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[(CH3CO2)Pt(μ-SO4)4Pt(H2O)](3-) | 170891-82-4

中文名称
——
中文别名
——
英文名称
[(CH3CO2)Pt(μ-SO4)4Pt(H2O)](3-)
英文别名
——
[(CH3CO2)Pt(μ-SO4)4Pt(H2O)](3-)化学式
CAS
170891-82-4
化学式
C2H5O19Pt2S4
mdl
——
分子量
851.474
InChiKey
YOWMVALQEHTPNM-UHFFFAOYSA-E
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:
    参考文献:
    名称:
    Reactions of Nitroplatinum Complexes. 2. Reactions of K2[Pt(NO2)4] and Related Complexes with Aqueous Acids (CH3CO2H, HClO4, CF3SO3H, HNO3, and H2SO4): Pathways to Platinum(III) Complexes with Acetate Bridges. Crystal Structure of K2[{Pt(NO2)2(.mu.-CH3CO2)}2].cntdot.H2O
    摘要:
    Reaction of K-2[Pt((NO2)-N-15)(4)] under argon with 1 M HClO4 or CF3SO3H gave an initial blue solution (lambda(max) = 627 nm), due to nitrosyl complexes of platinum(IV), With heating, the color faded, and Pt-195 and N-15 NMR peaks were observed from cis-[Pt((NO2)-N-15)(2)(H2O)(2)], [Pt((NO2)-N-15)(H2O)(3)](+), and fac-[Pt((NO2)-N-15)(3)(H2O)(3)](+). In air of oxygen, reaction was faster, giving [Pt(H2O)(4)](2+) as well as mixed nitrito-N/aqua platinum(II) complexes, and larger proportions of platinum(IV) complexes, including [Pt(OH)(6)](2-) in solution, and solid H-2[Pt(OH)(6)]. With 0.5 M H2SO4. reactions were similar, but a greater variety of platinum(IV) complexes were formed, some probably containing coordinated sulfate. With 1 M HNO3, K-2[Pt(NO2)(6)] formed. Reactions of K-2[Pt(NO2)(4)] with aqueous acetic acid gave mixtures of Pt(II) and PI(IV) mononuclear complexes and dinuclear Pt(III) complexes containing acetate bridges. The composition of the solution depended on the reaction conditions (heated for various times with argon, air, or oxygen above the solution or bubbled through). Crystals of K-2[{Pt-II(NO2)(2)(mu-CH3CO2)}(2)]. H2O were obtained from a reaction under argon, and the crystal structure was determined by X-ray diffraction: space group P $(1) over bar$$ (no. 2); a = 7.202(2) Angstrom; b = 8.987(2) Angstrom; c = 13.592(2) Angstrom; alpha = 94.01(2)degrees; beta = 90.68(2)degrees; gamma = 111.04(2)degrees; Z = 2; R = 0.0371, for 2875 reflections. The structure showed two acetate ligands bridging between cis-Pt(NO2)(2) units, with the Pt-Pt distance 2.986(1) Angstrom. Reactions of cis-[Pt(NO2)(2)(H2O)(2)] with various oxidants in the presence of acetic acid were studied. [{(CH3CO2)Pt-III(NO2)(2)(mu-CH3CO2)}(2)](2-) is formed by the oxidation of preformed [{Pt-II(NO2)(2)(mu-CH3CO2)}(2)](2-). Under anaerobic conditions, the major oxidant is HNO3 formed in the reaction mixture. Oxidation of [{Pt-II(NO2)(2)(mu-CH3CO2)}(2)](2-) with NO2 formed in the reaction mixture in the presence of oxygen provides one route to [(O2N)Pt-III(NO2)(2)(mu-CH3CO2)(2)Pt-III(NO2)(2)(O2CCH3)](2-). Continued heating of solutions containing these Pt(III) complexes eventually gave solutions containing [{(CH3CO2)Pt-III(NO2)}(2)(mu CH3CO2)(3)](-).
    DOI:
    10.1021/ic00128a015
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