Catalytic Reduction of CN-, CO, and CO2 by Nitrogenase Cofactors in Lanthanide-Driven Reactions

被引:46
|
作者
Lee, Chi Chung [1 ]
Hu, Yilin [1 ]
Ribbe, Markus W. [1 ,2 ]
机构
[1] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
关键词
carbon dioxide; CC coupling; enzyme catalysis; hydrocarbons; nitrogenase; IRON-MOLYBDENUM COFACTOR; CARBON-DIOXIDE; FEMO COFACTOR; PRECURSOR; PROTEIN; MECHANISM; NIFEN;
D O I
10.1002/anie.201410412
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nitrogenase cofactors can be extracted into an organic solvent to catalyze the reduction of cyanide (CN-), carbon monoxide (CO), and carbon dioxide (CO2) without using adenosine triphosphate (ATP), when samarium(II) iodide (SmI2) and 2,6-lutidinium triflate (Lut-H) are employed as a reductant and a proton source, respectively. Driven by SmI2, the cofactors catalytically reduce CN- or CO to C-1-C-4 hydrocarbons, and CO2 to CO and C-1-C-3 hydrocarbons. The CC coupling from CO2 indicates a unique Fischer-Tropsch-like reaction with an atypical carbonaceous substrate, whereas the catalytic turnover of CN-, CO, and CO2 by isolated cofactors suggests the possibility to develop nitrogenase-based electrocatalysts for the production of hydrocarbons from these carbon-containing compounds.
引用
收藏
页码:1219 / 1222
页数:4
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