The reaction of [Re₆Qⁱ ₈(OH)^a ₆]^{4 −} (Q = S, Se) with p-tert-butylpyridine (TBP) in water leads to neutral trans-[Re₆Q₈(TBP)₄(OH)₂] whose hydroxyl reactivity with carboxylic acid and TBP exchange reaction with functional pyridine have been investigated.

This work presents the synthesis and studies of a red-NIR luminescent liquid crystal compound based on an octahedral metallic cluster core orthogonally bounded to six non-mesogenic organic ligands. It evidences synergetic effects between the organic and inorganic parts of the hybrid, resulting in the generation of liquid crystal properties on cooling from the isotropic melt.

In this work we report our studies concerning the synthesis and characterisation of a series of imine derivatives that incorporate the 2-phenylpyridine (2-ppy) core. These derivatives were used in the cyclometalating reactions of platinum(II) or palladium(II) in order to prepare several complexes with liquid crystalline properties. Depending on the starting materials used as well as the solvents employed, different metal complexes were obtained, some of them showing both liquid crystalline behaviour and luminescence properties at room temperature. It was found that, even if there are two competing coordination sites, the cyclometalation process takes place always at the 2-ppy core with (for Pt) or without (for Pd) the imine bond cleavage. We successfully showed that it is possible to prepare emissive room temperature liquid crystalline materials based on double cyclopalladated heteroleptic complexes by varying the volume fraction of the long flexible alkyl tails on the ancillary benzoylthiourea (BTU) ligands.