo:eu-repo/semantics/closedAccesses_MX
dc.sourceChemphyschem (ISSN 1439-4235) 21, 3, 194-203es_MX
dc.titleLaplacian of the hamiltonian kinetic energy density as an indicator of binding and weak interactionses_MX
dc.typeinfo:eu-repo/semantics/articlees_MX
dc.creator.idinfo:eu-repo/dai/mx/orcid/0000-0002-6716-1621es_MX
dc.relation.alternativeidentifierhttps://doi.org/10.1002/cphc.201900769-
dc.subject.ctiinfo:eu-repo/classification/cti/2es_MX
dc.subject.keywordsChemical interactionses_MX
dc.subject.keywordsKinetic energy densityes_MX
dc.subject.keywordsLaplacianes_MX
dc.subject.keywordsShell structurees_MX
dc.subject.keywordsTopographic analysises_MX
dc.creator.twoJosé Enrique Barquera Lozada-
dc.creator.threePablo Carpio Martínez-
dc.creator.fourAngel Martín Pendás-
dc.creator.idtwoinfo:eu-repo/dai/mx/orcid/0000-0002-9668-5328es_MX
dc.creator.idthreeinfo:eu-repo/dai/mx/orcid/0000-0001-5733-2485es_MX
dc.creator.idfourinfo:eu-repo/dai/mx/orcid/0000-0002-4471-4000es_MX
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