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Perfluorocycloparaphenylenes

Perfluorinated aromatic compounds, the so-called perfluoroarenes, are widely used in materials science owing to their high electron affinity and characteristic intermolecular interactions. However, methods to synthesize highly strained perfluoroarenes are limited, which greatly limits their structur...

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Autores principales: Shudo, Hiroki, Kuwayama, Motonobu, Shimasaki, Masafumi, Nishihara, Taishi, Takeda, Youhei, Mitoma, Nobuhiko, Kuwabara, Takuya, Yagi, Akiko, Segawa, Yasutomo, Itami, Kenichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240036/
https://www.ncbi.nlm.nih.gov/pubmed/35764634
http://dx.doi.org/10.1038/s41467-022-31530-x
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author Shudo, Hiroki
Kuwayama, Motonobu
Shimasaki, Masafumi
Nishihara, Taishi
Takeda, Youhei
Mitoma, Nobuhiko
Kuwabara, Takuya
Yagi, Akiko
Segawa, Yasutomo
Itami, Kenichiro
author_facet Shudo, Hiroki
Kuwayama, Motonobu
Shimasaki, Masafumi
Nishihara, Taishi
Takeda, Youhei
Mitoma, Nobuhiko
Kuwabara, Takuya
Yagi, Akiko
Segawa, Yasutomo
Itami, Kenichiro
author_sort Shudo, Hiroki
collection PubMed
description Perfluorinated aromatic compounds, the so-called perfluoroarenes, are widely used in materials science owing to their high electron affinity and characteristic intermolecular interactions. However, methods to synthesize highly strained perfluoroarenes are limited, which greatly limits their structural diversity. Herein, we report the synthesis and isolation of perfluorocycloparaphenylenes (PFCPPs) as a class of ring-shaped perfluoroarenes. Using macrocyclic nickel complexes, we succeeded in synthesizing PF[n]CPPs (n = 10, 12, 14, 16) in one-pot without noble metals. The molecular structures of PF[n]CPPs (n = 10, 12, 14) were determined by X-ray crystallography to confirm their tubular alignment. Photophysical and electrochemical measurements revealed that PF[n]CPPs (n = 10, 12, 14) exhibited wide HOMO–LUMO gaps, high reduction potentials, and strong phosphorescence at low temperature. PFCPPs are not only useful as electron-accepting organic materials but can also be used for accelerating the creation of topologically unique molecular nanocarbon materials.
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spelling pubmed-92400362022-06-30 Perfluorocycloparaphenylenes Shudo, Hiroki Kuwayama, Motonobu Shimasaki, Masafumi Nishihara, Taishi Takeda, Youhei Mitoma, Nobuhiko Kuwabara, Takuya Yagi, Akiko Segawa, Yasutomo Itami, Kenichiro Nat Commun Article Perfluorinated aromatic compounds, the so-called perfluoroarenes, are widely used in materials science owing to their high electron affinity and characteristic intermolecular interactions. However, methods to synthesize highly strained perfluoroarenes are limited, which greatly limits their structural diversity. Herein, we report the synthesis and isolation of perfluorocycloparaphenylenes (PFCPPs) as a class of ring-shaped perfluoroarenes. Using macrocyclic nickel complexes, we succeeded in synthesizing PF[n]CPPs (n = 10, 12, 14, 16) in one-pot without noble metals. The molecular structures of PF[n]CPPs (n = 10, 12, 14) were determined by X-ray crystallography to confirm their tubular alignment. Photophysical and electrochemical measurements revealed that PF[n]CPPs (n = 10, 12, 14) exhibited wide HOMO–LUMO gaps, high reduction potentials, and strong phosphorescence at low temperature. PFCPPs are not only useful as electron-accepting organic materials but can also be used for accelerating the creation of topologically unique molecular nanocarbon materials. Nature Publishing Group UK 2022-06-28 /pmc/articles/PMC9240036/ /pubmed/35764634 http://dx.doi.org/10.1038/s41467-022-31530-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shudo, Hiroki
Kuwayama, Motonobu
Shimasaki, Masafumi
Nishihara, Taishi
Takeda, Youhei
Mitoma, Nobuhiko
Kuwabara, Takuya
Yagi, Akiko
Segawa, Yasutomo
Itami, Kenichiro
Perfluorocycloparaphenylenes
title Perfluorocycloparaphenylenes
title_full Perfluorocycloparaphenylenes
title_fullStr Perfluorocycloparaphenylenes
title_full_unstemmed Perfluorocycloparaphenylenes
title_short Perfluorocycloparaphenylenes
title_sort perfluorocycloparaphenylenes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240036/
https://www.ncbi.nlm.nih.gov/pubmed/35764634
http://dx.doi.org/10.1038/s41467-022-31530-x
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