Literature DB >> 16805506

Definition of a nucleophilicity scale.

Paula Jaramillo1, Patricia Pérez, Renato Contreras, William Tiznado, Patricio Fuentealba.   

Abstract

This 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, BF(3), and the other soft, BH(3)) 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.

Entities:  

Year:  2006        PMID: 16805506     DOI: 10.1021/jp057351q

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  13 in total

1.  The chemical biology of hydropersulfides (RSSH): Chemical stability, reactivity and redox roles.

Authors:  Simran S Saund; Victor Sosa; Stephanie Henriquez; Q Nhu N Nguyen; Christopher L Bianco; Shuhei Soeda; Robert Millikin; Corey White; Henry Le; Katsuhiko Ono; Dean J Tantillo; Yoshito Kumagai; Takaaki Akaike; Joseph Lin; Jon M Fukuto
Journal:  Arch Biochem Biophys       Date:  2015-11-05       Impact factor: 4.013

2.  On the intrinsic reactivity index for electrophilicity/nucleophilicity responses.

Authors:  Eduardo Chamorro; Junia Melin
Journal:  J Mol Model       Date:  2015-02-21       Impact factor: 1.810

3.  Influence of gauche effect on uncharged oxime reactivators for the reactivation of tabun-inhibited AChE: quantum chemical and steered molecular dynamics studies.

Authors:  Shibaji Ghosh; Kalyanashis Jana; Bishwajit Ganguly
Journal:  J Comput Aided Mol Des       Date:  2018-07-06       Impact factor: 3.686

Review 4.  Protein modifications by electrophilic lipoxidation products: adduct formation, chemical strategies and tandem mass spectrometry for their detection and identification.

Authors:  Yury V Vasil'ev; Shin-Chen Tzeng; Lin Huang; Claudia S Maier
Journal:  Mass Spectrom Rev       Date:  2014 May-Jun       Impact factor: 10.946

5.  β-dicarbonyl enolates: a new class of neuroprotectants.

Authors:  Richard M LoPachin; Terrence Gavin; Brian C Geohagen; Lihai Zhang; Diana Casper; Rukmani Lekhraj; David S Barber
Journal:  J Neurochem       Date:  2010-12-02       Impact factor: 5.372

Review 6.  Application of the Hard and Soft, Acids and Bases (HSAB) theory to toxicant--target interactions.

Authors:  Richard M Lopachin; Terrence Gavin; Anthony Decaprio; David S Barber
Journal:  Chem Res Toxicol       Date:  2011-11-16       Impact factor: 3.739

7.  A density functional reactivity theory (DFRT) based approach to understand the interaction of cisplatin analogues with protecting agents.

Authors:  Amrit Sarmah; Ram Kinkar Roy
Journal:  J Comput Aided Mol Des       Date:  2014-09-03       Impact factor: 3.686

8.  Cytocompatibility and Antibacterial Properties of Coaxial Electrospun Nanofibers Containing Ciprofloxacin and Indomethacin Drugs.

Authors:  Shahla Khalili; Nazanin Ghane; Saied Nouri Khorasani; Fariba Heydari; Arjan Atwal; Pooya Davoodi
Journal:  Polymers (Basel)       Date:  2022-06-24       Impact factor: 4.967

Review 9.  Molecular mechanisms of 4-hydroxy-2-nonenal and acrolein toxicity: nucleophilic targets and adduct formation.

Authors:  Richard M LoPachin; Terrence Gavin; Dennis R Petersen; David S Barber
Journal:  Chem Res Toxicol       Date:  2009-09       Impact factor: 3.739

10.  Synaptosomal toxicity and nucleophilic targets of 4-hydroxy-2-nonenal.

Authors:  Richard M Lopachin; Brian C Geohagen; Terrence Gavin
Journal:  Toxicol Sci       Date:  2008-11-07       Impact factor: 4.849

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