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[(η5-C5Me5)Fe(μ-S-2-(trimethylsilyl)phenyl)]2 | 1370318-37-8

中文名称
——
中文别名
——
英文名称
[(η5-C5Me5)Fe(μ-S-2-(trimethylsilyl)phenyl)]2
英文别名
——
[(η5-C5Me5)Fe(μ-S-2-(trimethylsilyl)phenyl)]2化学式
CAS
1370318-37-8
化学式
C38H56Fe2S2Si2
mdl
——
分子量
744.86
InChiKey
BXKLOKTXLVRDHJ-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:
    [(η5-C5Me5)Fe(μ-S-2-(trimethylsilyl)phenyl)]2四氢呋喃 为溶剂, 生成 [((η5-C5Me5)Fe)2(μ-S-2-(trimethylsilyl)phenyl)(μ-η2:η2-NHNMe)][OTf]
    参考文献:
    名称:
    Synthesis of Sulfur- and Nitrogen-Bridged Diiron Complexes and Catalytic Behavior toward Hydrazines
    摘要:
    Novel thiolate-bridged diiron complexes bearing diazenido and diazene ligands in a side-on manner have been prepared and characterized by X-ray analysis. These sulfur-bridged diiron complexes work as effective catalysts toward the reduction of hydrazines into amines and ammonia via a sequential process of protonation and reduction on the sulfur-bridged diiron skeleton, as is likely observed at the active site of nitrogenase.
    DOI:
    10.1021/om300134t
  • 作为产物:
    描述:
    [FeClCp*(TMEDA)] 、 K(S-2-(trimethylsilyl)phenyl) 以 四氢呋喃 为溶剂, 以77%的产率得到[(η5-C5Me5)Fe(μ-S-2-(trimethylsilyl)phenyl)]2
    参考文献:
    名称:
    Synthesis of Sulfur- and Nitrogen-Bridged Diiron Complexes and Catalytic Behavior toward Hydrazines
    摘要:
    Novel thiolate-bridged diiron complexes bearing diazenido and diazene ligands in a side-on manner have been prepared and characterized by X-ray analysis. These sulfur-bridged diiron complexes work as effective catalysts toward the reduction of hydrazines into amines and ammonia via a sequential process of protonation and reduction on the sulfur-bridged diiron skeleton, as is likely observed at the active site of nitrogenase.
    DOI:
    10.1021/om300134t
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