Article ID Journal Published Year Pages File Type
194366 Electrochimica Acta 2006 8 Pages PDF
Abstract

New insights into the electrochemical oxidative coupling of 4-hydroxycinnamate derivatives are delineated through the variation of the nature of the supporting electrolyte. In particular, replacement of a tetraethylammonium salt by a lithium salt markedly modified the outcome of the reaction, thus allowing the isolation of different coupling products. This effect could be ascribed to lithium ion-pairing phenomena, which affected both the starting materials and the bis-quinonemethide species generated during the oxidative coupling process.

Related Topics
Physical Sciences and Engineering Chemical Engineering Chemical Engineering (General)
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