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[PtCl2(η(2)-ethylene)(2,9-dimethyl-1,10-phenanthroline-5,6-dione)] | 671185-12-9

中文名称
——
中文别名
——
英文名称
[PtCl2(η(2)-ethylene)(2,9-dimethyl-1,10-phenanthroline-5,6-dione)]
英文别名
[PtCl2(η(2)-C2H4)(Me2phedon)]
[PtCl2(η(2)-ethylene)(2,9-dimethyl-1,10-phenanthroline-5,6-dione)]化学式
CAS
671185-12-9
化学式
C16H14Cl2N2O2Pt
mdl
——
分子量
532.285
InChiKey
HHFQHGWVEBDMBC-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):
    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:
    描述:
    参考文献:
    名称:
    Influence of steric and electronic factors in the stabilization of five-coordinate ethylene complexes of platinum(II): X-ray crystal structure of [PtCl2(2,9-dimethyl-1,10-phenanthroline-5,6-dione)]
    摘要:
    Reactions of Zeise's salt (K[Pt(eta(2)-C2H4)Cl-3]) with oxidized phenanthroline ligands (1, 10-phenanthroline-5,6-dione, phedon, and 2,9-dimethyl-1,10-phenanthroline-5,6-dione, Me(2)phedon) are reported. Comparison with analogous reactions involving unoxidized phen (1,10-phenanthroline) and Me phen (2,9-dimethyl-1,10-phenanthroline) ligands indicates that these latter ligands are less capable to stabilize the five-coordinate species [PtCl2 (eta(2)-C2H4)(phenanthroline)] in which the phenanthroline and the olefin share the trigonal plane and two chlorines are in the axial positions. The X-ray structure of the four-coordinate species [PtCl)(Me(2)phedon)] indicates that the major difference between oxidized and unoxidized phenanthrolines is the loss of aromaticity of the central ring of phenanthroline. As a consequence, the oxidized phenanthroline becomes more flexible and can undergo a bowlike distortion so to reduce steric interaction between ortho substituents of phenanthroline and cis chlorine ligands. The increase in stability of the four-coordinate species with Me(2)phedon is concomitant with an increase in stability of the five-coordinate precursor complex with ethylene. In the latter case the stabilization is not of sterical origin but stems from reduced electron-donor properties of oxidized phenanthrolines. The balance of the two effects is such that the equilibrium between five- and four-coordinate species is more shifted in favour of the former species in the case of Me2phedon than in the case of Me(2)phen. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(03)00382-7
  • 作为产物:
    描述:
    2,9-二甲基-1,10-菲��啉-5,6-二酮 、 potassium trichloro(ethylene)platinate(II) 以 甲醇 为溶剂, 以66%的产率得到[PtCl2(η(2)-ethylene)(2,9-dimethyl-1,10-phenanthroline-5,6-dione)]
    参考文献:
    名称:
    Influence of steric and electronic factors in the stabilization of five-coordinate ethylene complexes of platinum(II): X-ray crystal structure of [PtCl2(2,9-dimethyl-1,10-phenanthroline-5,6-dione)]
    摘要:
    Reactions of Zeise's salt (K[Pt(eta(2)-C2H4)Cl-3]) with oxidized phenanthroline ligands (1, 10-phenanthroline-5,6-dione, phedon, and 2,9-dimethyl-1,10-phenanthroline-5,6-dione, Me(2)phedon) are reported. Comparison with analogous reactions involving unoxidized phen (1,10-phenanthroline) and Me phen (2,9-dimethyl-1,10-phenanthroline) ligands indicates that these latter ligands are less capable to stabilize the five-coordinate species [PtCl2 (eta(2)-C2H4)(phenanthroline)] in which the phenanthroline and the olefin share the trigonal plane and two chlorines are in the axial positions. The X-ray structure of the four-coordinate species [PtCl)(Me(2)phedon)] indicates that the major difference between oxidized and unoxidized phenanthrolines is the loss of aromaticity of the central ring of phenanthroline. As a consequence, the oxidized phenanthroline becomes more flexible and can undergo a bowlike distortion so to reduce steric interaction between ortho substituents of phenanthroline and cis chlorine ligands. The increase in stability of the four-coordinate species with Me(2)phedon is concomitant with an increase in stability of the five-coordinate precursor complex with ethylene. In the latter case the stabilization is not of sterical origin but stems from reduced electron-donor properties of oxidized phenanthrolines. The balance of the two effects is such that the equilibrium between five- and four-coordinate species is more shifted in favour of the former species in the case of Me2phedon than in the case of Me(2)phen. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(03)00382-7
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