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| 395669-58-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
395669-58-6
化学式
C24H29FeNO2S
mdl
——
分子量
451.413
InChiKey
GABDBHAPHAVFGN-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:
    在 tert-butylammonium hexafluorophosphate(V) 作用下, 以 二氯甲烷 为溶剂, 生成
    参考文献:
    名称:
    In situ reversible electrochemical switching of the molecular first hyperpolarizability
    摘要:
    In situ reversible electrochemical switching of the molecular second-order nonlinear optical (NLO) polarizability, or first hyperpolarizability, has been implemented in a specially designed cell. The redox-switchable NLO chromophore is based on the octamethylferrocene/octamethylferrocenium redox system as electron-donor (D) group, in conjunction with nitrothiophene as the electron-acceptor (A) group and ethenyl as the pi-conjugation bridge. This D-pi-A chromophore has been shown to exhibit reversible redox switching of its linear and nonlinear optical properties. The importance and potential of this electrochemical switching of the first hyperpolarizability is discussed in the context of current and future applications of second-order NLO effects. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0009-2614(02)01890-0
  • 作为产物:
    描述:
    在 tert-butylammonium hexafluorophosphate(V) 作用下, 以 二氯甲烷 为溶剂, 生成
    参考文献:
    名称:
    In situ reversible electrochemical switching of the molecular first hyperpolarizability
    摘要:
    In situ reversible electrochemical switching of the molecular second-order nonlinear optical (NLO) polarizability, or first hyperpolarizability, has been implemented in a specially designed cell. The redox-switchable NLO chromophore is based on the octamethylferrocene/octamethylferrocenium redox system as electron-donor (D) group, in conjunction with nitrothiophene as the electron-acceptor (A) group and ethenyl as the pi-conjugation bridge. This D-pi-A chromophore has been shown to exhibit reversible redox switching of its linear and nonlinear optical properties. The importance and potential of this electrochemical switching of the first hyperpolarizability is discussed in the context of current and future applications of second-order NLO effects. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0009-2614(02)01890-0
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