聚合
链式转移
催化作用
活性聚合
聚乙烯
链端接
化学
摩尔质量分布
高分子化学
光化学
烯烃聚合
烯烃纤维
化学工程
材料科学
有机化学
自由基聚合
聚合物
工程类
作者
Xiao‐Qiang Hu,Xiaohui Kang,Zhongbao Jian
标识
DOI:10.1002/anie.202207363
摘要
Living polymerization by suppressing chain transfer is a very useful method for achieving precise molecular weight and structure control. However, the suppression of chain transfer at high temperatures is extremely challenging in any catalytic polymerization. This has been a severe limitation for catalytic olefin polymerization, which is one of the most important chemical reactions. Here, we report the unprecedented living polymerization of ethylene at 130 °C, with a narrow molecular weight distribution range of 1.04 to 1.08. This is a significant increase in the reaction temperature. Tailor-made α-diimine nickel catalysts that exhibit both the steric shielding and fluorine effects play an essential role in this breakthrough. These nickel catalysts are even active at 200 °C, and enable the formation of semi-crystalline, ultrahigh-molecular-weight polyethylene at 150 °C. Mechanistic insights into the key chain transfer reaction are elucidated by density functional theory calculations.
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