摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

AuCl2(2-C6H4Ph2PNC(O)Ph) | 1224428-84-5

中文名称
——
中文别名
——
英文名称
AuCl2(2-C6H4Ph2PNC(O)Ph)
英文别名
——
AuCl2(2-C6H4Ph2PNC(O)Ph)化学式
CAS
1224428-84-5
化学式
C25H19AuCl2NOP
mdl
——
分子量
648.278
InChiKey
HUQDWHWZOVVHEE-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:
    描述:
    Hg(2-C6H4P(NC(O)Ph)Ph2)2 、 tetramethyl-ammonium; tetrachloroaurate (III) 、 四甲基氯化铵乙腈 为溶剂, 以68%的产率得到AuCl2(2-C6H4Ph2PNC(O)Ph)
    参考文献:
    名称:
    Synthesis and characterisation of isomeric cycloaurated complexes derived from the iminophosphorane Ph3PNC(O)Ph
    摘要:
    Using different organomercury substrates, two isomeric cycloaurated complexes derived from the stabilised iminophosphorane Ph3P=NC(O)Ph were prepared. Reaction of Ph3P=NC(O)Ph with PhCH2Mn(CO)(5) gave the manganated precursor (CO)(4)Mn(2-C6H4C(O)N=PPh3), metallated on the C(O)Ph substituent, which yielded the organomercury complex ClHg(2-C6H4C(O)N=PPh3) by reaction with HgCl2 in methanol. Transmetallation of the mercurated derivative with Me4N[AuCl4] gave the cycloaurated iminophosphorane AuCl2(2-C6H4C(O)N=PPh3) with an exo PPh3 substituent. The endo isomer AuCl2(2-C6H4Ph2P=NC(O)Ph) [aurated on a PPh3 ring] was obtained by an independent reaction sequence, involving reaction of the diarylmercury precursor Hg(2-C6H4P(=NC(O)Ph)Ph-2)(2) [prepared from the known compound Hg(2-C6H4PPh2)(2) and PhC(O)N-3] with Me4N[AuCl4]. Both of the isomeric iminophosphorane derivatives were structurally characterised, together with the precursors (2-HgClC6H4)C(O)N=PPh3 and (CO)(4)Mn(2-C6H4C(O)N=PPh3). The utility of P-31 NMR spectroscopy in monitoring reaction chemistry in this system is described. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2009.12.019
点击查看最新优质反应信息