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Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups
The high-frequency and high-speed communication in the 5 G era puts forward requirements for the dielectric properties of polymers. Introducing fluorine into poly(ary ether ketone) can improve its dielectric properties. In this work, by introducing the fluorine group strategy, we successfully design...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150610/ https://www.ncbi.nlm.nih.gov/pubmed/37139095 http://dx.doi.org/10.1080/15685551.2023.2205733 |
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author | Liu, Xiaolong Sun, Yunlong Chen, Yue Zhao, Zhongfu Wang, Zhipeng Zhou, Guangyuan |
author_facet | Liu, Xiaolong Sun, Yunlong Chen, Yue Zhao, Zhongfu Wang, Zhipeng Zhou, Guangyuan |
author_sort | Liu, Xiaolong |
collection | PubMed |
description | The high-frequency and high-speed communication in the 5 G era puts forward requirements for the dielectric properties of polymers. Introducing fluorine into poly(ary ether ketone) can improve its dielectric properties. In this work, by introducing the fluorine group strategy, we successfully designed and synthesized three novel trifluoromethyl (−CF(3)) or trifluoromethoxy (−OCF(3))-containing bisphenol monomers and their F-substitution PEK-based polymers (PEK-Ins). All these PEK-Ins exhibited good thermal, mechanical and dielectric properties. The T d5% of the three polymers is all higher than 520℃. The free volume fraction of novel polymers increased from 3.75% to 5.72%. Among the three polymers, exhibited the lowest dielectric constant of the films is 2.839, and the dielectric loss is 0.0048, ascribing to the increasing free volume. The Young’s modulus of the polymer film is as high as 2.9 GPa and the tensile strength is as high as 84 MPa. PEK-Ins reduced the dielectric constant by introducing a low fluorine content. This study provides a new way to design PEK to synthesize low dielectric constant polymers. |
format | Online Article Text |
id | pubmed-10150610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-101506102023-05-02 Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups Liu, Xiaolong Sun, Yunlong Chen, Yue Zhao, Zhongfu Wang, Zhipeng Zhou, Guangyuan Des Monomers Polym Full Length Article The high-frequency and high-speed communication in the 5 G era puts forward requirements for the dielectric properties of polymers. Introducing fluorine into poly(ary ether ketone) can improve its dielectric properties. In this work, by introducing the fluorine group strategy, we successfully designed and synthesized three novel trifluoromethyl (−CF(3)) or trifluoromethoxy (−OCF(3))-containing bisphenol monomers and their F-substitution PEK-based polymers (PEK-Ins). All these PEK-Ins exhibited good thermal, mechanical and dielectric properties. The T d5% of the three polymers is all higher than 520℃. The free volume fraction of novel polymers increased from 3.75% to 5.72%. Among the three polymers, exhibited the lowest dielectric constant of the films is 2.839, and the dielectric loss is 0.0048, ascribing to the increasing free volume. The Young’s modulus of the polymer film is as high as 2.9 GPa and the tensile strength is as high as 84 MPa. PEK-Ins reduced the dielectric constant by introducing a low fluorine content. This study provides a new way to design PEK to synthesize low dielectric constant polymers. Taylor & Francis 2023-04-29 /pmc/articles/PMC10150610/ /pubmed/37139095 http://dx.doi.org/10.1080/15685551.2023.2205733 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Full Length Article Liu, Xiaolong Sun, Yunlong Chen, Yue Zhao, Zhongfu Wang, Zhipeng Zhou, Guangyuan Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups |
title | Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups |
title_full | Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups |
title_fullStr | Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups |
title_full_unstemmed | Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups |
title_short | Design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups |
title_sort | design and synthesis of novel poly (aryl ether ketones) containing trifluoromethyl and trifluoromethoxy groups |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150610/ https://www.ncbi.nlm.nih.gov/pubmed/37139095 http://dx.doi.org/10.1080/15685551.2023.2205733 |
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