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Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups

A series of soluble aromatic poly(amide-imide)s (PAIs) was prepared from a new diamide–diamine monomer having biphenyl units with two CF(3) groups. The diamide–diamine monomer was polymerized with 2,2′-bis(trifluoromethyl)benzidine and pyromelltic dianhydride through an imidization reaction to prepa...

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Detalles Bibliográficos
Autores principales: Byun, Taejoon, Kim, Seong Jong, Kim, Sang Youl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840246/
https://www.ncbi.nlm.nih.gov/pubmed/35160615
http://dx.doi.org/10.3390/polym14030624
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author Byun, Taejoon
Kim, Seong Jong
Kim, Sang Youl
author_facet Byun, Taejoon
Kim, Seong Jong
Kim, Sang Youl
author_sort Byun, Taejoon
collection PubMed
description A series of soluble aromatic poly(amide-imide)s (PAIs) was prepared from a new diamide–diamine monomer having biphenyl units with two CF(3) groups. The diamide–diamine monomer was polymerized with 2,2′-bis(trifluoromethyl)benzidine and pyromelltic dianhydride through an imidization reaction to prepare PAIs with a controlled imide/amide bond ratio in the main chains. While the PAIs with the highest imide bond content showed a limited solubility, other PAIs were soluble in polar organic solvents and can be solution-cast into flexible freestanding films. All PAIs exhibited high thermal stability with 5% weight loss temperature (T(d5)) from 464 to 497 °C in air, and no appearance of glass transition up to 400 °C. Notably, the linear coefficient of thermal expansion (CTE) value of the PAI films was linearly decreased with the imide bond content and varied from 44.8 to 7.8 ppm/°C.
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spelling pubmed-88402462022-02-13 Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups Byun, Taejoon Kim, Seong Jong Kim, Sang Youl Polymers (Basel) Article A series of soluble aromatic poly(amide-imide)s (PAIs) was prepared from a new diamide–diamine monomer having biphenyl units with two CF(3) groups. The diamide–diamine monomer was polymerized with 2,2′-bis(trifluoromethyl)benzidine and pyromelltic dianhydride through an imidization reaction to prepare PAIs with a controlled imide/amide bond ratio in the main chains. While the PAIs with the highest imide bond content showed a limited solubility, other PAIs were soluble in polar organic solvents and can be solution-cast into flexible freestanding films. All PAIs exhibited high thermal stability with 5% weight loss temperature (T(d5)) from 464 to 497 °C in air, and no appearance of glass transition up to 400 °C. Notably, the linear coefficient of thermal expansion (CTE) value of the PAI films was linearly decreased with the imide bond content and varied from 44.8 to 7.8 ppm/°C. MDPI 2022-02-06 /pmc/articles/PMC8840246/ /pubmed/35160615 http://dx.doi.org/10.3390/polym14030624 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Byun, Taejoon
Kim, Seong Jong
Kim, Sang Youl
Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups
title Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups
title_full Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups
title_fullStr Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups
title_full_unstemmed Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups
title_short Soluble Poly(amide-imide)s from Diamide–Diamine Monomer with Trifluoromethyl Groups
title_sort soluble poly(amide-imide)s from diamide–diamine monomer with trifluoromethyl groups
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840246/
https://www.ncbi.nlm.nih.gov/pubmed/35160615
http://dx.doi.org/10.3390/polym14030624
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