Huang Fang, Xing Qifeng, Liang Tongling, Flisak Zygmunt, Ye Bin, Hu Xinquan, Yang Wenhong, Sun Wen-Hua
College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, China.
Dalton Trans. 2014 Nov 28;43(44):16818-29. doi: 10.1039/c4dt02102a.
A series of 2-(1-arylimino)ethyl-9-arylimino-5,6,7,8-tetrahydrocycloheptapyridine derivatives was synthesized and fully characterized, and thereafter reacted with iron dichloride to form their corresponding iron(II) complexes. The single crystals of representative organic and iron complex compounds were obtained and analyzed by the X-ray diffraction analysis, indicating the distorted bipyramidal geometry around the iron core. Moreover, DFT calculations were performed on selected species to determine their structural features. On treatment with either MAO or MMAO, all iron complex pre-catalysts showed high activities (up to 1.56 × 10(7) gPE mol(-1)(Fe) h(-1)) toward ethylene polymerization. Regarding the nature of the ligands and reaction parameters, their catalytic activities and the characters of the obtained polyethylenes have been carefully investigated. The ring strain of the fused-cycloheptane of the ligands within iron complexes was considered to affect their catalytic performance in ethylene polymerization. The active species were activated and controlled by using a co-catalyst of MMAO preferred over MAO, and the obtained polyethylenes with MMAO showed narrower molecular polydispersity than the corresponding polyethylenes with MAO.
合成并全面表征了一系列2-(1-芳基亚氨基)乙基-9-芳基亚氨基-5,6,7,8-四氢环庚并吡啶衍生物,随后使其与二氯化铁反应以形成相应的铁(II)配合物。获得了代表性有机化合物和铁配合物的单晶,并通过X射线衍射分析进行了分析,结果表明铁核周围的几何形状为扭曲的双锥构型。此外,对选定的物种进行了密度泛函理论(DFT)计算,以确定其结构特征。在用甲基铝氧烷(MAO)或改性甲基铝氧烷(MMAO)处理时,所有铁配合物预催化剂对乙烯聚合均表现出高活性(高达1.56×10(7) gPE mol(-1)(Fe) h(-1))。关于配体的性质和反应参数,已对它们的催化活性和所得聚乙烯的特性进行了仔细研究。认为铁配合物中配体的稠合环庚烷的环应变会影响其在乙烯聚合中的催化性能。使用MMAO作为助催化剂比MAO更有利于活化和控制活性物种,并且用MMAO得到的聚乙烯比用MAO得到的相应聚乙烯具有更窄的分子多分散性。