Mechanistic pathways of aromatic nucleophilic substitution in conventional solvents and ionic liquids

Date

2014

Type:

Artículo

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1

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Journal Title

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Volume Title

Publisher

Royal Society of Chemistry

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Abstract

Solvation effects on the reaction mechanism of the title reactions have been kinetically evaluated in 21 conventional solvents and 17 ionic liquids. Solvent polarity affects the catalyzed and non-catalyzed SNAr pathways differently. The ambiphilic character of water and formamide, which act as a hydrogen bond donor/acceptor, induces nucleophilic activation at the nitrogen center of the nucleophile. The ionic liquid EMIMDCN appears to be the best solvent for the SNAr route probably due to the high polarizability of the dicyanamide anion.

Description

Centro de Química Médica

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Citation

New J. Chem., 2014,38, p:2611-2618

Keywords

Química, conventional solvents, ionic liquids, nucleophilic activation, SNAr reactions

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