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(CpMe5)HfCl2(O-2,6-Ph2C6H3) | 1203588-34-4

中文名称
——
中文别名
——
英文名称
(CpMe5)HfCl2(O-2,6-Ph2C6H3)
英文别名
——
(CpMe5)HfCl2(O-2,6-Ph2C6H3)化学式
CAS
1203588-34-4
化学式
C28H28Cl2HfO
mdl
——
分子量
629.926
InChiKey
AWTXPSZLCANIQB-UHFFFAOYSA-K
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:
    参考文献:
    名称:
    Ethylene polymerization and ethylene/1-octene copolymerization using group 4 half-metallocenes containing aryloxo ligands, CpMCl2(OAr) [M=Ti, Zr, Hf; Ar=O-2,6-R2C6H3, R=tBu, Ph]—MAO catalyst systems
    摘要:
    Effect of the centered metal toward the catalytic activity as well as comonomer incorporation has been explored in ethylene (co)polymerization using a series of Cp*MCl2(O-2,6-R2C6H3) [M = Ti (1), Zr (2), Hf (3); R Ph (a), Bu-t (b), Pr-i (C)] in the presence of methylaluminoxane (MAO) cocatalyst. Complexes 2a, 3a,b were prepared and identified, and the Structures for 2-3a,b were determined by X-ray crystallography as a distorted tetrahedral geometry around the metal center. The catalytic activity in ethylene polymerization was affected by the centered metal employed [Ti > Zr > Hf]; the complexes containing 2,6-diphenylphenoxy ligand (1-3a) showed higher catalytic activities than the complexes containing 2,6-di-tert-butylphenoxy analogues (1-3b). The molecular weights in the resultant polymers prepared by the Zr and the Hf analogues were lower than those prepared by the Ti-Ph (1a) and the Ti-Pr-i (1c) analogues. Although the copolymerizations of ethylene with 1-octene afforded the copolymers With uniform molecular weight distributions (except 1b), both the catalytic activities and the 1-octene incorporation were highly affected by the centered metal employed: the Ti-Pr-i analogue(1c) seems to be the most suited in terms of both the catalytic activity and the 1-octene incorporation. The attempted copolymerization of ethylene with 2-methyl-1-pentene using 2a,b and 3a-MAO catalysts afforded linear polyethylene. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molcata.2009.01.001
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