Juabite, CaCu10(Te4+O3)4(AsO4)4(OH)2(H2O)4:: Crystal structure and revision of the chemical formula

被引:6
作者
Burns, PC
Clark, CM
Gault, RA
机构
[1] Univ Notre Dame, Dept Civil Engn & Geol Sci, Notre Dame, IN 46556 USA
[2] Univ Manitoba, Dept Geol Sci, Winnipeg, MB R3T 2N2, Canada
[3] Canadian Museum Nat, Div Res, Ottawa, ON K1P 6P4, Canada
关键词
juabite; crystal structure; copper oxysalt; tellurite; arsenate;
D O I
10.2113/gscanmin.38.4.809
中图分类号
P57 [矿物学];
学科分类号
070901 ;
摘要
The crystal structure of juabite, CaCu10(Te4+O3)(4)(AsO4)(4)(OH)(2)(H2O)(4), triclinici, a 8.9903(7), b 10.1197(8), c 8.9959(7) Angstrom, alpha 102.654(1), beta 92.432(1), gamma 70.432(1)degrees, V 752.0(2) Angstrom (3), space group P (1) over bar, Z = 1, has been solved by direct methods and refined by least-squares techniques on the basis of F-2 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 greater than or equal to4 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 similar to1.9 Angstrom 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 (3) square pyramids [phi :O2-, (OH)(-), H2O], both Te(4+)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.
引用
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页码:809 / 816
页数:8
相关论文
共 14 条
  • [1] BOND-VALENCE PARAMETERS FOR SOLIDS
    BRESE, NE
    OKEEFFE, M
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1991, 47 : 192 - 197
  • [2] Burns PC, 1998, CAN MINERAL, V36, P847
  • [3] Burns PC, 1996, CAN MINERAL, V34, P1089
  • [4] ALPHA CUPRIC DIVANADATE
    CALVO, C
    FAGGIANI, R
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1975, 31 (FEB15): : 603 - 605
  • [5] STRUCTURAL RELATIONS IN COPPER OXYSALT MINERALS .1. STRUCTURAL HIERARCHY
    EBY, RK
    HAWTHORNE, FC
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1993, 49 : 28 - 56
  • [6] FISCHER R, 1975, CANADIAN MINERALOGIS, V0013
  • [7] STEREOCHEMISTRY OF ELEMENTS WHICH ARE UNBOUND PAIRS - GE (II), AS (III), SE (IV), BR (V), SN (II), SB (III), TE (IV), I (V), XE (VI), TL (I), PB (II), AND BI (III) (OXIDES, FLUORIDES AND OXYFLUORIDES)
    GALY, J
    MEUNIER, G
    ANDERSSON, S
    ASTROM, A
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 1975, 13 (1-2) : 142 - 159
  • [8] GRICE JD, 1989, CAN MINERAL, V27, P133
  • [9] THE ROLE OF OH AND H2O IN OXIDE AND OXYSALT MINERALS
    HAWTHORNE, FC
    [J]. ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 1992, 201 (3-4): : 183 - 206
  • [10] Ibers J.A., 1974, INT TABLES XRAY CRYS, VIV