Hydrogen-Bonding-Induced Heterogenization of Nickel and Palladium Catalysts for Copolymerization of Ethylene with Polar Monomers

被引:93
作者
Zhang, Hu [1 ]
Zou, Chen [2 ]
Zhao, Huipeng [1 ]
Cai, Zhengguo [1 ]
Chen, Changle [2 ]
机构
[1] Donghua Univ, Coll Mat Sci & Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[2] Univ Sci & Technol China, Dept Polymer Sci & Engn, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Soft Matter Chem, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
heterogenization; morphology; nickel; polar functionalization; polyolefins; OLEFIN POLYMERIZATION; DIIMINE CATALYST; SULFATED ZIRCONIA; RATIONAL DESIGN; LIGAND; SILICA; POLYETHYLENE; POLYOLEFINS; STRATEGIES; SUPPORT;
D O I
10.1002/anie.202106682
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The practical synthesis of polar-functionalized polyolefins using transition-metal-catalyzed copolymerization of olefins with polar monomers is a challenge; the use of heterogeneous catalysts is little explored. Herein, we report the synthesis of heterogeneous naphthoquinone-based nickel (Ni/SiO2) and palladium (Pd/SiO2) catalysts through hydrogen bonding interactions of the ligands with the silica surface. Ni/SiO2 exhibits high activities (up to 2.65x10(6) g mol(-1) h(-1)) during the copolymerization of ethylene with 5-hexene-1-yl-acetate, affording high-molecular-weight (M-n up to 630 000) polar-functionalized semicrystalline polyethylene (comonomer incorporation up to 2.8 mol %), along with great morphology control. The resulting copolymers possess improved surface properties and great mechanical properties. Pd/SiO2 can mediate ethylene copolymerization with polar monomers with moderate activity to produce high-molecular-weight copolymers with tunable comonomer incorporation.
引用
收藏
页码:17446 / 17451
页数:6
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