4.7 Article

Dehydration of Octacyanido-Bridged NiII-WIV Framework toward Negative Thermal Expansion and Magneto-Colorimetric Switching

Journal

INORGANIC CHEMISTRY
Volume 56, Issue 1, Pages 179-185

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.6b01883

Keywords

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Funding

  1. Japan Society for the Promotion of Science (JSPS) [15H05697]
  2. Polish National Science Centre [2014/15/B/ST5/04465, 2015/19/B/ST5/00922]
  3. Diamond Grant program of the Polish Ministry of Science and Higher Education [0195/DIA/2013/42]
  4. Krakow Scientific M. Smoluchowski Consortium Matter-Energy-Future within the KNOW framework
  5. Foundation for Polish Science within a START fellowship
  6. Grants-in-Aid for Scientific Research [15H05697] Funding Source: KAKEN

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An inorganic three-dimensional [Ni-II(H2O)(2)](2) [W-IV(CN)8]center dot 4H(2)O (1) framework undergoes a single-crystal-to-single-crystal transformation upon thermal dehydration, producing a fully anhydrous phase Ni-2(II)[W-IV(CN)(8)] (1d). The dehydration process induces changes in optical, magnetic, and thermal expansion properties. While 1 reveals typical positive thermal expansion of the crystal lattice, greenish-yellow color, and paramagnetic behavior, id is the first ever reported octacyanido-based solid revealing negative thermal expansion, also exhibiting a deep red color and diamagnetism. Such drastic shift in the physical properties is explained by the removal of water molecules, leaving the exclusively cyanido-bridged bimetallic network, which is accompanied by the transformation of the octahedral paramagnetic [Ni-II(H2O)(2)(NC)(4)](2-) to the square-planar diamagnetic [NiII(NC)(4)](2-) moieties.

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