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Chemoselective Polymerization of Polar Divinyl Monomers with Rare-Earth/Phosphine Lewis Pairs

机译:稀土/膦路易斯对对极性二乙烯基单体的化学选择性聚合

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摘要

This work reports the chemoselective polymerization of polar divinyl monomers, including allyl methacrylate (AMA), vinyl methacrylate (VMA), and 4-vinylbenzyl methacrylate (VBMA), by using simple Lewis pairs comprised of homoleptic rare-earth (RE) aryloxide complexes RE(OAr)3 (RE = Sc (>1), Y (>2), Sm (>3), La (>4), Ar = 2,6-tBu2C6H3) and phosphines PR3 (R = Ph, Cy, Et, Me). Catalytic activities of polymerizations relied heavily upon the cooperation of Lewis acid and Lewis base components. The produced polymers were soluble in common organic solvents and often had a narrow molecular weight distribution. A highly syndiotactic poly(allyl methacrylate) (PAMA) with rr ~88% could be obtained by the scandium complex >1/PEt3 pair at −30 °C. In the case of poly(4-vinylbenzyl methacrylate) (PVBMA), it could be post-functionalized with PhCH2SH. Mechanistic study, including the isolation of the zwitterionic active species and the end-group analysis, revealed that the frustrated Lewis pair (FLP)-type addition was the initiating step in the polymerization.
机译:这项工作报告了极性二乙烯基单体的化学选择性聚合,包括甲基丙烯酸烯丙酯(AMA),甲基丙烯酸乙烯酯(VMA)和甲基丙烯酸4-乙烯基苄酯(VBMA),这是通过使用由均相稀土(RE)芳氧基配合物RE组成的简单Lewis对进行的。 (OAr)3(RE = Sc(> 1 ),Y(> 2 ),Sm(> 3 ),La(> 4 < / strong>),Ar = 2,6-tBu2C6H3)和膦PR3(R = Ph,Cy,Et,Me)。聚合反应的催化活性在很大程度上取决于路易斯酸和路易斯碱组分的协同作用。产生的聚合物可溶于常见的有机溶剂,并且通常具有窄的分子量分布。 strong配合物> 1 / PEt3对在-30°C时可制得rr〜88%的高度间同立构的聚甲基丙烯酸烯丙酯(PAMA)。在聚(甲基丙烯酸4-乙烯基苄酯)(PVBMA)的情况下,可以用PhCH2SH将其后官能化。包括两性离子活性物质的分离和端基分析在内的机理研究表明,沮丧的路易斯对(FLP)型添加是聚合反应的起始步骤。

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