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2,2'-bis(2-hydroxy-5-trifluoro-benzylideneamino)-1.1'-naphthyl(III) complex | 1616063-27-4

中文名称
——
中文别名
——
英文名称
2,2'-bis(2-hydroxy-5-trifluoro-benzylideneamino)-1.1'-naphthyl(III) complex
英文别名
——
2,2'-bis(2-hydroxy-5-trifluoro-benzylideneamino)-1.1'-naphthyl(III) complex化学式
CAS
1616063-27-4
化学式
C36H21F6MnN2O5
mdl
——
分子量
730.502
InChiKey
FUISZADPHXWIFP-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:
    描述:
    manganese (II) acetate tetrahydrate 、 2,2'-bis(2-hydroxy-5-trifluoromethoxy-benzylideneamino)-1.1'-naphthyl 在 sodium methylate 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以82%的产率得到2,2'-bis(2-hydroxy-5-trifluoro-benzylideneamino)-1.1'-naphthyl(III) complex
    参考文献:
    名称:
    Synthesis, characterization and catalytic activity of chiral binaphthyl Schiff-base manganese complexes for the epoxidation of styrene
    摘要:
    Chiral binaphthyl Schiff base ligands were prepared by condensation of 2,2'-diamino-1,1'-binaphthalene with various salicylaldehydes. Ligands were coordinated with Mn(III) as catalysts. The catalytic efficiency of the complexes was tested on the epoxidation of styrene. The influences of the parameters such as reaction time, position of substituents with various oxidants on the epoxidation reactions were investigated. (C) 2014 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2014.04.004
  • 作为试剂:
    参考文献:
    名称:
    Synthesis, characterization and catalytic activity of chiral binaphthyl Schiff-base manganese complexes for the epoxidation of styrene
    摘要:
    Chiral binaphthyl Schiff base ligands were prepared by condensation of 2,2'-diamino-1,1'-binaphthalene with various salicylaldehydes. Ligands were coordinated with Mn(III) as catalysts. The catalytic efficiency of the complexes was tested on the epoxidation of styrene. The influences of the parameters such as reaction time, position of substituents with various oxidants on the epoxidation reactions were investigated. (C) 2014 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2014.04.004
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