Trialkylsilylethynyl-functionalized tetraceno[2,3-b]thiophene and anthra[2,3-b]thiophene organic transistors
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
A series of ethynyl-substituted molecules with the tetraceno[2,3-è] thiophene and anthra[2,3-b]thiophene core have been synthesized. The aim was to investigate the impact of differently bulky side-chain substituents on the packing of the molecule in thin film and hence its thin-film transistor (TFT) mobility. Three R groups were used, namely, the tri-isopropyl-, triethyl-, and trimethylsilylethynyl groups. We did not observe a direct correlation between substituent size and TFT mobility. However, the 5,12-bis(tri- isopropylsilylethynyl)tetraceno[2,3-b]thiophene has a mobility as high as 1.25 cm2/V·s, the 5,12-bis(trimethylsilylethynyl)tetraceno[2,3-b] thiophene has a mobility of about 0.00616 cm2/V·s, while 5,10-bis(triethylsilylethynyl)anthra[2,3-b]thiophene and 5,10- bis(trimethylsilylethynyl)anthra[2,3-è]thiophene have a mobility of 10-4cm2/V·s on phenylsilane- and octadecyltrichlorosilane-treated surfaces respectively.
Details
Original language | English |
---|---|
Pages (from-to) | 4669-4676 |
Number of pages | 8 |
Journal | Chemistry of materials |
Volume | 20 |
Issue number | 14 |
Publication status | Published - 20 Jun 2008 |
Peer-reviewed | Yes |
Externally published | Yes |