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N,N-bis[(E)-2-thienylmethylidene]-1,8-naphthalenediamine | 1325727-45-4

中文名称
——
中文别名
——
英文名称
N,N-bis[(E)-2-thienylmethylidene]-1,8-naphthalenediamine
英文别名
——
N,N-bis[(E)-2-thienylmethylidene]-1,8-naphthalenediamine化学式
CAS
1325727-45-4
化学式
C20H14N2S2
mdl
——
分子量
346.477
InChiKey
RZPFHEIHPNQKPQ-JFMUQQRKSA-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:
    2-噻吩甲醛1,8-二氨基萘甲醇 为溶剂, 反应 5.0h, 以53%的产率得到N,N-bis[(E)-2-thienylmethylidene]-1,8-naphthalenediamine
    参考文献:
    名称:
    Synthesis, spectroscopic and electrochemical studies of N,N-bis[(E)-2-thienylmethylidene]-1,8-naphthalenediamine and its Cu(II) complex: DNA cleavage and generation of superoxide anion
    摘要:
    A novel tetradentate Cu(II) complex of the type, [CuL](NO3)(2) was synthesized by the interaction of Schiff base ligand, N,N-bis[(E)-2-thienylmethylidene]-1,8-naphthalenediamine, L obtained by the condensation of thiophene-2-carboxaldehyde and 1,8-diaminonaphthalene. The formation of Schiff base ligand, L and its Cu(II) complex was confirmed on the basis of results of elemental analyses, mass, FT-IR, H-1 and C-13(H-1) NMR spectral studies. UV-Vis, EPR and magnetic susceptibility data support a square planar environment around Cu(II) ion. However, molar conductance values confirmed 1:2 electrolytic nature for the Cu(II) complex. The electrochemical studies of Cu(II) complex was carried out by using cyclic voltammetry which revealed the complex to exhibit quasi reversible process. The biological activity of Cu(II) complex such as ability to bind DNA and DNA cleavage were studied where the Cu(II) complex was shown to cause considerable DNA cleavage and also generated reactive oxygen species such as superoxide anion. Since it is known that various anticancer drugs act through induction of oxidative stress that is mediated by reactive oxygen species, our results suggest a putative role of Cu(II) complex similar to various anticancer drugs. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jphotobiol.2011.05.003
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