阴离子加成聚合
聚合
活性阴离子聚合
自由基聚合
离子聚合
高分子化学
链式转移
材料科学
机械化学
聚合物
分散性
活性聚合
本体聚合
活性自由基聚合
单体
链生长聚合
可逆加成-断裂链转移聚合
化学
化学工程
有机化学
复合材料
工程类
作者
Kwangho Yoo,Gue Seon Lee,Hyo Won Lee,Byeong‐Su Kim,Jeung Gon Kim
摘要
Mechanochemistry has been extended to various polymer syntheses to achieve efficiency, greenness, and new products. However, many fundamental polymerization reactions have not been explored, although anionic polymerization of vinyl compounds has been pursued under mechanochemical conditions. Two solid monomers, 4-biphenyl methacrylate and 4-vinyl biphenyl, representing methacrylate and styrenic classes, respectively, were reacted with secondary butyl lithium under high-speed ball-milling. The alkyl-anion-promoted polymerization process was established by excluding radical initiation and producing the expected polymers with good efficiency. However, the generally expected features of anionic polymerization, such as molecular weight control and narrow dispersity, were not observed. Analysis of the milling parameters, reaction monitoring, and microstructural analysis revealed that the mechanism of the mechanochemical process differs from that of conventional anionic polymerizations. The mechanical force fractured the newly formed polymer chains via anionic initiation and generated macroradicals, which participated in the polymerization process. The anionic process governs the initiation step and the radical process becomes dominant during the propagation step.
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