STEREOCHEMICAL CONTROL IN PROPYLENE POLYMERIZATION CATALYZED BY UNBRIDGED METALLOCENE CATALYSTS  

STEREOCHEMICAL CONTROL IN PROPYLENE POLYMERIZATION CATALYZED BY UNBRIDGED METALLOCENE CATALYSTS

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作  者:Yin-bang Zhu Zhi-qiang Fan Tariq Yasin Lin-xian Feng Department of Polymer Science and Engineering Zhejiang University Hangzhou 310027, China 

出  处:《Chinese Journal of Polymer Science》2001年第4期407-413,共7页高分子科学(英文版)

基  金:This project was supported by the National Natural Science Foundation of China and the Petrochemical Incorporation of China (Grant number: 29734144).

摘  要:Two unbridged metallocene catalysts, bis(2,4,7-trimethylindenyl)zirconium dichloride (met-I) and bis(2,4,6-trimethylindenyl)zirconium dichloride (met-II), which are different in the position of substituents on the six-membered ring of the indenyl ligands were synthesized. The effect of substituents in the two metallocenes on the propylene polymerization was studied in the presence of methylaluminoxane (MAO) and triisobutylaluminium (TIBA). From the analysis of microstructure determined by C-13-NMR, it was demonstrated that the polymers produced by met-II have higher [mmmm] isotactic sequences than that of met-I. Using a mechanism based on model statistical analysis, it was found that chain-end model was dominant for met-I. However, met-II obeys the concurrent two-sites model during polymerization, which can be attributed to the existence of 'racemic-like' conformer in its system.Two unbridged metallocene catalysts, bis(2,4,7-trimethylindenyl)zirconium dichloride (met-I) and bis(2,4,6-trimethylindenyl)zirconium dichloride (met-II), which are different in the position of substituents on the six-membered ring of the indenyl ligands were synthesized. The effect of substituents in the two metallocenes on the propylene polymerization was studied in the presence of methylaluminoxane (MAO) and triisobutylaluminium (TIBA). From the analysis of microstructure determined by C-13-NMR, it was demonstrated that the polymers produced by met-II have higher [mmmm] isotactic sequences than that of met-I. Using a mechanism based on model statistical analysis, it was found that chain-end model was dominant for met-I. However, met-II obeys the concurrent two-sites model during polymerization, which can be attributed to the existence of 'racemic-like' conformer in its system.

关 键 词:unbridged metallocene propylene polymerization elastomeric polypropylene stereochemical mechanism 

分 类 号:O631.5[理学—高分子化学]

 

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