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[Pb(η2-o-OOCC6H4Fc)(phen)](NO3) | 1123209-75-5

中文名称
——
中文别名
——
英文名称
[Pb(η2-o-OOCC6H4Fc)(phen)](NO3)
英文别名
[Pb(η2-o-ferrocenylbenzoate)(1,10-phenanthroline)]NO3
[Pb(η2-o-OOCC6H4Fc)(phen)](NO3)化学式
CAS
1123209-75-5
化学式
C29H21FeN2O2Pb*NO3
mdl
——
分子量
754.55
InChiKey
MAQZANUVAISYNG-UHFFFAOYSA-M
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:
    1,10-菲罗啉lead(II) nitrate 、 sodium o-ferrocenylbenzoate 以 甲醇 为溶剂, 以72%的产率得到[Pb(η2-o-OOCC6H4Fc)(phen)](NO3)
    参考文献:
    名称:
    Syntheses and structures’ influence on the nonlinear optical properties of o-ferrocenylbenzoate compounds
    摘要:
    Two complexes containing o-ferrocenylbenzoate [ o- OOCH(4)C(6)Fc, Fc = (eta(5)-C5H5)Fe(eta(5)-C5H4)] components: {[Pb(eta(2)-o-OOCH(4)C(6)Fc)(2)(phen)](NO3)} (phen = phenanthroline) (1) and {[Zn(eta(2)-o-OOCH(4)C(6)Fc)(2)(bpe)](CH3OH)}(n) (bpe = 1,2-bis(4-pyridyl)ethene) (2) have been synthesized and structurally characterized by single crystal X-ray diffraction. 1 gives a discrete mononuclear framework, 2 features an in. finite 1-D chain structure constructed by the bpe linking two adjacent zinc (II) ions. The third-order nonlinear optical (NLO) properties of complexes 1, 2 and the reactant o-NaOOCH(4)C(6)Fc were determined by Z-scan techniques in DMF solution. The results show that the structures of complexes have great impact on NLO properties. Complex 1 and o-NaOOCH(4)C(6)Fc display self-defocusing behaviors, while complex 2 exhibits strong self-focusing effect. The solution-state differential pulse voltammograms of complexes 1, 2 and o-NaOOCH(4)C(6)Fc were investigated as well. The results reveal that the half-wave potential of the ferrocenyl moieties is strongly influenced by the Pb(II) or Zn(II) ions in complexes 1 and 2. (C) 2008 Published by Elsevier B.V.
    DOI:
    10.1016/j.ica.2008.04.010
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