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[Mn(cyclopentadienyl)(CO)2(η1-Z-P(Mes)CHMe)] | 1071224-77-5

中文名称
——
中文别名
——
英文名称
[Mn(cyclopentadienyl)(CO)2(η1-Z-P(Mes)CHMe)]
英文别名
[Cp(CO)2Mn(η1-Z-P(Mes)CHMe)]
[Mn(cyclopentadienyl)(CO)2(η1-Z-P(Mes)CHMe)]化学式
CAS
1071224-77-5;1287312-72-4
化学式
C18H20MnO2P
mdl
——
分子量
354.267
InChiKey
WXAHTXAFIIKSLS-UHFFFAOYSA-N
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:
    Generation of α-Phosphinocarbene Complexes and Their Evolution: New Light on Relevant Isomerization Pathways
    摘要:
    The eta(1)-alpha-phosphinocarbene complex CP(CO)(2)Mn=CR(PHMes) (R = Ph, Me) is generated by nucleophilic attack of MesPH(2) at the electrophilic center of the cationic Mn-carbyne complex [Cp(CO)(2)Mn CR](+), followed by deprotonation. One of its identified isomerization pathways to eta(1)-phosphaalkene derivatives is shown to be both base-catalyzed and stereoselective, and to involve a transient phosphidocarbene species engaged in an acid-catalyzed migratory CO-insertion step.
    DOI:
    10.1021/om800884v
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文献信息

  • Synthesis of η<sup>1</sup>-α-Phosphinocarbene Complexes of Manganese and Mechanistic Insight into Their Base-Induced Transformations
    作者:Dmitry A. Valyaev、Noël Lugan、Guy Lavigne、Nikolai A. Ustynyuk
    DOI:10.1021/om2000772
    日期:2011.4.25
    η1-α-phosphinocarbene complexes of manganese, Cp(CO)2Mn═C(R)PR′R′′ (3; 3a: R = Ph, R′ = H, R′′ = Mes; 3b: R = Me, R′ = H, R′′ = Mes; 3c: R = Ph, R′ = R′′ = Ph; 3d: R = Ph, R′ = R′′ = N(i-Pr)2; 3e: R = Ph, R′ = Me, R′′ = Mes), was generated at low temperature upon nucleophilic addition of the primary phosphine H2PMes and secondary phosphines HPPh2, HP(N(i-Pr)2)2, or (±)-HPMeMes to the cationic carbyne complexes Cp(CO)2Mn+≡C−R
    一系列η的1,CP(CO)的-α-phosphinocarbene络合物2 Mn═C(R)PR'R''(3 ; 3a中:R = PH,R'= H,R''=的Mes;图3b:R = Me,R'= H,R''= Mes; 3c:R = Ph,R'= R''= Ph; 3d:R = Ph,R'= R''= N(i -Pr)2 ; 3e:亲核添加一级膦H 2 PMes和二级膦HPPh 2,HP(N(i- Pr)2)时,在低温下生成R = Ph,R'= Me,R''= Mes))2或(±)-HPMeMes与阳离子碳炔复合物CP(CO)2的Mn + ≡C-R([ 1 ] + ; [ 1A ] +:R = Ph值; [ 1B ] +:R = Me)时,接着将得到的α-phosphoniocarbene中间体CP的去质子化(CO)2 Mn═C( R)P +(H)R'R''([ 2a - e ] +)。在η
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