Mahmood Qaiser, Zeng Yanning, Wang Xinxin, Sun Yang, Sun Wen-Hua
Key Laboratory of Engineering Plastics and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Dalton Trans. 2017 May 30;46(21):6934-6947. doi: 10.1039/c7dt01295k.
A new family of nickel halides (bromides Ni1-Ni5 and chlorides Ni6-Ni10) ligated by 1-(2,6-dibenzhydryl-4-nitrophenylimino)-2-(arylimino)acenaphthylene (Aryl = 2,6-MeCHL1, 2,6-EtCHL2, 2,6-PrCHL3, 2,4,6-MeCHL4, and 2,6-Et-4-MeCHL5) have been prepared and well characterized, and the scope of their catalytic properties toward the polymerization of ethylene has been investigated. Upon activation with either EtAlCl or EASC, the nickel bromide complexes displayed better activities than their nickel chloride counterparts and produced higher-molecular-weight polyethylene in the range of 10 g mol with a very narrow range of molecular weight distributions. In comparison with reference precatalysts with non-nitro substituents (CH, F or Cl), the title complexes experienced a modest negative effect on catalytic activity upon replacement with a NO moiety (activity up to 4.61 × 10 g PE (mol Ni) h at 20 °C). Conversely, the NO moiety exerted a positive effect to increase the molecular weight of the resulting polyethylene, and Ni4/EtAlCl gave polyethylene with a maximum molecular weight of as high as 32.8 × 10 g mol, which is not only the highest among the title complexes but also higher than any literature values reported with 1,2-diiminoacenaphthylnickel halides.
已制备并充分表征了一类由1-(2,6-二苯甲基-4-硝基苯基亚氨基)-2-(芳基亚氨基)苊烯(芳基 = 2,6-甲基苄基L1、2,6-乙基苄基L2、2,6-丙基苄基L3、2,4,6-三甲基苄基L4和2,6-乙基-4-甲基苄基L5)配位的新型卤化镍(溴化物Ni1-Ni5和氯化物Ni6-Ni10),并研究了它们对乙烯聚合的催化性能范围。在用EtAlCl或EASC活化后,溴化镍配合物显示出比其氯化镍对应物更好的活性,并生成了分子量在10 g/mol范围内且分子量分布非常窄的高分子量聚乙烯。与具有非硝基取代基(CH、F或Cl)的参考预催化剂相比,用NO基团取代后,标题配合物对催化活性产生了适度的负面影响(在20°C下活性高达4.61×10 g PE/(mol Ni)·h)。相反,NO基团对增加所得聚乙烯的分子量产生了积极影响,Ni4/EtAlCl得到的聚乙烯最大分子量高达32.8×10 g/mol,这不仅是标题配合物中最高的,而且高于任何用1,2-二亚氨基苊基卤化镍报道的文献值。