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Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA

An alicyclic tetracarboxylic dianhydride having cyclopentanone bis-spironorbornane structure (CpODA) was polycondensated with aromatic dianhydrides to form the corresponding poly(amic acid)s which possessed logarithmic viscosities in the range 1.47–0.54 dL/g. The poly(amic acid) was imidized by thre...

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Autores principales: Ozawa, Hiroki, Ishiguro, Eriko, Kyoya, Yuri, Kikuchi, Yasuaki, Matsumoto, Toshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398836/
https://www.ncbi.nlm.nih.gov/pubmed/34451362
http://dx.doi.org/10.3390/polym13162824
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author Ozawa, Hiroki
Ishiguro, Eriko
Kyoya, Yuri
Kikuchi, Yasuaki
Matsumoto, Toshihiko
author_facet Ozawa, Hiroki
Ishiguro, Eriko
Kyoya, Yuri
Kikuchi, Yasuaki
Matsumoto, Toshihiko
author_sort Ozawa, Hiroki
collection PubMed
description An alicyclic tetracarboxylic dianhydride having cyclopentanone bis-spironorbornane structure (CpODA) was polycondensated with aromatic dianhydrides to form the corresponding poly(amic acid)s which possessed logarithmic viscosities in the range 1.47–0.54 dL/g. The poly(amic acid) was imidized by three methods: a chemical, a thermal, and a combined chemical and thermal process. In a thermal method, imidization temperature markedly influenced the film quality and molecular weight of the polyimide. When the poly(amic acid) was cured over the Tg of the corresponding polyimide, the flexible polyimide films were obtained and the molecular weights increased several times, which means that the post-polymerization took place. In spite of low-temperature cure below Tg flexible films with the imidization ratio of 100% were fabricated by a combined chemical and thermal imidization technique. The films possessed the decomposition temperatures in a range of 475–501 °C and Tgs over 330 °C. The high Tg results from a dipole–dipole interaction between the keto groups of the polymer chains as well as development of the rigid polyalicyclic unit. The polyimide films exhibited CTE between 17 and 57 ppm/K. All the films fabricated were entirely colorless and possessed the λcut-offs shorter than 337 nm. Notably, the films prepared by a chemical method exhibited outstanding optical properties.
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spelling pubmed-83988362021-08-29 Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA Ozawa, Hiroki Ishiguro, Eriko Kyoya, Yuri Kikuchi, Yasuaki Matsumoto, Toshihiko Polymers (Basel) Article An alicyclic tetracarboxylic dianhydride having cyclopentanone bis-spironorbornane structure (CpODA) was polycondensated with aromatic dianhydrides to form the corresponding poly(amic acid)s which possessed logarithmic viscosities in the range 1.47–0.54 dL/g. The poly(amic acid) was imidized by three methods: a chemical, a thermal, and a combined chemical and thermal process. In a thermal method, imidization temperature markedly influenced the film quality and molecular weight of the polyimide. When the poly(amic acid) was cured over the Tg of the corresponding polyimide, the flexible polyimide films were obtained and the molecular weights increased several times, which means that the post-polymerization took place. In spite of low-temperature cure below Tg flexible films with the imidization ratio of 100% were fabricated by a combined chemical and thermal imidization technique. The films possessed the decomposition temperatures in a range of 475–501 °C and Tgs over 330 °C. The high Tg results from a dipole–dipole interaction between the keto groups of the polymer chains as well as development of the rigid polyalicyclic unit. The polyimide films exhibited CTE between 17 and 57 ppm/K. All the films fabricated were entirely colorless and possessed the λcut-offs shorter than 337 nm. Notably, the films prepared by a chemical method exhibited outstanding optical properties. MDPI 2021-08-22 /pmc/articles/PMC8398836/ /pubmed/34451362 http://dx.doi.org/10.3390/polym13162824 Text en © 2021 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
Ozawa, Hiroki
Ishiguro, Eriko
Kyoya, Yuri
Kikuchi, Yasuaki
Matsumoto, Toshihiko
Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA
title Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA
title_full Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA
title_fullStr Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA
title_full_unstemmed Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA
title_short Colorless Polyimides Derived from an Alicyclic Tetracarboxylic Dianhydride, CpODA
title_sort colorless polyimides derived from an alicyclic tetracarboxylic dianhydride, cpoda
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398836/
https://www.ncbi.nlm.nih.gov/pubmed/34451362
http://dx.doi.org/10.3390/polym13162824
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