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(3-benzyl-1H-inden-1-yl)(2-methylbenz[e]-1H-inden-1-yl)-dimethylsilane | 1243064-10-9

中文名称
——
中文别名
——
英文名称
(3-benzyl-1H-inden-1-yl)(2-methylbenz[e]-1H-inden-1-yl)-dimethylsilane
英文别名
(3-benzyl-1H-inden-1-yl)(2-methylbenz[e]-1H-inden-1-yl)dimethylsilane;(3-benzyl-1H-inden-1-yl)-dimethyl-(2-methyl-3H-cyclopenta[a]naphthalen-3-yl)silane
(3-benzyl-1H-inden-1-yl)(2-methylbenz[e]-1H-inden-1-yl)-dimethylsilane化学式
CAS
1243064-10-9
化学式
C32H30Si
mdl
——
分子量
442.676
InChiKey
OCUMCGQRPMTXOB-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):
    8.55
  • 重原子数:
    33
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (3-benzyl-1H-inden-1-yl)(2-methylbenz[e]-1H-inden-1-yl)-dimethylsilane氯化锆(IV) 在 n-BuLi 作用下, 以 乙醚正己烷二氯甲烷 为溶剂, 以15%的产率得到(3-benzylinden-1-id-1-yl)-dimethyl-(2-methylcyclopenta[a]naphthalen-3-id-3-yl)silane;zirconium(4+);dichloride
    参考文献:
    名称:
    Rotating Benzyl Substituent in ansa-Bis(indenyl)zirconocenes Controls Propene Polymerization
    摘要:
    A series of benzyl-substituted, dual-site ansa-metallocenes were synthesized and characterized. Their isolated rac- and meso-diastereomers were studied in propene polymerization after methyl-aluminoxane or borate activation. Catalysts' polymerization behavior were investigated in various polymerization conditions, and produced polypropenes (PPs) were characterized with NMR, GPC, and DSC. The rac- and meso-diastereomers of these unsymmetric catalysts bearing a SiMe(2) bridge produced PP with similar activity, tacticity, and molar mass. According to quantum chemical calculations, the benzyl group in the catalysts can rotate, having significant energy minima. The reason that the diastereomers produce PP with similar molar mass is linked to these local energy minima and is further discussed.
    DOI:
    10.1021/om9009262
  • 作为产物:
    描述:
    2-甲基苯并[E]茚(1H-和3H-型的混合物)(3-benzylindenyl)-(chloro)dimethylsilane正丁基锂 作用下, 以 乙醚正己烷 为溶剂, 以48%的产率得到(3-benzyl-1H-inden-1-yl)(2-methylbenz[e]-1H-inden-1-yl)-dimethylsilane
    参考文献:
    名称:
    Rotating Benzyl Substituent in ansa-Bis(indenyl)zirconocenes Controls Propene Polymerization
    摘要:
    A series of benzyl-substituted, dual-site ansa-metallocenes were synthesized and characterized. Their isolated rac- and meso-diastereomers were studied in propene polymerization after methyl-aluminoxane or borate activation. Catalysts' polymerization behavior were investigated in various polymerization conditions, and produced polypropenes (PPs) were characterized with NMR, GPC, and DSC. The rac- and meso-diastereomers of these unsymmetric catalysts bearing a SiMe(2) bridge produced PP with similar activity, tacticity, and molar mass. According to quantum chemical calculations, the benzyl group in the catalysts can rotate, having significant energy minima. The reason that the diastereomers produce PP with similar molar mass is linked to these local energy minima and is further discussed.
    DOI:
    10.1021/om9009262
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文献信息

  • Rotating Benzyl Substituent in <i>ansa</i>-Bis(indenyl)zirconocenes Controls Propene Polymerization
    作者:Arto Puranen、Mikko Linnolahti、Tanja Piel、Pertti Elo、Ilpo Mutikainen、Tapani Pakkanen、Barbro Löfgren、Erkki Aitola、Jukka Seppälä、Markku Leskelä、Timo Repo
    DOI:10.1021/om9009262
    日期:2010.9.27
    A series of benzyl-substituted, dual-site ansa-metallocenes were synthesized and characterized. Their isolated rac- and meso-diastereomers were studied in propene polymerization after methyl-aluminoxane or borate activation. Catalysts' polymerization behavior were investigated in various polymerization conditions, and produced polypropenes (PPs) were characterized with NMR, GPC, and DSC. The rac- and meso-diastereomers of these unsymmetric catalysts bearing a SiMe(2) bridge produced PP with similar activity, tacticity, and molar mass. According to quantum chemical calculations, the benzyl group in the catalysts can rotate, having significant energy minima. The reason that the diastereomers produce PP with similar molar mass is linked to these local energy minima and is further discussed.
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