Oxidation of renewable polyol/sugar into formic acid using molecular O₂ over heterogeneous catalysts is still challenging due to the insufficient activation of both O₂ and organic substrates on coordination-saturated metal oxides. In this study, we develop a defective MnO₂ catalyst through a coordination number reduction strategy to enhance the aerobic oxidation of various polyols/sugars to formic acid. Compared to common MnO₂, the tri-coordinated Mn in the defective MnO₂ catalyst displays the electronic reconstruction of surface oxygen charge state and rich surface oxygen vacancies. These oxygen vacancies create more Mnδ+ Lewis acid site together with nearby oxygen as Lewis base sites. This combined structure behaves much like Frustrated Lewis pairs, serving to facilitate the activation of O₂, as well as C-C and C-H bonds. As a result, the defective MnO₂ catalyst shows high catalytic activity (turnover frequency: 113.5 h⁻¹) and formic acid yield (>80%) comparable to noble metal catalysts for glycerol oxidation. The catalytic system is further extended to the oxidation of other polyols/sugars to formic acid with excellent catalytic performance.
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Yan et al. (2023) studied this question.
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