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Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency
5-Amine-2-(4-amino-benzene)-1-phenyl-benzimidazole (N-PhPABZ) was successfully synthesized and polymerized with 3,3′,4,4′-biphenyl tetracarboxylic dianhydride (BPDA) to obtain a novel N-phenyl-poly(benzimidazole imide) (N-Ph-PBII). The successful incorporation of N-phenyl addressed the issue of high...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694182/ https://www.ncbi.nlm.nih.gov/pubmed/35424274 http://dx.doi.org/10.1039/d0ra10138a |
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author | Qian, Guangtao Dai, Fengna Chen, Haiquan Wang, Mengxia Hu, Mengjie Chen, Chunhai Yu, Youhai |
author_facet | Qian, Guangtao Dai, Fengna Chen, Haiquan Wang, Mengxia Hu, Mengjie Chen, Chunhai Yu, Youhai |
author_sort | Qian, Guangtao |
collection | PubMed |
description | 5-Amine-2-(4-amino-benzene)-1-phenyl-benzimidazole (N-PhPABZ) was successfully synthesized and polymerized with 3,3′,4,4′-biphenyl tetracarboxylic dianhydride (BPDA) to obtain a novel N-phenyl-poly(benzimidazole imide) (N-Ph-PBII). The successful incorporation of N-phenyl addressed the issue of high H(2)O-absorption of traditional PBIIs while retained the superheat resistance property. The resulting N-Ph-PBII possessed a high glass-transition temperature (T(g)) up to 425 °C and a low affinity for water of 1.4%. Furthermore, the loose molecular packing and noncoplanar structures led to an increase in optical transparency for the modified PBII. |
format | Online Article Text |
id | pubmed-8694182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86941822022-04-13 Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency Qian, Guangtao Dai, Fengna Chen, Haiquan Wang, Mengxia Hu, Mengjie Chen, Chunhai Yu, Youhai RSC Adv Chemistry 5-Amine-2-(4-amino-benzene)-1-phenyl-benzimidazole (N-PhPABZ) was successfully synthesized and polymerized with 3,3′,4,4′-biphenyl tetracarboxylic dianhydride (BPDA) to obtain a novel N-phenyl-poly(benzimidazole imide) (N-Ph-PBII). The successful incorporation of N-phenyl addressed the issue of high H(2)O-absorption of traditional PBIIs while retained the superheat resistance property. The resulting N-Ph-PBII possessed a high glass-transition temperature (T(g)) up to 425 °C and a low affinity for water of 1.4%. Furthermore, the loose molecular packing and noncoplanar structures led to an increase in optical transparency for the modified PBII. The Royal Society of Chemistry 2021-01-19 /pmc/articles/PMC8694182/ /pubmed/35424274 http://dx.doi.org/10.1039/d0ra10138a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Qian, Guangtao Dai, Fengna Chen, Haiquan Wang, Mengxia Hu, Mengjie Chen, Chunhai Yu, Youhai Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency |
title | Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency |
title_full | Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency |
title_fullStr | Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency |
title_full_unstemmed | Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency |
title_short | Incorporation of N-phenyl in poly(benzimidazole imide)s and improvement in H(2)O-absorbtion and transparency |
title_sort | incorporation of n-phenyl in poly(benzimidazole imide)s and improvement in h(2)o-absorbtion and transparency |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694182/ https://www.ncbi.nlm.nih.gov/pubmed/35424274 http://dx.doi.org/10.1039/d0ra10138a |
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