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 |
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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. |
doi_str_mv | 10.1021/acscatal.0c05053 |
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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. This work highlights the potential of MOFs in promoting earth-abundant metal-based photocatalysis.</description><identifier>ISSN: 2155-5435</identifier><identifier>EISSN: 2155-5435</identifier><identifier>DOI: 10.1021/acscatal.0c05053</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>ACS catalysis, 2021-02, Vol.11 (3), p.1024-1032</ispartof><rights>2021 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a346t-40078fcfadc9c547c0a793b6ac230d090bced94de9b69948e0ee7ab9f3b6190f3</citedby><cites>FETCH-LOGICAL-a346t-40078fcfadc9c547c0a793b6ac230d090bced94de9b69948e0ee7ab9f3b6190f3</cites><orcidid>0000-0003-4212-8814 ; 0000-0001-7035-7759 ; 0000-0003-1355-1445 ; 0000-0002-2796-9300</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acscatal.0c05053$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acscatal.0c05053$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids></links><search><creatorcontrib>Feng, Xuanyu</creatorcontrib><creatorcontrib>Pi, Yunhong</creatorcontrib><creatorcontrib>Song, Yang</creatorcontrib><creatorcontrib>Xu, Ziwan</creatorcontrib><creatorcontrib>Li, Zhong</creatorcontrib><creatorcontrib>Lin, Wenbin</creatorcontrib><title>Integration of Earth-Abundant Photosensitizers and Catalysts in Metal–Organic Frameworks Enhances Photocatalytic Aerobic Oxidation</title><title>ACS catalysis</title><addtitle>ACS Catal</addtitle><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. 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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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title | Integration of Earth-Abundant Photosensitizers and Catalysts in Metal–Organic Frameworks Enhances Photocatalytic Aerobic Oxidation |
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