Both the rac-and meso-dinuclear ansa-zirconocene catalysts (-C 12 H 8 {[SiPh(Ind) 2 ]ZrCl 2 } 2 ) were prepared by a coupling reaction between 2 equiv of diindenylphenylchlorosilane (rac-and meso-isomers) and 1 equiv of p-dilithiobiphenyl in diethyl ether at Οͺ80Β°C, followed by a successive reaction
Synthesis of a dinuclear ansa-zirconocene catalyst having a biphenyl bridge and application to ethene polymerization
β Scribed by Kazuo Soga; Hoang The Ban; Toshiya Uozumi
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 139 KB
- Volume
- 128
- Category
- Article
- ISSN
- 1381-1169
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β¦ Synopsis
Ε½ Γ w Ε½ . x 4 . Ε½ . A novel dinuclear ansa-zirconocene catalyst m-C H SiPh Ind ZrCl I was prepared by a Wurtz coupling 12 8 2 2 2 reaction between two equivalent of bisindenylphenylchlorosilane and one equivalent of 4,4 X -dibromobiphenyl in THF at reflux temperature for 12 h, followed by a successive reaction with ZrCl P 2THF in THF at y788C. Polymerization of 4 ethene was conducted in a 300 cm 3 glass reactor equipped with a stirrer at 40, 60, 80 and 1008C using MAO or w Ε½ . x Ε½ . Ph C B C F as cocatalyst and toluene as the solvent. The catalyst I gave linear polyethene with a broader molecular 3 6 54 Ε½ . mass distribution MMD in a much higher yield as compared to the corresponding mononuclear catalyst derived from w Ε½ . x Ε½ . Ph Si Ind ZrCl II . The apparent activity increased monotonously from 408C up to 1008C. The replacement of MAO 2 2 2 w Ε½ . x with Ph C B C F gave polyethene with a higher molecular weight. q 1998 Elsevier Science B.V.
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## Abstract In the polymerization of ethene cocatalyzed with modified methylaluminoxane, the catalyst activities of the siloxaneβbridged dinuclear zirconocenes, tetramethyldisiloxanediylbis(cyclopentadienylindenylzirconium dichloride) (3) and hexamethyltrisiloxanediylbis(cyclopentadienylindenylzirc
The titanocene complex shown in the scheme, which is generated by an asymmetric thermal transformation of the corresponding binaphthol complex and subsequent chlorination, is found to be an efficient catalyst for the hydrogenation of cyclic and noncyclic imines. -