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1,3-bis(tribromostannyl)propane | 351388-00-6

中文名称
——
中文别名
——
英文名称
1,3-bis(tribromostannyl)propane
英文别名
tribromo(3-tribromostannylpropyl)stannane
1,3-bis(tribromostannyl)propane化学式
CAS
351388-00-6
化学式
C3H6Br6Sn2
mdl
——
分子量
758.925
InChiKey
DDHDHVKCEZXVHF-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

计算性质

  • 辛醇/水分配系数(LogP):
    5.62
  • 重原子数:
    11.0
  • 可旋转键数:
    4.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为反应物:
    描述:
    1,3-bis(tribromostannyl)propane四乙基溴化铵氯仿 为溶剂, 以73%的产率得到[Et4N]2[1,3-bis(tetrabromostannyl)propane]
    参考文献:
    名称:
    α,ω-Bis(trichlorostannyl)alkanes as Bis(monodentate) Lewis Acids toward Halide Ions
    摘要:
    The reactions between X3Sn(CH2)(n)SnX3 (X = Cl, Br; n = 1, 3, 4, 8) and halide in solution are described. Sn-119 NMR spectroscopy (CD2Cl2) indicates formation of five-coordinate dinuclear 1:2 adducts, [X4Sn(CH2)(n)SnX4](2-), with chloride and bromide. A trigonal-bipyramidal geometry has been confirmed in, the solid state for the compound having X = CI and n = 4. In contrast, fluoride reacts with X3Sn(CH2)(n)SnX3 to give six-coordinate tin species, [F5Sn(CH2)(n)SnF5].(4-) There was no evidence indicating that the tin atoms could act as a bidentate acid.
    DOI:
    10.1021/om010246s
  • 作为产物:
    描述:
    bis(triphenyltin)propane溴化锡 以 neat (no solvent) 为溶剂, 以84%的产率得到1,3-bis(tribromostannyl)propane
    参考文献:
    名称:
    α,ω-Bis(trichlorostannyl)alkanes:  Unravelling the Hydrolysis Pathway to Organotin-oxo Oligomers
    摘要:
    New alpha,omega -bis(trichlorostannyl)alkanes, Cl3Sn(CH2)(n)SnCl3 [n = 3-5, 8], have been synthesized via tin-phenyl bond cleavage reactions on alpha,omega -bis(triphenylstannyl)alkanes, Ph3Sn(CH2)(n)SnPh3 [n = 3-5, 8], using either SnCl4 or concentrated hydrochloric acid. Some key missing links, (H2O)Cl3Sn(CH2)(3)SnCl3(H2O) (1a) and (H2O)(2)Cl3Sn(CH2)(3)SnCl3(H2O)(2) (6), in the hydrolysis pathway of organotin trichlorides were identified. Crystal structures of the nonassociated di-tin compounds (H2O)Cl3Sn(CH2)(3)SnCl3(H2O) (1a) and (H2O)(2)Cl3Sn(CH2)(3)SnCl3(H2O)(2) (6, isolated as the 18-crown-6 cocrystal acetonitrile solvate) as well as the polymeric hydrolysis product [H2O(OH)Cl2Sn(CH2)(3)SnCl2(OH)H2O . 2H(2)O](n) (7 . 2H(2)O) are reported.
    DOI:
    10.1021/om010202j
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