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Experimental study demonstrates efficient protoboration of carbon-carbon multiple bonds using copper nanoclusters, highlighting a robust platform for organoboron synthesis.
Although atomically precise metal nanoclusters bridge homogeneous and heterogeneous catalysis, their application in the protoboration of C–C unsaturated bonds remains challenging. Herein, we report a stable copper nanocluster (Cu6-1) featuring exposed active sites, which successfully enables efficient protoboration of alkynes. This catalyst can be readily synthesized on a gram scale and exhibits ultrahigh catalytic efficiency under ambient conditions (room temperature and air atmosphere), achieving a turnover number (TON) of up to 32,000. The reaction demonstrates excellent regio- and stereoselectivity, and the substrate scope has been successfully expanded to alkenes and enynes. More importantly, Cu6-1 overcomes the recyclability issues of traditional catalysts, retaining its activity over eight consecutive cycles with no significant deactivation, thus offering a highly efficient and robust platform for the synthesis of organoboron compounds.
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Zhang et al. (2026) studied this question.
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