Copper Nanoclusters with Exposed Active Sites for Highly Efficient Protoboration of C–C Multiple Bonds

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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Publication Details

Journal
Molecules
Published
2026-08-24
DOI
https://doi.org/10.3390/molecules31172956
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Copper Nanoclusters with Exposed Active Sites for Highly Efficient Protoboration of C–C Multiple Bonds

Shaoke Zhang, Songwei Wen
Molecules
Organoboron and organosilicon chemistry
article

Copper Nanoclusters with Exposed Active Sites for Highly Efficient Protoboration of C–C Multiple Bonds

Shaoke Zhang, Songwei Wen
article en

Abstract

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.

MoleculesVol. 31(17)
Southern University of Science and Technology (CN)
National Natural Science Foundation of China, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 19%
Organoboron and organosilicon chemistry
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