Issue 6, 2005

Dye-functionalized head-to-tail coupled oligo(3-hexylthiophenes)—perylene–oligothiophene dyads for photovoltaic applications

Abstract

A series of novel donor–acceptor systems, consisting of head-to-tail coupled oligo(3-hexylthiophene)s covalently linked to perylenemonoimide, is described. These hybrid molecules, which differ by the length of the oligothiophene units from a monothiophene up to an octathiophene, were created via effective palladium-catalyzed Negishi and Suzuki cross-coupling reactions in good to excellent yields. The optical and electrochemical properties of these compounds were determined and based on this series structure–property relationships have been established which give vital information for the fabrication of photovoltaic devices. Because the synthesized perylenyl–oligothiophenes distinguish themselves by a high absorption between 300 and 550 nm and an almost complete fluorescence quenching of the perylene acceptor, they meet the requirements for organic solar cells.

Graphical abstract: Dye-functionalized head-to-tail coupled oligo(3-hexylthiophenes)—perylene–oligothiophene dyads for photovoltaic applications

Article information

Article type
Paper
Submitted
29 Sep 2004
Accepted
14 Jan 2005
First published
21 Feb 2005

Org. Biomol. Chem., 2005,3, 985-995

Dye-functionalized head-to-tail coupled oligo(3-hexylthiophenes)—perylene–oligothiophene dyads for photovoltaic applications

J. Cremer, E. Mena-Osteritz, N. G. Pschierer, K. Müllen and P. Bäuerle, Org. Biomol. Chem., 2005, 3, 985 DOI: 10.1039/B414817G

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