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(η5-MeCO2C5H4Mo)2(μ-Br)(μ-PhTe)3 | 258823-82-4

中文名称
——
中文别名
——
英文名称
(η5-MeCO2C5H4Mo)2(μ-Br)(μ-PhTe)3
英文别名
——
(η5-MeCO2C5H4Mo)2(μ-Br)(μ-PhTe)3化学式
CAS
258823-82-4;259137-06-9
化学式
C32H29BrMo2O4Te3
mdl
——
分子量
1132.16
InChiKey
MBIISQLNSJPVAY-UHFFFAOYSA-J
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:
    描述:
    [(η(5)-CH3O2CC5H4)2Mo2(CO)4]联苯二碲四丁基溴化铵 以 xylene 为溶剂, 以26%的产率得到(η5-MeCO2C5H4Mo)2(μ-Br)(μ-PhTe)3
    参考文献:
    名称:
    Investigations on Novel Tandem Reaction of Three Components, [η5-RC5H4(CO)2Mo]2, Ph2Te2, and Cp2TiCl2, Cp2ZrCl2, or Cp2ZrBr2. Synthesis and Structural Characterization of Tetrakis- and Bis-Bridged Dimolybdenum Complexes (η5-RC5H4Mo)2(μ-PhTe)4 (R = MeCO, MeO2C, EtO2C), (η5-RC5H4Mo)2(μ-Cl)(μ-PhTe)3 (R = MeCO, MeO2C, EtO2C), (η5-RC5H4Mo)2(μ-Br)(μ-PhTe)3 (R = MeO2C, EtO2C), and [η5-RC5H4(CO)2Mo]2(μ-PhTe)2 (R = MeO2C, EtO2C)
    摘要:
    While reaction of triply bonded dimers [eta(5)-RC5H4(CO)(2)Mo](2) (R = MeCO, MeO2C) with Ph-2-Te-2 in xylene at 110 degrees C and subsequent treatment with Cp2TiCl2 at reflux gives novel tetrakis-bridged complexes (eta(5)-RC5H4Mo)(2)(mu-PhTe)(4) (1, R = MeCO; 3, R = MeO2C) and (eta(5)-RC5H4Mo)(2)(mu-Cl)(mu-PhTe)(3) (2a,b, R = MeCO; 4a,b, R = MeO2C), the dimers [eta(5)-RC5H4(CO)(2)Mo](2) (R = MeO2C, EtO2C) reacted with Ph2Te2 and Cp2ZrCl2 or Cp2ZrBr2 under similar conditions to afford novel tetrakis-bridged complexes (eta(5)-RC5H4Mo)(2)(mu-PhTe)(4) (3, R = MeO2C; 5, R = EtO2C), (eta(5)-RC5H4Mo)(2)(mu-Cl)(mu-PhTe)(3) (4a,b, R = MeO2C; 6a,b, R = EtO2C), and (eta(5)-RC5H4Mo)(2)(mu-Br)(mu-PhTe)(3) (7a,b, R = MeO2C; 8a,b, R = EtO2C). A possible pathway for production of such tetrakis-bridged complexes has been suggested primarily on the basis of the following facts: (i) Treatment of triply bonded dimers [eta(5)-RC5H4(CO)(2)Mo](2) (R = MeO2C, EtO2C) with Ph2Te2 in xylene at 110 degrees C produces bis-bridged complexes [eta(5)-RC5H4(CO)(2)Mo](2)(mu-PhTe)(2) (9, R = MeO2C; 10, R = EtO2C) and (ii) reaction of 9 with Cp2MCl2 (M = Ti, Zr) yields tetrakis-bridged complexes 3 and 4a,b. All the new products 1-10 are fully characterized by elemental analysis and IR, H-1, and Te-125 NMR spectroscopies, and 4b and 9 by single-crystal X-ray diffraction techniques.
    DOI:
    10.1021/om9904448
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