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Authordc.contributor.authorJaramillo, Paula 
Authordc.contributor.authorDomingo, Luis R. es_CL
Authordc.contributor.authorContreras Ramos, Renato es_CL
Authordc.contributor.authorTiznado Vásquez, William es_CL
Authordc.contributor.authorFuentealba Rosas, Patricio es_CL
Admission datedc.date.accessioned2009-04-13T17:23:37Z
Available datedc.date.available2009-04-13T17:23:37Z
Publication datedc.date.issued2006-07-06
Cita de ítemdc.identifier.citationJOURNAL OF PHYSICAL CHEMISTRY A Volume: 110 Issue: 26 Pages: 8181-8187 Published: JUL 6 2006en
Identifierdc.identifier.issn1089-5639
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/118813
Abstractdc.description.abstractThis work deals with exploring some empirical scales of nucleophilicity. We have started evaluating the experimental indices of nucleophilicity proposed by Legon and Millen on the basis of the measure of the force constants derived from vibrational frequencies using a probe dipole H-X (X = F, CN). The correlation among some theoretical parameters with this experimental scale has been evaluated. The theoretical parameters have been chosen as the minimum of the electrostatic potential V-min, the binding energy ( BE) between the nucleophile and the H-X dipole, and the electrostatic potential measured at the position of the hydrogen atom V-H when the complex nucleophile and dipole H-X is in the equilibrium geometry. All of them present good correlations with the experimental nucleophilicity scale. In addition, the BEs of the nucleophiles with two other Lewis acids (one hard, BF3, and the other soft, BH3) have been evaluated. The results suggest that the Legon and Millen nucleophilicity scale and the electrostatic potential derived scales can describe in good approximation the reactivity order of the nucleophiles only when the interactions with a probe electrophile is of the hard-hard type. For a covalent interaction that is orbital controlled, a new nucleophilicity index using information of the frontier orbitals of both, the nucleophile and the electrophile has been proposed.en
Lenguagedc.language.isoenen
Publisherdc.publisherAMER CHEMICAL SOCen
Keywordsdc.subjectDENSITY-FUNCTIONAL THEORYen
Títulodc.titleDefinition of a nucleophilicity scaleen
Document typedc.typeArtículo de revista


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