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| 1589084-53-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1589084-53-6
化学式
C24H36Fe2N10O4
mdl
——
分子量
640.308
InChiKey
MONKZSWXVKWPMM-AFLRZGNESA-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:
    甲醇Iron(III) nitrate nonahydrate(2-[1-(2-dimethylaminoethylimino)methyl]phenol) 、 sodium azide 在 ` 作用下, 以 为溶剂, 以75%的产率得到
    参考文献:
    名称:
    Structural and theoretical investigation on two dinuclear Fe(III) complexes of tridentate NNO-donor Schiff base ligands
    摘要:
    Two new Fe(III) complexes of formulas [FeL1(N-3)(OMe)](2) (1) and [FeL2(N-3)(OH)](2).H2O (2) have been synthesized by using two tridentate NNO-donor Schiff base ligands HL1{(2-[(3-methylaminoethylimino)-methyl]-phenol)} and HL2 {(2-[1-(2-dimethylarninoethylimino)methyl]-phenol)}, respectively. Substitution of the -CH3 group on the secondary amine group of the N,N-dimethyldiarnine fragment of the Schiff base by a H-atom leads to a structural change from a methoxido-bridged dimer (I) to a single hydroxido-bridged dimer (2). Both complexes have been characterized by single-crystal X-ray analyses, IR and UV-Vis spectroscopy and OFT studies. Both dimers are centrosymmetric containing two Fe-lll atoms which are bridged by two methoxido ions in compound 1 and by two hydroxido ions in compound 2. The chelating tridentate Schiff base and a terminal azido group complete the distorted octahedral environment around each iron center in both complexes. To explain the preferential bridging ability of methoxido and hydroxido groups in complexes 1 and 2, we have carried out theoretical calculations based on DFT to compare their formation energies and dimerization energies. In the case of complex 2, it is noticed that the close proximity of the azido group from the iron centers allow the hydroxido bridged complex to gain extra stability through H-bonds, whereas due to the steric crowding of the azido group and the methyl moiety of adjacent molecules, complex 1 disfavors the formation of hydrogen bonds as well as hydroxido bridging. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2014.01.012
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