Literature DB >> 25701090

On the intrinsic reactivity index for electrophilicity/nucleophilicity responses.

Eduardo Chamorro1, Junia Melin.   

Abstract

We present a critical discussion related to the recent definition of the intrinsic reactivity index, IRI, (Tetrahedron Lett. 2013, 54, 339-342; Tetrahedron 2013, 69, 4247-4258) formulated to describe both, electrophilicity (charge acceptance) and nucleophilicity (charge donation) reactivities. We here stress that such an IRI model, based on the quantity μ/η, should be properly related to theoretical approximations associated to the change in the global electronic energy of a given chemical system under interaction with a suitable electron bath (Gazquez JL et al. J Phys Chem A 2007, 111, 1966-1970). Further, the limitations of the IRI model are presented by emphasizing that the intrinsic relative scales of electrophilicity and nucleophilicity within a second-order perturbation approach must account for the further stabilization of the two interacting species (Chamorro E et al. J Phys Chem A 2013, 117, 2636-2643).

Entities:  

Year:  2015        PMID: 25701090     DOI: 10.1007/s00894-015-2608-2

Source DB:  PubMed          Journal:  J Mol Model        ISSN: 0948-5023            Impact factor:   1.810


  16 in total

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4.  The physical basis of the hard/soft acid/base principle.

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5.  Electrodonating and electroaccepting powers.

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Journal:  J Phys Chem A       Date:  2007-02-17       Impact factor: 2.781

6.  Philicity indices within the spin-polarized density-functional theory framework.

Authors:  E Chamorro; P Pérez; F De Proft; P Geerlings
Journal:  J Chem Phys       Date:  2006-01-28       Impact factor: 3.488

7.  Update 2 of: electrophilicity index.

Authors:  Pratim Kumar Chattaraj; Santanab Giri; Soma Duley
Journal:  Chem Rev       Date:  2011-02-09       Impact factor: 60.622

8.  Intrinsic relative scales of electrophilicity and nucleophilicity.

Authors:  Eduardo Chamorro; Mario Duque-Noreña; Rafael Notario; Patricia Pérez
Journal:  J Phys Chem A       Date:  2013-03-14       Impact factor: 2.781

9.  The nucleophilicity N index in organic chemistry.

Authors:  Luis R Domingo; Patricia Pérez
Journal:  Org Biomol Chem       Date:  2011-08-15       Impact factor: 3.876

10.  Comparison between experimental and theoretical scales of electrophilicity in benzhydryl cations.

Authors:  Patricia Pérez; Alejandro Toro-Labbé; Arie Aizman; Renato Contreras
Journal:  J Org Chem       Date:  2002-07-12       Impact factor: 4.354

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  3 in total

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Journal:  J Mol Model       Date:  2018-09-14       Impact factor: 1.810

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Journal:  J Mol Model       Date:  2018-11-09       Impact factor: 1.810

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Journal:  Comput Toxicol       Date:  2021-09-23
  3 in total

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