Carbon-Carbon Bond Formation in a Weak Ligand Field: Leveraging Open-Shell First-Row Transition-Metal Catalysts

被引:123
作者
Chirik, Paul J. [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
cobalt; cycloaddition; homogeneous catalysis; iron; polymerization; ETHYLENE POLYMERIZATION CATALYSTS; CROSS-COUPLING REACTIONS; ELECTRONIC-STRUCTURE; NOBEL LECTURE; ORGANIC-SYNTHESIS; OLEFIN POLYMERIZATION; COBALT CATALYSTS; CYCLOBUTANE DERIVATIVES; 2-PI+2-PI CYCLOADDITION; 2+2 PHOTOCYCLOADDITION;
D O I
10.1002/anie.201611959
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Unique features of earth-abundant transition-metal catalysts are reviewed in the context of catalytic carbon-carbon bond-forming reactions. Aryl-substituted bis(imino)pyridine iron and cobalt dihalide compounds, when activated with alkyl aluminum reagents, form highly active catalysts for the polymerization of ethylene. Open-shell iron and cobalt alkyl complexes have been synthesized that serve as single-component olefin polymerization catalysts. Reduced bis(imino)pyridine iron and cobalt dinitrogen compounds have also been discovered that promote the unique [2+2]cycloaddition of unactivated terminal alkenes. Studies of the electronic structure support open-shell intermediates, a deviation from traditional strong-field organometallic compounds that promote catalytic C-C bond formation.
引用
收藏
页码:5170 / 5181
页数:12
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