动态共价键:烷氧基胺中C-ON键的激活模式

IF 26 1区 化学 Q1 POLYMER SCIENCE
Gérard Audran , Elena G. Bagryanskaya , Raphaël Bikanga , Michelle L. Coote , Olga Guselnikova , Chelsey L. Hammill , Sylvain R.A. Marque , Philippe Mellet , Pavel S. Postnikov
{"title":"动态共价键:烷氧基胺中C-ON键的激活模式","authors":"Gérard Audran ,&nbsp;Elena G. Bagryanskaya ,&nbsp;Raphaël Bikanga ,&nbsp;Michelle L. Coote ,&nbsp;Olga Guselnikova ,&nbsp;Chelsey L. Hammill ,&nbsp;Sylvain R.A. Marque ,&nbsp;Philippe Mellet ,&nbsp;Pavel S. Postnikov","doi":"10.1016/j.progpolymsci.2023.101726","DOIUrl":null,"url":null,"abstract":"<div><p><span>The materials of future depend a lot on properties that are due to “non stable” molecules. Hence, Dynamic Covalent Bonds (DCB) are covalent bonds that are labile under specific stimuli and are integral to the design of next generation materials. Alkoxyamines R</span><sup>1</sup>R<sup>2</sup>NO—R<sup>3</sup> exhibit a unique C—O DCB that is nonsymmetric between the adjacent O- and C-atoms. This bond can be cleaved homolytically, heterolytically and mesolytically in response to a wide variety of physical, chemical and biological stimuli, and the kinetics and thermodynamics of cleavage can be tuned on-demand by varying the structure of R<sup>1</sup>, R<sup>2</sup> and R<sup>3</sup><span><span><span><span>. Alkoxyamines are easily incorporated into polymers via nitroxide mediated polymerisation (NMP) however, their dynamic covalent properties are yet to be fully exploited in materials sciences. This is in part because reports on C—ON activation are scattered through the broader synthetic, physical and biological </span>chemistry literature, and a comprehensive review of them has been lacking. Herein, 20 leading C—ON activation processes using UV-light, </span>surface plasmon resonance<span><span>, magnetothermy, electrochemistry, chemical </span>oxidation, protonation, non-covalent bonding, </span></span>sonication, enzymatic activation among others, are presented and discussed, along with primary examples of their application.</span></p></div>","PeriodicalId":413,"journal":{"name":"Progress in Polymer Science","volume":"144 ","pages":"Article 101726"},"PeriodicalIF":26.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dynamic Covalent Bond: Modes of Activation of the C—ON Bond in Alkoxyamines\",\"authors\":\"Gérard Audran ,&nbsp;Elena G. Bagryanskaya ,&nbsp;Raphaël Bikanga ,&nbsp;Michelle L. Coote ,&nbsp;Olga Guselnikova ,&nbsp;Chelsey L. Hammill ,&nbsp;Sylvain R.A. Marque ,&nbsp;Philippe Mellet ,&nbsp;Pavel S. Postnikov\",\"doi\":\"10.1016/j.progpolymsci.2023.101726\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>The materials of future depend a lot on properties that are due to “non stable” molecules. Hence, Dynamic Covalent Bonds (DCB) are covalent bonds that are labile under specific stimuli and are integral to the design of next generation materials. Alkoxyamines R</span><sup>1</sup>R<sup>2</sup>NO—R<sup>3</sup> exhibit a unique C—O DCB that is nonsymmetric between the adjacent O- and C-atoms. This bond can be cleaved homolytically, heterolytically and mesolytically in response to a wide variety of physical, chemical and biological stimuli, and the kinetics and thermodynamics of cleavage can be tuned on-demand by varying the structure of R<sup>1</sup>, R<sup>2</sup> and R<sup>3</sup><span><span><span><span>. Alkoxyamines are easily incorporated into polymers via nitroxide mediated polymerisation (NMP) however, their dynamic covalent properties are yet to be fully exploited in materials sciences. This is in part because reports on C—ON activation are scattered through the broader synthetic, physical and biological </span>chemistry literature, and a comprehensive review of them has been lacking. Herein, 20 leading C—ON activation processes using UV-light, </span>surface plasmon resonance<span><span>, magnetothermy, electrochemistry, chemical </span>oxidation, protonation, non-covalent bonding, </span></span>sonication, enzymatic activation among others, are presented and discussed, along with primary examples of their application.</span></p></div>\",\"PeriodicalId\":413,\"journal\":{\"name\":\"Progress in Polymer Science\",\"volume\":\"144 \",\"pages\":\"Article 101726\"},\"PeriodicalIF\":26.0000,\"publicationDate\":\"2023-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Progress in Polymer Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0079670023000801\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0079670023000801","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: 0

摘要

未来的材料在很大程度上取决于“不稳定”分子的特性。因此,动态共价键(DCB)是在特定刺激下不稳定的共价键,是下一代材料设计的组成部分。烷氧胺R1R2NO-R3表现出独特的C-O DCB,在相邻的O-和c -原子之间不对称。该键可以响应各种物理、化学和生物刺激进行均解、异解和中解裂解,并且可以通过改变R1、R2和R3的结构来按需调节裂解的动力学和热力学。烷氧胺很容易通过氮氧化物介导聚合(NMP)结合到聚合物中,然而,它们的动态共价性质尚未在材料科学中得到充分利用。部分原因是关于C-ON活化的报道分散在更广泛的合成、物理和生物化学文献中,缺乏对它们的全面回顾。本文介绍和讨论了20种主要的C-ON活化工艺,包括紫外线、表面等离子体共振、磁热、电化学、化学氧化、质子化、非共价键、超声、酶活化等,并给出了它们的应用实例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dynamic Covalent Bond: Modes of Activation of the C—ON Bond in Alkoxyamines

Dynamic Covalent Bond: Modes of Activation of the C—ON Bond in Alkoxyamines

The materials of future depend a lot on properties that are due to “non stable” molecules. Hence, Dynamic Covalent Bonds (DCB) are covalent bonds that are labile under specific stimuli and are integral to the design of next generation materials. Alkoxyamines R1R2NO—R3 exhibit a unique C—O DCB that is nonsymmetric between the adjacent O- and C-atoms. This bond can be cleaved homolytically, heterolytically and mesolytically in response to a wide variety of physical, chemical and biological stimuli, and the kinetics and thermodynamics of cleavage can be tuned on-demand by varying the structure of R1, R2 and R3. Alkoxyamines are easily incorporated into polymers via nitroxide mediated polymerisation (NMP) however, their dynamic covalent properties are yet to be fully exploited in materials sciences. This is in part because reports on C—ON activation are scattered through the broader synthetic, physical and biological chemistry literature, and a comprehensive review of them has been lacking. Herein, 20 leading C—ON activation processes using UV-light, surface plasmon resonance, magnetothermy, electrochemistry, chemical oxidation, protonation, non-covalent bonding, sonication, enzymatic activation among others, are presented and discussed, along with primary examples of their application.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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