Nucleophilicity Parameters for Nitroalkyl Anions in Methanol and Structure‐Reactivity Analysis

Author:

Necibi Feriel12,Ben Salah Saida1,Hierso Jean‐Cyrille2,Fleurat‐Lessard Paul2,Ayachi Sahbi3,Boubaker Taoufik1ORCID

Affiliation:

1. Laboratoire de Chimie hétérocyclique Produits Naturels et Réactivité (LR11ES39) Faculté des Sciences Université de Monastir Avenue de l'Environnement 5019 Monastir Tunisie

2. Institut de Chimie Moléculaire de l'Université de Bourgogne (UMR CNRS 6302) Université Bourgogne-Franche-Comté (UBFC) 9 Avenue Alain Savary 21000 Dijon France

3. Laboratoire de physico-chimie des matériaux (LR01ES19) Faculté des Sciences Université de Monastir Avenue de l'Environnement 5019 Monastir, Tunisie

Abstract

AbstractA kinetic study is reported for the addition of nitroalkyl anions 2 ac at the C‐7 position of the 4‐nitrobenzochalcogenadiazoles 1 ac in methanol at 20 °C. By using the Mayr approach, the nucleophilicity parameters N and the nucleophile specific parameters sN of these nitroalkyl anions 2 ac have been determined and discussed. The structure‐reactivity relationships are discussed, and it is shown that the measured nucleophilicity parameters (N) of anions 2 ac are linearly related (r2=0.9934) to their acidity constant (pKaHMeOH) in methanol. In addition, satisfactory linear correlation has been evidenced between the experimental nucleophilicity N parameter and the theoretical model of nucleophilicity ω−1 for the various nitroalkyl anions 2 ac in methanol.

Publisher

Wiley

Subject

General Chemistry

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