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[C4H2N(2,5-CH2NMe2)2Hf(pyrrole(-H))3] | 1338682-11-3

中文名称
——
中文别名
——
英文名称
[C4H2N(2,5-CH2NMe2)2Hf(pyrrole(-H))3]
英文别名
——
[C4H2N(2,5-CH2NMe2)2Hf(pyrrole(-H))3]化学式
CAS
1338682-11-3
化学式
C22H30HfN6
mdl
——
分子量
557.01
InChiKey
GVLVYZQCROGIGW-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):
    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:
    吡咯[C4H2N(2,5-CH2NMe2)2Hf(NEt2)3]正戊烷 为溶剂, 以62%的产率得到[C4H2N(2,5-CH2NMe2)2Hf(pyrrole(-H))3]
    参考文献:
    名称:
    Zirconium and hafnium amide, alkoxide, and pyrrolyl complexes manifesting with pyrrolyl-linked N-donor ligands: Syntheses, characterization, and ring opening polymerization of ε-caprolactone
    摘要:
    A series of zirconium and hafnium alkoxide and amide complexes containing symmetrical tridentate pyrrolyl ligand, [C4H2NH(2,5-CH2NMe2)(2)] have been synthesized conveniently by treatment of 2,6-di-tert-butylphenol, tert-butanol or pyrrole in pentane and their reactivity over ring opening polymerization of epsilon-caprolactone have been carried out. Reactions of [C4H2NH(2,5-CH2NMe2)(2)] with M(NEt2)(4) (M = Zr or Hf) originate [C4H2N(2,5-CH2NMe2)(2)]M(NEt2)(3) (1, M = Zr; 2, M = Hf). Furthermore, reactions of [C4H2N(2,5-CH2NMe2)(2)]M(NEt2)(3) with 2,6-di-tert-butylphenol, tert-butanol or pyrrole afford [C4H2N(2,5-CH2NMe2)(2)]M(OC6H3-2,6-Bu-t(2))(NEt2)(2) (3, M = Zr; 4, M = Hf), [C4H2N(2,5-CH2NMe2)(2)]M((OBu)-Bu-t)(3) (5, M = Zr; 6, M = Hf) and [C4H2N(2,5-CH2NMe2)(2)]M(C4H4N)(3) (7, M = Zr; 8, M = Hf), respectively, in satisfactory yield. All the complexes have been characterized by NMR spectra as well 3, 4 and 6 subjected to the X-ray diffraction analysis. Complexes 3-8 have been used as initiators for the ring-opening polymerization of epsilon-caprolactone and observed broad PDI values (1.84-2.75) representing multiple reactivity centers of these complexes. (C) 2011 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2011.09.001
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