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| 1414025-44-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1414025-44-7
化学式
C42H37FeNO3P2S2
mdl
——
分子量
785.687
InChiKey
CGHRLASRQJJKIE-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

  • 作为反应物:
    描述:
    在 sodium hydroxide 作用下, 以 1,4-二氧六环 为溶剂, 反应 5.0h, 以22%的产率得到
    参考文献:
    名称:
    Light-Driven Electron Transfer between a Photosensitizer and a Proton-Reducing Catalyst Co-adsorbed to NiO
    摘要:
    While intermolecular hole-hopping along the surface of semiconductors is known, there are no previous examples of electron-hopping between molecules on a surface. Herein, we present the first evidence of electron transfer from the photoreduced sensitizer, Coumarin-343 (C343) to complex 1, both bound on the surface of NiO. In solution, 1 has been shown to be a mononuclear Fe-based proton-reducing catalyst. The reduction of 1 is reversible and occurs within 50 ns after excitation of C343. Interfacial recombination between the reduced 1((-)) and NiO hole occurs on a 100 mu s time scale by non-exponential kinetics. The observed process is the first essential step in the photosensitized generation of Hz from a molecular catalyst in the absence of a sacrificial donor reagent.
    DOI:
    10.1021/ja3082268
  • 作为产物:
    描述:
    苯甲醇三乙胺 作用下, 以 甲醇 为溶剂, 反应 26.5h, 生成
    参考文献:
    名称:
    Light-Driven Electron Transfer between a Photosensitizer and a Proton-Reducing Catalyst Co-adsorbed to NiO
    摘要:
    While intermolecular hole-hopping along the surface of semiconductors is known, there are no previous examples of electron-hopping between molecules on a surface. Herein, we present the first evidence of electron transfer from the photoreduced sensitizer, Coumarin-343 (C343) to complex 1, both bound on the surface of NiO. In solution, 1 has been shown to be a mononuclear Fe-based proton-reducing catalyst. The reduction of 1 is reversible and occurs within 50 ns after excitation of C343. Interfacial recombination between the reduced 1((-)) and NiO hole occurs on a 100 mu s time scale by non-exponential kinetics. The observed process is the first essential step in the photosensitized generation of Hz from a molecular catalyst in the absence of a sacrificial donor reagent.
    DOI:
    10.1021/ja3082268
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