摘要
合成并表征了含RCOO-基团的单核(Ni^1~Ni^2)及双核(Ni^3)镍配合物[(2,6-R_2-C_6H_3)-N=C(H)-(3-Ph-5-Ph COO-2-O-C_6H_2)-κ~2-N,O]Ni(CH_3)(pyridine)](R=i Pr;3,5-t Bu_2C_6H_3)并用于催化乙烯均聚和共聚反应。作为单组分催化剂,这些配合物可以有效地催化乙烯聚合得到中等相对分子质量的支化聚乙烯(PE)。供电性的Ph COO—基团促进了催化剂Ni^1的引发,从而在低温下比Ni^0活性更高。引入大位阻的2,6-(3,5-二叔丁基苯基)苯胺基团,催化剂Ni^2在5×10~5Pa下的活性高达1.8×10~6g PE mol^(-1)·Ni^(-1)·h^(-1),是活性最高的水杨醛亚胺中性镍催化剂之一。与相应的单核催化剂相比,双核催化剂Ni^3对三苯基膦具有更好的耐受性。这些催化剂可催化乙烯与1,5-己二烯、1,7-辛二烯、6-溴-1-己烯或10-十一烯酸甲酯的共聚合,制备功能化聚乙烯。
Mononuclear nickel complexes [(2,6-R2-C6H3)—N=C(H)—(3-Ph-5-PhCOO-2-O-C6H2)-κ2-N,O]Ni(CH3)(pyridine)](R=iPr; 3,5-tBu2C6H3)(Ni1~Ni2) and binuclear nickel complex(Ni3) were synthesized, characterized and applied in ethylene (co)polymerization. As single-component catalysts, all these complexes are capable of converting ethylene to branched polyethylenes(PE) with moderate relative molecular mass. The electron-donating group PhCOO— facilitates the initiation of catalyst Ni1, leading to better catalytic activity at low temperature compared to nickel methyl pyridine comples(Ni0). Introducing bulky 2,6-(3,5-(t-Bu)2C6H3)2C6H3N— moiety, the activities of Ni2 up to 1.8×106 g of PE mol-1·Ni-1·h-1(at 5×105 Pa ethylene) were among the highest values using phenoxyiminato neutral nickel catalysts. Binuclear catalyst Ni3 showes better tolerance toward PPh3 donor additive than its mononuclear counterpart. In the presence of comonomers 1,5-hexadiene, 1,7-octadiene, 6-bromo-1-hexene, or methyl 10-undecenoate, these catalysts effectively enchain these comonomers into the polymer chain to give functionalized polyethylenes.
出处
《应用化学》
CAS
CSCD
北大核心
2018年第1期89-101,共13页
Chinese Journal of Applied Chemistry
基金
Supported by the National Natural Science Foundation of China(No.21304087)~~
关键词
中性镍催化剂
电子效应
烯烃聚合
功能化聚烯烃
, neutral nickel catalysts
electronic effects
olefin polymerization
functionlized polyolefin