Cu-Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp2)-N Coupling Reaction

Tianxiang Chen, Wenhua Yu, Ching Kit Tommy Wun, Tai-Sing Wu, Mingzi Sun, Sarah J. Day, Zehao Li, Bo Yuan, Yong Wang, Mingjie Li, Zi Wang, Yung-Kang Peng, Wing-Yiu Yu, Kwok-Yin Wong, Bolong Huang*, Taoyuan Liang*, Tsz Woon Benedict Lo*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

24 Citations (Scopus)

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. This study offers critical insights into the engineering of next-generation solid atomic catalysts with complex reaction steps. © 2023 American Chemical Society.
Original languageEnglish
Pages (from-to)8464–8473
JournalJournal of the American Chemical Society
Volume145
Issue number15
Online published6 Apr 2023
DOIs
Publication statusPublished - 19 Apr 2023

Funding

T.W.B.L. thanks the National Natural Science Foundation of China (no. 22172136), Hong Kong Research Grants Council (nos. 15301521, 15300819, and 15305722), Department of Science and Technology of Guangdong Province (no. 2021A1515010218), and PolyU start-up SHS fund (no. BDC3) for financial support. T.L. thanks the National Natural Science Foundation of China (no. 22201048) and the Natural Science Foundation of Guangxi Province (no. 2022GXNSFBA035480) for financial support.

RGC Funding Information

  • RGC-funded

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