NaAgMOF (M = Mo, W): An Ordered Oxyfluoride Derivative of the LiNbO Structure.

NaAgMoOF and NaAgWOF have been synthesized by solid state reactions and structurally characterized using synchrotron X-ray and neutron powder diffraction. Unlike the vast majority of salts containing [MOF] anions (M = Mo, W) the oxyfluoride groups in NaAgMoOF and NaAgWOF are orientationally ordered,...

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Published in:Journal of the American Chemical Society Vol. 134; no. 5; pp. 2621 - 2626
Main Authors: Fry, Allyson M., Seibel, Harry A., Lokuhewa, Indunil N., Woodward, Patrick M.
Format: Article
Published: American Chemical Society 2/8/2012
Subjects:
Online Access:View this record in EBSCOhost
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      dt: 2/8/2012
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        10.1021/ja208587e
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        atl: NaAgMOF (M = Mo, W): An Ordered Oxyfluoride Derivative of the LiNbO Structure.
      aug:
        au:
          Fry, Allyson M.
          Seibel, Harry A.
          Lokuhewa, Indunil N.
          Woodward, Patrick M.
        affil: Department of Chemistry, The Ohio State University, Columbus, Ohio 43210-1185, United States
      su:
        Oxyfluorides
        Lithium niobate
        Solid state chemistry
        Synchrotrons
        Optical diffraction
        Anions
        Salts
        Ions
      sug:
        subj:
          Oxyfluorides
          Lithium niobate
          Solid state chemistry
          Synchrotrons
          Optical diffraction
          Anions
          Salts
          Ions
      ab: NaAgMoOF and NaAgWOF have been synthesized by solid state reactions and structurally characterized using synchrotron X-ray and neutron powder diffraction. Unlike the vast majority of salts containing [MOF] anions (M = Mo, W) the oxyfluoride groups in NaAgMoOF and NaAgWOF are orientationally ordered, so that the Na ions are coordinated by fluorine and the Ag ions by oxygen. The resulting structure type, which has not previously been reported, is related to the LiNbO structure, but the combination of Na/Ag ordering and orientational ordering of the [MOF] anions produces a supercell that doubles the c-axis and changes the space group symmetry from R3 to R3¯. The use of hard (Na) and soft (Ag) cations to direct the orientational ordering of polar oxyfluoride building units provides a new approach to the design of polar materials.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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