TY - JOUR
T1 - Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
AU - Shimo, Yuma
AU - Mikami, Takahiro
AU - Hamao, Shino
AU - Goto, Hidenori
AU - Okamoto, Hideki
AU - Eguchi, Ritsuko
AU - Gohda, Shin
AU - Hayashi, Yasuhiko
AU - Kubozono, Yoshihiro
N1 - Funding Information:
This study was partly supported by Grants-in-Aid (22244045, 24550054, 26105004, and 26400361) from MEXT, from the LEMSUPER project (JST-EU Superconductor Project) and the JST-ACT-C project of the Japan Science and Technology Agency (JST), from the Okayama Foundation for Science and Technology, and by the Program for Promoting the Enhancement of Research Universities.
PY - 2016/2/19
Y1 - 2016/2/19
N2 - Many chemists have attempted syntheses of extended I €-electron network molecules because of the widespread interest in the chemistry, physics and materials science of such molecules and their potential applications. In particular, extended phenacene molecules, consisting of coplanar fused benzene rings in a repeating W-shaped pattern have attracted much attention because field-effect transistors (FETs) using phenacene molecules show promisingly high performance. Until now, the most extended phenacene molecule available for transistors was [8]phenacene, with eight benzene rings, which showed very high FET performance. Here, we report the synthesis of a more extended phenacene molecule, [9]phenacene, with nine benzene rings. Our synthesis produced enough [9]phenacene to allow the characterization of its crystal and electronic structures, as well as the fabrication of FETs using thin-film and single-crystal [9]phenacene. The latter showed a field-effect mobility as high as 18 cm 2 V â'1 s â'1, which is the highest mobility realized so far in organic single-crystal FETs.
AB - Many chemists have attempted syntheses of extended I €-electron network molecules because of the widespread interest in the chemistry, physics and materials science of such molecules and their potential applications. In particular, extended phenacene molecules, consisting of coplanar fused benzene rings in a repeating W-shaped pattern have attracted much attention because field-effect transistors (FETs) using phenacene molecules show promisingly high performance. Until now, the most extended phenacene molecule available for transistors was [8]phenacene, with eight benzene rings, which showed very high FET performance. Here, we report the synthesis of a more extended phenacene molecule, [9]phenacene, with nine benzene rings. Our synthesis produced enough [9]phenacene to allow the characterization of its crystal and electronic structures, as well as the fabrication of FETs using thin-film and single-crystal [9]phenacene. The latter showed a field-effect mobility as high as 18 cm 2 V â'1 s â'1, which is the highest mobility realized so far in organic single-crystal FETs.
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U2 - 10.1038/srep21008
DO - 10.1038/srep21008
M3 - Article
AN - SCOPUS:84959036833
SN - 2045-2322
VL - 6
JO - Scientific reports
JF - Scientific reports
M1 - 21008
ER -