Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/107566
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorDepartment of Applied Physicsen_US
dc.creatorChen, Ten_US
dc.creatorYu, Wen_US
dc.creatorWun, CKTen_US
dc.creatorWu, TSen_US
dc.creatorSun, Men_US
dc.creatorDay, SJen_US
dc.creatorLi, Zen_US
dc.creatorYuan, Ben_US
dc.creatorWang, Yen_US
dc.creatorLi, Men_US
dc.creatorWang, Zen_US
dc.creatorPeng, YKen_US
dc.creatorYu, WYen_US
dc.creatorWong, KYen_US
dc.creatorHuang, Ben_US
dc.creatorLiang, Ten_US
dc.creatorLo, TWBen_US
dc.date.accessioned2024-07-04T01:54:49Z-
dc.date.available2024-07-04T01:54:49Z-
dc.identifier.issn0002-7863en_US
dc.identifier.urihttp://hdl.handle.net/10397/107566-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2023 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © 2023 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/jacs.3c00114.en_US
dc.titleCu-Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp²)-N Coupling Reactionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage8464en_US
dc.identifier.epage8473en_US
dc.identifier.volume145en_US
dc.identifier.issue15en_US
dc.identifier.doi10.1021/jacs.3c00114en_US
dcterms.abstractA cross-coupling reaction via the dehydrogenative route over heterogeneous solid atomic catalysts offers practical solutions toward an economical and sustainable elaboration of simple organic substrates. The current utilization of this technology is, however, hampered by limited molecular definition of many solid catalysts. Here, we report the development of Cu-M dual-atom catalysts (where M = Co, Ni, Cu, and Zn) supported on a hierarchical USY zeolite to mediate efficient dehydrogenative cross-coupling of unprotected phenols with amine partners. Over 80% isolated yields have been attained over Cu-Co-USY, which shows much superior reactivity when compared with our Cu1 and other Cu-M analogues. This amination reaction has hence involved simple and non-forceful reaction condition requirements. The superior reactivity can be attributed to (1) the specifically designed bimetallic Cu-Co active sites within the micropore for “co-adsorption-co-activation” of the reaction substrates and (2) the facile intracrystalline (meso/micropore) diffusion of the heterocyclic organic substrates. This study offers critical insights into the engineering of next-generation solid atomic catalysts with complex reaction steps.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of the American Chemical Society, 19 Apr. 2023, v. 145, no. 15, p. 8464-8473en_US
dcterms.isPartOfJournal of the American Chemical Societyen_US
dcterms.issued2023-04-19-
dc.identifier.scopus2-s2.0-85152137121-
dc.identifier.pmid37023113-
dc.identifier.eissn1520-5126en_US
dc.description.validate202407_adaen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera2935-
dc.identifier.SubFormID48829-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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