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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...

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Autores principales: Liu, Xiaolong, Sun, Yunlong, Chen, Yue, Zhao, Zhongfu, Wang, Zhipeng, Zhou, Guangyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
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.
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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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