能源化学(英文) ›› 2003, Vol. 12 ›› Issue (2): 98-104.
Jianjun Yi, Xugeng Huang, Wei Zhang, Xiaoyu Hong, Zhenhua Jing
Jianjun Yi, Xugeng Huang, Wei Zhang, Xiaoyu Hong, Zhenhua Jing
摘要: Several nickel complexes [N,N]NiBr2, in which [N,N] indicates bidentate nitrogencontaining ligands (1: [N,N]=N-(2,6-diisopropylphenyl)pyridine-2-carboxaldimine (C18H22N2); 2: N-(2,6- diisopropylphenyl)-6-methylpyridine-2-carboxaldimine (C19H24N2); 3: N-(2,4,6-trimethylphenyl)pyridine- 2-carboxaldimine(C15H16N2); 4: N-(2,4,6-trimethylphenyl)-6-methylpyridine-2-carboxaldimine (C16H18- N2) were synthesized. Some of the nickel complexes exhibit high activity for ethylene oligomerization in the presence of an organoaluminum activator. The main factor aecting the activity and the structure of oligomers is the steric eect of substituents on [N,N] ligands. Methylaluminoxane (MAO) -activated catalysts showed higher activities and produced oligomers with higher molecular weight than Et2AlClactivated ones. The oligomerization in toluene rather than hexane results in much higher activity, and the oligomers produced in toluene have relatively high molecular weight. With activation of MAO or Et2AlCl, the [N,N]NiBr2 system tended to produce highly branched oligomers with low a-olefin content, but the a-olefin content could be increased by changing the reaction conditions.