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The Canadian Mineralogist; August 2000; v. 38; no. 4; p. 809-816; DOI: 10.2113/gscanmin.38.4.809
© 2000 Mineralogical Association of Canada
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JUABITE, CaCu10(Te4+O3)4(AsO4)4(OH)2(H2O)4: CRYSTAL STRUCTURE AND REVISION OF THE CHEMICAL FORMULA

Peter C. Burns1,§, Christine M. Clark2 and Robert A. Gault3

1 Department of Civil Engineering and Geological Sciences, University of Notre Dame, 156 Fitzpatrick Hall, Notre Dame, Indiana 46556-0767, U.S.A.
2 Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada
3 Research Division, Canadian Museum of Nature, P.O. Box 3443, Station "D", Ottawa, Ontario K1P 6P4, Canada

§ E-mail address: pburns{at}nd.edu

The crystal structure of juabite, CaCu10(Te4+O3)4(AsO4)4(OH)2(H2O)4, triclinic, a 8.9903(7), b 10.1197(8), c 8.9959(7) Å, {alpha} 102.654(1), ß 92.432(1), {gamma} 70.432(1)°, V 752.0(2) Å3, space group PFormula, Z = 1, has been solved by direct methods and refined by least-squares techniques on the basis of F2 for 3358 unique reflections collected for a microcrystal using graphite-monochromated MoK{alpha} X-radiation and a CCD area detector. The agreement index (R1) was 7.3%, calculated for 2288 unique observed [F ≥ 4{sigma}F] reflections, and the goodness-of-fit (S) was 1.03. The structure determination has shown that the formula originally proposed for juabite is incorrect with regards to the oxidation state of Te, as well as the absence of Ca. The structure contains five unique Cu2+ positions that are each in square pyramidal coordination. The two symmetrically distinct Te4+ cations are in the usual one-sided coordination owing to the presence of a lone pair of electrons on the cation; there are three short Te4+–O bonds with lengths ~1.9 Å in each polyhedron, as well as two or three longer bonds. The structure contains two unique As5+ cations that are tetrahedrally coordinated by O2– anions, and one Ca position that is octahedrally coordinated by O2– anions. Juabite possesses a layered heteropolyhedral framework structure; layers parallel to (010) are weakly bonded in the [010] direction, resulting in a perfect {010} cleavage. Each layer contains all of the cation polyhedra of the structure, and involves two symmetrically identical sheets that contain four of the Cu{phi}5 square pyramids [{phi}: O2–, (OH), H2O], both Te4+{phi}n polyhedra, and both AsO4 tetrahedra. The sheets are parallel to (010), and chains of edge-sharing CaO6 octahedra and Cu{phi}5 square pyramids extending parallel to [001] are sandwiched between adjacent symmetrically identical sheets, such that all anions contained within the chains are also linked to the sheets on either side, resulting in the heteropolyhedral layers.

Keywords: juabite, crystal structure, copper oxysalt, tellurite, arsenate.




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S. V. Krivovichev, L. P. Vergasova, G. L. Starova, S. K. Filatov, S. N. Britvin, A. C. Roberts, and I. M. Steele
BURNSITE, KCdCu7O2(SeO3)2Cl9, A NEW MINERAL SPECIES FROM THE TOLBACHIK VOLCANO, KAMCHATKA PENINSULA, RUSSIA
Can Mineral, August 1, 2002; 40(4): 1171 - 1175.
[Abstract] [Full Text] [PDF]




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