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Zn(II)-3-hydroxyflavone | 916887-15-5

中文名称
——
中文别名
——
英文名称
Zn(II)-3-hydroxyflavone
英文别名
[Zn(3-hydroxyflavone(1-))](1+)
Zn(II)-3-hydroxyflavone化学式
CAS
916887-15-5
化学式
C15H9O3Zn
mdl
——
分子量
302.625
InChiKey
MXPZRSZKFIAEBG-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):
    2.53
  • 重原子数:
    19.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    53.27
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为产物:
    描述:
    3-羟基黄酮 、 zinc(II) chloride 以 甲醇 为溶剂, 生成 Zn(II)-3-hydroxyflavone
    参考文献:
    名称:
    Spectroscopic and Theoretical Studies of the Zn(II) Chelation with Hydroxyflavones
    摘要:
    The Zn(II) complexation of three naturally occurring organic compounds (3-hydroxyflavone, 5-hydroxyflavone, and 3',4'-dihydroxyflavone) has been investigated by electronic spectroscopy combined with quantum chemical calculations. These three ligands, which differ in the nature of their chelating site, lead to the formation of a complex of 1:1 stoichiometry. The experimental results show that it is possible to class the three studied sites, according to their chelating power toward Zn(II), in the following way: alpha-hydroxy-carbonyl > beta-hydroxy-carbonyl > catechol. Time-dependent density functional theory (TD-DFT) calculations were performed to obtain the excitation energies and oscillator strengths of the different complexes. Several effective core potentials (Los Alamos and Stuttgart/Dresden) were used for the description of the Zn ion. Calculations were also performed without any pseudopotential, and they give very satisfying results in the simulation of UV-vis spectra of the three complexes. Only the MWB28 ECP leads globally to a good quality description of the spectral features, roughly comparable to that obtained when the 6-31G(d,p) basis set is used to describe the Zn(II) orbitals. The analysis of the results shows that the nature of electronic transitions involved in the UV-vis spectra greatly differs according to the substitution pattern of the flavonoid.
    DOI:
    10.1021/jp064362q
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文献信息

  • Annan, Theodore A.; Peppe, Clovis; Tuck, Dennis G., Canadian Journal of Chemistry, 1990, vol. 68, # 3, p. 423 - 430
    作者:Annan, Theodore A.、Peppe, Clovis、Tuck, Dennis G.
    DOI:——
    日期:——
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