The ability of zirconium metal–organic frameworks (MOFs) to gelate under specific synthetic conditions opens up new opportunities in the preparation and shaping of hierarchically porous MOF monoliths, which could be directly implemented for catalytic and adsorptive applications.
Over
the past decade, the zirconium-terephthalate UiO-66 has evolved
into one of the most intensely studied metal–organic frameworks
(MOFs) to date. Among the most fascinating and pervasive features
of this material are defects, and their influence on a multitude of
its properties. However, the simultaneous occurrence of two defect
types, missing linkers and missing nodes, limits the extent to which
certain material properties can be accurately matched to the framework’s
defect structure. In this contribution, we present a strategy to unequivocally
create missing linker defects in UiO-66, by first synthesizing terephthalate
frameworks doped with a thermolabile linker, trans-1,4-cyclohexane-dicarboxylate (cdc), followed by postsynthetic thermal
decomposition of the latter. Characterization of the mixed-linker
materials before and after cdc removal by powder X-ray diffraction,
thermogravimetric analysis, N2 physisorption, and NMR spectroscopy
confirmed a homogeneous distribution of cdc, and thus also of the
formed defects, throughout the materials. The UiO-66 structure is
shown to tolerate up to 4.3 missing linker defects per [Zr6O4(OH)4]12+ node, with higher defect
densities compromising the framework’s structural integrity
and porosity. Importantly, no increase in specific surface area was
seen after additional missing linker defects were formed, providing
compelling evidence that high porosity often observed in modulated
UiO-66 samples should rather be attributed to missing cluster defects.
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