Cyclization Polymerization of Elemental Sulfur and Diisocyanate: New Polymerization Toward High-Performance Polymer

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2025-04-22 DOI:10.1002/anie.202502207
Jikai Zhang, Yongkang Zuo, Hongxin Yao, Jianwei Zhang, Wenyan Huang, Hongjun Yang, Guangzhao Zhang
{"title":"Cyclization Polymerization of Elemental Sulfur and Diisocyanate: New Polymerization Toward High-Performance Polymer","authors":"Jikai Zhang,&nbsp;Yongkang Zuo,&nbsp;Hongxin Yao,&nbsp;Jianwei Zhang,&nbsp;Wenyan Huang,&nbsp;Hongjun Yang,&nbsp;Guangzhao Zhang","doi":"10.1002/anie.202502207","DOIUrl":null,"url":null,"abstract":"<p>The development of polymer materials heavily relies on new polymerization reactions. Herein, we report the discovery of cyclization polymerization of element sulfur (S<sub>8</sub>) and aliphatic diisocyanate at room temperature with 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) organic base as the catalyst, where the two monomers are covalently linked via the formation of thiadiazolidinone (TDZD) or a cyclic isocyanurate ring. The polymer of S<sub>8</sub> and 1,6-diisocyanatohexane (HDI) exhibits remarkable thermal stability and mechanical properties. Particularly, it has exceptionally high adhesion to various substrates in air or under water, e.g., the underwater adhesion strength is as high as ∼26.5 MPa for poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate) (PETG) and ∼2.3 MPa for poly(tetrafluoroethylene) (Teflon). The cyclization polymerization provides the basis for the synthesis of high-performance polymers with elemental sulfur.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"64 26","pages":""},"PeriodicalIF":16.9000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.202502207","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The development of polymer materials heavily relies on new polymerization reactions. Herein, we report the discovery of cyclization polymerization of element sulfur (S8) and aliphatic diisocyanate at room temperature with 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) organic base as the catalyst, where the two monomers are covalently linked via the formation of thiadiazolidinone (TDZD) or a cyclic isocyanurate ring. The polymer of S8 and 1,6-diisocyanatohexane (HDI) exhibits remarkable thermal stability and mechanical properties. Particularly, it has exceptionally high adhesion to various substrates in air or under water, e.g., the underwater adhesion strength is as high as ∼26.5 MPa for poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate) (PETG) and ∼2.3 MPa for poly(tetrafluoroethylene) (Teflon). The cyclization polymerization provides the basis for the synthesis of high-performance polymers with elemental sulfur.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
单质硫和二异氰酸酯的环化聚合:制备高性能聚合物的新聚合方法
高分子材料的发展在很大程度上依赖于新的聚合反应。本文报道了在1,5,7-三氮杂环[4.4.0]十二-5烯(TBD)有机碱催化下,元素硫(S8)和脂肪族二异氰酸酯在室温下环化聚合的发现,其中两个单体通过形成噻唑烷酮(TDZD)或环异氰脲酸环共价连接。S8 - 1,6-二异氰酸酯己烷(HDI)聚合物具有良好的热稳定性和力学性能。特别是,它在空气或水下对各种底物具有极高的附着力,例如,聚乙二醇-co-1,4-环己二甲醇对苯二甲酸乙二醇酯(PETG)的水下附着力高达~26.5 MPa,聚四氟乙烯(Teflon)的水下附着力高达~2.3 MPa。环合聚合为单质硫高性能聚合物的合成提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
期刊最新文献
Unraveling Synthetase's Mode of Action: The Pyrrolysyl-tRNA Synthetase Dimer Uses Secondary Binding Sites in the Cell. Chemically Synthesized H3K14Ub Unveils Clr4's IDR-Mediated Multivalent Nucleosome Recognition in H3K9 Methylation. One-Pot Amidation/C─H Halogenation by an Efficient Electrochemical Cascade. Shallow-Trap Perovskite Scintillators for High-Resolution, Ghosting-Free X-Ray Imaging. Molecular-Gate Strategy for Solid-State Selective Recognition of Dioxane Isomers via Reversible Host-Guest and Charge-Transfer Modulation.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1