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ID 70792
FullText URL
Author
Takahashi, Naoki Graduate School of Environmental, Life, Natural Science and Technology, Okayama University
Ohkura, Kentaro Research Institute for Interdisciplinary Science, Okayama University
Nishina, Yuta Research Institute for Interdisciplinary Science, Okayama University ORCID Kaken ID publons researchmap
Abstract
Lewis acidic boron-containing π-conjugated polymer materials have been demonstrated to be promising for sensing and catalysis; however, the synthetic approaches and the number of installed boron atoms have been limited. Herein, we report the synthesis of a BC6 polymer structure via cyclotrimerization of alkynes. The resulting polymer exhibited superior catalytic activity to small-molecule analogues such as BPh3 and previously reported boron-containing polymers. This enhanced performance is attributed to the high boron content and increased Lewis acidity of BC6, as supported by theoretical and experimental analyses. Owing to its polymeric nature, the catalyst was readily recovered and reused in the catalytic system. These findings demonstrate that building rigid polymer frameworks with a high density of Lewis acidic boron sites is a promising approach to developing recyclable heterogeneous Lewis acid catalysts, and offers a broadly applicable design principle for functional boron-containing polymeric materials.
Published Date
2026
Publication Title
Polymer Chemistry
Volume
volume17
Issue
issue23
Publisher
Royal Society of Chemistry (RSC)
Start Page
2473
End Page
2478
ISSN
1759-9954
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Royal Society of Chemistry
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publisher
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.1039/d6py00177g
License
http://creativecommons.org/licenses/by/3.0/
助成情報
JPMJCR24S6: 未利用有機物の炭素化:資源循環のためのマルチナリーカーボンの創出 ( 国立研究開発法人科学技術振興機構 / Japan Science and Technology Agency )