Synthesis, characterization, and styrene polymerization catalysis of pyridyl-functionalized indenyl rare earth metal bis(silylamide) complexes

被引:21
作者
Lei, Yinlin [1 ]
Wang, Yibin [1 ]
Luo, Yunjie [1 ]
机构
[1] Zhejiang Univ, Ningbo Inst Technol, Organometall Chem Lab, Ningbo 315100, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Rare earth metal bis(amide) complex; Indenyl ligand; Syndiospecific polymerization; Styrene; ALLYL ANSA-LANTHANIDOCENES; SINGLE-SITE CATALYSTS; SYNDIOSPECIFIC STYRENE; SYNDIOTACTIC POLYSTYRENE; OLEFIN POLYMERIZATION; BIS(AMIDE) COMPLEXES; ETHYLENE COPOLYMERS; RAC-LACTIDE; SCANDIUM; BEARING;
D O I
10.1016/j.jorganchem.2013.04.014
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Amine elimination of rare earth metal tris(silylamide) complexes Ln[N(SiHMe2)(2)](3)(THF)(2) with 1 equiv of the pyridyl-functionalized indenyl ligand C9H7CMe2CH2C5H4N-alpha afforded the neutral mono-indenyl-ligated rare earth metal bis(silylamide) complexes (C9H6CMe2CH2C5H4N-alpha)Ln[N(SiHMe2)(2)](2) (Ln = Sc (1), Y (2), Nd (3)) in 70-82% isolated yields. These complexes were characterized by elemental analysis, FT-IR, NMR, and X-ray single crystal structural diffraction. X-ray determination showed that the metal centers are coordinated by one indenyl ring, one nitrogen atom from the pendent pyridyl group, and two amide groups to form a distorted tetrahedral geometry. In the presence of excess (AlBu3)-Bu-i and on activation with 1 equiv of [Ph3C][B(C6F5)(4)] in toluene, 1-3 became active for syndiospecific polymerization of styrene in toluene at room temperature. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:24 / 28
页数:5
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