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ruthenium(II)(η3-2-C3H4Me)(CO)Cl(1,1'bis(diphenylphosphino)ferrocene) | 640721-17-1

中文名称
——
中文别名
——
英文名称
ruthenium(II)(η3-2-C3H4Me)(CO)Cl(1,1'bis(diphenylphosphino)ferrocene)
英文别名
RuCl(η3-C3H4CH3)(CO)(1,1'-bis(diphenylphosphino)ferrocene)
ruthenium(II)(η3-2-C3H4Me)(CO)Cl(1,1'bis(diphenylphosphino)ferrocene)化学式
CAS
640721-17-1
化学式
C39H35ClFeOP2Ru
mdl
——
分子量
774.024
InChiKey
GJBFQXRPICAYNL-UHFFFAOYSA-M
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:
    silver hexafluoroantimonate 、 ruthenium(II)(η3-2-C3H4Me)(CO)Cl(1,1'bis(diphenylphosphino)ferrocene)二氯甲烷 为溶剂, 以97%的产率得到[Ru(η3-2-C3H4Me)(CO)(1,1'-bis(diphenylphosphino)ferrocene)][SbF6]
    参考文献:
    名称:
    [Ru(η3-2-C3H4Me)(CO)(dppf)][SbF6]: a mononuclear 16eruthenium(ii) catalyst for propargylic substitution and isomerization of HCCCPh2(OH)
    摘要:
    16e−衍生物[Ru(η3-2-C3H4Me)(CO)(dppf)][SbF6]催化:(i)1,1-二苯基-2-丙炔-1-醇与醇类发生丙炔基取代反应,生成丙炔基醚;(ii)1,1-二苯基-2-丙炔-1-醇发生形式异构化反应,生成3,3-二苯基-2-丙烯醛。
    DOI:
    10.1039/b410812d
  • 作为产物:
    描述:
    1,1'-双(二苯基膦)二茂铁(η3-2-methylallyl)Ru(CO)3Cl四氢呋喃 为溶剂, 以75%的产率得到ruthenium(II)(η3-2-C3H4Me)(CO)Cl(1,1'bis(diphenylphosphino)ferrocene)
    参考文献:
    名称:
    An Easy Entry to Dimers [{RuX(μ-X)(CO)(P⌒P)}2] (X = Cl, Br; P⌒P = 1,1‘-Bis(diphenylphosphino)ferrocene, 1,1‘-Bis(diisopropylphosphino)ferrocene) from η3-Allylruthenium(II) Derivatives [RuX(η3-2-C3H4R)(CO)(P⌒P)] (R = H, Me):  Efficient Catalyst Precursors in Transfer Hydrogenation of Ketones
    摘要:
    Complexes [RuX(eta(3)-2-C3H4R)(CO)(P<^>P)] (X = Cl, Br; R = H, Me; P<^>P = dppf, dippf) (2a-d and 3a-d) have been prepared by reaction of the eta-allylruthenium(II) derivatives [RuX(eta(3)-2-C3H4R)(CO)(3)] (1a-d) with 1 equiv of the appropriate diphosphine. Treatment of 2a-d and 3a-d with HX allows the high-yield preparation of the dimeric compounds [{RUX(mu-X)(CO)(P<^>P) }(2)] (P<^>P = dppf, X = Cl (4a), Br (4b); P<^>P = dippf, X = Cl (5a), Br (5b)). Complex [{RuCl(mu-Cl)(CO)(dppf)}(2)] reacts with neutral ligands, via chloride bridge cleavage, affording the mononuclear derivatives [RuCl2(CO)(L)(dppf)] (L = CO (6a), BzNC (6b), Py (6c), PhNH2 (6d)). The structures of compounds [RUCl(eta(3)-C3H5)(CO)(dPPf)] (2a), [{RuCl(mu-Cl)(CO)(dppf)}(2)] (4a), and [RuCl2(CO)(Py)(dppf)] (6c) have been confirmed by X-ray crystallography. The catalytic activity of dimers 4a,b and 5a,b in transfer hydrogenation of ketones by propan-2-ol has also been studied.
    DOI:
    10.1021/om030530e
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