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RAFT mediated polymerization of methyl methacrylate initiated by bergman cyclization: Access to high molecular weight narrow polydispersity polymers

机译:伯曼环化引发的RAFT介导的甲基丙烯酸甲酯聚合:获得高分子量的窄多分散性聚合物

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摘要

The first RAFT mediated polymerization of methyl methacrylate initiated by diradicals derived from Bergman cyclization was performed employing 3,4-benzocyclodec-3-ene-1,5-diyne (BCDY) as diradical source and cyanoisopropyldithiobenzoate (CPDB) as RAFT agent. The polymerization was conducted in bulk at 80°C for 3h. The concentration of the enediyne was kept constant at 3.0× 10-2 mol ·L-1 and the RAFT agent concentration was varied between 0.0mol ·L-1 and 2.4× 10-1 mol ·L-1. A detailed ESI-MS analysis reveals the absence of intramolecular termination reactions (ring formation) in the RAFT mediated system, which usually makes diradicalic initiation unfavorable. The presence of polymeric chains propagating at both ends could be confirmed. The conversion of the RAFT mediated polymerization was up to more than two times higher than the RAFT free polymerization at identical conditions. Thus, polymers with narrow polydispersities (1.1 ≤ PDI ≤ 1.5) even at very high molecular weights (near 400000Da) were obtained within modest reaction times.
机译:由3,4-苯并环癸-3-烯-1,5-二炔(BCDY)作为双自由基源,氰基异丙基二硫代苯甲酸酯(CPDB)作为RAFT试剂,进行了由Bergman环化衍生的双自由基引发的甲基丙烯酸甲酯的第一个RAFT介导的聚合反应。聚合在80℃下本体进行3小时。二烯炔的浓度保持恒定在3.0×10-2mol·L-1,RAFT剂的浓度在0.0mol·L-1和2.4×10-1mol·L-1之间变化。详细的ESI-MS分析表明,RAFT介导的系统中不存在分子内终止反应(环形成),这通常会使双自由基引发反应变得不利。可以确认在两端均存在传播的聚合物链。在相同条件下,RAFT介导的聚合反应的转化率比不含RAFT的聚合反应高出两倍以上。因此,即使在非常高的分子量(接近400000Da)下,也能在适当的反应时间内获得具有窄多分散性(1.1≤PDI≤1.5)的聚合物。

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