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(η5-C5H4CH2Ph)Fe(CO)2SiPh3 | 1589503-55-8

中文名称
——
中文别名
——
英文名称
(η5-C5H4CH2Ph)Fe(CO)2SiPh3
英文别名
5-C5H4CH2Ph)Fe(CO)2SiPh3
(η5-C5H4CH2Ph)Fe(CO)2SiPh3化学式
CAS
1589503-55-8
化学式
C32H26FeO2Si
mdl
——
分子量
526.49
InChiKey
OARLCPUNQFRCMB-UHFFFAOYSA-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

  • 作为产物:
    描述:
    五羰基铁5-benzylcyclopentadiene三苯基硅烷对二甲苯 为溶剂, 反应 24.0h, 以28%的产率得到(η5-C5H4CH2Ph)Fe(CO)2SiPh3
    参考文献:
    名称:
    A New Approach to Directly Synthesize (η5-C5H4R)Fe(CO)2SiR′3 by Reaction of Cyclopentadienes with Pentacarbonyliron and Hydrosilanes
    摘要:
    A new approach to the direct synthesis of Fe Si-bonded complexes (eta(5)-C5H4R)Fe(CO)(2)SiR'(3) (1) by the reaction of cyclopentadienes C5H5R (2) with pentacarbonyliron in the presence of hydrosilanes R'3SiH (5) has been developed. Thus, when the reaction of 2 and pentacarbonyliron in refluxing p-xylene was performed in the presence of 5, the desired complexes were successfully obtained in good yields, providing a simple one-step synthetic route to obtain 1 from the readily available starting materials, wherein the substituents R and R' could vary over a wide range: C5H5R = C3H5SiMe2SiMe3, R'(3) = Ph-3 (la); C5H5R = C5H5SiMe2SiMe2Ph, R'(3) = Ph-3 (1h); C5H5R = C5H5SiMe2SiMePh2, = Ph-3 (1f); C5H5R = C5H5SiMe2SiPh3, R'(3) = Ph-3 (1d); C5H5R = C(5)H(5)SiPh(2)StPh(3), R'(3) = Ph-3 (1e); C5H5R = C5H5SiMe3, R'(3) = Ph-3 (1o; C5H5R = C5H6, R'(3) = Ph-3 (1g);C5H5R = CsHsMe, R'(3) = Ph3 (1h);C5H5R = C5H5CH2Ph, R'(3) = Ph-3 (1i);C5H5R = MeC5H4SiM03, R'(3) = Ph3 (10; C5H5R=C9H8, R'(3) = Ph3 (1k);C5H5R = C5H5SiMe2SiMe2Ph, R'(3) = Me2Ph (1i); C5H5R = C5H5SiMe2Ph3, R'(3) = Me2Ph (1m); C5H5R = C(5)H(5)SiPh(2)StPh(3), R'(3) = Me2Ph (In);C5H5R = C5H5CH2Ph, R'(3) = MezPh (10). A plausible mechanism involving interception of coordinatively unsaturated iron species (eta(4)-C5H5R)Fe(CO)(2) by oxidative addition of the Si H bond is believed to be responsible for the preferred formation of the desired product.
    DOI:
    10.1021/om500066y
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