Structure-Activity Relationship in Olefin Polymerization Catalysis: Is Entropy the Key?

被引:32
|
作者
Ciancaleoni, Gianluca [2 ,3 ]
Fraldi, Natascia [1 ,3 ]
Budzelaar, Peter H. M. [3 ,4 ]
Busico, Vincenzo [1 ,3 ]
Cipullo, Roberta [1 ,3 ]
Macchioni, Alceo [2 ,3 ]
机构
[1] Univ Naples Federico 2, Dipartimento Chim, I-80126 Naples, Italy
[2] Univ Perugia, Dipartimento Chim, I-06123 Perugia, Italy
[3] Dutch Polymer Inst, NL-5600 AX Eindhoven, Netherlands
[4] Univ Manitoba, Dept Chem, Winnipeg, MB R3T 2N2, Canada
关键词
PROPENE POLYMERIZATION; ISOTACTIC POLYPROPYLENE; LIVING POLYMERIZATION; 1-HEXENE; COPOLYMERS; KINETICS; SYSTEM;
D O I
10.1021/ja105965x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Activation parameters for propene polymerization mediated by a bis(phenoxyamine)Zr-dibenzyl catalyst in combination with MAO have been measured experimentally and calculated by DFT; experiment and calculation consistently indicate that the entropic term is the most important reason for the low chain propagation rate with this system. Based on this finding and a review of literature data on a variety of olefin polymerization catalysts, we propose a strong correlation between the propagation rate and how catalysts deal with the entropy loss of monomer capture.
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页码:13651 / 13653
页数:3
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