摘要
Copolymerizations of ethylene and 1-dodecene were conducted with a series of ansa-fluorenylamidodimethyltitanium complexes, [t-BuNSiMe2Flu]TiMe2（1a）, [t-BuNSiMe2（2,7-^tBu2Flu）]TiMe2（1 b）, and [（1-adamantyl）NSiMe2（2,7-^tBu2Flu）]TiMe2（1c） activated by modified methylaluminoxane. The activity increased by the introduction of the alkyl groups on the fluorenyl and amido ligands, and 1c produced the highest molecular weight copolymers. Complex 1c also promoted copolymerization of ethylene and ^iBu3 Al protected 10-undecen-1-ol with high activity（～2000 kg·mol^-1·h^-1）, affording hydroxy-functionalized ultrahigh molecular weight polyethylene. The hydroxy content of the copolymers obtained was controllable by changing comonomer feed ratio. The introduction of a small amount of hydroxy group can alter the surface properties of polyethylene.
Copolymerizations of ethylene and 1-dodecene were conducted with a series of ansa-fluorenylamidodimethyltitanium complexes, [t-BuNSiMe2Flu]TiMe2（1a）, [t-BuNSiMe2（2,7-^tBu2Flu）]TiMe2（1 b）, and [（1-adamantyl）NSiMe2（2,7-^tBu2Flu）]TiMe2（1c） activated by modified methylaluminoxane. The activity increased by the introduction of the alkyl groups on the fluorenyl and amido ligands, and 1c produced the highest molecular weight copolymers. Complex 1c also promoted copolymerization of ethylene and ^iBu3 Al protected 10-undecen-1-ol with high activity（～2000 kg·mol^-1·h^-1）, affording hydroxy-functionalized ultrahigh molecular weight polyethylene. The hydroxy content of the copolymers obtained was controllable by changing comonomer feed ratio. The introduction of a small amount of hydroxy group can alter the surface properties of polyethylene.
基金
financially supported by the National Natural Science Foundation of China (No. 21174026)
Program for New Century Excellent Talents in University
the Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning
"Shu Guang" project supported by Shanghai Municipal Education Commission
Shanghai Education Development Foundation
the Fundamental Research Funds for the Central Universities (No. CUSF-DH-D-2017041)
