Abstract: | The phase diagram of the system [Ph4P]Br/BiBr3 was investigated with the aid of DSC, TG and temperature dependent X‐ray powder diffraction measurements. By varying the reaction conditions, stoichiometry and crystallisation conditions of the reaction between BiBr3 and [Ph4P]Br four polynuclear bromobismuthates are formed. We report here the crystal structure of the solvation product [Ph4P]3[Bi2Br9] · CH3COCH3, which crystallises with monoclinic symmetry in the S. G. P21/n No. 14, a = 12.341(1), b = 32.005(3), c = 19.929(3) Å, β = 99.75(2)°, V = 7758(7) Å3, Z = 4 and the crystal structures of two modifications of the compound [Ph4P]4[Bi6Br22]. The α‐form, crystallises with triclinic symmetry in the S. G. P1 No. 2, a = 13.507(4) Å, b = 14.434(4) Å, c = 17.709(5) Å, α = 81.34(2)°, β = 72.42(2)°, γ = 72.53(2)°, V = 3132.7(1) Å3, Z = 2. The high‐temperature β‐form, crystallises with triclinic symmetry in the S. G. P1 No. 2, a = 13.893(4) Å, b = 14.267(3) Å, c = 16.580(3), α = 100.13(2)°, β = 96.56(2)°, γ = 110.01(2)°, V = 2985.5(1) Å3, Z = 2. Lattice parameters of [Ph4P]4[Bi8Br28] are also given. The thermal behaviour of the compounds and in addition the vibrational spectra of [Ph4P]3[Bi2Br9] · CH3COCH3 are presented and discussed. |