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cesium tetrafluorochlorate(III) | 15321-04-7

中文名称
——
中文别名
——
英文名称
cesium tetrafluorochlorate(III)
英文别名
——
cesium tetrafluorochlorate(III)化学式
CAS
15321-04-7
化学式
ClF4*Cs
mdl
——
分子量
244.352
InChiKey
SUWKJPYPDHZMIV-UHFFFAOYSA-N
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    cesium tetrafluorochlorate(III) 以 neat (no solvent) 为溶剂, 生成 cesium fluoride
    参考文献:
    名称:
    Popov, A. I.; Kiselev, Yu. M.; Sukhoverkhov, V. F., Russian Journal of Inorganic Chemistry, 1988, vol. 33, p. 789 - 791
    摘要:
    DOI:
  • 作为产物:
    描述:
    三氟化氯caesium carbonate 以 neat (no solvent) 为溶剂, 生成 cesium tetrafluorochlorate(III)
    参考文献:
    名称:
    Popov, A. I.; Kiselev, Yu. M.; Sukhoverkhov, V. F., Russian Journal of Inorganic Chemistry, 1988, vol. 33, p. 789 - 791
    摘要:
    DOI:
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文献信息

  • The reaction of fluoroxidizers with rare earth elements, zirconium and hafnium oxides
    作者:M.N. Brechovskich、A.I. Popov、V.A. Fedorov、Yu.M. Kiselev
    DOI:10.1016/0025-5408(88)90266-8
    日期:1988.10
    Reactions between XeF2 or alkali metal tetrafluorohalogenates(III) and Rare Earth elements oxides, ZrO2, and HfO2 have been studied. The formation conditions of the binary and complex fluorides have been investigated. The comparison of the fluorination activity of Xe(II), Cl(III), and Br(III) fluorides has been proposed.
    已经研究了 XeF2 或碱属四卤酸盐 (III) 与稀土元素化物、ZrO2 和 HfO2 之间的反应。研究了二元和复合化物的形成条件。已提议比较 Xe(II)、Cl(III) 和 Br(III) 化物的化活性。
  • Synthesis and Characterization of the Tetrafluoridochlorates(III) <i>A</i> [ClF <sub>4</sub> ] ( <i>A</i> = K, Rb, Cs)
    作者:Benjamin Scheibe、Sergei I. Ivlev、Antti J. Karttunen、Florian Kraus
    DOI:10.1002/ejic.202000106
    日期:2020.4.16
    Single-crystalline tetrafluoridochlorates(III) A[ClF4] (A = K, Rb, Cs) were synthesized from solvolysis reactions of alkali metal fluorides in liquid chlorine trifluoride. The structures were examined by means of single-crystal X-ray diffraction. K[ClF4] crystallizes in the K[BrF4] structure type, whereas the Rb and Cs compounds crystallize in the Li[AuF4] structure type.
    单晶四酸盐 (III) A[ClF4] (A = K, Rb, Cs) 是由碱化物在液态三氟化氯中的溶剂分解反应合成的。通过单晶X射线衍射检查结构。K[ClF4] 以 K[BrF4] 结构类型结晶,而 Rb 和 Cs 化合物以 Li[AuF4] 结构类型结晶。
  • Syntheses and properties of FOIF4O, ClOIF4O, HOIF4O, and tetrafluoroperiodates
    作者:Karl O. Christe、Richard D. Wilson、Carl J. Schack
    DOI:10.1021/ic50221a034
    日期:1981.7
  • Popov, A. I.; Sukhoverkhov, V. F.; Chumaevskii, N. A., Russian Journal of Inorganic Chemistry, 1990, vol. 35, p. 626 - 632
    作者:Popov, A. I.、Sukhoverkhov, V. F.、Chumaevskii, N. A.
    DOI:——
    日期:——
  • Preparation and Structures of Salts with the Anions of IF2?, ClF4? IF4?, TeF7?, and AsF4?
    作者:Xiongzhi Zhang、Konrad Seppelt
    DOI:10.1002/zaac.19976230178
    日期:——
    AbstractSingle crystal structures are presented for the IF2, ClF4, IF4, TeF7, and AsF4 fluoroanions. The 1,1,3,3,5,5 hexamethylpiperidinium (pip+) ion was used as cation in order to obtain good crystallinity and to avoid twinning and disorder which are notorious with the tetramethylammonium ion. Precise structural data are obtained for the first time, and the ions have the expected geometries. The pip+ has the further advantage that cation‐anion interactions are weak, which results in fairly ideal structures of the anions. Pip+BrF2 is too unstable to be obtained in single crystal form, and pip+BrOF4 as well as NO+BrOF4 show disordered anions and cations.
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