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tetra-para-tolylstibonium iodide | 1298132-11-2

中文名称
——
中文别名
——
英文名称
tetra-para-tolylstibonium iodide
英文别名
tetra-p-tolylantimony iodide;iodo-tetrakis(4-methylphenyl)-λ5-stibane
tetra-para-tolylstibonium iodide化学式
CAS
1298132-11-2
化学式
C28H28Sb*I
mdl
——
分子量
613.185
InChiKey
UMJDXVGITTUWFX-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):
    5.18
  • 重原子数:
    30
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    tetra-para-tolylstibonium iodide碘化锑丙酮 为溶剂, 以89%的产率得到[tetra-p-tolylantimony]3[Sb3I12]
    参考文献:
    名称:
    Synthesis and structure of tetra-p-tolylantimony complexes [(4-MeC6H4)4Sb] 2 + [Hg2I6]2−, [(4-MeC6H4)4Sb] 2 + [HgI4]2−, [(4-MeC6H4)4Sb] 3 + [Sb3I12]2−, and [(4-MeC6H4)4Sb]+[ReO4]−
    摘要:
    Complexes [(4-MeC6H4)(4)Sb] (2) (+) [Hg2I6](2-) (I), [(4-MeC6H4)(4)Sb] (2) (+) [HgI4](2-) (II), [(4-MeC6H4)(4)Sb] (3) (+) [Sb3I12](2-) (III), were synthesized by reactions of tetra-p-tolylantimony iodide with mercury iodide and antimony iodide, respectively. Tetra-p-tolylantimony perrhenate [(4-MeC6H4)(4)Sb](+)[ReO4](-) (IV) was prepared from tetra-p-tolylantimony chloride and sodium perrhenate in acetone. Crystal structures of complexes I, II, and IV were determined by X-ray crystallography. Mercury and rhenium atoms have tetrahedral coordinations in these complexes. The Hg-I and Re-O distances in the structures of I, II, and IV vary within 2.7719(13)-2.7908(12), 2.7028(3)-2.9163(3) , and 1.693(3)-1.744(3) , respectively. Antimony atoms in two crystallographically independent trinuclear centrosymmetric [Sb3I12](2-) anions of complex III have an octahedral environment. Each terminal SbI3 fragment (Sb-I-t, 2.8265(9)-2.8333(10)) is bound to the central atom through tree bridging iodine atoms (Sb(2)-I-br, 3.2275(9)-3.3620(10)). The distances between the central Sb atom and bridging iodine atoms are much shorter (Sb(1)-I-br, 3.0153(6)-3.0316(6) ; Sb(3)-I-br, 2.9926(6)-3.0074(6) ).
    DOI:
    10.1134/s0036023610071010
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文献信息

  • Bismuth complexes [p-Tol4P] 2 + [Bi2I8(THF)2]2–, [p-Tol4Sb] 2 + [Bi2I8(THF)2]2–, [p-Tol4P] 2 + [Bi2I8(DMSO)2]2–, [Bu4P] n + [(Bi2I7) n ] n–, [p-Tol4P] n + [(Bi2I7) n ] n–, and [p-Tol4Sb] n + [(Bi2I7) n ] n–: Synthesis and structure
    作者:V. V. Sharutin、O. K. Sharutina、R. M. Khisamov、V. S. Senchurin
    DOI:10.1134/s0036023617060201
    日期:2017.6
    The complexes [p-Tol(4)P] (2) (+) [Bi2I8(THF)(2)](2-), [p-Tol(4)Sb] (2) (+) [Bi2I8(THF)(2)](2-), [p-Tol(4)P] (2) (+) [Bi2I8(DMSO)(2)](2-), [Bu4P] (n) (+) [(Bi2I7) (n) ] (n-), [p-Tol(4)P] (n) (+)[(Bi2I7) (n) ] (n-), and [p-Tol(4)Sb] (n) (+) [(Bi2I7) (n) ] (n-) were synthesized by the reaction between bismuth iodides and tetrabutyl- and tetraphenylphosphonium, tetra-para-tolylphosphonium and -stibonium iodides in tetrahydrofuran, dimethyl sulfoxide, acetone, and ethyl cellosolve. The crystal structures of the synthesized complexes containing bi- and polynuclear anions with an octahedral coordination of bismuth atoms were characterized by X-ray diffraction.
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