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Article: Visible light-mediated intermolecular crossed [2+2] cycloadditions using a MOF-supported copper triplet photosensitizer

TitleVisible light-mediated intermolecular crossed [2+2] cycloadditions using a MOF-supported copper triplet photosensitizer
Authors
Issue Date23-Feb-2024
PublisherNature Research
Citation
Nature Catalysis, 2024, v. 7, n. 3, p. 307-320 How to Cite?
Abstract

The photochemical [2+2] cycloaddition of styrenes provides a frequently used route for the synthesis of multi-substituted cyclobutanes. Despite the extensive studies in noble-metal and organo-photocatalysis, developing sustainable cycloaddition methods with copper photosensitizers is still in its infancy, largely owing to their low reactivity and photostability. Here we show that the introduction of a binap-ligated heteroleptic copper(I) complex to the linker of a microporous zirconium-based metal−organic framework produces a highly stable and reusable heterogeneous photocatalyst with an extended excited-state lifetime. Under visible light irradiation, this robust copper triplet photosensitizer efficiently promotes multiple intermolecular crossed [2+2] cycloadditions, including an underdeveloped cycloaddition reaction of simple styrenes with electron-deficient alkenes. Our findings suggest that metal–organic framework-based heterogenization strategies have the potential to advance copper photocatalysis and foster a variety of visible light-mediated energy-transfer processes.


Persistent Identifierhttp://hdl.handle.net/10722/343842

 

DC FieldValueLanguage
dc.contributor.authorGuo, Jun-
dc.contributor.authorXia, Qi-
dc.contributor.authorTang, Wing Yi-
dc.contributor.authorLi, Zekun-
dc.contributor.authorWu, Xia-
dc.contributor.authorLiu, Li-Juan-
dc.contributor.authorTo, Wai-Pong-
dc.contributor.authorShu, Hui-Xing-
dc.contributor.authorLow, Kam-Hung-
dc.contributor.authorChow, Philip C Y-
dc.contributor.authorLo, Tsz Woon Benedict-
dc.contributor.authorHe, Jian-
dc.date.accessioned2024-06-11T07:52:02Z-
dc.date.available2024-06-11T07:52:02Z-
dc.date.issued2024-02-23-
dc.identifier.citationNature Catalysis, 2024, v. 7, n. 3, p. 307-320-
dc.identifier.urihttp://hdl.handle.net/10722/343842-
dc.description.abstract<p>The photochemical [2+2] cycloaddition of styrenes provides a frequently used route for the synthesis of multi-substituted cyclobutanes. Despite the extensive studies in noble-metal and organo-photocatalysis, developing sustainable cycloaddition methods with copper photosensitizers is still in its infancy, largely owing to their low reactivity and photostability. Here we show that the introduction of a binap-ligated heteroleptic copper(I) complex to the linker of a microporous zirconium-based metal−organic framework produces a highly stable and reusable heterogeneous photocatalyst with an extended excited-state lifetime. Under visible light irradiation, this robust copper triplet photosensitizer efficiently promotes multiple intermolecular crossed [2+2] cycloadditions, including an underdeveloped cycloaddition reaction of simple styrenes with electron-deficient alkenes. Our findings suggest that metal–organic framework-based heterogenization strategies have the potential to advance copper photocatalysis and foster a variety of visible light-mediated energy-transfer processes.</p>-
dc.languageeng-
dc.publisherNature Research-
dc.relation.ispartofNature Catalysis-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleVisible light-mediated intermolecular crossed [2+2] cycloadditions using a MOF-supported copper triplet photosensitizer-
dc.typeArticle-
dc.identifier.doi10.1038/s41929-024-01112-9-
dc.identifier.scopuseid_2-s2.0-85187280795-
dc.identifier.volume7-
dc.identifier.issue3-
dc.identifier.spage307-
dc.identifier.epage320-
dc.identifier.eissn2520-1158-
dc.identifier.issnl2520-1158-

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