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Macromolecular coupling in seconds of triazolinedione end-functionalized polymers prepared by RAFT polymerization

机译:通过RaFT聚合制备的三唑二酮末端官能化聚合物在数秒内的大分子偶联

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摘要

The ultrafast and additive-free triazolinedione-click reaction with electron rich (di)enes is a powerful method for the ultrafast ligation of polymer segments. A versatile method is described for the introduction of dickable TAD end groups in various polymer segments, using reversible addition-fragmentation chain transfer polymerization. These triazolinedione-functionalized prepolymers were subsequently used for macromolecular functionalization with a low molecular weight diene and block copolymer synthesis of different types within seconds, at ambient conditions, through the coupling with diene-functionalized polymers such as poly(ethylene glycol) and poly(isobornyl acrylate).
机译:与富电子(二)烯的超快且无添加剂的三唑啉二酮点击反应是超快速连接聚合物链段的有效方法。描述了使用可逆的加成-断裂链转移聚合在各种聚合物链段中引入可滴答TAD端基的通用方法。这些三唑啉二酮官能化的预聚物随后用于与低分子量二烯的高分子官能化,并在几秒钟内于环境条件下通过与二烯官能化的聚合物(如聚乙二醇和聚异冰片基酯)偶联,合成不同类型的嵌段共聚物。丙烯酸酯)。

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