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首页> 外文期刊>Angewandte Chemie >Coordination Polymerization of Renewable 3-Methylenecyclopentene with Rare-Earth-Metal Precursors
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Coordination Polymerization of Renewable 3-Methylenecyclopentene with Rare-Earth-Metal Precursors

机译:具有稀土金属前体可再生3-甲基癸烯烯的配位聚合

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摘要

Coordination polymerization of renewable 3-methylenecyclopentene has been investigated for the first time using rare-earth metal-based precursors bearing various bulky ligands. All the prepared complexes catalyze controllable polymerization of 3-methylenecyclopentene into high molecular weight polymers, of which the NPN-and NSN-tridentate non-Cp ligated lutetium-based catalytic systems exhibited extremely high activities up to 11 520 kg/(mol(Lu) . h) in a dilute toluene solution (3.2 g/100 mL) at room temperature. The resultant polymers have pure 1,4-regioregularity (>99%) and tailorable number average molecular weights (1-20 X 10(4)) with narrow molecular weight distributions (polydispersity index (PDI)= 1.45-1.79). DFT simulations were employed to study the polymerization mechanism and stereoregularity control.
机译:使用含有各种庞大配体的稀土金属基前体首次研究了可再生3-甲基癸烯烯的配位聚合。 所有制备的复合物将3-甲基二氯丁的可控聚合催化到高分子量聚合物中,其中NPN-and NSN三级非CP连接的乳液基催化体系呈现出高达11 520 kg /(摩尔(Lu)的最高活性 。H)在室温下在稀甲苯溶液(3.2g / 100ml)中。 所得聚合物具有纯1,4-℃(> 99%)和可定制的数均分子量(1-20×10(4)),分子量分布窄(多分散指数(PDI)= 1.45-1.79)。 使用DFT模拟来研究聚合机制和立体调控。

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