Synthesis and olefin polymerization catalysis of new trivalent samarium and yttrium complexes with bridging bis(cyclopentadienyl) ligands

被引:39
作者
Ihara, E
Yoshioka, S
Furo, M
Katsura, K
Yasuda, H
Mohri, S
Kanehisa, N
Kai, Y
机构
[1] Osaka Univ, Fac Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan
[2] Hiroshima Univ, Fac Engn, Dept Appl Chem, Higashihiroshima 7398527, Japan
关键词
D O I
10.1021/om000226a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New trivalent samarium and 5-ytrium complexes with bridging bis(cyclopentadienyl) ligands mere synthesized, and olefin polymerization catalysis of the complexes having an alkyl group [R = CH(SiMe3)(2)] on the metal was investigated. Three types of the rare earth halides (I ac, C-1, and meso) whose structures differed with respect to the bridging group and the positions of substituents on the cyclopentadienyl (Cp) rings were prepared: rac-Sm-Cl, Me2Si[2,4-Me3Si)(2)C5H2](2)SmCl2Li(THF)(2) (1a); C-1-Sm-Cl, Me2Si[2,4-(Me3Si)(2)C5H2][3,4-(Me3Si)(2)C5H2]-SmCl2Li(THF)(2) (2a); C-1(Ph2Si)-Sm-Cl, Ph2Si[2,4-(Me3Si)(2)C5H2][3,4-(Me3Si)(2)C5H2]SmCl2-Li(THF)(2) (3); meso-Sm-Cl, [1,2-(Me2Si)(Me2SiOSiMe2)](4-Me3CC5H2)(2)SmCl2Li(THF)(2) (4a); rac-Y-Cl, Me2Si[2,4-(Me3Si)(2)C5H2](2) YCL2Li(THF)(2) (5a); C-1-Y-Cl, Me2Si[2,4-(Me3Si)(2)C5H2][3,4-(Me3Si)(2)C5H2]YCl2Li(THF)(2) (6a); meso-Y-Cl, [1,2-Me2Si)(Me2SiOSiMe2)](4-Me3SiC5H2)(2)YCl-(THF) (7a). Although the rac and C-1 complexes (1a, 2a and 5a, 6a) were obtained as an isomeric mixture by the reaction of LnCl(3) (Ln = Sm, Y) with a dilithium salt of the ligand Me2Si[(Me3Si)(2)C5H3](2), it could be separated into both the pure complexes by utilizing the difference of solubility in hexane in each case. Structural data were obtained on Ist, aa, 3, and 7a to confirm the structures expected from NMR spectroscopy. The (ring centroid)metal-(ring centroid) angles in these complexes are ca. 10-20 degrees smaller than those in nonbridging bis(cyclopentadienyl) rare earth complexes. The rare earth halides la, 2a, 4a, 5a, 6a, and 7a reacted with LiCH(SiMe3)(2) to afford rare earth alkyl complexes, rac-Sm-R, Me2Si[2,4-(Me3Si)(2)C5H2](2)SmCH(SiMe3)(2) (1b); C-1-Sm-R, Me2Si[2,4-(Me3Si)(2)C5H2][3,4-(Me-3-Si)(2)C5H2]SmCH(SiMe3)(2) (2b); meso-Sm-R, [1,2-(Me2Si)(Me2SiOSiMe2)](4-Me3CC5H2)(2)SmCH-(SiMe3)(2) (4b); rac-Y-R, Me2Si[2/4-(Me3Si)(2)C5H2](2) YCH(SiMe3)(2) (5b); C-1-Y-R, Me2Si[2,4-(Me3Si)(2)C5H2] [3,4-(Me3Si)(2)C5H2]YCH(SiMe3)(2) (6b); meso-Y-R, and [1,2-(Me2Si)(Me2SiOSiMe2)] (4-Me3SiC5H2)(2)YCH(SiMe3)(2) (7b), respectively. Only C-1 type alkyl complexes (2b and Gb) polymerize ethylene, giving high molecular weight polyethylenes, and the precise structure of the active Sm complex 2b was determined by X-ray crystallography.
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页码:1752 / 1761
页数:10
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