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首页> 外文期刊>Organometallics >In situ formation of bis(phosphinimino)methanide rare earth alkoxide initiators for the ring-opening polymerization of epsilon-caprolactone
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In situ formation of bis(phosphinimino)methanide rare earth alkoxide initiators for the ring-opening polymerization of epsilon-caprolactone

机译:双(膦基氨基)甲烷甲烷稀土醇盐引发剂的原位形成用于ε-己内酯的开环聚合

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摘要

A series of pentamethylcyclopentadienyl bis(phosphinimino)methanide complexes of yttrium and the lanthanides, [{CH(PPh2NSiMe3)(2)}Ln(eta(5)-C5Me5)Cl] (Ln = Y (1a), Sm (1b), Yb (1c)), were prepared by two different synthetic approaches. The compounds can be obtained either from [{CH(PPh2NSiMe3)(2)}LnCl(2)](2) (Ln = Y, Sm, Yb) and K(C5Me5) or in a one-pot reaction when K{CH(PPh2NSiMe3)(2)} is reacted with anhydrous rare earth trichlorides in the presence of K(C5Me5). When 1a-c were combined in situ with 1 equiv of 2-propanol, an active [Ln]-OiPr initiator was formed that enabled the pseudo-living ring-opening polymerization of epsilon-caprolactone to polymers with controlled molecular features (end groups,
机译:钇和镧系元素[[CH(PPh2NSiMe3)(2)} Ln(eta(5)-C5Me5)Cl]的一系列五甲基环戊二烯基双(膦基氨基)甲烷络合物(Ln = Y(1a),Sm(1b), Yb(1c)),是通过两种不同的合成方法制备的。化合物可以从[{CH(PPh2NSiMe3)(2)} LnCl(2)](2)(Ln = Y,Sm,Yb)和K(C5Me5)或一锅反应中从K {CH (PPh2NSiMe3)(2)}在K(C5Me5)存在下与无水稀土三氯化物反应。当1a-c与1当量的2-丙醇原位混合时,形成了一种活性[Ln] -OiPr引发剂,该引发剂使ε-己内酯能够假居化开环聚合成具有可控分子特征(端基,

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