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首页> 外文期刊>Angewandte Chemie >Catalytic Reduction of CN-, CO, and CO2 by Nitrogenase Cofactors in Lanthanide-Driven Reactions
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Catalytic Reduction of CN-, CO, and CO2 by Nitrogenase Cofactors in Lanthanide-Driven Reactions

机译:镧系元素驱动的固氮酶辅助因子催化还原CN,CO和CO2

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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.
机译:当碘化sa(II)和二碘化and(SmI2)和二碘化and(II)一起使用时,无需使用三磷酸腺苷(ATP),就可以将氮酶辅助因子提取到有机溶剂中,以催化氰化物(CN-),一氧化碳(CO)和二氧化碳(CO2)的还原。 2,6-lut啶鎓三氟甲磺酸盐(Lut-H)分别用作还原剂和质子源。在SmI2的驱动下,辅因子催化将CN-或CO还原为C-1-C-4烃,并将CO2还原为CO和C-1-C-3烃。来自CO2的CC偶合表明与非典型碳质底物的独特的费-托式反应,而分离的辅因子对CN-,CO和CO2的催化转化表明,有可能开发基于固氮酶的电催化剂以从中生产烃这些含碳化合物。

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