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[Me3Sb(1-phenyl-1H-tetrazole-5-thiol(-1H))2] | 894107-49-4

中文名称
——
中文别名
——
英文名称
[Me3Sb(1-phenyl-1H-tetrazole-5-thiol(-1H))2]
英文别名
——
[Me3Sb(1-phenyl-1H-tetrazole-5-thiol(-1H))2]化学式
CAS
894107-49-4
化学式
C17H19N8S2Sb
mdl
——
分子量
521.273
InChiKey
RSLHEFRPYPFKOF-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):
    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

  • 作为产物:
    描述:
    三甲基二氯化锑1-苯基-5-巯基四氮唑 在 NaOC2H5 作用下, 以 为溶剂, 以85%的产率得到[Me3Sb(1-phenyl-1H-tetrazole-5-thiol(-1H))2]
    参考文献:
    名称:
    Syntheses, characterizations and crystal structures of new organoantimony(V) complexes with heterocyclic (S,N) ligand
    摘要:
    Eight new organoantimony(V) complexes with 1-phenyl-H-1-tetrazole-5-thiol [(LH)-H-1] and 2,5-dimercapto-4-phenyl-1,3,4-thiodiazole [(LH)-H-2] of the type RnSbL5-n(L=L-1: n=4, R=n-Bu 1, Ph 2, n=3, R=Me 3, Ph 4; L=L-2: n=4, R=n-Bu 5, Ph 6, n=3, R=Me 7, Ph 8) have been synthesized. All the complexes 1-8 have been characterized by elemental, FT-IR, H-1 and C-13 NMR analyses. Among them complexes 2, 6 and 8 have also been confirmed by X-ray crystallography. The structure analyses show that the antimony atoms in complexes 2 and 6 display a trigonal bipyramid geometry, while it displays a distorted capped trigonal prism in complex 8 with two intramolecular Sb...N weak interactions. Furthermore, the supramolecular structure of 2 has been found to consist of one-dimensional linear molecular chain built up by intermolecular C-H...N weak-hydrogen bonds, while a macrocyclic dimer has been found in complex 6 linked by intermolecular C-H...S weak hydrogen bonds with head-to-tail arrangement. Interestingly, one-dimensional helical chain is recognized in complex 8, which is connected by intermolecular C-H...S weak hydrogen bonds. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2006.01.049
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