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Synthesis of novel asymmetric oligomers based on oligothiophene-naphthalene molecules and solution-processable p-channel organic thin film transistors
- Authors
- Jang, S.H.; Shin, M.-G.; Park, J.H.; Chung, D.S.; Park, C.E.; Kim, Y.-H.; Lee, S.-G.; Kwon, S.-K.
- Issue Date
- Dec-2009
- Citation
- Proceedings of International Meeting on Information Display, pp 699 - 700
- Pages
- 2
- Indexed
- SCOPUS
- Journal Title
- Proceedings of International Meeting on Information Display
- Start Page
- 699
- End Page
- 700
- ISSN
- 1738-7558
- Abstract
- A series of novel thiophene-naphthalene based asymmetric oligomers for organic thin film transistors (OTFTs) were synthesized by Suzuki cross-coupling reaction between 2-bromo-6-decylnaphthalene and 2-decylthiophene, 2-decyl bithiophene, or 1-decylbenzene, respectively. Remarkably, AON-1 and AON-3 showed good solubility in common solvents. The fabricated devices showed the hole field-effect mobility of 1.4 × 10-2 cm2/Vs for AO, 1.5 × 10-2 cm2/Vs for AON-1, and 3.7 ×10 2 cm-2/Vs for AON-3.
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