Highly Crystalline 2,6,9,10-Tetrakis((4-hexylphenyl)ethynyl)anthracene for Efficient Solution-Processed Field-effect Transistors

A new anthracene-containing conjugated molecule was synthesized through the Sonogashira coupling and reduction reactions. 1-Ethynyl-4-hexylbenzene was coupled to 2,6-bis((4-hexylphenyl) ethynyl)anthracene- 9,10-dione through a reduction reaction to generate 2,6,9,10-tetrakis((4-hexylphenyl)ethynyl)...

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Published inBulletin of the Korean Chemical Society Vol. 33; no. 5; pp. 1653 - 1658
Main Authors Hur, Jung-A, Shin, Ji-Cheol, Lee, Tae-Wan, Kim, Kyung-Hwan, Cho, Min-Ju, Choi, Dong-Hoon
Format Journal Article
LanguageEnglish
Published 대한화학회 20.05.2012
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Summary:A new anthracene-containing conjugated molecule was synthesized through the Sonogashira coupling and reduction reactions. 1-Ethynyl-4-hexylbenzene was coupled to 2,6-bis((4-hexylphenyl) ethynyl)anthracene- 9,10-dione through a reduction reaction to generate 2,6,9,10-tetrakis((4-hexylphenyl)ethynyl) anthracene. The semiconducting properties were evaluated in an organic thin film transistor (OTFT) and a single-crystal fieldeffect transistor (SC-FET). The OTFT showed a mobility of around 0.13 cm2 V−1 s−1 (ION/IOFF > 106), whereas the SC-FET showed a mobility of 1.00-1.35 cm2 V−1 s−1, which is much higher than that of the OTFT. Owing to the high photoluminescence quantum yield of 2,6,9,10-tetrakis((4-hexylphenyl)ethynyl) anthracene, we could observe a significant increase in drain current under irradiation with visible light (λ = 538 nm, 12.5 μW/ cm2). KCI Citation Count: 6
Bibliography:http://journal.kcsnet.or.kr/main/j_search/j_abstract_view.htm?code=B120540&qpage=j_search&spage=b_bkcs&dpage=ar
G704-000067.2012.33.5.021
ISSN:0253-2964
1229-5949
DOI:10.5012/bkcs.2012.33.5.1653