Literature DB >> 23832651

Protophilicity index and protofelicity equalization principle: new measures of Brønsted-Lowry-Lewis acid-base interactions.

Francisco Méndez1, Julio A Alonso, Arlette Richaud.   

Abstract

The simultaneous contributions of proton and electron transfer to the Brønsted-Lowry and Lewis acid-base properties of a set of p-substituted phenols are reported in this work. As a result of the analysis, a novel protophilicity index considered as the second-order energy change of a Brønsted-Lowry base as it is saturated with protons, a combined Brønsted-Lowry-Lewis acidity index (with a corresponding basicity index), and a protofelicity equalization principle (a parallel of the electronegativity equalization principle) are presented.

Entities:  

Year:  2013        PMID: 23832651     DOI: 10.1007/s00894-013-1881-1

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


  17 in total

1.  Conceptual Density-Functional Theory for General Chemical Reactions, Including Those That Are Neither Charge- nor Frontier-Orbital-Controlled. 2. Application to Molecules Where Frontier Molecular Orbital Theory Fails.

Authors:  James S M Anderson; Junia Melin; Paul W Ayers
Journal:  J Chem Theory Comput       Date:  2007-03       Impact factor: 6.006

2.  Conceptual Density-Functional Theory for General Chemical Reactions, Including Those That Are Neither Charge- nor Frontier-Orbital-Controlled. 1. Theory and Derivation of a General-Purpose Reactivity Indicator.

Authors:  James S M Anderson; Junia Melin; Paul W Ayers
Journal:  J Chem Theory Comput       Date:  2007-03       Impact factor: 6.006

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

Authors:  Paul W Ayers
Journal:  Faraday Discuss       Date:  2007       Impact factor: 4.008

4.  Nucleophilicity index from perturbed electrostatic potentials.

Authors:  A Cedillo; R Contreras; M Galván; A Aizman; J Andrés; V S Safont
Journal:  J Phys Chem A       Date:  2007-03-08       Impact factor: 2.781

5.  Elucidating the hard/soft acid/base principle: a perspective based on half-reactions.

Authors:  Paul W Ayers; Robert G Parr; Ralph G Pearson
Journal:  J Chem Phys       Date:  2006-05-21       Impact factor: 3.488

6.  Indices for predicting the quality of leaving groups.

Authors:  Paul W Ayers; James S M Anderson; Juan I Rodriguez; Zobia Jawed
Journal:  Phys Chem Chem Phys       Date:  2005-05-07       Impact factor: 3.676

7.  Molecular acidity: A quantitative conceptual density functional theory description.

Authors:  Shubin Liu; Cynthia K Schauer; Lee G Pedersen
Journal:  J Chem Phys       Date:  2009-10-28       Impact factor: 3.488

8.  The Basicity of p-Substituted Phenolates and the Elimination-Substitution Ratio in p-Nitrophenethyl Bromide: A HSAB Theoretical Study.

Authors:  Francisco Méndez; María de L. Romero; Frank De Proft; Paul Geerlings
Journal:  J Org Chem       Date:  1998-08-21       Impact factor: 4.354

9.  Predicting the reactivity of ambidentate nucleophiles and electrophiles using a single, general-purpose, reactivity indicator.

Authors:  James S M Anderson; Paul W Ayers
Journal:  Phys Chem Chem Phys       Date:  2007-03-27       Impact factor: 3.676

10.  Influence of fluorine atoms and aromatic rings on the acidity of ethanol.

Authors:  Ramsés E Ramírez; Cirilo García-Martínez; Francisco Méndez
Journal:  J Phys Chem A       Date:  2009-10-08       Impact factor: 2.781

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