Zubar Viktoriia, Lebedev Yury, Azofra Luis Miguel, Cavallo Luigi, El-Sepelgy Osama, Rueping Magnus
Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.
KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Angew Chem Int Ed Engl. 2018 Oct 8;57(41):13439-13443. doi: 10.1002/anie.201805630. Epub 2018 Sep 3.
The first base-metal-catalysed hydrogenation of CO -derived carbonates to alcohols is presented. The reaction proceeds under mild conditions in the presence of a well-defined manganese complex with a loading as low as 0.25 mol %. The non-precious-metal homogenous catalytic system provides an indirect route for the conversion of CO into methanol with the co-production of value-added (vicinal) diols in yields of up to 99 %. Experimental and computational studies indicate a metal-ligand cooperative catalysis mechanism.
首次报道了碱金属催化由CO衍生的碳酸盐加氢制醇的反应。该反应在温和条件下进行,使用一种结构明确的锰配合物,负载量低至0.25 mol %。这种非贵金属均相催化体系为将CO转化为甲醇提供了一条间接途径,同时联产增值(邻位)二醇,产率高达99%。实验和计算研究表明其催化机理为金属-配体协同催化。