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The crystal structure of titanium-tin tellurium oxide Sn 0.59 Ti 0.41 Te 3 O 8 has been determined using X-ray powder diffraction techniques. At room temperature, the title compound crystallizes in cubic space group Ia-3, with lattice parameter a = 11.05515͑6͒ Å. Rietveld refinement of the structure led to final confidence factors R p = 0.0395 and R wp = 0.0577. The structure of Sn 0.59 Ti 0.41 Te 3 O 8 consists of isolated Ti/ SnO 6 -octahedra slightly deformed in the a direction. The TeO 4 E ͓E = lone pair of Te͑IV͒ atoms͔ groups are located between the octahedra ensuring the stability of the structure by Ti/ Sn-O-Te bonding contacts. Only one peak in thermal behavior was detected for this compound at 488 K by differential scanning calorimetry experiment. An IR spectroscopic study is employed as a means to obtain preliminary structural information and shows the presence of the Ti/ SnO 6 and TeO 4 E groups. This result is later confirmed by X-ray diffraction studies.

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Synthesis, crystal structure, thermal characterization, FTIR and Raman measurements are given for a new mixed compound cesium-ammonium tellurate. X-ray study showed that the [Cs 0.92 (NH 4) 0.08 ] 2 TeCl 4 Br 2 compound crystallizes in the tetragonal space group P4/mnc, with a = 7.452 (1) Å, c = 10.544 (3) Å and Z = 2. The refinement converged at room temperature to R p = 0.093 and R wp = 0.076. The structure is considered as isolated octahedral TeCl 4 Br 2− 2. These anions show a 4 • rotation around the fourfold axis against the cubic arrangement of the K 2 PtCI 6 type structure. The monovalent cations (Cs + /NH + 4) are located between the octahedra ensuring the stability of the structure by ionic and hydrogen bonding contacts: Cs...Cl/Br and N-H.. .. .. Cl/Br. A DTA/TGA experiment at high temperature reveals one endothermic peak at 780 K for this compound. At low temperature a transition from phase I to phase II was detected at 213 K by DSC. This transition, confirmed by Raman analysis, can be attributed to an order-disorder phase transition.

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