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二氢铀酰 | 211573-15-8

中文名称
二氢铀酰
中文别名
——
英文名称
uranyl hydroxide
英文别名
Uranylhydroxyd;dioxouranium(2+);dihydroxide
二氢铀酰化学式
CAS
211573-15-8
化学式
H2O4U
mdl
——
分子量
304.042
InChiKey
VWIQIIGYDAPONF-UHFFFAOYSA-L
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):
    -1.35
  • 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:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    哌啶二氢铀酰二硫化碳 作用下, 以 further solvent(s) 为溶剂, 以88%的产率得到
    参考文献:
    名称:
    Shukla, P. R.; Srivastava, Sanjay Kumar, Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical, 1987, vol. 26, # 10, p. 891 - 893
    摘要:
    DOI:
  • 作为产物:
    描述:
    uranium(IV) hydroxideair 作用下, 以 为溶剂, 生成 二氢铀酰
    参考文献:
    名称:
    Solubility of mixed-valence U(IV–VI) and Np(IV–V) hydroxides in simulated groundwater and 0.1 M NaClO4 solutions
    摘要:
    The kinetics of U(VI) accumulation in the phase of U(IV) hydroxide and of Np(V) in the phase of neptunium(IV) hydroxide, and also the solubility of the formed mixed-valence U(IV)-U(IV) and Np(IV)-Np(V) hydroxides in simulated groundwater (SGW, pH 8.5) and 0.1 M NaClO4 (pH 6.9) solutions was studied. It was found that the structure of the mixed U(IV-VI) hydroxide obtained by both oxidation of U(IV) hydroxide with atmospheric oxygen and alkaline precipitation from aqueous solution containing simultaneously U(IV) and U(VI) did not affect its solubility at the U(VI) content in the system exceeding 16%. The solubility of mixed-valence U(IV-VI) hydroxides in SGW and 0.1 M NaClO4 is (3.6 +/- 1.9) x 10(-4) and (4.3 +/- 1.7) x 10(-4) M, respectively. The mixed Np(IV-V) hydroxide containing from 8 to 90% Np(V) has a peculiar structure controlling its properties. The solubility of the mixed-valence Np(IV-V) hydroxide in SGW [(6.5 +/- 1.5) x 10(-6) M] and 0.1 M NaClO4 [(6.1 +/- 2.4) x 10(-6) M] is virtually equal. Its solubility is about three orders of magnitude as high as that of pure Np(OH)(4) (10(-9)-10(-8) M), but considerably smaller than that of NpO2(OH) (similar to 7 x 10(-4) M). The solubility is independent of the preparation procedure [oxidation of Np(OH)(4) with atmospheric oxygen or precipitation from Np(IV) + Np(V) solutions]. The solubility of the mixed-valence Np hydroxide does not increase and even somewhat decreases [to (1.4 +/- 0.7) x 10(-6) M] in the course of prolonged storage (for more than a year).
    DOI:
    10.1134/s1066362206050122
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文献信息

  • Synthesis and characterization of mono- and bis-(tetraalkylmalonamide)uranium(VI) complexes
    作者:Gregg J Lumetta、Bruce K McNamara、Brian M Rapko、Richard L Sell、Robin D Rogers、Grant Broker、James E Hutchison
    DOI:10.1016/s0020-1693(00)00253-x
    日期:2000.11
    The complex [UO 2 (NO 3 ) 2 (TMMA)] (TMMA= N , N , N ′, N-tetramethylmalonamide) was structurally characterized by single-crystal X-ray diffraction. The complex consists of two bidentate nitrate ions and one bidentate TMMA ligand coordinated to the UO 2 2+ ion. The complex [UO 2 (THMA) 2 ] 2+ (THMA= N , N , N ′, N ′-tetrahexylmalonamide) was prepared as the BF 4 − salt; this material tended to form
    通过单晶X射线衍射对复合物[UO 2(NO 3)2(TMMA)](TMMA = N,N,N',N'-四甲基丙二酰胺)进行结构表征。该络合物由两个二齿硝酸根离子和一个与UO 2 2+离子配位的二齿TMMA配体组成。制备复合物[UO 2(THMA)2] 2+(THMA = N,N,N',N'-四己基丙二酰胺)作为BF 4-盐;这种材料倾向于形成油。但是,分离出[UO 2(TMMA)2](OTf)2(OTf =三氟甲磺酸盐),为结晶固体。将这些配合物的傅立叶变换红外光谱与液-液萃取系统中形成的配合物光谱进行比较,支持以下假设:[UO 2(NO 3)2 L]和[UO 2 L 2](NO 3 )在萃取系统中以2(L =二酰胺萃取剂)形式存在。
  • Preparation and properties of Cr2UO6
    作者:Henry R. Hoekstra、Stanley Siegel
    DOI:10.1016/0022-1902(71)80048-9
    日期:1971.9
    Cr2UO6 has been prepared hydrothermally by the reaction of uranium trioxide with a chromium(III) nitrate solution at 325–425°C. The crystal symmetry is hexagonal, space group D3d1-P31m, with a = 4·988[1] and c = 4·620[1]Å. The i.r. spectrum is shown to be in accord with predictions of factor group analysis. Thermal analysis indicates that Cr2UO6 is stable in air to 950°C.
    Cr 2 UO 6是通过三氧化铀硝酸(III)在325–425°C下的反应热制备的。晶体对称性为六边形,空间群D3d1-P31m,a = 4·988 [1],c = 4·620 [1]Å。红外光谱显示与因子组分析的预测一致。热分析表明,Cr 2 UO 6在空气中至950°C都是稳定的。
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: K: MVol.3, 1.1.2.7, page 536 - 538
    作者:
    DOI:——
    日期:——
  • Schoenbein, C. F., Annalen der Physik, 1849, vol. 78, p. 519
    作者:Schoenbein, C. F.
    DOI:——
    日期:——
  • Chaikhorskii, A. A., Radiokhimiya, 1986, vol. 28, p. 425 - 429
    作者:Chaikhorskii, A. A.
    DOI:——
    日期:——
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