ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOS

In this study two new global descriptors for chemical reactivity are proposed, namely the electrophilic power and nucleophilic power. These have been developed by performing the normalization of the local electrophilic power and local nucleophilic power respectively, which were recently proposed elsewhere. In particular, the usefulness of both global and local electrophilic power was evaluated by studying the chemical reactivity of six series of α,β-unsaturated carbonyl compounds whose experimental reactivity measures toward the nucleophile glutathione are available. It was observed in the majority of the cases the global and local electrophilic powers work as better than the popular global and local electrophilicity indices, respectively.

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Main Authors: Figueredo,Said F., Páez,Manuel S., Torres,Francisco
Format: Digital revista
Language:Spanish / Castilian
Published: Sociedade Brasileira de Química 2017
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422017000500513
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spelling oai:scielo:S0100-404220170005005132017-07-04ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOSFigueredo,Said F.Páez,Manuel S.Torres,Francisco conceptual DFT electrophilic power nucleophilic power chemical reactivity unsaturated carbonyl compounds In this study two new global descriptors for chemical reactivity are proposed, namely the electrophilic power and nucleophilic power. These have been developed by performing the normalization of the local electrophilic power and local nucleophilic power respectively, which were recently proposed elsewhere. In particular, the usefulness of both global and local electrophilic power was evaluated by studying the chemical reactivity of six series of α,β-unsaturated carbonyl compounds whose experimental reactivity measures toward the nucleophile glutathione are available. It was observed in the majority of the cases the global and local electrophilic powers work as better than the popular global and local electrophilicity indices, respectively.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaQuímica Nova v.40 n.5 20172017-06-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422017000500513es10.21577/0100-4042.20170031
institution SCIELO
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country Brasil
countrycode BR
component Revista
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databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language Spanish / Castilian
format Digital
author Figueredo,Said F.
Páez,Manuel S.
Torres,Francisco
spellingShingle Figueredo,Said F.
Páez,Manuel S.
Torres,Francisco
ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOS
author_facet Figueredo,Said F.
Páez,Manuel S.
Torres,Francisco
author_sort Figueredo,Said F.
title ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOS
title_short ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOS
title_full ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOS
title_fullStr ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOS
title_full_unstemmed ÍNDICES DE PODER ELECTROFÍLICO GLOBAL Y LOCAL PARA EL ESTUDIO TEÓRICO DE LA REACTIVIDAD QUÍMICA: APLICACIÓN A DERIVADOS CARBONILO α,β-INSATURADOS
title_sort índices de poder electrofílico global y local para el estudio teórico de la reactividad química: aplicación a derivados carbonilo α,β-insaturados
description In this study two new global descriptors for chemical reactivity are proposed, namely the electrophilic power and nucleophilic power. These have been developed by performing the normalization of the local electrophilic power and local nucleophilic power respectively, which were recently proposed elsewhere. In particular, the usefulness of both global and local electrophilic power was evaluated by studying the chemical reactivity of six series of α,β-unsaturated carbonyl compounds whose experimental reactivity measures toward the nucleophile glutathione are available. It was observed in the majority of the cases the global and local electrophilic powers work as better than the popular global and local electrophilicity indices, respectively.
publisher Sociedade Brasileira de Química
publishDate 2017
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422017000500513
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AT paezmanuels indicesdepoderelectrofilicoglobalylocalparaelestudioteoricodelareactividadquimicaaplicacionaderivadoscarboniloabinsaturados
AT torresfrancisco indicesdepoderelectrofilicoglobalylocalparaelestudioteoricodelareactividadquimicaaplicacionaderivadoscarboniloabinsaturados
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