Issue 10, 2011

Straightforward access to aryl-substituted tetrathiafulvalenes by palladium-catalysed direct C–H arylation and their photophysical and electrochemical properties

Abstract

Treatment of tetrathiafulvalene (TTF) with aryl bromides in the presence of cesium carbonate and a palladium catalyst results in direct arylation of TTF. The direct arylation is inherently straightforward and efficient, hence easily creating a large library of aryl TTFs for systematic investigations of structure–property relationships. The present protocol will thus represent an efficient method for exploiting TTF-based interesting functional materials.

Graphical abstract: Straightforward access to aryl-substituted tetrathiafulvalenes by palladium-catalysed direct C–H arylation and their photophysical and electrochemical properties

Supplementary files

Article information

Article type
Edge Article
Submitted
16 Jun 2011
Accepted
04 Jul 2011
First published
01 Aug 2011

Chem. Sci., 2011,2, 2017-2021

Straightforward access to aryl-substituted tetrathiafulvalenes by palladium-catalysed direct C–H arylation and their photophysical and electrochemical properties

Y. Mitamura, H. Yorimitsu, K. Oshima and A. Osuka, Chem. Sci., 2011, 2, 2017 DOI: 10.1039/C1SC00372K

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