Metal-rich phosphides RE5Ir19P12 with Sc5Co19P12 type structure

The iridium-rich phosphides RE5Ir19P12 (RE=Sc, Y, La–Nd, Sm–Lu) with Sc5Co19P12 type structure, space group P62̄m were synthesized by solid state reactions of the elements in tantalum crucibles. Well shaped single crystals were obtained in bismuth fluxes. All phosphides were characterized on the basis of X-ray powder data. The structures of RE5Ir19P12 with RE=Sc, La, Ce, Dy, Er, Tm, and Yb were refined from single crystal diffractometer data. The complex structure of these phosphides can be described by an intergrowth of simpler ThCr2Si2 and SrPtSb related slabs. Striking structural motifs of the RE5Ir19P12 structures are slightly distorted tricapped trigonal prisms of the metal atoms around the phosphorus atoms. The iridium and phosphorus atoms build up three-dimensional [Ir19P12] polyanionic networks (230–286 pm Ir–P and 282–296 pm Ir–Ir in La5Ir19P12) which leave cavities of coordination numbers 16 and 15 for the rare earth atoms.

Graphical AbstractThe intergrowth structure La5Ir19P12.Figure optionsDownload as PowerPoint slideHighlights
► Metal flux syntheses of intermetallic compounds.
► Synthesis and structure of new phosphides RE5Ir19P12.
► Crystal chemistry of metal-rich phosphides.
► Description of the RE5Ir19P12 structure as an intergrowth variant.