Oxygen, light, and mechanical force mediated radical polymerization toward precision polymer synthesis

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-01-02 DOI:10.1039/d4cc05772d
Zhujun Huang , Jin Dong , Kaiwen Liu , Xiangcheng Pan
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Abstract

The synthesis of polymers with well-defined composition, architecture, and functionality has long been a focal area of research in the field of polymer chemistry. The advancement of controlled radical polymerization (CRP) has facilitated the synthesis of precise polymers, which are endowed with new properties and functionalities, thereby exhibiting a wide range of applications. However, radical polymerization faces several challenges, such as oxygen intolerance, and common thermal initiation methods may lead to side reactions and depolymerization. Therefore, we have developed some oxygen-tolerant systems that directly utilize oxygen for initiating and regulating polymerization. We utilize oxygen/alkylborane as an effective radical initiator system in the polymerization, and also as a reductant for the removal of polymer chain ends. Moreover, we employ the gentler photoinduced CRP to circumvent side reactions caused by high temperatures and achieve temporal and spatial control over the polymerization. To enhance the penetration of the light source for polymerization, we have developed near-infrared light-induced atom transfer radical polymerization. Additionally, we have extended photochemistry to reversible addition–fragmentation chain transfer polymerization involving ion-pair inner-sphere electron transfer mechanism, metal-free radical hydrosilylation polymerization, as well as carbene-mediated polymer modification through C–H activation and insertion mechanisms. Furthermore, we propose a new method for polymerization initiation synergistically triggered by oxygen and mechanical energy. This review not only showcases the current advancements in CRP but also outlines future directions, such as the potential for 3D printing and surface coatings, and the exploration of new heteroatom radical polymerizations. By expanding the boundaries of polymer synthesis, these innovations could lead to the creation of new materials with enhanced functionality and applications.

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氧、光和机械力介导的自由基聚合用于精密聚合物合成
合成具有明确的组成、结构和功能的聚合物一直是高分子化学领域的研究热点。可控自由基聚合(CRP)技术的发展促进了精密聚合物的合成,使其具有新的性能和功能,具有广泛的应用前景。然而,自由基聚合面临着一些挑战,如氧不耐受,常见的热引发方法可能导致副反应和解聚。因此,我们开发了一些耐氧系统,直接利用氧来引发和调节聚合。我们利用氧/烷基硼烷作为聚合反应中有效的自由基引发体系,同时也作为聚合物链端去除的还原剂。此外,我们采用更温和的光诱导CRP来规避高温引起的副反应,并实现对聚合的时间和空间控制。为了提高聚合的光源穿透性,我们发展了近红外光诱导原子转移自由基聚合。此外,我们已经将光化学扩展到可逆加成-破碎链转移聚合,包括离子对球内电子转移机制,金属自由基氢硅化聚合,以及通过C−H活化和插入机制的碳介导的聚合物改性。此外,我们还提出了一种由氧和机械能协同引发聚合的新方法。这一观点不仅展示了CRP的当前进展,而且概述了未来的发展方向,例如3D打印和表面涂层的潜力,以及新的杂原子自由基聚合的探索。通过扩大聚合物合成的边界,这些创新可能导致具有增强功能和应用的新材料的创造。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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