LAUSR

Activation and selective functionalization of inert C(sp3)-H bonds remain one of the most challenging tasks in current synthetic chemistry. Herein, by decorating vanadium(VIV)-porphyrin into metal-organic frameworks (MOFs) to stabilize the active tertbutyl peroxide radical, we reported a new approach to accomplish inert C(sp3)-H bond activation by a synergistic bimetallic strategy via a hydrogen atom transfer process under mild conditions. The stabilized peroxide radical by VIV-porphyrin-based MOFs abstracted a hydrogen atom from the inert C(sp3)-H bonds for direct oxidization transformation utilizing environmentally friendly oxygen. Taking advantage of the high stability of Zr6 clusters, the new Zr-MOF was recyclable six times without a conversion efficiency decrease. From this foundation, {Mn3(μ3-O)} cluster nodes with potential unsaturated coordinated sites were introduced into MOFs to replace Zr6 clusters, realizing the pre-activation of substrates through the interaction between Mn nodes and substrates. The synergistic bimetallic activation effect of VIV-porphyrin and Mn nodes dramatically promoted the conversion efficiency and product selectivity for inert C(sp3)-H bond functionalization.