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可逆硫自由基加成-断裂链转移聚合

Reversible Thiyl Radical Addition-Fragmentation Chain Transfer Polymerization.

作者信息

Wang Yongjin, Du Jiaman, Huang Hanchu

机构信息

School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Sun Yat-Sen University, Guangzhou, 510006, China.

出版信息

Angew Chem Int Ed Engl. 2024 Mar 18;63(12):e202318898. doi: 10.1002/anie.202318898. Epub 2024 Feb 16.

Abstract

Developing reversible-deactivation radical polymerization (RDRP) methods that could directly control the thiyl radical propagation is highly desirable yet remains challenging in modern polymer chemistry. Here, we reported the first reversible thiyl radical addition-fragmentation chain transfer (SRAFT) polymerization strategy, which utilizes allyl sulfides as chain transfer agents for reversibly deactivating the propagating thiyl radicals, thus allowing us to directly control a challenging thiyl radical chain polymerization to afford polymers with well-defined architectures. A linear dependence of molecular weight on conversion, high chain-end fidelity, and efficient chain extension proved good controllability of the polymerization. In addition, density functional theory calculations provided insight into the reversible deactivation ability of allyl sulfides. The SRAFT strategy developed in this work represents a promising platform for discovering new controlled polymerizations based on thiyl radical chemistry.

摘要

开发能够直接控制硫自由基增长的可逆失活自由基聚合(RDRP)方法是非常理想的,但在现代高分子化学中仍然具有挑战性。在此,我们报道了首个可逆硫自由基加成-断裂链转移(SRAFT)聚合策略,该策略利用烯丙基硫醚作为链转移剂来可逆失活增长的硫自由基,从而使我们能够直接控制具有挑战性的硫自由基链式聚合反应,以获得具有明确结构的聚合物。分子量与转化率的线性关系、高链端保真度和高效的链增长证明了聚合反应具有良好的可控性。此外,密度泛函理论计算深入了解了烯丙基硫醚的可逆失活能力。这项工作中开发的SRAFT策略代表了一个基于硫自由基化学发现新型可控聚合反应的有前景的平台。

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