摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-[1-(2,6-diisopropylphenylimino)ethyl]-2,2'-bipyridine iron dichloride | 300343-29-7

中文名称
——
中文别名
——
英文名称
6-[1-(2,6-diisopropylphenylimino)ethyl]-2,2'-bipyridine iron dichloride
英文别名
——
6-[1-(2,6-diisopropylphenylimino)ethyl]-2,2'-bipyridine iron dichloride化学式
CAS
300343-29-7
化学式
C24H27Cl2FeN3
mdl
——
分子量
484.251
InChiKey
CMHQAWSINFNMTO-DMVWOWLWSA-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:
    N-(1-[2,2′-bipyridin-6-yl]ethylidene)-2,6-diisopropylbenzenamine 、 iron(II) chloride 以 正丁醇 为溶剂, 以76%的产率得到6-[1-(2,6-diisopropylphenylimino)ethyl]-2,2'-bipyridine iron dichloride
    参考文献:
    名称:
    The role of bulky substituents in the polymerization of ethylene using late transition metal catalysts: a comparative study of nickel and iron catalyst systems
    摘要:
    A series of nickel(II) and iron(II) complexes of the general formula [LMX2] containing bidentate (for M = Ni) and tridentate (for M = Fe) heterocycle-imine ligands L have been synthesized and characterized. Compared to the well-known alpha-diimine nickel and bis(imino)pyridine iron catalysts, these systems contain a bulky imine substituent on one side and a non-bulky N-heterocycle on the other. Depending on the ligand and the conditions used, either four- or five-coordinate complexes are obtained in the case of nickel. Iron complexes are generally five-coordinate, even with potentially tetradentate ligands. Activation of these precatalysts with MAO affords active catalyst systems for the oligomerization/polymerization of ethylene. Compared to alpha-diimine nickel and bis(imino)pyridine iron catalysts, both- metal systems provide only half of the steric protection and consequently the catalytic activities and the degree of polymerization are significantly lower. Lower activities are attributed to a reduced stability of the active species under polymerization conditions, whereas the lower molecular weights are a result of increased beta-H transfer rates. Variations within the heterocyclic component of the ligand reveal that both steric and electronic factors influence the polymerization behavior of these catalysts. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(02)01293-8
点击查看最新优质反应信息