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  • [Na4(H2O)14]SnS4  (1)
  • antiferrodistortive  (1)
  • magnetochemistry  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 26 (1996), S. 261-265 
    ISSN: 1572-8854
    Keywords: Bimetallic chain-type compounds ; magnetochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound is a mixed valence compound obtained as one of the products of the reaction of Cu(15-ane N4)Br2 with CoBr2·6H2O in water/acetone solvent (15-ane N4=1,4,8,12-tetraazacyclopentadecane). The compound is tetragonal, space group P42/mbc witha=16.675(2)Å,c=13.185(3)Å,V=3666(1)Å3, withZ=8, for pcalc=2.106 g/cc. Refinement of 674 unique observed reflection yielded final values ofR=0.088 andR w=0.083. The compound contains chains of alternating Cu(15-ane N4)2+ cations and CuBr 3 2− anions. The chains run perpendicular to thec axis, and are arranged in alternate layers running parallel toa andb. The chains lie athwart the mirror planes atz=0 andz=1/2, with disorder observed for both the (15-ane N4) rings and the CuBr 3 2− anions. The Cu(II) ion is coordinated by the tetradentate macrocycle to yield an approximate square planar coordination. The CuBr 3 2− anions are nearly planar with Cu−Br(ave.)=2.37Å. Long semi-coordinate Cu(II)...Br bonds of ∼3.0Å link the cations and anions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 25 (1995), S. 537-542 
    ISSN: 1572-8854
    Keywords: Perovskite ; antiferrodistortive ; EPR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound is a member of the (RNH3)2CuCl4 layer perovskite family, space group C2/c, witha=21.624(5),b=7.511(1),c=7.431(2)Å, β=89.56(2)° andV=1206.9(4)Å3 withZ=4. In the antiferrodistortive structure, the Cu(II) ion assumes an elongated octahedral coordination (unique Cu−Cl distances=2.274(2), 2.288(2), and 3.010(2)Å). The octahedra share corners with four neighbors to form a two-dimensional network. The −NH3 moieties hydrogen bond to the layers, so that the −C2H5OH moieties form sheathes about each metal halide layer. A twofold disorder of the −C2H5OH groups is observed. The EPR spectrum is investigated to help understand the magnetic properties of the systems. Theg-values are consistent with strong intralayer exchange coupling. The EPR linewidths show evidence of spin diffusion effects at liquid nitrogen temperature. However, at room temperature, the spin anisotropies lead to broadening of the EPR lines through a phonon modulation mechanism.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-8854
    Keywords: Hydrated salt ; tin(IV)tetrasulfide ; chain structure ; [Na4(H2O)14]SnS4
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract [Na4(H2O)14]SnS4 is obtained by the reaction of Na2S·9H2O with SnCl4·5H2O in aqueous solution at 21°C. It crystallizes in the space group Cc with a = 8.621(2) Å, b = 23.543(5) Å, c = 11.358(2) Å, β = 110.58(3)° and V = 2158.2 Å3 with Z = 2. Refinement of 3826 unique reflections from a racemically twinned crystal yielded a final value of R1 = 0.0464 (|F| 〉 4σ) and wR2 = 0.104 and a goodness of fit of 1.125. The structure consists of a Na+/H2O network supporting the tetrahedral SnS4 4− anions. Water molecules or sulfide ions octahedrally coordinate each of the four crystallographically independent Na+ ions. The dominant feature of the structure is the existence of zigzag chains of edgeshared Na octahedra. These chains are tied together into a three-dimensional network by bridging Na(H2O)6 octahedra and individual H2O molecules.
    Type of Medium: Electronic Resource
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