Photocatalytic (Het)arylation of C(sp3)-H Bonds with Carbon Nitride

被引:80
作者
Das, Saikat [1 ]
Murugesan, Kathiravan [1 ]
Rodriguez, Gonzalo J. Villegas [1 ]
Kaur, Jaspreet [1 ]
Barham, Joshua P. [1 ]
Savateev, Aleksandr [2 ]
Antonietti, Markus [2 ]
Koenig, Burkhard [1 ]
机构
[1] Univ Regensburg, Fak Chem & Pharm, D-93040 Regensburg, Germany
[2] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14424 Potsdam, Germany
基金
欧洲研究理事会;
关键词
heterogeneous photocatalysis; carbon nitride; hydrogen atom transfer; C(sp(3))-H arylation; dual photo nickel; drug molecule functionalization; C-H BONDS; LIGHT PHOTOREDOX CATALYSIS; HYDROGEN-PRODUCTION; FUNCTIONALIZATION; ARYLATION; PHOTOCHEMISTRY; ALKYLATION; CO2;
D O I
10.1021/acscatal.0c05694
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Graphitic carbon nitride materials have attracted significant interest in recent years and found applications in diverse light-to-energy conversions such as artificial photosynthesis, CO2 reduction, or degradation of organic pollutants. However, their utilization in synthetic photocatalysis, especially in the direct functionalization of C(sp(3))-H bonds, remains underexplored. Herein, we report mesoporous graphitic carbon nitride (mpg-CN as a heterogeneous organic semiconductor photocatalyst for direct arylation of C(sp(3))-H bonds in combination with nickel catalysis. Our protocol has a broad synthetic scope (>70 examples including late-stage functionalization of drugs and agrochemicals), is operationally simple, and shows high chemo- and regioselectivities. Facile separation and recycling of the mpg-CN catalyst in combination with its low preparation cost, innate photochemical stability, and low toxicity are beneficial features overcoming typical shortcomings of homogeneous photocatalysis. Detailed mechanistic investigations and kinetic studies indicate that an unprecedented energy-transfer process (EnT) from the organic semiconductor to the nickel complex is operating.
引用
收藏
页码:1593 / 1603
页数:11
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