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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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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
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author Shimo, Yuma
Mikami, Takahiro
Hamao, Shino
Goto, Hidenori
Okamoto, Hideki
Eguchi, Ritsuko
Gohda, Shin
Hayashi, Yasuhiko
Kubozono, Yoshihiro
author_facet Shimo, Yuma
Mikami, Takahiro
Hamao, Shino
Goto, Hidenori
Okamoto, Hideki
Eguchi, Ritsuko
Gohda, Shin
Hayashi, Yasuhiko
Kubozono, Yoshihiro
author_sort Shimo, Yuma
collection PubMed
description 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.
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spelling pubmed-47595502016-02-26 Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene Shimo, Yuma Mikami, Takahiro Hamao, Shino Goto, Hidenori Okamoto, Hideki Eguchi, Ritsuko Gohda, Shin Hayashi, Yasuhiko Kubozono, Yoshihiro Sci Rep Article 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. Nature Publishing Group 2016-02-19 /pmc/articles/PMC4759550/ /pubmed/26893188 http://dx.doi.org/10.1038/srep21008 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Shimo, Yuma
Mikami, Takahiro
Hamao, Shino
Goto, Hidenori
Okamoto, Hideki
Eguchi, Ritsuko
Gohda, Shin
Hayashi, Yasuhiko
Kubozono, Yoshihiro
Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
title Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
title_full Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
title_fullStr Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
title_full_unstemmed Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
title_short Synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
title_sort synthesis and transistor application of the extremely extended phenacene molecule, [9]phenacene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759550/
https://www.ncbi.nlm.nih.gov/pubmed/26893188
http://dx.doi.org/10.1038/srep21008
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