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| 174781-28-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
174781-28-3
化学式
C14H20Nb
mdl
——
分子量
281.219
InChiKey
NJLJHFMFNHFWRB-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

  • 作为反应物:
    描述:
    、 lead(II) chloride 以 为溶剂, 以62%的产率得到
    参考文献:
    名称:
    Thermolysis of (MeCp) 2Nb(η2−CO2)R complexes: decarbonylation vs. insertion
    摘要:
    A series of carbon dioxide complexes of the type Cp(2)'Nb(eta(2)-CO2)R (Cp' = MeC(5)H(4); R = -CH(2)SiMe(3), 1a; -CH(2)CMe(3), 1b; -CH(2)Ph, 1c; -CH3, 1d) was prepared and the thermolyses of 1a-1c investigated. When heated at 60 degrees C in THF, complexes 1a and 1b are converted to the corresponding oxo derivatives (MeC(5)H(4))(2)Nb(=O)R (2a, 2b) and CO. The structure of 2a was established by X-ray diffraction and consists of a pseudotetrahedral Cp(2)MXY arrangement. That the oxo group of 2 is derived from coordinated CO2 was confirmed by C-13 labeling. Thermolysis of benzyl derivative Ic exhibits concentration dependent behavior, converting to the corresponding oxoalkyl derivative 2c in dilute solutions but forming a mixture of 2c and the carbonyl complex (MeC(5)H(4))(2)Nb(CO)CH(2)Ph (4) in more concentrated solutions. With extended reaction times 2c and 4 decompose producing PhCH(3), PhCH(2)CH(2)Ph, PhCH(2)OH, and PhCHO, the products of apparent M-C homolysis and oxidation.
    DOI:
    10.1016/0022-328x(95)05667-e
  • 作为产物:
    描述:
    (η5-C5H4Me)2NbCl2 、 甲基锂乙醚 为溶剂, 以75%的产率得到
    参考文献:
    名称:
    Thermolysis of (MeCp) 2Nb(η2−CO2)R complexes: decarbonylation vs. insertion
    摘要:
    A series of carbon dioxide complexes of the type Cp(2)'Nb(eta(2)-CO2)R (Cp' = MeC(5)H(4); R = -CH(2)SiMe(3), 1a; -CH(2)CMe(3), 1b; -CH(2)Ph, 1c; -CH3, 1d) was prepared and the thermolyses of 1a-1c investigated. When heated at 60 degrees C in THF, complexes 1a and 1b are converted to the corresponding oxo derivatives (MeC(5)H(4))(2)Nb(=O)R (2a, 2b) and CO. The structure of 2a was established by X-ray diffraction and consists of a pseudotetrahedral Cp(2)MXY arrangement. That the oxo group of 2 is derived from coordinated CO2 was confirmed by C-13 labeling. Thermolysis of benzyl derivative Ic exhibits concentration dependent behavior, converting to the corresponding oxoalkyl derivative 2c in dilute solutions but forming a mixture of 2c and the carbonyl complex (MeC(5)H(4))(2)Nb(CO)CH(2)Ph (4) in more concentrated solutions. With extended reaction times 2c and 4 decompose producing PhCH(3), PhCH(2)CH(2)Ph, PhCH(2)OH, and PhCHO, the products of apparent M-C homolysis and oxidation.
    DOI:
    10.1016/0022-328x(95)05667-e
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