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sodium lithium hexafluorotitanate(IV) | 137165-30-1

中文名称
——
中文别名
——
英文名称
sodium lithium hexafluorotitanate(IV)
英文别名
——
sodium lithium hexafluorotitanate(IV)化学式
CAS
137165-30-1
化学式
F6Ti*Li*Na
mdl
——
分子量
191.801
InChiKey
VIIIZSIOKVXMMU-UHFFFAOYSA-H
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为产物:
    描述:
    sodium hexafluorotitanate 、 lithium hexafluorotitanate 为溶剂, 生成 sodium lithium hexafluorotitanate(IV)
    参考文献:
    名称:
    Crystal Structure of Na3Li(TiF6)2
    摘要:
    Single crystals of Na3Li(TiF6)(2) were synthesized and studied by X-ray diffraction analysis (DAR UMBk diffractometer, MoKalpha. radiation, graphite monochromator); space group P (4) over bar2(1)c, a = 5.130(1), c = 18.046(4) Angstrom. The structure was solved by the heavy-atom method and refined by the full-matrix least-squares method in anisotropic approximation to R = 0.053 and wR = 0.048 for 468 independent reflections with1 > 3sigma(1). The Madelung's constant for the lattice energy was calculated and the structure was compared to structures of other hexafluoro complexes of Group IV elements.
    DOI:
    10.1023/b:ruco.0000011638.48963.c9
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文献信息

  • Antokhina, T. F.; Lysun, T. V.; Sergienko, V. I., Russian Journal of Inorganic Chemistry, 1991, vol. 36, p. 1171 - 1173
    作者:Antokhina, T. F.、Lysun, T. V.、Sergienko, V. I.、Kaidalova, T. A.、Kir'yanova, I. V.
    DOI:——
    日期:——
  • Synthesis and physicochemical investigation of LiMTif6
    作者:T. F. Antokhina、T. V. Lysun、L. N. Ignat'eva、V. Ya. Kavun、V. I. Sergienko
    DOI:10.1007/bf00863353
    日期:1992.11
    Mixed alkali hexafluorotitanates of the composition LiMTiF6 are synthesized, which crystallize with the orthorhombic symmetry. The lattice parameters of these materials are determined It is shown that substitution of the Li+ cation in Li2TiF6 by Na+, K+, Rb+, and Cs+ leads to various degrees of distortion of the hexafluoro-ion It is determined (F-19 NMR data) that the change in the dynamic state of the octahedral [TiF6]2- ions is related to their transition from the hindered-rotational to the isotropic state.
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