Controlling the molecular diffusion in MOFs with the acidity of monocarboxylate modulators

Abstract

The catalytic performance of metal-organic frameworks (MOFs) is related to their physicochemical properties, such as particle size, defect chemistry and porosity, which can be potentially controlled by coordination modulation. By combining PXRD, 1HNMR, FT-IR, and N2 uptake measurements we have gained insights into the control of different types of defects (missing linker or missing cluster consequence of the spatial distribution of missing linkers, and a combination of both) by the type of modulator employed. We show that the molar percent of defects, either as missing linkers or as a part of missing cluster defects, is related to the acidity of a modulator and its subsequent incorporation into the UiO-66 structure. Modulators with strong acidity and small size result in a considerable defect induction that causes an increase in the external surface area and mesopore volume, which is beneficial for the ring-opening of epoxides with amines, using UiO-66 defect-modulated MOFs as heterogeneous catalysts.