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bis(triphenylphosphine)(carbonyl)(allylamine)(hydrido)ruthenium chloride | 155516-26-0

中文名称
——
中文别名
——
英文名称
bis(triphenylphosphine)(carbonyl)(allylamine)(hydrido)ruthenium chloride
英文别名
——
bis(triphenylphosphine)(carbonyl)(allylamine)(hydrido)ruthenium chloride化学式
CAS
155516-26-0
化学式
C40H38ClNOP2Ru
mdl
——
分子量
747.218
InChiKey
YBIOVYSVKBUYRR-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

反应信息

  • 作为产物:
    描述:
    [RuHCl(CO)(PPh3)3] 、 丙烯胺四氢呋喃 为溶剂, 以60%的产率得到bis(triphenylphosphine)(carbonyl)(allylamine)(hydrido)ruthenium chloride
    参考文献:
    名称:
    RuClH(CO)(PPh3)3与烯丙基胺的反应:烯丙基胺的插入和不寻常的碳氮键裂解
    摘要:
    Reactions between RuClH(CO)(PPh3)3 and primary or secondary allylamines give olefin-insertion products: Ru(CH2CH2CH2NHR)Cl(CO)(PPh3)2(R=H(1),CH3(4), and CH2CH=CH2 (5)). Analytical and spectroscopic studies on these products show they have an octahedral six-coordinate structure in which two triphenylphosphines are located mutually cis, and a phosphine-trans isomer is obtained only in the case of R=H. The insertion of the primary allylamine occurs after the initial ligand exchange of the allylamine with one PPh3 of the starting complex. The variable-temperature NMR analyses reveal that the complexes derived from the secondary allylamines liberate one of the two PPh3 ligands at high temperatures. When R = CH3, an isolable dichloro-bridged dinuclear complex [Ru(mu-Cl)(CH2CH2CH2NHCH3)(CO)(PPh3)-]2 (6) is formed by the liberation of PPh3. A carbon-nitrogen bond of some tertiary allylic amines is cleaved in the reaction with RuClH(CO) (PPh3)3 to give the (pi-allyl)ruthenium(II) complex Ru(eta3-C3H5)CI(CO)(PPh3)2 (7) and its analog. The direct interaction between the Ru-H bond and the allylic amine leads to the formation of the (pi-allyl)ruthenium(II) complex, and the corresponding secondary amine without an increase of the oxidation state. Catalytic isomerization of some allylic amines to the enamines is also recognized during the insertion and the carbon-nitrogen bond cleavage.
    DOI:
    10.1021/om00017a051
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