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(η(5)-1-(Me2BrSi)-4,5,6,7-tetrahydroindenyl)(η(5)-C5H5)ZrBr2 | 244765-90-0

中文名称
——
中文别名
——
英文名称
(η(5)-1-(Me2BrSi)-4,5,6,7-tetrahydroindenyl)(η(5)-C5H5)ZrBr2
英文别名
bromo-dimethyl-(4,5,6,7-tetrahydroinden-1-id-1-yl)silane;cyclopenta-1,3-diene;dibromozirconium(2+)
(η(5)-1-(Me2BrSi)-4,5,6,7-tetrahydroindenyl)(η(5)-C5H5)ZrBr2化学式
CAS
244765-90-0
化学式
C16H21Br3SiZr
mdl
——
分子量
572.364
InChiKey
YGQLANPTHJTPMH-UHFFFAOYSA-L
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)-1-(trimethylsilyl)-4,5,6,7-tetrahydroindenyl)(η(5)-C5H5)ZrCl2三溴化硼二氯甲烷 为溶剂, 以49%的产率得到(η(5)-1-(Me2BrSi)-4,5,6,7-tetrahydroindenyl)(η(5)-C5H5)ZrBr2
    参考文献:
    名称:
    Electrophile-Functionalized Metallocene Intermediates. Application in the Diastereoselective Synthesis of a Tetramethyldisiloxane-Bridged C2-Symmetric ansa-Zirconocene Dibromide
    摘要:
    The reactivity of group 4 zirconocene dichlorides incorporating (1-trimethylsilyl)-eta(5)-indenyl (Me(3)SiInd) and eta(5)-1-(trimethylsilyl)-4,5,6,7-tetrahydro (Me3SiTHI) ligands toward boron tribromide was investigated. Whereas the reaction of (Me(3)SiInd)CpZrCl2 (1) with BBr3 in CH2Cl2 immediately cleaved the indenyl ligand from the metal, (Me3SiTHI)CpZrCl2 (3) reacted with BBr3 in CH2Cl2 at 70 degrees C for 2 days to obtain [1-(BrSiMe2)THI]CpZrBr2 (6) in 49% yield. The reaction of (Me(3)SiInd)Li (2 equiv) with ZrCl4(THF)(2) afforded pure rac-(Me(3)SiInd)(2)ZrCl2 (2) in 60% yield. Hydrogenation of (2) (50 bar, PtO2 catalyst) afforded rac-(Me3SiTHI)(2)ZrCl2 (4) in 81% yield. Single-crystal X-ray diffraction analysis of 4 showed that the Zr atom Lies on a crystallographic C-2 axis with the C4H8 annelated rings projecting into the ZrCl2 hemisphere of the pseudotetrahedral coordination environment. The reaction of 4 with MeLi in toluene afforded rac-(Me3SiTHI)(2)ZrMe2 (5) in 62% yield. H-1 NMR and C-13 NMR analysis confirmed the rac assignment for 5. Treatment of 4 with BBr3 in CH2Cl2 at 70 degrees C for 2 days afforded rac-[1-(BrMe2Si)THI](2)ZrBr2 (7) in 78% yield. The reaction of 7 with moisture in ambient air gave the ansa-metallocene rac-[mu-O-(1-Me2SiTKI)(2)]ZrBr2 (8) in 97% yield. In solution, 8 showed time-averaged C-2 symmetry (H-1 NMR); however, single-crystal X-ray diffraction analysis showed that 8 adopts an asymmetric conformation in which only one of the C4H8 annelated rings projects into the ZrCl2 coordination hemisphere. Neither 4 nor 8 served as a precatalyst for alumoxane-cocatalyzed, homogeneous propylene polymerization.
    DOI:
    10.1021/om9903339
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