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Published on: November 21, 2017
A Spirobifluorene-Based Covalent Organic Framework for Dual Photoredox and Nickel Catalysis
Yingjie Fan1, Dong Won Kang1,2, Steven Labalme1
1Department of Chemistry, The University of Chicago, Chicago, Illinois 60637, United States.
Abstract:
Covalent organic frameworks (COFs) have emerged as tunable, crystalline, and porous functional organic materials, but their application in photocatalysis has been limited by rapid excited-state quenching. Herein, we report the first example of dual photoredox/nickel catalysis by an sp2 carbon-conjugated spirobifluorene-based COF. Constructed from spirobifluorene and nickel-bipyridine linkers, the NiSCN COF adopted a two-dimensional structure with staggered stacking. Under light irradiation, NiSCN catalyzed amination and etherification/esterification reactions of aryl halides through the photoredox mechanism, with a catalytic efficiency more than 23-fold higher than that of its homogeneous control. NiSCN was used in five consecutive reactions without a significant loss of catalytic activity.
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