Supramolecular polymer materials based on ureidopyrimidinone quadruple hydrogen bonding units

IF 26 1区 化学 Q1 POLYMER SCIENCE
Jente Verjans, Richard Hoogenboom
{"title":"Supramolecular polymer materials based on ureidopyrimidinone quadruple hydrogen bonding units","authors":"Jente Verjans,&nbsp;Richard Hoogenboom","doi":"10.1016/j.progpolymsci.2023.101689","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Supramolecular polymer materials are polymeric structures that are physically crosslinked by non-covalent interactions such as ionic interactions, host-guest complexation and </span>hydrogen bonding<span>. The resulting materials generally display stimuli-responsive behavior and/or healable properties, which makes them excellent candidates for the design of dynamic materials. Inspired by its omnipresence in natural systems, hydrogen bonding has proven to be useful for the development of synthetic materials with dynamic properties. Inspired by the base-pairing in the DNA<span> double helix, Meijer et al. developed the self-complementary quadruple hydrogen bonding unit ureidopyimidinone (UPy), which has a strong dimerization constant (K</span></span></span><sub>dim</sub> &gt; 10<sup>7</sup> <em>M</em> <sup>−1</sup><span> ). The incorporation of UPy motifs in polymeric precursors led to a plethora of hydrogen bonded materials with applications ranging from artificial arteries to reversible adhesives. This review will focus on design strategies to synthesize these UPy-containing polymer materials, which can be split into three main categories based on the location of the UPy arrays: UPy in the main-chain, UPy in the side-chains or UPy at the chain-ends. In addition to the synthetic routes, the material properties of the resulting UPy-containing supramolecular polymer materials will be discussed.</span></p></div>","PeriodicalId":413,"journal":{"name":"Progress in Polymer Science","volume":"142 ","pages":"Article 101689"},"PeriodicalIF":26.0000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0079670023000448","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 2

Abstract

Supramolecular polymer materials are polymeric structures that are physically crosslinked by non-covalent interactions such as ionic interactions, host-guest complexation and hydrogen bonding. The resulting materials generally display stimuli-responsive behavior and/or healable properties, which makes them excellent candidates for the design of dynamic materials. Inspired by its omnipresence in natural systems, hydrogen bonding has proven to be useful for the development of synthetic materials with dynamic properties. Inspired by the base-pairing in the DNA double helix, Meijer et al. developed the self-complementary quadruple hydrogen bonding unit ureidopyimidinone (UPy), which has a strong dimerization constant (Kdim > 107 M −1 ). The incorporation of UPy motifs in polymeric precursors led to a plethora of hydrogen bonded materials with applications ranging from artificial arteries to reversible adhesives. This review will focus on design strategies to synthesize these UPy-containing polymer materials, which can be split into three main categories based on the location of the UPy arrays: UPy in the main-chain, UPy in the side-chains or UPy at the chain-ends. In addition to the synthetic routes, the material properties of the resulting UPy-containing supramolecular polymer materials will be discussed.

Abstract Image

基于脲嘧啶四重氢键单元的超分子高分子材料
超分子高分子材料是通过离子相互作用、主客体络合作用和氢键等非共价相互作用进行物理交联的高分子结构。所得到的材料通常表现出刺激响应行为和/或可治愈性,这使它们成为动态材料设计的优秀候选人。受其在自然系统中无处不在的启发,氢键已被证明对开发具有动态特性的合成材料是有用的。受到DNA双螺旋碱基配对的启发,Meijer等人开发了自互补的四重氢键单元脲嘧啶(UPy),它具有很强的二聚化常数(Kdim >107 m−1)。UPy基序在聚合物前体中的结合导致了大量的氢键材料,其应用范围从人造动脉到可逆粘合剂。本文将重点介绍合成这些含UPy聚合物材料的设计策略,根据UPy阵列的位置可将其分为三大类:主链上的UPy,侧链上的UPy或链端上的UPy。除了合成路线外,还将讨论所得含upy的超分子高分子材料的材料性质。
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 求助全文
来源期刊
Progress in Polymer Science
Progress in Polymer Science 化学-高分子科学
CiteScore
48.70
自引率
1.10%
发文量
54
审稿时长
38 days
期刊介绍: Progress in Polymer Science is a journal that publishes state-of-the-art overview articles in the field of polymer science and engineering. These articles are written by internationally recognized authorities in the discipline, making it a valuable resource for staying up-to-date with the latest developments in this rapidly growing field. The journal serves as a link between original articles, innovations published in patents, and the most current knowledge of technology. It covers a wide range of topics within the traditional fields of polymer science, including chemistry, physics, and engineering involving polymers. Additionally, it explores interdisciplinary developing fields such as functional and specialty polymers, biomaterials, polymers in drug delivery, polymers in electronic applications, composites, conducting polymers, liquid crystalline materials, and the interphases between polymers and ceramics. The journal also highlights new fabrication techniques that are making significant contributions to the field. The subject areas covered by Progress in Polymer Science include biomaterials, materials chemistry, organic chemistry, polymers and plastics, surfaces, coatings and films, and nanotechnology. The journal is indexed and abstracted in various databases, including Materials Science Citation Index, Chemical Abstracts, Engineering Index, Current Contents, FIZ Karlsruhe, Scopus, and INSPEC.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信