A new MIL-101 material based on aluminum and containing amine functional groups has been synthesized. The pure phase NH2-MIL-101(Al) can only be formed in very specific synthesis conditions, where both the metal source and the solvent used play a key role. The resulting porous solid shows a high thermal and chemical stability, decomposing at temperatures above 650 K in air. The NH2-MIL-101(Al) framework offers an excellent trade off for separation of CO2: the combination of high stability, acceptable capacity at low adsorbate partial pressures, high selectivity, and fast regenerability makes this new material a very attractive candidate for applications like natural gas or biogas upgrading. CO2 capacities up to 62 wt % are obtained at room temperature and 3 MPa. In addition to an excellent separation performance, the NH2-MIL-101(Al) shows a high activity in the basic catalyzed Knoevenagel condensation of benzaldehyde with ethyl cyanoacetate at 313 K even in an as apolar a solvent as toluene (turn over frequency, TOF = 1.8 h–1).

Several archetypical metal organic frameworks (MOFs), namely, HKUST-1, ZIF-8, MIL-100(Al), MIL-53(Al), and NH2-MIL-53(Al), were synthesized via anodic dissolution in an electrochemical cell. The influence of different reaction parameters such as solvent, electrolyte, voltage–current density, and temperature on the synthesis yield and textural properties of the MOFs obtained was investigated. The characterization of the samples involved X-ray diffraction, gas adsorption, atomic force microscopy, diffuse reflectance infrared Fourier transform spectroscopy, and scanning electron microscopy. In the present article, we demonstrate that electrochemical synthesis is a robust method offering additional degrees of freedom in the synthesis of these porous materials. The main advantages are the shorter synthesis time, the milder conditions, the facile synthesis of MOF nanoparticles, the morphology tuning and the high Faraday efficiencies. The synthesized MIL-53 and NH2-MIL-53 samples exhibit suppressed framework flexibility compared to samples synthesized solvothermally.

Mixed matrix membranes (MMMs) composed of a glassy polymer (polysulfone) and the flexible metal organic framework NH(2)-MIL-53(Al) exhibit excellent separation properties. In contrast to most reported membranes, CO(2)/CH(4) separation selectivity increases with pressure, related to the flexibility of the filler.

Hybrid materials bearing organic and inorganic motives have been extensively discussed as playgrounds for the implementation of atomically resolved inorganic sites within a confined environment, with an exciting similarity to enzymes. Here, we present the successful design of a site-isolated mixed-metal Metal Organic Framework that mimics the reactivity of soluble methane monooxygenase enzyme and demonstrates the potential of this strategy to overcome current challenges in selective methane oxidation. We describe the synthesis and characterisation of an Fe-containing MOF that comprises the desired antiferromagnetically coupled high spin species in a coordination environment closely resembling that of the enzyme. An electrochemical synthesis method is used to build the microporous MOF matrix while integrating the atomically dispersed Fe active sites in the crystalline scaffold. The model mimics the catalytic C-H activation behaviour of the enzyme to produce methanol, and shows that the key to this reactivity is the formation of isolated oxobridged Fe units.

Mixed matrix membranes (MMMs) composed of metal organic framework (MOF) fillers embedded in a polymeric matrix represent a promising alternative for CO2 removal from natural gas and biogas. Here, MMMs based on NH2‐MIL‐53(Al) MOF and polyimide are successfully synthesized with MOF loadings up to 25 wt% and different thicknesses. At 308 K and ΔP = 3 bar, the incorporation of the MOF filler enhances CO2 permeability with respect to membranes based on the neat polymer, while preserving the relatively high separation factor. The rate of solvent evaporation after membrane casting proves key for the final configuration and dispersion of the MOF in the membrane. Fast solvent removal favours the contraction of the MOF structure to its narrow pore framework configuration, resulting in enhanced separation factor and, particularly, CO2 permeability. The study reveals an excellent filler‐polymer contact, with ca. 0.11% void volume fraction, for membranes based on the amino‐functionalized MOF, even at high filler loadings (25 wt%). By providing precise and quantitative insight into key structural features at the nanoscale range, the approach provides feedback to the membrane casting process and therefore it represents an important advancement towards the rational design of mixed matrix membranes with enhanced structural features and separation performance.