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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4759550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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