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[Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O | 1417424-10-2

中文名称
——
中文别名
——
英文名称
[Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O
英文别名
[Ni(Nap-tsc)(PPh3)]Cl.H2O
[Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O化学式
CAS
1417424-10-2
化学式
C30H25N3NiOPS*Cl*H2O
mdl
——
分子量
618.746
InChiKey
JCEWIAJUKXVYQJ-FCTFBDSLSA-L
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:
    bis(triphenylphosphine)nickel(II) chloride2-hydroxy-1-naphthaldehyde thiosemicarbazone乙醇二氯甲烷 为溶剂, 反应 96.0h, 以86%的产率得到[Ni(2-hydroxy-1-naphthaldehyde thiosemicarbazone)(triphenylphosphine)]Cl*H2O
    参考文献:
    名称:
    DNA binding, antioxidant, cytotoxicity (MTT, lactate dehydrogenase, NO), and cellular uptake studies of structurally different nickel(II) thiosemicarbazone complexes: synthesis, spectroscopy, electrochemistry, and X-ray crystallography
    摘要:
    Three new nickel(II) thiosemicarbazone complexes have been synthesized and characterized by analytical, spectral, and single-crystal X-ray diffraction studies. In complex 1, the ligand 2-hydroxy-1-naphthaldehydethiosemicarbazone coordinated as a monobasic tridentate donor, whereas in complexes 2 and 3, the ligands salicylaldehyde-4(N)-ethylthiosemicarbazone and 2-hydroxy-1-naphthaldehyde-4(N)-ethylthiosemicarbazone coordinated as a dibasic tridentate donor. The DNA binding ability of the complexes in calf thymus DNA was explored by absorption and emission titration experiments. The antioxidant property of the new complexes was evaluated to test their free-radical scavenging ability. In vitro cytotoxicity assays were performed for the new complexes in A549 and HepG2 cell lines. The new compounds overcome cisplatin resistance in the A549 cell line and they were also active in the HepG2 cell line. The cellular uptake study showed the accumulation of the complexes in tumor cells depended on the nature of the ligand attached to the nickel ion.Structurally different nickel(II) thiosemicarbazone complexes for which DNA binding, antioxidant, cytotoxicity, and cellular uptake studies were performed.
    DOI:
    10.1007/s00775-012-0969-x
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