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sodium iodate monohydrate | 22451-04-3

中文名称
——
中文别名
——
英文名称
sodium iodate monohydrate
英文别名
sodium iodate * H2O;sodium;iodate;hydrate
sodium iodate monohydrate化学式
CAS
22451-04-3
化学式
H2O*IO3*Na
mdl
——
分子量
215.908
InChiKey
GJPIEQXZYPOTHU-UHFFFAOYSA-M
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):
    -10.38
  • 重原子数:
    6
  • 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:
    58.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    sodium iodate monohydrate 以 neat (no solvent) 为溶剂, 生成 sodium iodate
    参考文献:
    名称:
    Rammelsberg, Annalen der Physik, 1838, vol. 44, p. 548 - 548
    摘要:
    DOI:
  • 作为产物:
    描述:
    sodium iodate 为溶剂, 生成 sodium iodate monohydrate
    参考文献:
    名称:
    Herlach, F., Helvetica Physica Acta, 1961, vol. 34, p. 305 - 330
    摘要:
    DOI:
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文献信息

  • Binding of inorganic oxo-anions to cationic cobaltammine: Synthesis, characterization, X-ray structures determination and DFT calculations of [Co(NH3)6]Cl2(ClO3), [Co(NH3)6]Br2(ClO3) and [Co(NH3)6]Cl2(IO3)·H2O
    作者:Raj Pal Sharma、Ritu Bala、Rajni Sharma、Valeria Ferretti
    DOI:10.1016/j.ica.2005.05.022
    日期:2005.8
    Single crystals of [Co(NH 3 ) 6 ]Cl 2 (ClO 3 ) ( 1 ), [Co(NH 3 ) 6 ]Br 2 (ClO 3 ) ( 2 ) and [Co(NH 3 ) 6 ]Cl 2 (IO 3 ) · H 2 O ( 3 ) suitable for X-ray structure determinations were obtained directly by reacting hexaamminecobalt(III) halide with appropriate metal halates in 1:1 molar ratio in hot aqueous medium. These hexaamminecobalt(III) complexes have been characterized by spectroscopic studies (e.g.
    摘要[Co(NH 3)6] Cl 2(ClO 3)(1),[Co(NH 3)6] Br 2(ClO 3)(2)和[Co(NH 3)6] Cl 2的单晶通过使六氨合钴(III)卤化物与适当的金属卤化物在热的水性介质中以1:1的摩尔比直接反应,可直接获得适用于X射线结构测定的(IO 3)·H 2 O(3)。这些六氨合钴(III)配合物已通过光谱研究(例如UV / Visible和IR)进行了表征。标题络合物盐的单晶X射线结构测定表明存在离散离子,即阳离子[Co(NH 3)6] 3+和混合的阴离子Cl-和ClO 3-或Br-和ClO 3-或Cl-和IO 3-处于固态。晶格通过静电吸引力和氢键相互作用(N–H⋯O-,N–H⋯Cl-或N–H⋯Br-)稳定。与卤化物离子组成的确定的盐的形成表明,[Co(NH 3)6] 3+可用作这些弱配位氧代阴离子的纯无机阴离子结合剂。已经进行了DFT计算以计算含氧阴
  • Solvolyses of thiocyanates by trifluoroethanoic acid
    作者:R.D. Gillard、Nordin Garif、Julio Pedrosa de Jesus
    DOI:10.1016/s0277-5387(00)83847-4
    日期:1989.1
    trifluoroethanoic (“trifluoroacetic” TFA) acid of several known and new thiocyanates have been studied using proton magnetic resonance. For the organic linkage isomers of RNCS (R = alkyl groups) isothiocyanates react (via N-alkyl monothiocarbamato trifluoroethanoates) to form alkylamines RNH 2 , whereas the thiocyanates RSCN yield thiols, RSH and ammonia. The coordinated thiocyanates include isomers (some new) of
    摘要利用质子磁共振研究了三氟乙酸(“三氟乙酸” TFA)对几种已知的和新型的硫氰酸盐的溶剂分解作用。对于RNCS的有机键合异构体(R =烷基),异硫氰酸酯反应(通过N-烷基单硫代氨基甲酸酯三氟乙酸酯)形成烷基胺RNH 2,而硫氰酸酯RSCN则生成硫醇,RSH和氨。配位的硫氰酸盐包括二硫氰酸根合双二氨基乙烷铑(III)盐的异构体(一些新的),通过光谱和通过它们的反应(添加的汞(II)离子,碘酸盐(V)的还原,异构化)进行表征。配位硫氰酸酯与TFA的两种键合异构形式均形成氨(在δ= 6.6 ppm时显示出尖锐的三重态)。
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Na: SVol.5, 9.1, page 1820 - 1829
    作者:
    DOI:——
    日期:——
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Na: MVol., 142, page 460 - 461
    作者:
    DOI:——
    日期:——
  • Hydrothermal synthesis and crystal structures of two NLO compounds, NaIO3·H2O and In(IO3)3
    作者:Xuean Chen、Haiping Xue、Xinan Chang、Li Zhang、Hegui Zang、Weiqiang Xiao
    DOI:10.1016/j.jallcom.2005.07.061
    日期:2006.5
    Two metal iodates. (NaIO3H2O)-H-. and In(IO3)(3), have been prepared by hydrothermal reactions at 170 degrees C. The X-ray structural analysis showed that (NaIO3H2O)-H-. crystallizes in a inonoclinic space group C2 with a = 14.175(3) angstrom, b = 3.6688(3) angstrom, c = 9.666(1) angstrom, beta = 124.41 (1)degrees, Z = 4 and In(IO3)(3) in a hexagonal group P6(3) with a = 9.5463(8) angstrom, c= 5.2745(8) angstrom, Z = 2. (NaIO3H2O)-H-. represents anew structure type and it can be viewed as a layered compound consisting of two-dimensional layers of edge-sharing NaO7 monocapped octahedra that are capped by IO3- groups, while In(IO3)(3) S a new compound containing slightly distorted InO6 octahedra that are bridged by IO3- groups giving rise to a three-dimensional polar network. Both compounds crystallize in non-centrosymmetric, chiral space groups. (c) 2005 Elsevier B.V. All rights reserved.
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