Al3+ Dopants Induced Mg2+ Vacancies Stabilizing Single-Atom Cu Catalyst for Efficient Free-Radical Hydrophosphinylation of Alkenes
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY(2022)
Abstract
Utilizing heterogeneous catalysts to overcome obstacles for homogeneous reactions is fascinating but very challenging owing to the difficult fabrication of such catalysts based on the character of target reactions. Herein, we report a Al3+ doping strategy to construct single-atom Cu on MgO nanosheets (Cu-1/MgO(Al)) for boosting the free-radical hydrophosphinylation of alkenes. Al3+ dopants in MgO bring about abundant Mg2+ vacancies for stabilizing dense independent Cu atoms (6.3 wt %), while aggregated Cu nanoparticles are formed without Al3+ dopants (Cu/MgO). Cu-1/MgO(Al) exhibits preeminent activity and durability in the hydrophosphinylation of various alkenes with great anti-Markovnikov selectivity (99%). The turnover frequency (TOF) value reaches up to 1272 h(-1), exceeding those of Cu/MgO by similar to 6-fold and of traditional homogeneous catalysts drastically. Further experimental and theoretical studies disclose that the prominent performance of Cu-1/MgO(Al) derives from the accelerated initiating step of phosphinoyl radical triggered by individual Cu atoms.
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Key words
alkenes,single-atom,free-radical
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