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Cp*(η4-1,4-Me2C4H4)Cr

中文名称
——
中文别名
——
英文名称
Cp*(η4-1,4-Me2C4H4)Cr
英文别名
——
Cp*(η4-1,4-Me2C4H4)Cr化学式
CAS
——
化学式
C16H25Cr
mdl
——
分子量
269.37
InChiKey
LUZCGMZCEZODMW-DURVFHFYSA-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

  • 作为反应物:
    描述:
    Cp*(η4-1,4-Me2C4H4)Cr三甲基膦正戊烷 为溶剂, 生成 Cp*(η4-1,4-Me2C4H4)CrPMe3
    参考文献:
    名称:
    Organochromium π-complexes—VIII. Reactions of the (η5-Me5C5)Cr-system with 1,3-dienes and alkynes
    摘要:
    Cp*(eta4-1,3-diene)Cr compounds have been prepared either by reacting Cp*(eta3-C3H5)2Cr with a diene or by reducing Cp*Cr(THF)Cl2 with activated-Mg in the presence of the diene. These coordinatively and electronically unsaturated species readily form adducts with CO or P-donor ligands. The reaction of Cp*(eta4-1,3-C4H6)Cr with further butadiene leads to the formation of Cp*(eta3,eta3-octadienediyl)Cr which in tum reacts with a disubstitued alkyne (RC2R) with addition to the 2,7-positions of the octadienediyl chain to give Cp*(eta1,eta2,eta1-R2C10H12)Cr species. The crystal structures of representative compounds have been established by X-ray diffraction.
    DOI:
    10.1016/s0277-5387(00)80117-5
  • 作为产物:
    描述:
    2,4-已二烯 、 (η5-Me5C5)(η3-C3H5)2Cr 以 正戊烷 为溶剂, 以63%的产率得到Cp*(η4-1,4-Me2C4H4)Cr
    参考文献:
    名称:
    Organochromium π-complexes—VIII. Reactions of the (η5-Me5C5)Cr-system with 1,3-dienes and alkynes
    摘要:
    Cp*(eta4-1,3-diene)Cr compounds have been prepared either by reacting Cp*(eta3-C3H5)2Cr with a diene or by reducing Cp*Cr(THF)Cl2 with activated-Mg in the presence of the diene. These coordinatively and electronically unsaturated species readily form adducts with CO or P-donor ligands. The reaction of Cp*(eta4-1,3-C4H6)Cr with further butadiene leads to the formation of Cp*(eta3,eta3-octadienediyl)Cr which in tum reacts with a disubstitued alkyne (RC2R) with addition to the 2,7-positions of the octadienediyl chain to give Cp*(eta1,eta2,eta1-R2C10H12)Cr species. The crystal structures of representative compounds have been established by X-ray diffraction.
    DOI:
    10.1016/s0277-5387(00)80117-5
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文献信息

  • Organochromium π-complexes—VIII. Reactions of the (η5-Me5C5)Cr-system with 1,3-dienes and alkynes
    作者:A. Döhring、R. Emrich、R. Goddard、P.W. Jolly、C. Krüger
    DOI:10.1016/s0277-5387(00)80117-5
    日期:1993.11
    Cp*(eta4-1,3-diene)Cr compounds have been prepared either by reacting Cp*(eta3-C3H5)2Cr with a diene or by reducing Cp*Cr(THF)Cl2 with activated-Mg in the presence of the diene. These coordinatively and electronically unsaturated species readily form adducts with CO or P-donor ligands. The reaction of Cp*(eta4-1,3-C4H6)Cr with further butadiene leads to the formation of Cp*(eta3,eta3-octadienediyl)Cr which in tum reacts with a disubstitued alkyne (RC2R) with addition to the 2,7-positions of the octadienediyl chain to give Cp*(eta1,eta2,eta1-R2C10H12)Cr species. The crystal structures of representative compounds have been established by X-ray diffraction.
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