Zhao Yanan, Xu Xianming, Wang Yulong, Liu Tong, Li Hongpeng, Zhang Yongjun, Wang Libo, Wang Xiuhui, Zhao Simeng, Luo Yi
State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology Dalian 116024 China
Daqing Petrochemical Research Center of PetroChina Daqing 163714 China.
RSC Adv. 2022 Aug 1;12(33):21111-21121. doi: 10.1039/d2ra03180a. eCollection 2022 Jul 21.
The polymerization of α-olefins catalyzed by zirconium metallocene catalyst was systematically studied through experiments and density functional theory (DFT) calculations. Having achieved an agreement between theory and experiment, it was found that the effect of the catalyst ligand on the C[double bond, length as m-dash]C insertion reaction was significantly greater than that on the β-H elimination reaction. Therefore, the molecular weight of polymers can be increased by improving the activity of the C[double bond, length as m-dash]C insertion. In addition, in comparison with propylene, the chain length of α-olefins can directly affect the stereotacticity of polymerization products, owing to steric hindrance between the polymer chain and monomer.
通过实验和密度泛函理论(DFT)计算,对锆茂催化剂催化的α-烯烃聚合反应进行了系统研究。在理论与实验达成一致后发现,催化剂配体对C═C插入反应的影响明显大于对β-H消除反应的影响。因此,可以通过提高C═C插入反应的活性来提高聚合物的分子量。此外,与丙烯相比,由于聚合物链与单体之间的空间位阻,α-烯烃的链长会直接影响聚合产物的立构规整性。