The crystal structure of the Ba-Al phosphate mineral gorceixite, a 7.0538(3), c 17.2746(6) Å, V 744.4(2) Å 3 , space group R3m, Z = 3, has been refi ned to an R 1 index of 2.3% on the basis of 253 unique refl ections measured using MoK␣ radiation on an automated single-crystal diffractometer. The specimen, from the Rapid Creek area, Yukon Territory, has rhombohedral rather than monoclinic Cm symmetry previously reported for the species. The crystal-structure refi nement shows that the atomic arrangement of gorceixite is similar to that of other members of the alunite supergroup. The Ba-O and Ba-OH distances are 2.825 and 2.859 Å (both ϫ6), respectively, and the volume of the Ba(O,OH) 12 polyhedron is 55.64 Å 3. Energy-dispersion spectra and electronmicroprobe analyses indicate that the site is completely occupied by Ba, but the site occupancy refi nes to 88% occupancy; the reason for this is unclear. The average Al-O,OH and P-O distances are 1.906 and 1.544 Å, respectively, and the OH-H distance is 0.980 Å. Interatomic distances [H...O(2) = 1.904 Å and OH...O(2) = 2.884 Å] and a bond-valence analysis suggest that each O(2) atom is involved in hydrogen bonding (as an acceptor) with three different OH groups. However, the low bond-valence sum for O(2) suggests that it not only acts as an acceptor but functions as a donor as well. No hydrogen-atom sites could be identifi ed from the difference-Fourier map, but the presence of OH groups at the O(2) site would help resolve the problem of charge balance. Assuming equal occupancy of the O(2) site by O and OH, the general formula of gorceixite is BaAl 3 [PO 3 (O,OH)] 2 (OH) 6. Although R3m is the most appropriate space-group for the gorceixite sample studied here, we do not claim that all gorceixite samples crystallize in this space group. Different conditions of formation and compositions might be responsible for the lower symmetry observed previously, but the mechanism to achieve the symmetry lowering remains unclear.
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