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| 1600500-94-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1600500-94-4
化学式
C60H52Cu2N4O8
mdl
——
分子量
1084.19
InChiKey
CEKHEWZAMXDGIS-YBKWXBMWSA-J
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:
    copper(II) acetate monohydrate 、 2-[[2-[(2-Hydroxy-3-methoxyphenyl)methylideneamino]-1,2-diphenylethyl]iminomethyl]-6-methoxyphenol 以 乙醇 为溶剂, 生成
    参考文献:
    名称:
    Mononuclear and dinuclear salen type copper(II) Schiff base complexes: Synthesis, characterization, crystal structures and catalytic epoxidation of cyclooctene
    摘要:
    A series of salen type Schiff base ligands and their mononuclear (CuLn, n = 1-4) or dinuclear Cu(II) complexes (Cu-2(L-5)(2)) were synthesized and characterized by H-1 NMR, IR and UV-Vis spectroscopy as well as elemental analyses. The ligands were synthesized from the condensation of meso-1,2-diphenyl-1,2-ethylenediamine with various salicylaldehyde derivatives (x-salicylaldehyde for H2Ln, x = H (n = 1), 5-Br (n = 2), 5-Br-3-NO2 (n = 3), 3-OMe, (n = 5)) and 20-hydroxyacetophenone (n = 4). Crystal structures of two complexes (CuL4 and Cu-2(L-5)(2)) were determined. Catalytic performance of the complexes was studied in the epoxidation of cyclooctene using tert-butylhydroperoxide (TBHP) as oxidant. Various factors including reaction temperature, solvent type, time, catalyst amount and substrate to oxidant ratio were optimized. High catalytic activity and epoxides selectivity was found. Solvent free epoxidation of cyclooctene was also studied and higher catalytic activity, epoxide selectivity and lower reaction times were observed. (C) 2014 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2014.01.047
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