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Synthesis of novel zirconium complexes bearing mono-Cp and tridentate Schilf hase [ONO] ligands and their catalytic activities for olefin polymerization  ( EI收录)  

文献类型:期刊文献

英文题名:Synthesis of novel zirconium complexes bearing mono-Cp and tridentate Schilf hase [ONO] ligands and their catalytic activities for olefin polymerization

作者:Chen, Qihui[1]; Huang, Jiling[1]

机构:[1] Laboratory of Organometallic Chemistry, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China

年份:2006

卷号:20

期号:11

起止页码:758

外文期刊名:Applied Organometallic Chemistry

收录:EI(收录号:20064510220694)

语种:英文

外文关键词:Catalyst activity - Complexation - Ethylene - Olefins - Organometallics - Polymerization

摘要:A series of novel zirconium complexes (R2Cp[2-R 1-6-(2-CH3OC6H4N=CH)C 6H3O]ZrCl2 (1, R1 = H, R2 = H, 2: R1 = CH3, R2 = H;4, R1 = H. Bu, R2 = H; 4, R1 = H, R2 = CH3; 5, R1 = H, R2 = n-Bu)} bearing mono-Cp and tridentate Schiff base [ONO] ligands are prepared by the reaction of corresponding lithium salt of Schiff base ligands with R2CpZrCl3-DME. All complexes were well characterized by 1H NMR, MS, IR and elemental analysis. The molecular structure of complex 1 was further confirmed by X-ray diffraction study, where the bond angle of Cl-Zr-Cl is extremely wide [151.71(3)°]. A nine-membered zirconoxacycle complex Cp(O-2-C6H4N=CHC 6H4-2-O)ZrCl2 (6) can be obtained by an intramolecular elimination of CH3Cl from complex 1 or by the reaction of CpZrCl3 · DME with dilithium salt of ligand. When activated by excess methylaluminoxane (MAO), complexes 1-6 exhibit high catalytic activities for ethylene polymerization. The influence of polymerization temperature on the activities of ethylene polymerization is investigated, and these complexes show high thermal stability. Complex 6 is also active for the copolymerization of ethylene and 1-hexene with low 1-hexene incorporation ability (1.10%). Copyright ? 2006 John Wiley & Sons, Ltd.

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