Synthesis, crystal structure and thermal properties of poly[di-μ-bromido-(μ-2,5-di-methyl-pyrazine)cadmium(II)].

The title compound, [CdBr(CHN)] , was prepared by the reaction of cadmium bromide with 2,5-di-methyl-pyrazine in water. Its asymmetric unit consists of one Cd cation and one 2,5-di-methyl-pyrazine ligand that are located on a crystallographic mirror plane as well as one bromide anion that occupies a general position. The Cd cations are sixfold coordinated by four bromide anions and two 2,5-di-methyl-pyrazine ligands within slightly distorted -CdBrN octa-hedra. The cations are linked into [100] chains pairs of bridging bromide anions that are further connected into (001) layers by the bridging 2,5-di-methyl-pyrazine ligands. Powder X-ray diffraction (PXRD) shows that a pure crystalline phase has been obtained. Thermogravimetry coupled to differential thermoanalysis (TG-TDA) reveal that the 2,5-di-methyl-pyrazine ligands are removed in two separate steps leading to the formation of a compound with the composition (CdBr)(2,5-di-methyl-pyrazine) that decomposes into CdBr upon further heating. PXRD measurements of the residue obtained after the first mass loss show that a new crystalline phase has been formed.