Zhu Yuan-Yuan, Lan Guangxu, Fan Yingjie, Veroneau Samuel S, Song Yang, Micheroni Daniel, Lin Wenbin
Department of Chemistry, the University of Chicago, 929 E 57th Street, Chicago, IL, 60637, USA.
School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, 230009, China.
Angew Chem Int Ed Engl. 2018 Oct 22;57(43):14090-14094. doi: 10.1002/anie.201809493. Epub 2018 Oct 8.
Metal-organic frameworks (MOFs) have been extensively used for single-site catalysis and light harvesting, but their application in multicomponent photocatalysis is unexplored. We report here the successful incorporation of an Ir photoredox catalyst and a Ni cross-coupling catalyst into a stable Zr MOF, Zr -Ir-Ni, to efficiently catalyze C-S bond formation between various aryl iodides and thiols. The proximity of the Ir and Ni catalytic components to each other (ca. 0.6 nm) in Zr -Ir-Ni greatly facilitates electron and thiol radical transfers from Ir to Ni centers to reach a turnover number of 38 500, an order of magnitude higher than that of its homogeneous counterpart. This work highlights the opportunity in merging photoredox and organometallic catalysts in MOFs to effect challenging organic transformations.
金属有机框架材料(MOFs)已被广泛用于单中心催化和光捕获,但它们在多组分光催化中的应用尚未得到探索。我们在此报告了将铱光氧化还原催化剂和镍交叉偶联催化剂成功引入到一种稳定的锆基金属有机框架材料Zr-Ir-Ni中,以有效催化各种芳基碘化物与硫醇之间的C-S键形成。在Zr-Ir-Ni中,铱和镍催化组分彼此接近(约0.6纳米),极大地促进了电子和硫醇自由基从铱中心转移到镍中心,从而实现了38500的转化数,比其均相类似物高出一个数量级。这项工作突出了在金属有机框架材料中融合光氧化还原催化剂和有机金属催化剂以实现具有挑战性的有机转化的机会。