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[3]-ferrocenophane-2-phenylimine | 262300-29-8

中文名称
——
中文别名
——
英文名称
[3]-ferrocenophane-2-phenylimine
英文别名
——
[3]-ferrocenophane-2-phenylimine化学式
CAS
262300-29-8
化学式
C19H17FeN
mdl
——
分子量
315.198
InChiKey
URIBWLLEGJBOOD-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

  • 作为反应物:
    描述:
    [3]-ferrocenophane-2-phenylimine 、 lithium aluminium tetrahydride 以 乙醚 为溶剂, 以95%的产率得到2-(n-phenyl)amino-[3]-ferrocenophane
    参考文献:
    名称:
    Dissociative Intramolecular Charge Transfer after Local Two-Photon Ionization of Ferrocene Derivatives with Aromatic Chromophores
    摘要:
    Experimental evidence for dissociative intramolecular charge transfer processes is found for gas-phase ferrocene-aniline derivatives after local ionization at the aniline chromophore site via intermediate states with predominant aniline character. The direct ionization at the ferrocene site can be excluded since there is a rapid dissociation of ferrocene in the intermediate state prior to ionization so that no ferrocene ions would be produced in this case. Because of the higher local ionization energy of the chromophore, charge transfer takes place after local ionization. The released energy and additional photon absorption leads to breaking of bonds and results in a dissociation into intact ferrocene or ferrocene-containing cations and neutral fragments.
    DOI:
    10.1021/jp992963u
  • 作为产物:
    描述:
    [3]-ferrocenophan-6-one苯胺 在 zinc(II) chloride 作用下, 以 甲苯 为溶剂, 以78%的产率得到[3]-ferrocenophane-2-phenylimine
    参考文献:
    名称:
    Dissociative Intramolecular Charge Transfer after Local Two-Photon Ionization of Ferrocene Derivatives with Aromatic Chromophores
    摘要:
    Experimental evidence for dissociative intramolecular charge transfer processes is found for gas-phase ferrocene-aniline derivatives after local ionization at the aniline chromophore site via intermediate states with predominant aniline character. The direct ionization at the ferrocene site can be excluded since there is a rapid dissociation of ferrocene in the intermediate state prior to ionization so that no ferrocene ions would be produced in this case. Because of the higher local ionization energy of the chromophore, charge transfer takes place after local ionization. The released energy and additional photon absorption leads to breaking of bonds and results in a dissociation into intact ferrocene or ferrocene-containing cations and neutral fragments.
    DOI:
    10.1021/jp992963u
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