dc.creatorCárdenas, Carlos
dc.creatorRabi, Nataly
dc.creatorAyers, Paul W.
dc.creatorMorell, Christophe
dc.creatorJaramillo, Paula
dc.creatorFuentealba Rosas, Patricio
dc.date.accessioned2018-12-20T14:05:58Z
dc.date.available2018-12-20T14:05:58Z
dc.date.created2018-12-20T14:05:58Z
dc.date.issued2009
dc.identifierJournal of Physical Chemistry A, Volumen 113, Issue 30, 2018, Pages 8660-8667
dc.identifier10895639
dc.identifier10.1021/jp902792n
dc.identifierhttps://repositorio.uchile.cl/handle/2250/153839
dc.description.abstractThe second-order response of the electron density with respect to changes in electron number, known as the dual descriptor, has been established as a key reactivity indicator for reactions like pericyclic reactions, where reagents accept and donate electrons concurrently. Here we establish that the dual descriptor is also the key reactivity indicator for ambiphilic reagents: reagents that can act either as electrophiles or as nucleophiles, depending on the reaction partner. Specifically, we study dual atoms (which are proposed to act, simultaneously, as an electron acceptor and an electron donor), dual molecules (which react with both electrophiles and nucleophiles, generally at different sites), and dual ion-molecule complexes (which react with both cations and anions). On the basis of our analysis, the dual atom (an A1(I) that has been purported to be dual in the literature) is actually pseudodual in the sense that it does not truly accept electrons from a nucleophiles; rather, it se
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceJournal of Physical Chemistry A
dc.subjectPhysical and Theoretical Chemistry
dc.titleChemical reactivity descriptors for ambiphilic reagents: Dual descriptor, local hypersoftness, and electrostatic potential
dc.typeArtículo de revista


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