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(μ-SCH2)2N(CH2C6H5)[Fe2(CO)4(tris(N-pyrrolyl)phosphine)2] | 1021186-13-9

中文名称
——
中文别名
——
英文名称
(μ-SCH2)2N(CH2C6H5)[Fe2(CO)4(tris(N-pyrrolyl)phosphine)2]
英文别名
——
(μ-SCH2)2N(CH2C6H5)[Fe2(CO)4(tris(N-pyrrolyl)phosphine)2]化学式
CAS
1021186-13-9
化学式
C37H35Fe2N7O4P2S2
mdl
——
分子量
879.503
InChiKey
UCKYTLFHAJVFSS-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:
    (μ-SCH2)2N(CH2C6H5)[Fe2(CO)4(tris(N-pyrrolyl)phosphine)2]三(2,2'-联吡啶)钌II 作用下, 以 乙腈 为溶剂, 生成 (μ-SCH2)2N(CH2C6H5)[Fe2(CO)4(tris(N-pyrrolyl)phosphine)2](1-)
    参考文献:
    名称:
    Visible Light-Driven Electron Transfer and Hydrogen Generation Catalyzed by Bioinspired [2Fe2S] Complexes
    摘要:
    Complexes [{(mu-SCH2)(2)NCH2C6H5){Fe(CO)(2)L-1){Fe(CO)(2)L-2}] (L-1 = CO, L-2 = P(Pyr)(3), 2; L-1 = L-2 = P(Pyr)(3), 3) were prepared, which have the lowest reduction potentials for the mono- and double-CO-displaced diiron complexes reported so far. Hydrogen evolution, driven by visible light, was successfully observed for a three-component system, consisting of a ruthenium polypyridine complex, the biomimetic model complex 2 or 3, and ascorbic acid as both electron and proton donor in CH3CN/H2O. The electron transfer from photogenerated Ru(bPY)(3)(+) to 2 or 3 was detected by laser flash photolysis. Under optimal conditions, the total turnover number for hydrogen evolution was 4.3 based on 2 and 86 based on Ru(bPY)(3)(2+) in a three-hour photolysis.
    DOI:
    10.1021/ic702010w
  • 作为产物:
    描述:
    tri-1-pyrrolylphosphine{(μ-SCH2)2NCH2C6H5}Fe2(CO)5P(Pyr)3甲苯 为溶剂, 以65%的产率得到(μ-SCH2)2N(CH2C6H5)[Fe2(CO)4(tris(N-pyrrolyl)phosphine)2]
    参考文献:
    名称:
    Visible Light-Driven Electron Transfer and Hydrogen Generation Catalyzed by Bioinspired [2Fe2S] Complexes
    摘要:
    Complexes [{(mu-SCH2)(2)NCH2C6H5){Fe(CO)(2)L-1){Fe(CO)(2)L-2}] (L-1 = CO, L-2 = P(Pyr)(3), 2; L-1 = L-2 = P(Pyr)(3), 3) were prepared, which have the lowest reduction potentials for the mono- and double-CO-displaced diiron complexes reported so far. Hydrogen evolution, driven by visible light, was successfully observed for a three-component system, consisting of a ruthenium polypyridine complex, the biomimetic model complex 2 or 3, and ascorbic acid as both electron and proton donor in CH3CN/H2O. The electron transfer from photogenerated Ru(bPY)(3)(+) to 2 or 3 was detected by laser flash photolysis. Under optimal conditions, the total turnover number for hydrogen evolution was 4.3 based on 2 and 86 based on Ru(bPY)(3)(2+) in a three-hour photolysis.
    DOI:
    10.1021/ic702010w
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