We rationalize the thermodynamics behind the guest-induced structural transitions of hybrid material MIL-53, showing that the existence of a double transition depends on the relative guest affinities for the two phases, rather than absolute adsorption enthalpies. Based on a simple model, we interpret recent experimental data on alkane adsorption and predict transition pressures.

The flexible metal-organic framework MIL-53(Cr) undergoes a dramatic volume expansion upon immersion in water at room temperature to form a crystalline hydrate in which water is held as a hydrogen-bonded tube: the hydration is readily reversible under ambient conditions as shown by time-resolved powder X-ray diffraction.

Two new unsymmetrical N-heterocyclic carbene ligand (uNHC)-based ruthenium complexes featuring phenolic OH function were obtained and fully characterised. The more active one was then immobilised on the metal–organic framework (MOF) solid support (Al)MIL-101-NH2. catalytic activity of such a heterogeneous system tested, showing that, while catalyst is less than corresponding homogeneous in solu...

The direct conversion reaction of glucose to 5-hydroxymethylfurfural (HMF) is studied using metal organic framework (MOF) as Lewis-acid catalysts and a polyoxometalate (POM), silicotungstic acid, Brønsted-type acid with mixture 1% solution in ?-valerolactone (GVL)-10% H2O at 140 °C. study carried out two routes: one MOF POM tandem added independently the other through synthesis composite materi...

The thermal behaviour of the nanoporous iron(iii) terephthalate MIL-53 is in stark contrast to its chromium and aluminium analogues which show an expansion of the cell during dehydration; with iron, reversible dehydration occurs via evolution of the structure through a highly distorted metastable anhydrous phase to a more regular phase above 423 K in which pore volume remains approximately cons...

The MIXMOF concept has been applied to the metal-organic framework compound MIL-53(Al). The random incorporation of two different linker molecules (benzene-1,4-dicarboxylate and 2-aminobenzene-1,4-dicarboxylate) in the framework structure and its influence on thermal stability were proven using several complementary techniques (XRD, ATR-IR, MAS-NMR and TG).