Abstract
The natural sII-type clathrasil chibaite [chemical formula SiO(2)·(M(12),M(16)), where M(x) denotes a guest mol-ecule] was investigated using single-crystal X-ray diffraction and Raman spectroscopy in the temperature range from 273 to 83 K. The O atoms of the structure at room temperature, which globally conforms to space group [V = 7348.9 (17) Å(3), a = 19.4420 (15) Å], have anomalous anisotropic displacement parameters indicating a static or dynamic disorder. With decreasing temperature, the crystal structure shows a continuous symmetry-lowering transformation accompanied by twinning. The intensities of weak superstructure reflections increase as temperature decreases. A monoclinic twinned superstructure was derived at 100 K [A2/n, V = 7251.0 (17) Å(3), a' = 23.7054 (2), b' = 13.6861 (11), c' = 23.7051 (2) Å, β' = 109.47°]. The transformation matrix from the cubic to the monoclinic system is a(i) ' = (½ 1 ½ / ½ 0 -½ / ½ -1 ½). The A2/n host framework has Si-O bond lengths and Si-O-Si angles that are much closer to known values for stable silicate-framework structures compared with the averaged model. As suggested from band splitting observed in the Raman spectra, the [5(12)]-type cages (one crystallographically unique in , four different in A2/n) entrap the hydro-carbon species (CH(4), C(2)H(6), C(3)H(8), i-C(4)H(10)). The [5(12)6(4)]-type cage was found to be unique in both structure types. It contains the larger hydro-carbon mol-ecules C(2)H(6), C(3)H(8) and i-C(4)H(10).