TY - JOUR
T1 - Cu-Co Dual-Atom Catalysts Supported on Hierarchical USY Zeolites for an Efficient Cross-Dehydrogenative C(sp2)-N Coupling Reaction
AU - Chen, Tianxiang
AU - Yu, Wenhua
AU - Wun, Ching Kit Tommy
AU - Wu, Tai-Sing
AU - Sun, Mingzi
AU - Day, Sarah J.
AU - Li, Zehao
AU - Yuan, Bo
AU - Wang, Yong
AU - Li, Mingjie
AU - Wang, Zi
AU - Peng, Yung-Kang
AU - Yu, Wing-Yiu
AU - Wong, Kwok-Yin
AU - Huang, Bolong
AU - Liang, Taoyuan
AU - Lo, Tsz Woon Benedict
PY - 2023/4/19
Y1 - 2023/4/19
N2 - 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.
AB - 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.
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U2 - 10.1021/jacs.3c00114
DO - 10.1021/jacs.3c00114
M3 - RGC 21 - Publication in refereed journal
C2 - 37023113
SN - 0002-7863
VL - 145
SP - 8464
EP - 8473
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 15
ER -