Colloidal Ag particles decorated with Fe3O4 islands can be activated as inverse catalysts for C(sp(2))-H heteroarylation either electrochemically or photochemically. The silver-iron oxide (SIO) particles are reduced into redox-active forms by cathodic charging at mild potentials or short-term light exposure, and can be reused multiple times by magnetic cycling without further activation. The reduction peak shift is attributed to the overpotential produced by surface Fe3O4, which separates residual Ag ions or clusters from bulk silver. The catalytic efficiency of SIO is maintained even with acid degradation, and can be counteracted by simple addition of water to the reaction medium.
Colloidal Ag particles decorated with Fe3O4 islands can be electrochemically or photochemically activated as inverse catalysts for C(sp(2))-H heteroarylation. The silver-iron oxide (SIO) particles are reduced into redox-active forms by cathodic charging at mild potentials or by short-term light exposure, and can be reused multiple times by magnetic cycling without further activation. A negative shift in the reduction peak is attributed to an overpotential produced by surface Fe3O4 which separates residual Ag ions or clusters from bulk silver. The catalytic efficiency of SIO is maintained even with acid degradation, which can be countered simply by adding water to the reaction medium.
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