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出 处:《Chinese Science Bulletin》2008年第18期2764-2769,共6页
基 金:the National Natural Science Foundation of China (Grant Nos. 20531020, 20721063, and 20771028);Shanghai Leading Academic Discipline Project (Grant No. B108);the National Basic Research Program of China (Grant No. 2005CB623800) ;Shanghai Science and Technology Committee (Grant No. 06XD14002)
摘 要:Activated by methylaluminoxane, mononuclear bis(hydroxyindanone-iminate)nickel complexes Ni[ArN == CC_2H_3(CH3)C_6H_2(R)O]_2 (Ar = 2,6-i-Pr2C6H3, R = Me (1), R = Cl (2), and R = H (3)) showed good activity for the styrene polymerization. The effect of many reaction parameters including the Al/Ni ratio, tempera- ture, and reaction time on catalytic activities of catalytic systems and the molecular weights of the ob- tained polystyrene was ascertained. The highest activity of 1.34×105 g(PS)·mol^(-1)(Ni)·h^(-1) was obtained under the optimum reaction condition. The 13C NMR spectra of the polymers revealed that the polymer was isotactic-rich atactic polystyrene. And the coordination mechanism was confirmed by the analyses of the polymer chain end-groups.Activated by methylaluminoxane, mononuclear bis(hydroxyindanone-iminate)nickel complexes Ni[ArN=CC2H3(CH3)C6H2(R)O]2 (Ar = 2,6-i-Pr2C6H3, R=Me(1), R=CI(2), and R=H(3)) showed good activity for the styrene polymerization. The effect of many reaction parameters including the AI/Ni ratio, temperature, and reaction time on catalytic activities of catalytic systems and the molecular weights of the obrained polystyrene was ascertained. The highest activity of 1.34×10^5g(PS)·mol^-1(Ni)·h^-1 was obtained under the optimum reaction condition. The ^13C NMR spectra of the polymers revealed that the polymer was isotactic-rich atactic polystyrene. And the coordination mechanism was confirmed by the analyses of the polymer chain end-groups.
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