In analogy to the synthesis of polycrystalline M₂NaIO₆ (M = Ca, Sr, Ba) by precipitation in water at 90 °C, the title compound was first prepared as a metastable compound. The stable modification of Pb₂NaIO₆ was obtained by a heat treatment to 400 °C followed by cooling to room temperature. The crystal structure was refined from powder diffraction data [space group P2₁/c (14), a = 5.9040(2), b = 5.7526(2), c = 10.1104(3) Ã…, β = 125.341(1)°]. On heating, at ca. 125 °C, a phase transition to a cubic high temperature modification was observed. The crystal structure was refined from XRD data measured at 200 °C [space group Fm3m (225), a = 8.2678(1) Ã…]. Depending on the precipitation temperature between 90 °C and 0 °C, several metastable modifications were obtained, which can be distinguished by significantly different lattice parameters. The XRD pattern of a powder precipitated at room temperature is pseudocubic. The crystal structure was refined at room temperature in P2₁/c with a = 5.8201(4), b = 5.8473(4), c = 10.0798(5) Ã…, β = 125.074(3)°. This modification behaves almost as a cubic lattice on heating as found from XRD and DSC measurements.

The compound Ba₅I₂O₁₂ was synthesized by heating a precipitate of dissolved Ba(OH)₂·8H₂O and H₅IO₆. Rb₂O was added to increase the crystallite size. The crystal structure was determined from conventional laboratory X-ray diffraction data by using a real-space structure solution approach followed by a Rietveld refinement. No constraints on positions were used. The structure analysis gave an orthorhombic symmetry with a = 19.7474(2) Ã…, b = 5.9006(1) Ã… and c = 10.5773(1) Ã…. The final R_Bragg value in space group Pnma (62) was 1.0 %. The structure can be described by layers of a metal and iodine arrangement forming almost pentagonal holes. Raman measurements were correlated with the two IO₆ octahedra. Two further barium periodate patterns were observed and indexed.

The crystal structures of the M₂NaIO₆ series (M = Ca, Sr, Ba), prepared at 650 °C by ceramic methods, were determined from conventional laboratory X-ray powder diffraction data. Synthesis and crystal growth were made by oxidizing I^– with O₂^(air) to I⁷⁺ followed by crystal growth in the presence of NaF as mineralizator, or by the reaction of the alkali-metal periodate with the alkaline-earth metal hydroxide. All three compounds are insoluble and stable in water. The barium compound crystallizes in the cubic space group Fm3m (no. 225) with lattice parameters of a = 8.3384(1) Ã…, whereas the strontium and calcium compounds crystallize in the monoclinic space group P2₁/c (no. 14) with a = 5.7600(1) Ã…, b = 5.7759(1) Ã…, c = 9.9742(1) Ã…, β = 125.362(1)° and a = 5.5376(1) Ã…, b = 5.7911(1) Ã…, c = 9.6055(1) Ã…, β = 124.300(1)°, respectively. The crystal structure consists of either symmetric (for Ba) or distorted (for Sr and Ca) perovskite superstructures. Ba₂NaIO₆ contains the first perfectly octahedral [IO₆]^5– unit reported. The compounds of the ortho-periodates are stable up to 800 °C. Spectroscopic measurements as well as DFT calculations show a reasonable agreement between calculated and observed IR- and Raman-active vibrations.

Barium calcium magnesium fluoride (Ba₂(Ba_xCa_1-x)Mg₄F₁₄, x=0.19-0.26) has been synthesized at 850 °C from precursors prepared by the solution precipitation method. Single crystals with composition of Ba_2.200(2)Ca_0.800(2)Mg₄F₁₄were obtained after prolonged heating. Lattice parameters from single crystal data are a = 12.4203(8) and c = 7.4365(5) Ã… [tetragonal, space group P4₂/mnm (No. 136)]. They increase with increasing barium concentration within a given stability window. The structure is built of a network of MgF₆ octahedra forming a pyrochlore related channel system and isolated fluorine ions. Within the channels, heavy alkaline earth ions are located. The wide channel is filled with off-center positioned barium ions. The channel with a narrow cross section hosts both ions, Ca²⁺and Ba²⁺. The structure is isotypic with Pb₃Nb₄O₁₂F₂ but has a different coordination around Ba/Ca and Pb, respectively. Doped with ∼1% Eu(II), the compound shows intense blue luminescence under UV activation.