Electroenzymatic C-C Bond Formation from CO2

被引：62

作者：

Cai, Rong ^{[1
]}

Milton, Ross D. ^{[1
,2
]}

Abdellaoui, Sofiene ^{[1
]}

Park, Terry ^{[1
]}

Patel, Janki ^{[1
]}

Alkotaini, Bassam ^{[1
]}

Minteer, Shelley D. ^{[1
]}

机构：

[1] Univ Utah, Dept Chem, 315 S 1400 E, Salt Lake City, UT 84112 USA

[2] Stanford Univ, Dept Civil & Environm Engn, James H Clark Ctr E250,318 Campus Dr, Stanford, CA 94305 USA

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2018年 / 140卷 / 15期

关键词：

VANADIUM NITROGENASE; CARBON-DIOXIDE; AZOTOBACTER-VINELANDII; REDUCTION; DEHYDROGENASE; MECHANISM; EVOLUTION; CATALYSTS; PROTEIN;

D O I：

10.1021/jacs.8b02319

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Over the past decade, there has been significant research in electrochemical reduction of CO2, but it has been difficult to develop catalysts capable of C-C bond formation. Here, we report bioelectrocatalysis of vanadium nitrogenase from Azotobacter vinelandii, where cobaltocenium derivatives transfer electrons to the catalytic VFe protein, independent of ATP-hydrolysis. In this bioelectrochemical system, CO2 is reduced to ethylene (C2H4) and propene (C3H6), by a single metalloenzyme.

引用

页码：5041 / 5044

页数：4

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