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Trigonal rare-earth dioxymonocyanamides Ln2O2CN2 (Ln=Dy,Ho,Er,Tm,Yb) were synthesized by the modified solid-state metathesis (SSM) method, in which Ln2O3 and melamine C3N6H6 were mixed and heated at 8...
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Crystal structure of dehydrated chlorartinite by X-ray powder diffraction

Powder Diffr. Volume 22, Issue 1, pp. 64-67 (March 2007)

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Kunihisa Sugimoto and Robert E. Dinnebier
Max-Planck-Institute for Solid State Research, Heisenbergstraße 1, D-70569 Stuttgart, Germany

Thomas Schlecht
Wilhelm-Röntgen-Straße 25/1, D-73760 Ostfildern, Germany
In the course of an investigation of cracks in certain magnesia floors containing the mineral chlorartinite [Mg2(CO3)(H2O)(OH)]Cl·H2O, the dehydration process of chlorartinite was carried out in high vacuum. The crystal structure of dehydrated chlorartinite [Mg2(CO3)(H2O)(OH)]Cl was refined from laboratory X-ray powder diffraction data using the Rietveld method [R3c, a=22.6791(5)  Å, c=7.22336(14)  Å, V=3217.52(11)  Å3, Z=18, Rp=4.13%, Rwp=5.82%]. Dehydrated chlorartinite exhibits the same type of 3D honeycomb zeolite-like crystal structure with large channels as the hydrated form. Compared to the hydrated form, the channels of dehydrated chlorartinite are empty because of the removal of all non-coordinating water molecules with the cell volume shrinking by 4.0%, leading to a more distorted environment of the magnesium atoms. ©2007 International Centre for Diffraction Data
History: Received 23 October 2006; accepted 4 January 2007
Permalink: http://dx.doi.org/10.1154/1.2436546

KEYWORDS and PACS

Keywords
PACS
  • 61.66.Fn
    Crystal structure of specific inorganic compounds
  • YEAR: 2007

PUBLICATION DATA

ISSN:
0885-7156 (print)  
Publisher:
AIP is a member of CrossRef ICDD

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