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[Fe(N'-phenyl-N'-(pyridin-2-yl)picolinohydrazide)(MeOH)Cl2] | 1569105-56-1

中文名称
——
中文别名
——
英文名称
[Fe(N'-phenyl-N'-(pyridin-2-yl)picolinohydrazide)(MeOH)Cl2]
英文别名
[Fe(Pamp)(MeOH)Cl2]
[Fe(N'-phenyl-N'-(pyridin-2-yl)picolinohydrazide)(MeOH)Cl<sub>2</sub>]化学式
CAS
1569105-56-1
化学式
C18H17Cl2FeN4O2
mdl
——
分子量
448.112
InChiKey
VFMZESGXGGAPOL-UHFFFAOYSA-K
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:
    iron(III) chloride 、 N’-phenyl-N’-(pyridin-2-yl)picolinohydrazide甲醇 为溶剂, 反应 3.0h, 以42%的产率得到[Fe(N'-phenyl-N'-(pyridin-2-yl)picolinohydrazide)(MeOH)Cl2]
    参考文献:
    名称:
    Synthesis, structure, redox properties and DNA interaction studies on mononuclear iron(III) complexes with amidate ligand
    摘要:
    A new family of mononuclear Fe(III) complexes [Fe(Pamp)(MeOH) Cl-2], 1 and [Fe(Pamp)(2)](ClO4), 2 were synthesized using designed tridentate ligand PampH having pyridine and amide nitrogen donors (PampH is NO-phenyl-NO-(pyridin-2-yl) picolinohydrazide) and H stands for dissociable proton). Both the complexes (1 and 2) were characterized by different spectroscopic studies and molecular structure of [Fe(Pamp)(2)](ClO4), 2 was determined by single crystal X-ray diffraction. Geometry around metal centre was described as distorted octahedral with two meridionally oriented Pamp ligands. Electrochemical studies afforded E1/2 values of Fe(III)/Fe(II) couple + 0.065 V (for 1) and 0.077 V (for 2) versus Ag/AgCl electrode. DNA binding properties of these complexes were investigated and complex 1 exhibited nuclease activity. Mechanistic investigation revealed the possible participation of hydroxyl radical in nuclease activity which was supported by rhodamine B assay. (C) 2013 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2013.11.034
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