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dicarbonyldichlorobis(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)dirhodium(I) | 881735-96-2

中文名称
——
中文别名
——
英文名称
dicarbonyldichlorobis(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)dirhodium(I)
英文别名
——
dicarbonyldichlorobis(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)dirhodium(I)化学式
CAS
881735-96-2
化学式
C92H88Cl2N4O2P4Rh2S4
mdl
——
分子量
1810.61
InChiKey
HDENVTZFBCBVSW-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:
    tetrakis(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)tetrarhodium(I) tetrakis[3,5-bis(trifluoromethyl)phenyl]borate 、 tris(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)trirhodium(I) tetrakis[3,5-bis(trifluoromethyl)phenyl]borate 、 一氧化碳苄基三乙基氯化铵二氯甲烷-D2 为溶剂, 生成 tetracarbonyltetrachlorotetrakis(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)tetrarhodium(I) 、 dicarbonyldichlorobis(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)dirhodium(I) 、 tricarbonyltrichlorotris(2,8-bis[2-(diphenylphosphino)ethylthio]-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]diazocine)trirhodium(I)
    参考文献:
    名称:
    Metallomacrocycles Incorporating a Hemilabile Tröger's Base Derived Ligand
    摘要:
    Troger's base, a chiral molecule with a rigid 900 backbone, has been incorporated into a novel hemilabile phosphinoalkyl thioether ligand. Using the Weak Link Approach, this ligand has been reacted with Cu(CH3CN)(4)PF6 and [Rh(COE)(2)Cl](x) (COE = cyclooctene) to form metallomacrocycles. Upon reaction of the ligand with Cu-I, which prefers a tetrahedral coordination geometry, a bimetallic macrocycle was formed. Alternatively, owing to the steric restrictions imposed by the 900 backbone of the ligand and the square-planar geometry of Rh-I, when the ligand was reacted with [Rh(COE)(2)CI](x), the formation of bimetallic closed macrocycles was not observed, and instead a mixture of tri- and tetrametallic closed macrocycles is formed. Introducing pyridine to the Cu-I complex causes the weak thioether-Cu bonds to break, generating a large bimetallic open macrocycle. Upon reaction of the mixture of Rh-I metallornacrocycles with CO and CI-, the cyclic structure of these complexes becomes flexible enough that the dimeric bimetallic macrocycle forms, along with tri- and tetrameric open complexes. The mixture of differently sized Rh-I macrocyclic complexes has been analyzed using gel permeation chromatography, and the tetramer has been characterized by a single-crystal X-ray diffraction study. These are the first examples of metallomacrocycles containing a Troger's base derivative.
    DOI:
    10.1021/ic052000b
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