[Cp*Fe(η6-o-dipropylbenzene)]PF6 | 872104-38-6

• 英文名称: [Cp*Fe(η6-o-dipropylbenzene)]PF6
• 英文别名: [Cp*Fe(η⁶-o-dipropylbenzene)]PF6
• CAS: 872104-38-6
• 化学式: C₂₂H₃₃Fe*F₆P
• 分子量: 498.315
• InChiKey: APULTJDFTFNQAZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
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• 可旋转键数：
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• 环数：
  None
• sp3杂化的碳原子比例：
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• 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：

  [Cp*Fe(η6-o-dipropylbenzene)]PF6 、 氘代乙腈 以 氘代乙腈 为溶剂， 以92%的产率得到[(η5-C5Me5)Fe(CD3CN)3]PF6
  参考文献：
  名称：

  A Transition-Metal-Catalyzed Enediyne Cycloaromatization

  摘要：

  The pentamethylcyclopentadienyl iron cation, generated from [(eta5-C5Me5)Fe(NCMe)3]PF6, triggers the room temperature cycloaromatization of acyclic and alicyclic enediynes, in the presence of either 1,4-cyclohexadiene or terpinene as the hydrogen-atom donor, to give metal-arene products in good to excellent yields. Photolysis of the metal-arene complexes liberates the arene from the metal in excellent yield. The first demonstration of a transition-metal-catalyzed cycloaromatization of conjugated enediynes has been achieved under photochemical conditions utilizing either [(eta5-C5Me5)Fe(NCMe)3]PF6 or [(eta5-C5Me5)Fe(eta6-1,2-(Prn)2C6H4)]PF6 as the catalyst precursor. The use of a metal and light has led to a convenient method for cycloaromatization of a trans-enediyne.

  DOI：

  10.1021/ja050060a
• 作为产物：
  描述：

  [Cp*Fe(NCMe)₃]PF₆ 、 (Z)-dodeca-4,8-diyn-6-ene 以 丙酮 为溶剂， 生成 [Cp*Fe(η6-o-dipropylbenzene)]PF6
  参考文献：
  名称：

  A Transition-Metal-Catalyzed Enediyne Cycloaromatization

  摘要：

  The pentamethylcyclopentadienyl iron cation, generated from [(eta5-C5Me5)Fe(NCMe)3]PF6, triggers the room temperature cycloaromatization of acyclic and alicyclic enediynes, in the presence of either 1,4-cyclohexadiene or terpinene as the hydrogen-atom donor, to give metal-arene products in good to excellent yields. Photolysis of the metal-arene complexes liberates the arene from the metal in excellent yield. The first demonstration of a transition-metal-catalyzed cycloaromatization of conjugated enediynes has been achieved under photochemical conditions utilizing either [(eta5-C5Me5)Fe(NCMe)3]PF6 or [(eta5-C5Me5)Fe(eta6-1,2-(Prn)2C6H4)]PF6 as the catalyst precursor. The use of a metal and light has led to a convenient method for cycloaromatization of a trans-enediyne.

  DOI：

  10.1021/ja050060a
• 作为试剂：
  描述：

  (Z)-dodeca-4,8-diyn-6-ene 在 [Cp*Fe(η6-o-dipropylbenzene)]PF6 、 γ-松油烯 作用下， 以 丙酮 为溶剂， 反应 144.0h， 以91%的产率得到1,2-dipropylbenzene
  参考文献：
  名称：

  A Transition-Metal-Catalyzed Enediyne Cycloaromatization

  摘要：

  The pentamethylcyclopentadienyl iron cation, generated from [(eta5-C5Me5)Fe(NCMe)3]PF6, triggers the room temperature cycloaromatization of acyclic and alicyclic enediynes, in the presence of either 1,4-cyclohexadiene or terpinene as the hydrogen-atom donor, to give metal-arene products in good to excellent yields. Photolysis of the metal-arene complexes liberates the arene from the metal in excellent yield. The first demonstration of a transition-metal-catalyzed cycloaromatization of conjugated enediynes has been achieved under photochemical conditions utilizing either [(eta5-C5Me5)Fe(NCMe)3]PF6 or [(eta5-C5Me5)Fe(eta6-1,2-(Prn)2C6H4)]PF6 as the catalyst precursor. The use of a metal and light has led to a convenient method for cycloaromatization of a trans-enediyne.

  DOI：

  10.1021/ja050060a