Cu–Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp2)–N Coupling Reaction
A 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...
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Veröffentlicht in: | Journal of the American Chemical Society 2023-04, Vol.145 (15), p.8464-8473 |
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creator | Chen, Tianxiang Yu, Wenhua Wun, Ching Kit Tommy Wu, Tai-Sing Sun, Mingzi Day, Sarah J. Li, Zehao Yuan, Bo Wang, Yong Li, Mingjie Wang, Zi Peng, Yung-Kang Yu, Wing-Yiu Wong, Kwok-Yin Huang, Bolong Liang, Taoyuan Lo, Tsz Woon Benedict |
description | A 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. |
doi_str_mv | 10.1021/jacs.3c00114 |
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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.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/jacs.3c00114</identifier><identifier>PMID: 37023113</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Journal of the American Chemical Society, 2023-04, Vol.145 (15), p.8464-8473</ispartof><rights>2023 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-aca6ba01910c08f31fe34cbfbf3c997dfe749497db145292bb03f9f8a3a9afb13</citedby><cites>FETCH-LOGICAL-a324t-aca6ba01910c08f31fe34cbfbf3c997dfe749497db145292bb03f9f8a3a9afb13</cites><orcidid>0000-0003-0417-5089 ; 0000-0002-4853-0196 ; 0000-0002-2526-2002 ; 0000-0003-3181-8908 ; 0000-0003-4984-7109 ; 0000-0002-7509-5927 ; 0000-0001-9590-6902</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/jacs.3c00114$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jacs.3c00114$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37023113$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Tianxiang</creatorcontrib><creatorcontrib>Yu, Wenhua</creatorcontrib><creatorcontrib>Wun, Ching Kit Tommy</creatorcontrib><creatorcontrib>Wu, Tai-Sing</creatorcontrib><creatorcontrib>Sun, Mingzi</creatorcontrib><creatorcontrib>Day, Sarah J.</creatorcontrib><creatorcontrib>Li, Zehao</creatorcontrib><creatorcontrib>Yuan, Bo</creatorcontrib><creatorcontrib>Wang, Yong</creatorcontrib><creatorcontrib>Li, Mingjie</creatorcontrib><creatorcontrib>Wang, Zi</creatorcontrib><creatorcontrib>Peng, Yung-Kang</creatorcontrib><creatorcontrib>Yu, Wing-Yiu</creatorcontrib><creatorcontrib>Wong, Kwok-Yin</creatorcontrib><creatorcontrib>Huang, Bolong</creatorcontrib><creatorcontrib>Liang, Taoyuan</creatorcontrib><creatorcontrib>Lo, Tsz Woon Benedict</creatorcontrib><title>Cu–Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp2)–N Coupling Reaction</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>A 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.</description><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNptkEFPGzEQha2qVQlpbz0jH4PEUo-9yWaP0QKlUgRSaQ5wWc064-Bos15sL1JunPgD_Yf8EjYiLZeeZkb65j29x9g3EKcgJHxfow6nSgsBkH5gAxhLkYxBTj6ygRBCJtl0og7YYQjr_kzlFD6zA5UJqQDUgD0X3cvTn8Lxsw7rZBbdhhcYsd6GGPhN17bOR1py1_BLSx69vrcaa764ueV35GobKXDjPMeGnxtjtaUm8sK7EJIzut8uvVtRg9E-Ei9GoZXHvdsVL1zX1rZZ8V-EOlrXfGGfDNaBvu7nkC0uzn8Xl8n8-sfPYjZPUMk0JqhxUqGAHIQWU6PAkEp1ZSqjdJ5nS0NZmqf9UkE6lrmsKqFMbqaoMEdTgRqy0Ztu691DRyGWGxs01TU25LpQyizPoBfIJj168obqXRpPpmy93aDfliDKXfPlrvly33yPH-2Vu2pDy3_w36rfrXdfa9f5pg_6f61XtTaPRQ</recordid><startdate>20230406</startdate><enddate>20230406</enddate><creator>Chen, Tianxiang</creator><creator>Yu, Wenhua</creator><creator>Wun, Ching Kit Tommy</creator><creator>Wu, Tai-Sing</creator><creator>Sun, Mingzi</creator><creator>Day, Sarah J.