Structure of triaquatris(1,1,1-trifluoro-4-oxopentan-2-olato)cerium(III) as a possible fluorescent compound

Abstract

Luminescence due to the d-f transition of Ce 3+ is quite rare in metal-organic complexes where concentrate quenching frequently occurs. One of the possible ways to avoid this is to design an architecture with elongated metal-metal distances. In the structure of the title complex, triaquatris(1,1,1-trifluoro-4-oxopentan-2-olato-complex is linked to neighbouring ones by hydrogen bonding. Within the complex, the Ce III atom is coordinated by nine O atoms from three 1,1,1-trifluoro-4-oxopentan-2-olate (tfa) anions as bidentate ligands and three water molecules as monodentate ligands. Thus, the coordination number of Ce III atom is nine in a monocapped square-antiprismatic polyhedron. The F atoms of all three independent CF 3 groups in tfa are disordered over two positions with occupancy ratios of about 0.8:0.2. The intermolecular hydrogen bonds between the ligands involve tfa-water interactions along the [110] and [110] directions, generating an overall two-dimensional layered network structure. The presence of the F atoms in the tfa anion is responsible for an increased intermolecular metal-metal distance compared to that in the analogous acetylacetonate (acac) derivatives. Fluorescence from Ce 3+ is, however, not observed.