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[(CO)2Rh2(μ-(S(t)Bu)2)(μ-P,P-Fc[P(Fu(Me))2]2)] | 756824-23-4

中文名称
——
中文别名
——
英文名称
[(CO)2Rh2(μ-(S(t)Bu)2)(μ-P,P-Fc[P(Fu(Me))2]2)]
英文别名
——
[(CO)2Rh2(μ-(S(t)Bu)2)(μ-P,P-Fc[P(Fu(Me))2]2)]化学式
CAS
756824-23-4
化学式
C40H46FeO6P2Rh2S2
mdl
——
分子量
1010.54
InChiKey
GDCBYSLSFHKLIO-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:
    Rh2{μ-SC(CH3)3}2(CO)4 、 1,1'-bis[(5-methyl-2-furanyl)phosphino]ferrocene二氯甲烷 为溶剂, 以76%的产率得到[(CO)2Rh2(μ-(S(t)Bu)2)(μ-P,P-Fc[P(Fu(Me))2]2)]
    参考文献:
    名称:
    Enlarging the family of ferrocenylphosphine dinuclear rhodium complexes: synthesis and X-ray structure of a novel “A-frame”-type trimetallic Rh/Fe/Rh complex
    摘要:
    The symmetrically substituted ligand 1,1'-bis[di(5-methyl-2-furyl)phosphino]ferrocene (1) has been obtained from the bromo-phosphine BrP(Fu(Me))(2) and the dilithioferrocene/TMEDA adduct. The quantitative addition of this ferrocene derivative to the tetracarbonyl dimer [(CO)(4)Rh-2{mu-(S'Bu)(2)}] leads, through decarbonylation, to the dinuclear rhodium complex [(CO)(2)Rh-2 {mu-(S'Bu)(2)} {mu-P,P-Fc[P(Fu(Me))(2)](2)}] (2) in high yield. A X-ray structure [orthorhombic, space group P2(1)2(1)2(1); a = 11.2982(2) Angstrom, b = 13.3165(3) Angstrom, c = 27.2687(7) Angstrom] and the solution multinuclear NMR characterization are reported, which show that the rare "quasi-closed bridging" A-frame structure of the complex is rather similar to the one reported for [(CO)(2)Rh-2{mu-(S'Bu)(2)}{mu-P,P-dppf}] in solid state. However, in solution the furyl-containing ferrocenylphosphine complex presents a greater fluxionality, together with an electronic environment at phosphorus very different from the dppf analogue (delta(p) = -10 and 27 ppm, respectively). (C) 2004 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2004.01.012
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