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
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.3c00114