The deliberate engineering of cooperative catalytic microenvironments within metal-organic frameworks (MOFs) offers a powerful strategy for promoting sustainable catalysis. Herein, we report a robust nitro-functionalized trinuclear metal-organic framework, formulated as Cu3 (NTCB) 2 (4, 4'-bip) (DMF) 2·4DMF·3H2On (NUC-180; H3NTCB = 1, 3, 5-tri (4-carboxy-2-nitrophenyl) -2, 4, 6-trinitrobenzene, 4, 4'-bip = 4, 4'-bipyridine), featuring a high void fraction and dual nanoscale channel systems. Upon activation, NUC-180a exposes coordinatively unsaturated metal centers and strongly electron-withdrawing nitro functionalities that collectively regulate the local electronic environment and enhance substrate polarization. As a result, NUC-180a exhibits excellent heterogeneous catalytic performance for the solvent-free cycloaddition of CO2 with epoxides under mild conditions, delivering cyclic carbonates with high efficiency, selectivity, and recyclability. Beyond CO2 fixation, the framework also efficiently catalyzes tandem deacetalization-Knoevenagel condensation reactions. Mechanistic insights reveal that the catalytic activity originates from the synergistic interplay between Lewis-acidic metal sites and polar functional groups within the confined micropores. This work highlights nitro-functionalized MOFs as versatile platforms for cooperative catalysis without invoking classical Lewis basicity from nitro groups.
Li et al. (Mon,) studied this question.