Abstract
AbstractYellow single‐crystals of Na2[Ir(OH)6] were obtained by hydrothermal synthesis in 20 m sodium hydroxide solution at 473 K within 5 hours. X‐ray diffraction on a single‐crystal revealed the trigonal space group (no. 148) with lattice parameters a=582.76(3) pm and c=1399.30(8) pm at 100(1) K. Na2[Ir(OH)6] crystallizes in a hettotype of Mg(OH)2 (brucite) and is isostructural to Na2[Sn(OH)6]. The oxygen atoms are arranged in a hexagonal close packing, Na+ and Ir4+ ions occupy the octahedral voids in every second layer in an ordered manner, the voids of the next layers remain empty. The hydroxidometalate layer can be seen as isolated [Ir(OH)6]2− octahedra, which are embedded in a honeycomb net of alkali metal cations. Temperature‐dependent magnetic measurements revealed paramagnetic behavior with an effective moment of 1.9 μB per iridium ion. The thermal decomposition of Na2[Ir(OH)6] in air starts at about 220 °C and results in pure Na2IrO3.
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