Pieber Bartholomäus, Malik Jamal A, Cavedon Cristian, Gisbertz Sebastian, Savateev Aleksandr, Cruz Daniel, Heil Tobias, Zhang Guigang, Seeberger Peter H
Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
Department of Chemistry and Biochemistry, Freie Universität Berlin, Arnimallee 22, 14195, Berlin, Deutschland.
Angew Chem Int Ed Engl. 2019 Jul 8;58(28):9575-9580. doi: 10.1002/anie.201902785. Epub 2019 Jun 6.
Cross-coupling reactions mediated by dual nickel/photocatalysis are synthetically attractive but rely mainly on expensive, non-recyclable noble-metal complexes as photocatalysts. Heterogeneous semiconductors, which are commonly used for artificial photosynthesis and wastewater treatment, are a sustainable alternative. Graphitic carbon nitrides, a class of metal-free polymers that can be easily prepared from bulk chemicals, are heterogeneous semiconductors with high potential for photocatalytic organic transformations. Here, we demonstrate that graphitic carbon nitrides in combination with nickel catalysis can induce selective C-O cross-couplings of carboxylic acids with aryl halides, yielding the respective aryl esters in excellent yield and selectivity. The heterogeneous organic photocatalyst exhibits a broad substrate scope, is able to harvest green light, and can be recycled multiple times. In situ FTIR was used to track the reaction progress to study this transformation at different irradiation wavelengths and reaction scales.
由双镍/光催化介导的交叉偶联反应在合成方面具有吸引力,但主要依赖于昂贵的、不可回收的贵金属配合物作为光催化剂。常用于人工光合作用和废水处理的多相半导体是一种可持续的替代方案。石墨相氮化碳是一类可通过大宗化学品轻松制备的无金属聚合物,是具有光催化有机转化高潜力的多相半导体。在此,我们证明石墨相氮化碳与镍催化相结合可以诱导羧酸与芳基卤化物的选择性C-O交叉偶联,以优异的产率和选择性生成相应的芳基酯。这种多相有机光催化剂具有广泛的底物范围,能够吸收绿光,并且可以多次循环使用。原位傅里叶变换红外光谱用于跟踪反应进程,以研究在不同照射波长和反应规模下的这种转化。