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(η(6)-p-cymene)Os(NAcC(N=Ac)NAc)(triphenylphosphine) | 210820-27-2

中文名称
——
中文别名
——
英文名称
(η(6)-p-cymene)Os(NAcC(N=Ac)NAc)(triphenylphosphine)
英文别名
——
(η(6)-p-cymene)Os(NAcC(N=Ac)NAc)(triphenylphosphine)化学式
CAS
210820-27-2
化学式
C35H38N3O3OsP
mdl
——
分子量
769.879
InChiKey
DOFWAQNFANLRMG-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

  • 作为产物:
    参考文献:
    名称:
    Organometallic complexes of platinum-group metals incorporating substituted guanidine dianion (triazatrimethylenemethane) ligands
    摘要:
    Reactions of the platinum-group metal halide complexes [PtCl2(COD)] (COD = 1,5-cyclo-octadiene), [Cp*RhCl2(PPh3)] (Cp* = eta(5)-C5Me5), [Cp*IrCl2(PPh3)], [(p-cymene)RuCl2(PPh3)] and [(p-cymene)OsCl2(PPh3)] with symmetrically trisubstituted (acetyl or phenyl) guanidines, mediated by silver(I) oxide, give complexes formally containing the triazatrimethylenemethane ligand. A full X-ray crystal structure determination is reported for the N,N',N "-triphenylguanidine dianion complex [Pt{NPhC(=NPh)NPh}(COD)] 4a which shows the presence of a planar Pt-NR-C(=NR)-NR four-membered platinacycle. At room temperature (r.t.), the H-1- and C-13{H-1}-NMR spectra of 4a yield a single set of COD CH and CH2 resonances. At 240 K however, two sets of resonances are observed, interpreted in terms of fluxionality of the C=N-Ph moiety. Attempted synthesis of the analogous platinum triacetylguanidine complex yields the new ureylene complex [Pt{NAcC(=O)NAc}(COD)], via a hydrolysis reaction. Starting with the osmium compound, both the guanidine complex [(p-cymene)Os{NAcC(=NAc)NAc}(PPh3)] 9 and the ureylene complex [(p-cymene)Os{NAcC(=O)NAc}(PPh3)] 10 were formed; similar results were obtained for the iridium system. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0022-328x(97)00654-2
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