Liang Hong-Qing, Beweries Torsten, Francke Robert, Beller Matthias
Leibniz-Institute for Catalysis, Albert-Einstein-Strasse 29a, 18059, Rostock, Germany.
Angew Chem Int Ed Engl. 2022 May 2;61(19):e202200723. doi: 10.1002/anie.202200723. Epub 2022 Mar 24.
The conversion of CO into multicarbon (C ) compounds by reductive homocoupling offers the possibility to transform renewable energy into chemical energy carriers and thereby create "carbon-neutral" fuels or other valuable products. Most available studies have employed heterogeneous metallic catalysts, but the use of molecular catalysts is still underexplored. However, several studies have already demonstrated the great potential of the molecular approach, namely, the possibility to gain a deep mechanistic understanding and a more precise control of the product selectivity. This Minireview summarizes recent progress in both the thermo- and electrochemical reductive homocoupling of CO toward C products mediated by molecular catalysts. In addition, reductive CO homocoupling is discussed as a model for the further conversion of intermediates obtained from CO reduction, which may serve as a source of inspiration for developing novel molecular catalysts in the future.
通过还原均偶联将一氧化碳转化为多碳(C)化合物,为将可再生能源转化为化学能载体提供了可能,从而创造出“碳中和”燃料或其他有价值的产品。大多数现有研究采用多相金属催化剂,但分子催化剂的应用仍未得到充分探索。然而,一些研究已经证明了分子方法的巨大潜力,即深入理解反应机理并更精确地控制产物选择性的可能性。本综述总结了由分子催化剂介导的一氧化碳向C产物的热还原均偶联和电化学还原均偶联方面的最新进展。此外,还讨论了还原一氧化碳均偶联作为一氧化碳还原所得中间体进一步转化的模型,这可能为未来开发新型分子催化剂提供灵感。