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chlorochromium(III) meso-tetrakis(4-methoxyphenyl)porphyrinate | 84151-94-0

中文名称
——
中文别名
——
英文名称
chlorochromium(III) meso-tetrakis(4-methoxyphenyl)porphyrinate
英文别名
——
chlorochromium(III) meso-tetrakis(4-methoxyphenyl)porphyrinate化学式
CAS
84151-94-0
化学式
C48H36ClCrN4O4
mdl
——
分子量
820.287
InChiKey
OQEXWGIPVMYVEB-HTMHXADGSA-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):
    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

  • 作为反应物:
    描述:
    chlorochromium(III) meso-tetrakis(4-methoxyphenyl)porphyrinate 在 zinc amalgam 、 O2 作用下, 以 四氢呋喃 为溶剂, 以30%的产率得到(5,10,15,20-tetrakis(p-methoxyphenyl)porphyrinato)oxo-chromium(IV)
    参考文献:
    名称:
    Liston, David J.; West, Bruce O., Inorganic Chemistry, 1985, vol. 24, # 10, p. 1568 - 1576
    摘要:
    DOI:
  • 作为产物:
    描述:
    六羰基铬 、 5,10,15,20-meso-tetra(p-methoxyphenyl) porphyrin 以 N,N-二甲基甲酰胺 为溶剂, 以81%的产率得到chlorochromium(III) meso-tetrakis(4-methoxyphenyl)porphyrinate
    参考文献:
    名称:
    Liston, David J.; West, Bruce O., Inorganic Chemistry, 1985, vol. 24, # 10, p. 1568 - 1576
    摘要:
    DOI:
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文献信息

  • Neely, Frank L.; Bottomley, Lawrence A., Inorganic Chemistry, 1997, vol. 36, # 24, p. 5432 - 5434
    作者:Neely, Frank L.、Bottomley, Lawrence A.
    DOI:——
    日期:——
  • Stereoelectronic Aspects of Inter-Metal Nitrogen Atom Transfer Reactions between Nitridomanganese(V) and Chromium(III) Porphyrins
    作者:Lawrence A. Bottomley、Frank L. Neely
    DOI:10.1021/ic960919c
    日期:1997.11.1
    Reactions of nitridomanganese(V) porphyrins with chromium(III) porphyrins resulted in the irreversible formation of nitridochromium(V) porphyrins and manganese(III) porphyrins. The progress of these reactions has been followed spectrophotometrically, electrochemically, and spectroscopically by EPR. Kinetic analysis of the spectrophotometric data obtained during these reactions for a variety of substituted porphyrins showed the reactions to be first order in each of the reactants. Rate constants were dependent upon the electronic and steric effects of the porphyrin substituent, upon the identity of the anion bound to the chromium(III) reactant, and upon the solvent dielectric constant. We propose that the mechanism of these nitrogen atom transfer reactions involves the nucleophilic attack of the nitridomanganese porphyrin donor on the cationic chromium(III) porphyrin acceptor facilitating a net, two-electron redox process mediated by a heterobimetallic mu-nitrido intermediate. This report represents the first systematic study of the stereoelectronic effects involved in the complete, inter-metal nitrogen atom transfer between two metalloporphyrins.
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