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mono(oxovanadium(IV)) mono(2-methyl-4-oxo-4H-pyran-3-olate) | 307493-34-1

中文名称
——
中文别名
——
英文名称
mono(oxovanadium(IV)) mono(2-methyl-4-oxo-4H-pyran-3-olate)
英文别名
——
mono(oxovanadium(IV)) mono(2-methyl-4-oxo-4H-pyran-3-olate)化学式
CAS
307493-34-1
化学式
C6H5O3*OV
mdl
——
分子量
192.045
InChiKey
YSFZMILJVZIYCH-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):
    -0.1
  • 重原子数:
    11.0
  • 可旋转键数:
    0.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    70.34
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    参考文献:
    名称:
    Kinetics of ligand substitution reactions in the oxovanadium(IV)–maltol system
    摘要:
    The kinetics of the complex formation between oxovanadium(IV) and maltol was studied by the stopped-flow method at 25 degreesC in 0.2 M KCl The formation of the bis-complex is about an order of magnitude faster than that of the mono-complex under the same conditions. The results confirm that parallel paths are operative in these reactions via the acid (HA) and base (A(-)) forms of the ligand. The relevant rate constants were determined and mechanistic implications of the results are also discussed. It is concluded that the oxovanadium(IV) ion can easily form the thermodynamically most favorable complexes in ligand rich environments such as biological liquids. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(02)01094-0
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文献信息

  • Kinetics of ligand substitution reactions in the oxovanadium(IV)–maltol system
    作者:Erzsébet Kiss、István Fábián、Tamás Kiss
    DOI:10.1016/s0020-1693(02)01094-0
    日期:2002.11
    The kinetics of the complex formation between oxovanadium(IV) and maltol was studied by the stopped-flow method at 25 degreesC in 0.2 M KCl The formation of the bis-complex is about an order of magnitude faster than that of the mono-complex under the same conditions. The results confirm that parallel paths are operative in these reactions via the acid (HA) and base (A(-)) forms of the ligand. The relevant rate constants were determined and mechanistic implications of the results are also discussed. It is concluded that the oxovanadium(IV) ion can easily form the thermodynamically most favorable complexes in ligand rich environments such as biological liquids. (C) 2002 Elsevier Science B.V. All rights reserved.
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