Issue 37, 2006

Highly soluble acenes as semiconductors for thin film transistors

Abstract

Acene derivatives 3, 5, 7 and 9 bearing two trimethoxyphenylethynyl substituents have been synthesized. The optical properties of these acenes have been investigated by UV/Vis and fluorescence spectroscopy and their eletrochemical properties have been elucidated by cyclic voltammetry (CV). X-Ray analysis of the anthracene and tetracene derivatives 3 and 5 has revealed a 1-D π-stacking in crystals of 3 and 5. In contrast to their parent hydrocarbons, the present disubstituted acenes are highly soluble in different solvents. Spin-coating has afforded amorphous thin films that exhibit field effect mobility. Best performance has been achieved for the OTFTs prepared from the pentacene derivative 7 with a field effect mobility of 1.9 × 10−5 cm2 V−1 s−1 and an on/off ratio of 103.

Graphical abstract: Highly soluble acenes as semiconductors for thin film transistors

Supplementary files

Article information

Article type
Paper
Submitted
19 May 2006
Accepted
09 Aug 2006
First published
21 Aug 2006

J. Mater. Chem., 2006,16, 3708-3714

Highly soluble acenes as semiconductors for thin film transistors

R. Schmidt, S. Göttling, D. Leusser, D. Stalke, A. Krause and F. Würthner, J. Mater. Chem., 2006, 16, 3708 DOI: 10.1039/B607172D

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