Abstract
New candidates composed of anthracene and 4-alkylethynylbenzene end-capped oligomers for OTFTs were synthesized under Sonogashira coupling reaction conditions. All oligomers were characterized by FT-IR, mass, UV-visible, and PL emission spectrum analyses, cyclic voltammetry (CV), differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA), 1H-NMR, and 13C-NMR. Investigation of their physical properties showed that the oligomers had high oxidation potential and thermal stability. Thin films of DHPEAnt and DDPEAnt were characterized by spin coating them onto Si/SiO 2 to fabricate top-contact OTFTs. The devices prepared using DHPEAnt and DDPEAnt showed hole field-effect mobilities of 4.0 × 10-3 cm2/Vs and 2.0 × 10-3 cm2/Vs, respectively, for solution-processed OTFTs.
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CITATION STYLE
Jang, S. H., Kim, H., Hwang, M. J., Jeong, E. B., Yun, H. J., Lee, D. H., … Lee, S. G. (2012). Solution processable symmetric 4-alkylethynylbenzene end-capped anthracene derivatives. Bulletin of the Korean Chemical Society, 33(2), 541–548. https://doi.org/10.5012/bkcs.2012.33.2.541
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