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dichloro-(2-(p-chlorophenylazo)pyridine)platinum(II) | 341495-09-8

中文名称
——
中文别名
——
英文名称
dichloro-(2-(p-chlorophenylazo)pyridine)platinum(II)
英文别名
——
dichloro-(2-(p-chlorophenylazo)pyridine)platinum(II)化学式
CAS
341495-09-8
化学式
C11H8Cl3N3Pt
mdl
——
分子量
483.644
InChiKey
DYESCRQDXFGIHF-RBIFHYOVSA-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

  • 作为反应物:
    参考文献:
    名称:
    Synthesis, spectral characterization and electrochemical studies of mixed-ligand complexes of platinum(II) with 2-(arylazo)pyridines and catechols. Single-crystal X-ray structure of dichloro{2-(phenylazo) pyridine}platinum(II)
    摘要:
    The reaction of 2-(arylazo)pyridines, RH4C6N=NC5H4N (aap, 1 where R=H (pap), p-Me (p-tap), p-Cl (p-Clpap)) with K2PtCl4 in 1:2 boiling acetonitrile-water affords orange-red complexes of the type Pt(aap)Cl-2 (2). The IR spectrum shows two v(Pt-Cl) stretches suggesting cis-PtCl2 configuration. The structural confirmation was carried out by an X-ray diffraction study of Pt(pap)Cl-2 (2a). The addition of catechols to a chloroform-methanol solution of Pl(aap)Cl-2 in the presence of Et3N yielded green colored mixed-ligand complexes of the formula Pt(aap)(O,O) (O,O = catecholate (cat) (3), 4-tert-butylcatecholate (tbcat), (4), 3,5-di-tert-butylcatecholate (dtbcat) (5) and tetrachlorocatecholate (tccat) (6)). The complexes were characterized by elemental analyses, IR, W-Vis-NIR and H-1 NMR spectral data. Electronic spectra exhibit a ligand-ligand charge transfer (LLCT) transition at NIR region; the position and symmetry of the band depend on the type of substituent on the catechol frame. This is qualitatively assigned as 3b(1)(cat)-->pi*(aap) transition. Cyclic voltammogram of the complexes show four successive redox responses: two couples positive to SCE are referred to as oxidation of catechol to semiquinone and semiquinone to quinone, respectively and two couples negative to SCE correspond to azo reductions. (C) 2001 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0277-5387(00)00530-1
  • 作为产物:
    描述:
    potassium tetrachloroplatinate(II)2-((4-氯苯基)偶氮)吡啶乙腈 为溶剂, 以79%的产率得到dichloro-(2-(p-chlorophenylazo)pyridine)platinum(II)
    参考文献:
    名称:
    Synthesis, spectral characterization and electrochemical studies of mixed-ligand complexes of platinum(II) with 2-(arylazo)pyridines and catechols. Single-crystal X-ray structure of dichloro{2-(phenylazo) pyridine}platinum(II)
    摘要:
    The reaction of 2-(arylazo)pyridines, RH4C6N=NC5H4N (aap, 1 where R=H (pap), p-Me (p-tap), p-Cl (p-Clpap)) with K2PtCl4 in 1:2 boiling acetonitrile-water affords orange-red complexes of the type Pt(aap)Cl-2 (2). The IR spectrum shows two v(Pt-Cl) stretches suggesting cis-PtCl2 configuration. The structural confirmation was carried out by an X-ray diffraction study of Pt(pap)Cl-2 (2a). The addition of catechols to a chloroform-methanol solution of Pl(aap)Cl-2 in the presence of Et3N yielded green colored mixed-ligand complexes of the formula Pt(aap)(O,O) (O,O = catecholate (cat) (3), 4-tert-butylcatecholate (tbcat), (4), 3,5-di-tert-butylcatecholate (dtbcat) (5) and tetrachlorocatecholate (tccat) (6)). The complexes were characterized by elemental analyses, IR, W-Vis-NIR and H-1 NMR spectral data. Electronic spectra exhibit a ligand-ligand charge transfer (LLCT) transition at NIR region; the position and symmetry of the band depend on the type of substituent on the catechol frame. This is qualitatively assigned as 3b(1)(cat)-->pi*(aap) transition. Cyclic voltammogram of the complexes show four successive redox responses: two couples positive to SCE are referred to as oxidation of catechol to semiquinone and semiquinone to quinone, respectively and two couples negative to SCE correspond to azo reductions. (C) 2001 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0277-5387(00)00530-1
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