A microporous Al trimesate-based Metal Organic Framework (MOF), denoted MIL-96(Al), was selected as a porous hybrid filler for the processing of Mixed Matrix Membranes (MMMs) for CO 2 /N 2 post combustion separation. First, the structural model of MIL-96(Al) initially reported was revisited using a combination of synchrotron-based single crystal X-ray diffraction (XRD), solid state Nuclear Magnetic Resonance (NMR) spectroscopy and Density Functional Theory (DFT) calculations. In a second step, pure MIL-96 (Al) crystals differing by their size and aspect ratio, including anisotropic hexagonal platelets and nanoparticles of about 70 nm in diameter, were prepared. Then, a combination of in situ IR spectroscopy, single gas and CO 2 /N 2 co-adsorption experiments, calorimetry and molecular simulations revealed that MIL-96(Al) nanoparticles show a relatively high CO 2 affinity over N 2 owing to strong interactions between CO 2 molecules and several adsorption sites such as Al 3+ Lewis centers, coordinated water and hydroxyl groups. Finally, the high compatibility between MIL-96(Al) nanoparticles and the 6FDA-DAM polymer allowed the processing of homogeneous and defect-free MMMs with a high MOF loading (up to 25 wt%) that outperform pure polymer membranes for CO 2 /N 2 separation.

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The syntheses and biological evaluation of the first anti-protozoa imidazole N-oxide and benzimidazole N-oxide and their derivatives are reported. They were tested in vitro against two different protozoa, Trypanosoma cruzi and Trichomonas vaginalis. Derivative 7c, ethyl-1-(i-butyloxycarbonyloxy)-6-nitrobenzimid-azole-2-carboxylate, displayed activity on both protozoa. Lipophilicity and redox potential were experimentally determined in order to study the relationship with activity of the compounds. These properties are well related with the observed bioactivity. Imidazole and benzimidazole N-oxide derivatives are becoming leaders for further chemical modifications and advanced biological studies.

Due to the increasing use of nanometric cerium oxide in applications, concerns about the toxicity of these particles have been raised and have resulted in a large number of studies. We report here on the interactions between 7 nm anionically charged cerium oxide particles and living mammalian cells. By a modification of the particle coating including low-molecular weight ligands and polymers, two generic behaviours are compared: particles coated with citrate ions that precipitate in biofluids and particles coated with poly(acrylic acid) that are stable and remain nanometric. We find that nanoceria covered with both coating agents are taken up by mouse fibroblasts and localized into membrane-bound compartments. However, flow cytometry and electron microscopy reveal that as a result of their precipitation, citrate-coated particles interact more strongly with cells. At cerium concentration above 1 mM, only citrate-coated nanoceria (and not particles coated with poly(acrylic acid)) display toxicity and moderate genotoxicity. The results demonstrate that the control of the surface chemistry of the particles and its ability to prevent aggregation can affect the toxicity of nanomaterials.