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{Pt(PMe3)}3(μ-Ge-nBu2)3 | 1609208-02-7

中文名称
——
中文别名
——
英文名称
{Pt(PMe3)}3(μ-Ge-nBu2)3
英文别名
——
{Pt(PMe<sub>3</sub>)}<sub>3</sub>(μ-Ge-nBu<sub>2</sub>)<sub>3</sub>化学式
CAS
1609208-02-7
化学式
C33H81Ge3P3Pt3
mdl
——
分子量
1373.94
InChiKey
XEBREISYHWXYNV-UHFFFAOYSA-N
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):
    13.45
  • 重原子数:
    42.0
  • 可旋转键数:
    21.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为反应物:
    描述:
    四氟硼酸-二乙醚络合物{Pt(PMe3)}3(μ-Ge-nBu2)3甲苯 为溶剂, 反应 0.5h, 生成 [{Pt(PMe3)}3(μ-GenBu2)33-H)]*BF4
    参考文献:
    名称:
    Cationic Hydridotriplatinum Complex with Bridging Germylene Ligands
    摘要:
    Triplatinum complexes with bridging secondary germylene ligands, [(Pt(PMe3)}(3)(mu-GeR2)(3)] (R = Ph, Bu-n), were prepared from the reaction of H2GeR2 with [Pt(PMe3)4] in a 1:1 ratio. Protonation of the triplatinum complexes with HBF4 led to formation of the cationic hydride complexes [{Pt(PMe3)}(3)(mu-GeR2)(3)(mu(3)-H)D3F4 (R = Ph, Bu-n). The results of multinuclear NMR spectra and DFT calculations of the cationic complexes revealed that the Pt3H core has a trigonal-pyramidal structure with rapid exchange of the mu(3)-hydride ligand position between the two possible positions on the opposite side of the Pt-3 plane.
    DOI:
    10.1021/om500309k
  • 作为产物:
    描述:
    四(三甲基膦)铂(0)dibutylgermane甲苯 为溶剂, 反应 24.0h, 以47%的产率得到{Pt(PMe3)}3(μ-Ge-nBu2)3
    参考文献:
    名称:
    Cationic Hydridotriplatinum Complex with Bridging Germylene Ligands
    摘要:
    Triplatinum complexes with bridging secondary germylene ligands, [(Pt(PMe3)}(3)(mu-GeR2)(3)] (R = Ph, Bu-n), were prepared from the reaction of H2GeR2 with [Pt(PMe3)4] in a 1:1 ratio. Protonation of the triplatinum complexes with HBF4 led to formation of the cationic hydride complexes [{Pt(PMe3)}(3)(mu-GeR2)(3)(mu(3)-H)D3F4 (R = Ph, Bu-n). The results of multinuclear NMR spectra and DFT calculations of the cationic complexes revealed that the Pt3H core has a trigonal-pyramidal structure with rapid exchange of the mu(3)-hydride ligand position between the two possible positions on the opposite side of the Pt-3 plane.
    DOI:
    10.1021/om500309k
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