Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
194366 | Electrochimica Acta | 2006 | 8 Pages |
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.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Anne Neudörffer, Maurice-Bernard Fleury, Jean-Pierre Desvergne, Martine Largeron,