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{Pt(SC6F5)2(P,P'-dppm)} | 154624-58-5

中文名称
——
中文别名
——
英文名称
{Pt(SC6F5)2(P,P'-dppm)}
英文别名
——
{Pt(SC6F5)2(P,P'-dppm)}化学式
CAS
154624-58-5
化学式
C37H22F10P2PtS2
mdl
——
分子量
977.725
InChiKey
OYZFKBXSLAKJTF-UHFFFAOYSA-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):
    11.08
  • 重原子数:
    52.0
  • 可旋转键数:
    8.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.03
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    cis-[Pd(pentafluorophenyl)2(THF)2] 、 {Pt(SC6F5)2(P,P'-dppm)}二氯甲烷 为溶剂, 以73%的产率得到{dppmPt(μ-SC6F5)2Pd(C6F5)2}
    参考文献:
    名称:
    Stereospecific reactions of the “M(C6F5)2” (M  Pd or Pt synthons towards cis-dithiolato complexes
    摘要:
    Complexes of the general formula cis-[M(SC6F5)2L2] (M = Ni, Pd, or Pt; L2 = dppm [bis(diphenylphosphino)methane], dppe [1,2-bis(diphenylphosphino)ethane], or 2PPh3) were synthesized by the reaction (1: 2) between the corresponding cis-[MCl2L2] and Tl(SC6F5). When treated with cis-[M(C6F5)2(THF)2] (M = Pd or Pt; THF = OC4H8) they yield geminal homo- or hetero-binuclear compounds, which were characterized by IR, NMR and mass spectroscopy.
    DOI:
    10.1016/0022-328x(93)80283-h
  • 作为产物:
    描述:
    dichloro(bis(diphenylphosphino)methane)platinum(II) 在 TlSC6F5 作用下, 以 丙酮 为溶剂, 以94%的产率得到{Pt(SC6F5)2(P,P'-dppm)}
    参考文献:
    名称:
    Stereospecific reactions of the “M(C6F5)2” (M  Pd or Pt synthons towards cis-dithiolato complexes
    摘要:
    Complexes of the general formula cis-[M(SC6F5)2L2] (M = Ni, Pd, or Pt; L2 = dppm [bis(diphenylphosphino)methane], dppe [1,2-bis(diphenylphosphino)ethane], or 2PPh3) were synthesized by the reaction (1: 2) between the corresponding cis-[MCl2L2] and Tl(SC6F5). When treated with cis-[M(C6F5)2(THF)2] (M = Pd or Pt; THF = OC4H8) they yield geminal homo- or hetero-binuclear compounds, which were characterized by IR, NMR and mass spectroscopy.
    DOI:
    10.1016/0022-328x(93)80283-h
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文献信息

  • Synthesis and characterisation of mono- and binuclear palladium and platinum complexes with organochalcogenides
    作者:Anshu Singhal、Vimal K. Jain、Babu Varghese、Edward R.T. Tiekink
    DOI:10.1016/s0020-1693(98)00335-1
    日期:1999.2
    Mononuclear palladium and platinum complexes of the type M(ER)(2)((PP)-P-boolean AND) [M = Pd or Pt; ER = SPh, SC6H4Cl-4, SC6H4Me-4, SC6F5, SePh, TeC6H4OEt-4; (PP)-P-boolean AND = dppm or dppe] have been prepared and their ability to form dinuclear metal species has been demonstrated. All complexes have been characterised by multinuclear magnetic resonance (H-1, C-13, Se-77, Pt-195) spectral data. The effects of phosphine ligands and organochalcogenides are reflected in the Se-77 and Pt-195 NMR shifts. The shielding of Pt-195 NMR chemical shifts has been interpreted in terms of their binding ability to platinum. The structures of two derivatives, namely [Pd(SC6F5)(2)(dppe)] and [Pd(SePh)(2)(dppe)], have been established by X-ray crystallography. The palladium atom in each of the monomeric structures exists in a square planar geometry. (C) 1999 Elsevier Science S.A. All rights reserved.
  • Anionic pentafluorothiophenolato complexes of palladium(II) or platinum(II)
    作者:R. Usón、J. Forniés、M.A. Usón、J.A. Apaolaza
    DOI:10.1016/s0020-1693(00)90391-8
    日期:1991.9
    By reacting Tl(SC6F5) with halide containing complexes of palladium(II) or platinum(II), mono- or binuclear compounds with terminal and/or bridging pentafluorothiophenolato groups can be obtained. Treatment of the latter ones with triphenylphosphine causes bridge-cleavage affording cis-mononuclear compounds.
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