Chemical reactivity descriptors for ambiphilic reagents: Dual descriptor, local hypersoftness, and electrostatic potential
Author
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Cárdenas, Carlos
Author
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Rabi, Nataly
Author
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Ayers, Paul W.
Author
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Morell, Christophe
Author
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Jaramillo, Paula
Author
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Fuentealba Rosas, Patricio
Admission date
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2018-12-20T14:05:58Z
Available date
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2018-12-20T14:05:58Z
Publication date
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2009
Cita de ítem
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Journal of Physical Chemistry A, Volumen 113, Issue 30, 2018, Pages 8660-8667
Identifier
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10895639
Identifier
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10.1021/jp902792n
Identifier
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https://repositorio.uchile.cl/handle/2250/153839
Abstract
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The 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