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Single-Site Photocatalytic H2 Evolution from Covalent Organic Frameworks with Molecular Cobaloxime Co-Catalysts

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dc.contributor.author Banerjee, Tanmay
dc.date.accessioned 2021-11-11T11:21:24Z
dc.date.available 2021-11-11T11:21:24Z
dc.date.issued 2017-10-12
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jacs.7b07489
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3477
dc.description.abstract We demonstrate photocatalytic hydrogen evolution using COF photosensitizers with molecular proton reduction catalysts for the first time. With azine-linked N2-COF photosensitizer, chloro(pyridine)cobaloxime co-catalyst, and TEOA donor, H2 evolution rate of 782 μmol h–1 g–1 and TON of 54.4 has been obtained in a water/acetonitrile mixture. PXRD, solid-state spectroscopy, EM analysis, and quantum-chemical calculations suggest an outer sphere electron transfer from the COF to the co-catalyst which subsequently follows a monometallic pathway of H2 generation from the CoIII-hydride and/or CoII-hydride species. en_US
dc.language.iso en en_US
dc.publisher ACS en_US
dc.subject Chemistry en_US
dc.subject Covalent organic frameworks en_US
dc.subject Charge transfer en_US
dc.subject Mixtures en_US
dc.title Single-Site Photocatalytic H2 Evolution from Covalent Organic Frameworks with Molecular Cobaloxime Co-Catalysts en_US
dc.type Article en_US


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