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Bimetallic Coordination Insertion Polymerization of Unprotected Polar Monomers: Copolymerization of Amino Olefins and Ethylene by Dinickel Bisphenoxyiminato Catalysts

机译:未保护的极性单体的双金属配位插入聚合:氨基烯烃和乙烯的双镍双苯氧基亚胺基催化剂共聚合

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摘要

Dinickel bisphenoxyiminato complexes based on highly substituted p- and m-terphenyl backbones were synthesized, and the corresponding atropisomers were isolated. In the presence of a phosphine scavenger, Ni(COD)_2, the phosphine-ligated syn-dinickel complexes copolymerized α-olefins and ethylene in the presence of amines to afford 0.2–1.3% α-olefin incorporation and copolymerized amino olefins and ethylene with a similar range of incorporation (0.1–0.8%). The present rigid catalysts provide a bimetallic strategy for insertion polymerization of polar monomers without masking of the heteroatom group. The effects of the catalyst structure on the reactivity were studied by comparisons of the syn and anti atropisomers and the p- and m-terphenyl systems.
机译:合成了基于高度取代的对-和间-三苯基骨架的二镍双苯氧基亚氨基配合物,并分离了相应的阻转异构体。在膦清除剂Ni(COD)_2的存在下,磷化氢连接的顺二烯基络合物在胺的存在下使α-烯烃和乙烯共聚,从而引入0.2-1.3%的α-烯烃,并与氨基烯烃和乙烯共聚。相似的掺入范围(0.1–0.8%)。本发明的刚性催化剂提供了极性单体的插入聚合而不掩盖杂原子基团的双金属策略。通过比较顺式和反式阻转异构体以及对-和间-三联苯体系,研究了催化剂结构对反应活性的影响。

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