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2-methyl-2'-6-t-butoxyhexylmethylene[cyclopentadienyl-fluoren-9-yl]-zirconocenedichloride | 670222-37-4

中文名称
——
中文别名
——
英文名称
2-methyl-2'-6-t-butoxyhexylmethylene[cyclopentadienyl-fluoren-9-yl]-zirconocenedichloride
英文别名
——
2-methyl-2'-6-t-butoxyhexylmethylene[cyclopentadienyl-fluoren-9-yl]-zirconocenedichloride化学式
CAS
670222-37-4
化学式
C30H36Cl2OZr
mdl
——
分子量
574.745
InChiKey
UKJMJIBNJXMRLZ-IAHZSBLGSA-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:
    氯化锆(IV)2-methyl-2'-6-t-butoxyhexylmethylene[cyclopentadienyl-fluorene-9-yl]正丁基锂 作用下, 以 正己烷 为溶剂, 以31%的产率得到2-methyl-2'-6-t-butoxyhexylmethylene[cyclopentadienyl-fluoren-9-yl]-zirconocenedichloride
    参考文献:
    名称:
    The effect that 6-tert-butoxyhexyl functionalization has on ethylene polymerization in ansa-zirconocene dichlorides
    摘要:
    New ansa-zirconocene dichloride derivatives have been prepared, which have a 6-t-butoxyhexyl pendant introduced either on a Cp-ring-carbon or at the silicon and carbon ansa-bridging atom. Ethylene polymerization studies have been carried out with novel precatalysts of the type: [(eta(5)-C13H8)-X(t-BuOC6H12)Me-(eta(5)-C5H4)]ZrCl, [X=C [1a], Si [2a]], [(eta(5)-C13H8)-XMe2-(eta(5)-(t-BuOC6H12C5H3))] ZrCl, [X = C [3a], Si [4a]] in the presence of excess methylalumoxane (MAO) to compare their catalytic activity and to delineate the effect of the 6-t-butoxyhexyl functionality on ethylene polymerization. The precatalysts [1a] and [2a] with the bridge functionality showed higher activity in ethylene polymerization than the corresponding complexes [3a] and [4a] which have it on the Cp ring moiety. On the other hand the silyl bridged complexes [2a] and [4a] produced a higher molecular weight polyethylene than the carbon-bridged one, regardless of the location of functional group. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2003.10.006
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