Defects
in solid materials vitally determine their physicochemical
properties; however, facile regulation of the defect density is still
a challenge. Herein, we demonstrate that the ligand defect density
of metal–organic frameworks (MOFs) with a UiO-66 structural
prototype is precisely regulated by tuning the linker groups (X =
OMe, Me, H, F). Detailed analyses reveal that the ligand defect concentration
is positively correlated with the electronegativity of linker groups,
and Ce-UiO-66-F, constructed by F-containing ligands and Ce-oxo nodes,
possesses the superior ligand defect density (>25%) and identifiable
irregular periodicity. The increase in ligand defect density results
in the reduction of the valence state and the coordination number
of Ce sites in Ce-UiO-66-X, and this merit further validates the relationship
between the defective structure and catalytic performance of CO2 cycloaddition reaction. This facile, efficient, and reliable
strategy may also be applicable to precisely constructing the defect
density of porous materials in the future.