</creator><creator>Li, Zehao</creator><creator>Yuan, Bo</creator><creator>Wang, Yong</creator><creator>Li, Mingjie</creator><creator>Wang, Zi</creator><creator>Peng, Yung-Kang</creator><creator>Yu, Wing-Yiu</creator><creator>Wong, Kwok-Yin</creator><creator>Huang, Bolong</creator><creator>Liang, Taoyuan</creator><creator>Lo, Tsz Woon Benedict</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0417-5089</orcidid><orcidid>https://orcid.org/0000-0002-4853-0196</orcidid><orcidid>https://orcid.org/0000-0002-2526-2002</orcidid><orcidid>https://orcid.org/0000-0003-3181-8908</orcidid><orcidid>https://orcid.org/0000-0003-4984-7109</orcidid><orcidid>https://orcid.org/0000-0002-7509-5927</orcidid><orcidid>https://orcid.org/0000-0001-9590-6902</orcidid></search><sort><creationdate>20230406</creationdate><title>Cu–Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp2)–N Coupling Reaction</title><author>Chen, Tianxiang ; Yu, Wenhua ; Wun, Ching Kit Tommy ; Wu, Tai-Sing ; Sun, Mingzi ; Day, Sarah J. ; Li, Zehao ; Yuan, Bo ; Wang, Yong ; Li, Mingjie ; Wang, Zi ; Peng, Yung-Kang ; Yu, Wing-Yiu ; Wong, Kwok-Yin ; Huang, Bolong ; Liang, Taoyuan ; Lo, Tsz Woon Benedict</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-aca6ba01910c08f31fe34cbfbf3c997dfe749497db145292bb03f9f8a3a9afb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Tianxiang</creatorcontrib><creatorcontrib>Yu, Wenhua</creatorcontrib><creatorcontrib>Wun, Ching Kit Tommy</creatorcontrib><creatorcontrib>Wu, Tai-Sing</creatorcontrib><creatorcontrib>Sun, Mingzi</creatorcontrib><creatorcontrib>Day, Sarah J.</creatorcontrib><creatorcontrib>Li, Zehao</creatorcontrib><creatorcontrib>Yuan, Bo</creatorcontrib><creatorcontrib>Wang, Yong</creatorcontrib><creatorcontrib>Li, Mingjie</creatorcontrib><creatorcontrib>Wang, Zi</creatorcontrib><creatorcontrib>Peng, Yung-Kang</creatorcontrib><creatorcontrib>Yu, Wing-Yiu</creatorcontrib><creatorcontrib>Wong, Kwok-Yin</creatorcontrib><creatorcontrib>Huang, Bolong</creatorcontrib><creatorcontrib>Liang, Taoyuan</creatorcontrib><creatorcontrib>Lo, Tsz Woon Benedict</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Tianxiang</au><au>Yu, Wenhua</au><au>Wun, Ching Kit Tommy</au><au>Wu, Tai-Sing</au><au>Sun, Mingzi</au><au>Day, Sarah J.</au><au>Li, Zehao</au><au>Yuan, Bo</au><au>Wang, Yong</au><au>Li, Mingjie</au><au>Wang, Zi</au><au>Peng, Yung-Kang</au><au>Yu, Wing-Yiu</au><au>Wong, Kwok-Yin</au><au>Huang, Bolong</au><au>Liang, Taoyuan</au><au>Lo, Tsz Woon Benedict</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cu–Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp2)–N Coupling Reaction</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2023-04-06</date><risdate>2023</risdate><volume>145</volume><issue>15</issue><spage>8464</spage><epage>8473</epage><pages>8464-8473</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>A 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. 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title | Cu–Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp2)–N Coupling Reaction |
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