Integration of Earth-Abundant Photosensitizers and Catalysts in Metal–Organic Frameworks Enhances Photocatalytic Aerobic Oxidation

We report here the construction of two metal–organic frameworks (MOFs), Zr6-Cu/Fe-1 and Zr6-Cu/Fe-2, by integrating earth-abundant cuprous photosensitizers (Cu-PSs) and Fe catalysts for photocatalytic aerobic oxidation. Site isolation and pore confinement stabilize both Cu-PSs and Fe catalysts, whil...

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Veröffentlicht in:ACS catalysis 2021-02, Vol.11 (3), p.1024-1032
Hauptverfasser: Feng, Xuanyu, Pi, Yunhong, Song, Yang, Xu, Ziwan, Li, Zhong, Lin, Wenbin
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creator Feng, Xuanyu
Pi, Yunhong
Song, Yang
Xu, Ziwan
Li, Zhong
Lin, Wenbin
description We report here the construction of two metal–organic frameworks (MOFs), Zr6-Cu/Fe-1 and Zr6-Cu/Fe-2, by integrating earth-abundant cuprous photosensitizers (Cu-PSs) and Fe catalysts for photocatalytic aerobic oxidation. Site isolation and pore confinement stabilize both Cu-PSs and Fe catalysts, while the proximity between active centers facilitates electron and mass transfer. Upon visible light irradiation and using O2 as the only oxidant, Zr 6 -Cu/Fe-1 and Zr 6 -Cu/Fe-2 efficiently oxidize alcohols and benzylic compounds to afford corresponding carbonyl products with broad substrate scopes, high turnover numbers of up to 500 with a 9.4-fold enhancement over homogeneous analogues, and excellent recyclability in four consecutive runs. Control experiments, spectroscopic evidence, and computational studies revealed the photo-oxidation mechanism: oxidative quenching of [Cu-PS]* by O2 affords [CuII-PS], which efficiently oxidizes FeIII–OH to generate a hydroxyl radical for substrate oxidation. This work highlights the potential of MOFs in promoting earth-abundant metal-based photocatalysis.
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Site isolation and pore confinement stabilize both Cu-PSs and Fe catalysts, while the proximity between active centers facilitates electron and mass transfer. Upon visible light irradiation and using O2 as the only oxidant, Zr 6 -Cu/Fe-1 and Zr 6 -Cu/Fe-2 efficiently oxidize alcohols and benzylic compounds to afford corresponding carbonyl products with broad substrate scopes, high turnover numbers of up to 500 with a 9.4-fold enhancement over homogeneous analogues, and excellent recyclability in four consecutive runs. Control experiments, spectroscopic evidence, and computational studies revealed the photo-oxidation mechanism: oxidative quenching of [Cu-PS]* by O2 affords [CuII-PS], which efficiently oxidizes FeIII–OH to generate a hydroxyl radical for substrate oxidation. 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