In situ formation of bis(phosphinimino)methanide rare earth alkoxide initiators for the ring-opening polymerization of ε-caprolactone

被引:81
作者
Gamer, Michael T.
Roesky, Peter W.
Palard, Isabelle
Le Hellaye, Maude
Guillaume, Sophie M.
机构
[1] Free Univ Berlin, Inst Chem, D-14195 Berlin, Germany
[2] Univ Bordeaux 1, CNRS ENSCPB, Lab Chim Polymeres Organ, F-33607 Pessac, France
关键词
D O I
10.1021/om0608307
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
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, $$(M) over bar (n)) and very narrow molar mass distributions.
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收藏
页码:651 / 657
页数:7
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