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三氟-镍酸钾盐 | 13845-06-2

中文名称
三氟-镍酸钾盐
中文别名
——
英文名称
potassium trifluoronickelate
英文别名
Nickel potassium fluoride;potassium;nickel(2+);trifluoride
三氟-镍酸钾盐化学式
CAS
13845-06-2
化学式
F3Ni*K
mdl
——
分子量
154.784
InChiKey
GFHFDGDZKAYMPS-UHFFFAOYSA-K
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

计算性质

  • 辛醇/水分配系数(LogP):
    -11.99
  • 重原子数:
    5
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    在 KF 作用下, 以 氢氟酸 为溶剂, 以63%的产率得到三氟-镍酸钾盐
    参考文献:
    名称:
    Electrosynthesis of transition metal fluoro complexes by the dissolution of a sacrificial metal anode
    摘要:
    A general method for the electrosynthesis of anionic fluoro complexes of transition metals has been developed by the oxidation of sacrificial metal anodes in 20% HF medium at room temperature and at an applied potential of 2-8 V. Some mixed-valent complexes, e.g. Fe2F5.2H2O and Fe2F5.7H2O, have also been obtained by the same method. K2[MnF5].H2O was obtained by subsequent electrolytic oxidation of the Mn(II) fluoro complex obtained in situ in the first step. The method is rapid and gives a good yield with high purity.
    DOI:
    10.1016/s0277-5387(00)81335-2
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文献信息

  • Hydrothermal crystal growth of perovskite-type fluorides
    作者:Shigeyuki S¯omiya、Shin -Ichi Hirano、Masahiro Yoshimura、Kazumichi Yanagisawa
    DOI:10.1007/bf02402800
    日期:1981.3
  • Chakravorti; Subrahmanyam; Bandyopadhyay, Journal of the Indian Chemical Society, 1990, vol. 67, # 10, p. 835 - 836
    作者:Chakravorti、Subrahmanyam、Bandyopadhyay
    DOI:——
    日期:——
  • Babel, D.; Herdtweck, E., Zeitschrift fur Anorganische und Allgemeine Chemie
    作者:Babel, D.、Herdtweck, E.
    DOI:——
    日期:——
  • Electrosynthesis of transition metal fluoro complexes by the dissolution of a sacrificial metal anode
    作者:M.C. Chakravorti、Gampa.V.B. Subrahmanyam、D. Bandyopadhyay
    DOI:10.1016/s0277-5387(00)81335-2
    日期:1991.1
    A general method for the electrosynthesis of anionic fluoro complexes of transition metals has been developed by the oxidation of sacrificial metal anodes in 20% HF medium at room temperature and at an applied potential of 2-8 V. Some mixed-valent complexes, e.g. Fe2F5.2H2O and Fe2F5.7H2O, have also been obtained by the same method. K2[MnF5].H2O was obtained by subsequent electrolytic oxidation of the Mn(II) fluoro complex obtained in situ in the first step. The method is rapid and gives a good yield with high purity.
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