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(1,1'-di(2-tert-butyl-6-diphenylphosphiniminophenoxy)ferrocene)InCl | 1309956-42-0

中文名称
——
中文别名
——
英文名称
(1,1'-di(2-tert-butyl-6-diphenylphosphiniminophenoxy)ferrocene)InCl
英文别名
——
(1,1'-di(2-tert-butyl-6-diphenylphosphiniminophenoxy)ferrocene)InCl化学式
CAS
1309956-42-0
化学式
C54H52ClFeInN2O2P2
mdl
——
分子量
1029.09
InChiKey
YJKUOTPTUNTSRQ-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

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

  • 作为反应物:
    描述:
    (1,1'-di(2-tert-butyl-6-diphenylphosphiniminophenoxy)ferrocene)InClsodium phenoxide乙醚 为溶剂, 以85%的产率得到(1,1'-di(2-tert-butyl-6-diphenylphosphiniminophenoxy)ferrocene)In(OPh)
    参考文献:
    名称:
    Redox Control of a Ring-Opening Polymerization Catalyst
    摘要:
    The activity of an yttrium alkoxide complex supported by a ferrocene-based ligand was controlled using redox reagents during the ring-opening polymerization of L-lactide. The oxidized complex was characterized by X-ray crystallography and H-1 NMR, XANES, and Mossbauer spectroscopy. Switching in situ between the oxidized and reduced yttrium complexes resulted in a change in the rate of polymerization of L-lactide. Synthesized polymers were analyzed by gel permeation chromatography. Polymerization of trimethylene carbonate was also performed with the reduced and oxidized forms of an indium alkoxide complex. The indium system showed the opposite behavior to that of yttrium, revealing a metal-based dependency on the rate of polymerization.
    DOI:
    10.1021/ja2036089
  • 作为产物:
    描述:
    trichlorobis(tetrahydrofuran)indium(III) 、 sodium 1,1'-di(2-tert-butyl-6-diphenylphosphiniminophenolato)ferrocene bis(tetrahydrofuran) 以 四氢呋喃 为溶剂, 以85%的产率得到(1,1'-di(2-tert-butyl-6-diphenylphosphiniminophenoxy)ferrocene)InCl
    参考文献:
    名称:
    Redox Control of a Ring-Opening Polymerization Catalyst
    摘要:
    The activity of an yttrium alkoxide complex supported by a ferrocene-based ligand was controlled using redox reagents during the ring-opening polymerization of L-lactide. The oxidized complex was characterized by X-ray crystallography and H-1 NMR, XANES, and Mossbauer spectroscopy. Switching in situ between the oxidized and reduced yttrium complexes resulted in a change in the rate of polymerization of L-lactide. Synthesized polymers were analyzed by gel permeation chromatography. Polymerization of trimethylene carbonate was also performed with the reduced and oxidized forms of an indium alkoxide complex. The indium system showed the opposite behavior to that of yttrium, revealing a metal-based dependency on the rate of polymerization.
    DOI:
    10.1021/ja2036089
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