摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-(ferrocen-1-yl)benzylidene-malononitrile | 1239880-28-4

中文名称
——
中文别名
——
英文名称
4-(ferrocen-1-yl)benzylidene-malononitrile
英文别名
——
CAS
1239880-28-4
化学式
C20H14FeN2
mdl
——
分子量
338.192
InChiKey
OHMZJSMKHJFJON-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

反应信息

  • 作为产物:
    描述:
    4-formylphenylferrocene丙二腈 在 piperidine 作用下, 以 ethanol 为溶剂, 生成 4-(ferrocen-1-yl)benzylidene-malononitrile
    参考文献:
    名称:
    Ultrafast excited-state dynamics of ferrocene-bridge-acceptor system
    摘要:
    We employed both femtosecond fluorescence up-conversion and transient absorption techniques with similar to 150 fs time resolution to study the excited-state deactivation process of an intra-molecular charge transfer model compound, 4-(ferrocen-1-yl)benzylidene-malononitrile (Fc-ph-DCV), which consists of ferrocene (Fc) unit as an electron donor, dicyanovinly (DCV) as an electron acceptor and phenyl (ph) ring as the central bridge. The results showed that after photoexcitation into the higher excited S(2) state, ultrafast internal conversion into S(1) takes place. The rate of S(2) -> S(1) internal conversion is markedly faster (with a typical time of 120 fs +/- 20 fs) than the diffusive solvation process. On the other hand, the lifetime of the relaxed S(1) state was strongly dependent on the solvent polarity, changing from 40 to 50 ps in acetonitrile to similar to 20 ps in cyclohexane. Time-resolved. fluorescence data also showed subpicosecond transient component that is attributable to the spectral relaxation caused by solvation and/or vibrational relaxation in the S(1) state. Published by Elsevier B. V.
    DOI:
    10.1016/j.chemphys.2010.04.014
点击查看最新优质反应信息