Well-defined phosphino-phenolate neutral nickel(II) catalysts for efficient (co)polymerization of norbornene and ethylene

被引:27
作者
Zhang, Yan-Ping [1 ,2 ]
Li, Wei-Wei [1 ,2 ]
Li, Bai-Xiang [1 ]
Mu, Hong-Liang [1 ]
Li, Yue-Sheng [1 ,3 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Changchun Branch, Changchun 130022, Peoples R China
[3] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
VINYL-POLYMERIZATION; ADDITION POLYMERIZATION; COMPLEXES BEARING; REMOTE ACTIVATION; METAL-CATALYSTS; COPOLYMERIZATION; OLIGOMERIZATION; MONOMERS; LIGANDS; HOMOPOLYMERIZATION;
D O I
10.1039/c5dt00074b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Phosphino-phenolate neutral nickel catalysts 1-3/B(C6F5)(3), without the help of any organoaluminum compound, were found to be efficient catalytic systems for norbornene polymerization and its copolymerization with norbornene derivatives. The amount of B(C6F5)(3) required for achieving a high efficiency (3 equiv.) was markedly lower compared to previous reports, and high molecular weight polymers were obtained (>10(6) g mol(-1)). Efficient incorporation of polar monomers NBC, NBA, and NBM was also achieved in a controllable fashion, yielding high molecular weight copolymers. Catalysts 1-3 were highly active for ethylene polymerization as single component catalysts, with an activity of up to 10(7) g mol(Ni)(-1) h(-1), and catalyst 3 was more readily initiated at lower temperature. Catalysts 1-3 were also efficient in incorporating norbornene (up to 30%) into the polyethylene backbone. Bisligated phosphino-phenolate nickel complex 4 and salicylaldimine complex 5 were also studied for comparison, which further verified the unique performance of catalysts 1-3. Preliminary NMR analyses were conducted to explore the norbornene polymerization mechanism.
引用
收藏
页码:7382 / 7394
页数:13
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