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Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene

Many chemists have attempted syntheses of extended π-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 rin...

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Detalles Bibliográficos
Autores principales: Shimo, Yuma, Mikami, Takahiro, Hamao, Shino, Goto, Hidenori, Okamoto, Hideki, Eguchi, Ritsuko, Gohda, Shin, Hayashi, Yasuhiko, Kubozono, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759550/
https://www.ncbi.nlm.nih.gov/pubmed/26893188
http://dx.doi.org/10.1038/srep21008
Descripción
Sumario:Many chemists have attempted syntheses of extended π-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(−1) s(−1), which is the highest mobility realized so far in organic single-crystal FETs.