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trans-dichloro-bis[tris(2-diethylacetal formyl phenyl)stibine] platinum(II) | 879397-94-1

中文名称
——
中文别名
——
英文名称
trans-dichloro-bis[tris(2-diethylacetal formyl phenyl)stibine] platinum(II)
英文别名
——
trans-dichloro-bis[tris(2-diethylacetal formyl phenyl)stibine] platinum(II)化学式
CAS
879397-94-1
化学式
C66H90Cl2O12PtSb2
mdl
——
分子量
1584.92
InChiKey
VLHXVARQEINXQT-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:
    参考文献:
    名称:
    New stibines containing acetal and formyl group: Platinum complex and unexpected oxastibol derivative
    摘要:
    A new tertiary stibine ligand (1) containing acetal group at the ortho-position has been synthesized. This new stibine was then complexed with PtCl42- to obtain trans-PtCl2L2 (2) where stibine acts as a monodentate ligand. The acetal was hydrolyzed in a slightly acidic 4 medium and forms a very new stibine (3) containing formyl group at the ortho-position. When (3) was reduced with NaBH4 an unusual oxastibol (4) derivative was obtained under the experimental conditions used.All the compounds were characterized by IR, mass, H-1, C-13, COSY and HETCOR NMR spectroscopy. The molecular structures of (2), (3) and (4) were determined. Compound (3) crystallizes in two different polymorphs (3a) and (3b) and both the polymorphs show hypervalent antimony with three Sb(...)0 interactions and the molecule exists in O-cis-exo configuration. Compound (4) shows intramolecular Sb(...)0 interactions. To the best of our knowledge this is the first report on organoantimony compounds containing carbonyl groups though their phosphorus and bismuth analogues are well known. Compound (2) shows helicoidal chirality, which is a very new concept in antimony chemistry. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.09.037
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