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[η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2-][η5-C5(CH3)5]ZrH | 861143-68-2

中文名称
——
中文别名
——
英文名称
[η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2-][η5-C5(CH3)5]ZrH
英文别名
——
[η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2-][η5-C5(CH3)5]ZrH化学式
CAS
861143-68-2
化学式
C23H37NZr
mdl
——
分子量
418.777
InChiKey
ZXHOPUMNXQOBGU-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

反应信息

  • 作为反应物:
    描述:
    [η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2-][η5-C5(CH3)5]ZrH 、 ammonium chloride 以 四氢呋喃 为溶剂, 以72%的产率得到[η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2-][η5-C5(CH3)5]ZrCl
    参考文献:
    名称:
    Reduction of 2-(N,N-dimethylamino)ethyl substituted zirconocene dichlorides: Intramolecular activation of NCH2–H bond. The crystal structures of [η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2][η5-C5(CH3)5]ZrX (X=Cl, H)
    摘要:
    Treatment of zirconocene dichloride [eta(5)-C-5(CH3)(4)CH2CH2N(CH3)(2)][eta(5)-C-5(CH3)(3)]ZrCl2 (1) with amalgamated magnesium in THF results in cleavage of a C-H bond in one of the methyl groups of the N(CH3)(2) fragment yielding [eta(5):eta(2)(C,N)C-5(CH3)(4)CH2CH2N(CH3)CH2][eta(5)-C-5(CH3)(2)]ZrH (2). An analogous reduction of [eta(5)-C-5(CH3)(4)CH2CH2N(CH3)(2)](2)ZrCl2 (4) proceeds similarly only in the presence of great excess of P(CH3)(3), otherwise no identifiable products are formed. Heterogeneous reaction of the hydride complex 2 with NH4Cl in THF produces the corresponding chloride complex [eta(5):eta(2)(C,N)-C-5(CH3)(4)CH2CH2N(CH3)CH2][eta(5)-C-5(CH3)(5)]ZrCl (3), with the Zr-CH2 bond retained. The molecular structures of compounds 2 and 3 were established by X-ray diffraction analyses. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.03.055
  • 作为产物:
    描述:
    [η5-C5(CH3)4CH2CH2N(CH3)2][η5-C5(CH3)5]ZrCl2 在 amalgamated magnesium 作用下, 以 四氢呋喃 为溶剂, 以67%的产率得到[η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2-][η5-C5(CH3)5]ZrH
    参考文献:
    名称:
    Reduction of 2-(N,N-dimethylamino)ethyl substituted zirconocene dichlorides: Intramolecular activation of NCH2–H bond. The crystal structures of [η5:η2(C,N)-C5(CH3)4CH2CH2N(CH3)CH2][η5-C5(CH3)5]ZrX (X=Cl, H)
    摘要:
    Treatment of zirconocene dichloride [eta(5)-C-5(CH3)(4)CH2CH2N(CH3)(2)][eta(5)-C-5(CH3)(3)]ZrCl2 (1) with amalgamated magnesium in THF results in cleavage of a C-H bond in one of the methyl groups of the N(CH3)(2) fragment yielding [eta(5):eta(2)(C,N)C-5(CH3)(4)CH2CH2N(CH3)CH2][eta(5)-C-5(CH3)(2)]ZrH (2). An analogous reduction of [eta(5)-C-5(CH3)(4)CH2CH2N(CH3)(2)](2)ZrCl2 (4) proceeds similarly only in the presence of great excess of P(CH3)(3), otherwise no identifiable products are formed. Heterogeneous reaction of the hydride complex 2 with NH4Cl in THF produces the corresponding chloride complex [eta(5):eta(2)(C,N)-C-5(CH3)(4)CH2CH2N(CH3)CH2][eta(5)-C-5(CH3)(5)]ZrCl (3), with the Zr-CH2 bond retained. The molecular structures of compounds 2 and 3 were established by X-ray diffraction analyses. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.03.055
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