异氰酸酯
链式转移
可逆加成-断裂链转移聚合
化学
柯蒂斯重排
木筏
叠氮化物
聚合
高分子化学
点击化学
聚合物
单体
活性聚合
组合化学
自由基聚合
有机化学
聚氨酯
作者
Guillaume Gody,Christian Roßner,John Moraes,Philipp Vana,Thomas Maschmeyer,Sébastien Perrier
摘要
A new methodology has been developed for preparing α-functional polymers in a one-pot simultaneous polymerization/isocyanate "click" reaction. Our original synthetic strategy is based on the preparation of a carbonyl-azide chain transfer agent (CTA) precursor that undergoes the Curtius rearrangement in situ during reversible addition-fragmentation chain transfer (RAFT) polymerization yielding well-controlled α-isocyanate modified polymers. This strategy overcomes numerous difficulties associated with the synthesis of a polymerization mediator bearing an isocyanate at the R group and with the handling of such a reactive functionality. This new carbonyl-azide CTA can control the polymerization of a wide range of monomers, including (meth)acrylates, acrylamides, and styrenes (M(n) = 2-30 kDa; Đ = 1.16-1.38). We also show that this carbonyl-azide CTA can be used as a universal platform for the synthesis of α-end-functionalized polymers in a one-pot RAFT polymerization/isocyanate "click" procedure.
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