A microporous magnesium gallate MOF was prepared from highly biocompatible reagents under environmentally friendly conditions. Its slow degradation in physiological fluids leads to the release of gallic acid and hence a high antioxidant activity, which was illustrated in the HL-60 cell line.

Novel biocompatible Ca-gallate MOFs with progressive release of gallic acid associated with a significantin vitroantioxidant effect.

The ability of two structurally related small pore Metal Organic Frameworks (MOFs) to capture CO2 was investigated by a combination of gas sorption measurements, X-ray powder diffraction (XRPD) analysis, microcalorimetry experiments and Ideal Adsorbed Solution Theory (IAST) calculations. The title solids, formulated Mg(H2gal) and Fe(Hgal) (H4gal = gallic acid) are made of a naturally occurring ligand, and were both prepared on the multigram scale under mild conditions. They both present very similar structures, with identical channels of ca 3.5 Å diameter, but present different amounts of acidic protons on the surface of the pores. These compounds were found to be extremely hydrophilic, and exhibit a moderate stability towards water. Whilst their ability to adsorb CH4 and N2 is very limited, they both adsorb significant amounts of CO2 even at atmospheric pressure (3 and 5 mmol g-1 at 303 K for the Fe and Mg derivatives respectively). As a consequence, these compounds present high CO2/N2 and CO2/CH4 selectivities (380-910 and 190-460 respectively) together with good working capacities, making them of interest for the capture of CO2 from flue gas or for landfill gas upgrading in pressure swing adsorption or vacuum swing adsorption processes. Finally, the analysis of the Mg derivative by X-Ray Diffraction (XRD) and adsorption microcalorimetry revealed that its high affinity for CO2 relies on a strong and specific site of adsorption involving double hydrogen bonds between the CO2 molecules and the acidic protons of the framework.