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[Zr(1-Me2Si(3-η5-C9H5nBu)2)Me2] | 946507-95-5

中文名称
——
中文别名
——
英文名称
[Zr(1-Me2Si(3-η5-C9H5nBu)2)Me2]
英文别名
——
[Zr(1-Me2Si(3-η5-C9H5nBu)2)Me2]化学式
CAS
946507-95-5
化学式
C30H40SiZr
mdl
——
分子量
519.957
InChiKey
BIFYPRLNNIWJGU-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

  • 作为产物:
    描述:
    [ZrCl2(1-(CH3)2Si(3-η5-C9H5(C4H9)))2]甲基溴化镁四氢呋喃 为溶剂, 以42%的产率得到[Zr(1-Me2Si(3-η5-C9H5nBu)2)Me2]
    参考文献:
    名称:
    Activation process of 3-alkyl-substituted ansa-bis(indenyl) zirconocenes by MAO
    摘要:
    The ansa-indene compound {1-Me2Si(3-C9H6Et)(2)} (1) was prepared by alkylation of the unsubstituted ansa-indene. This compound was converted. by reaction with nBuLi, to the dilithium compound [Li-2{1-Me2Si(3-C9H5Et)(2)}] (2). ansa-Zirconocene [Zr{1-Me2Si(3-eta(5)-C9H5Et)(2)}Cl-2] (3) was prepared by the reaction of ZrCl4 with 2 in ether/toluene at -78 degrees C. The molecular structure of meso-3 was determined by single crystal X-ray diffraction studies. The ansa-zirconocene 3 exhibits a greater activity in ethylene polymerization than reference complexes such as [Zr{1-Me2Si(eta(5)-C9H6)(2)}Cl-2] and [Zr{1-C2H4(eta(5)-C9H5)(2)}Cl-2] and, in addition, it maintained a reasonable level of activity after 12h of contact with MAO solution. Furthermore, the different elementary steps in the activation process of ethylene polymerization for substituted complexes [Zr{1-Me2Si(3-eta(5)-C9H5R)(2)}Cl-2] (R=Et 3, Me 4, nPr 5 and nBu 6) by commercial methylaluminoxane (MAO) have been studied by UV-vis spectroscopy. Addition of MAO in large excess ([Al]/[Zr] = 2000) at -78 degrees C yields a previously unreported intermediate in the activation process of metallocenes: this intermediate has an absorption band centered at lambda = 639 nm. We report here the influence of the type of catalyst, ring substitution, type of cocatalyst and addition of THF on the activation process of these metallocenes. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molcata.2006.07.041
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