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carbonyl(ethanol)(2,3,7,8,12,13,17,18-octaethylporphyrinato)osmium | 52629-19-3

中文名称
——
中文别名
——
英文名称
carbonyl(ethanol)(2,3,7,8,12,13,17,18-octaethylporphyrinato)osmium
英文别名
——
carbonyl(ethanol)(2,3,7,8,12,13,17,18-octaethylporphyrinato)osmium化学式
CAS
52629-19-3
化学式
C39H50N4O2Os
mdl
——
分子量
797.052
InChiKey
IJEIBZFILMLNPJ-SBYLDBAISA-N
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:
    参考文献:
    名称:
    Che, Chi-Ming; Chung, Wai-Cheung; Lai, Ting-Fong, Inorganic Chemistry, 1988, vol. 27, # 16, p. 2801 - 2804
    摘要:
    DOI:
  • 作为产物:
    描述:
    乙醇 作用下, 以 乙醇 为溶剂, 以>99的产率得到carbonyl(ethanol)(2,3,7,8,12,13,17,18-octaethylporphyrinato)osmium
    参考文献:
    名称:
    Che, Chi-Ming; Poon, Chung-Kwong; Chung, Wai-Cheung, Inorganic Chemistry, 1985, vol. 24, # 8, p. 1277 - 1278
    摘要:
    DOI:
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文献信息

  • Synthesis, Characterization, and Spectral Properties of New Perpendicularly Linked Osmium(II) Porphyrin Oligomers<sup>1</sup>
    作者:Nobuko Kariya、Taira Imamura、Yoichi Sasaki
    DOI:10.1021/ic960878k
    日期:1997.2.1
    A series of new osmium(II) porphyrin oligomers having tetraarylporphyrins with mixed 4-pyridyl (Py) and phenyl (P) groups, H(2)Py(n)P(4-n)P, as an axial or a bridging ligand, Os(OEP)(CO)(H(2)PyP(3)P), 1, cis-[Os(OEP)(CO)](2)(H(2)Py(2)P(2)P), 2, trans-[Os(OEP)(CO)](2)(H(2)Py(2)P(2)P), 3, [Os(OEP)(CO)](3)(H(2)Py(3)PP), 4, and [Os(OEP)(CO)](4)(H(2)TPyP), 5, were synthesized and characterized by spectroscopic methods. The oligomerizations were confirmed by H-1 NMR. The construction of the oligomers enabled to observe directly the tautomerization of internal N-H protons in the axial porphyrins at low temperatures. The activation energy of the tautomerism: E(a) = 40.5 kJ mol(-1), and the exchanging rate constant, k = 7200 +/- 100 s(-1) at 298 K, were comparable to the values previously reported for various porphyrin monomers. The absorption spectra of these oligomers are essentially superpositions of the spectra of the constituent monomeric porphyrins. The cyclic voltammograms of all the oligomers showed the redox waves of parent porphyrins and the osmium ions, each current reflecting the number of constituents. The peak separations of these Os(II/III) redox waves are nearly the same among the five oligomers. The redox and electronic spectral measurements of the oligomers indicated that there are no distinct interactions between the macrocycles in the ground state electrochemically and visible spectrally.
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