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chloro(5,10,15,20-tetrakis(2-chloro-6-fluoro-3-sulfonatophenyl)porphyrinato)iron(III) | 834856-83-6

中文名称
——
中文别名
——
英文名称
chloro(5,10,15,20-tetrakis(2-chloro-6-fluoro-3-sulfonatophenyl)porphyrinato)iron(III)
英文别名
——
chloro(5,10,15,20-tetrakis(2-chloro-6-fluoro-3-sulfonatophenyl)porphyrinato)iron(III)化学式
CAS
834856-83-6
化学式
C44H16Cl5F4FeN4O12S4
mdl
——
分子量
1230.0
InChiKey
QSENSELNHRVUPW-YQGGSDPOSA-I
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:
    iron(III) chloride hexahydrate 、 5,10,15,20-tetrakis(2-chloro-6-fluoro-3-SO3Na-phenyl)porphyrin 以 not given 为溶剂, 生成 chloro(5,10,15,20-tetrakis(2-chloro-6-fluoro-3-sulfonatophenyl)porphyrinato)iron(III)
    参考文献:
    名称:
    Catalytic activity of anionic iron(III) porphyrins immobilized on grafted disordered silica obtained from acidic leached chrysotile
    摘要:
    Hydrated disordered silica obtained by leaching chrysotile with hydrochloric acid was grafted with 3-APTS and reacted with aqueous iron porphyrins solutions of [Fe(TDFSPP) and Fe(TCFSPP)]. The obtained materials were characterized by powder X-ray diffraction (PXRD), Uv-vis, FTIR and electron paramagnetic resonance (EPR) spectroscopies and investigated as catalysts in oxidation reaction of cyclohexane using iodosylbenzene as oxidant. The catalytic activities obtained in heterogeneous media for Fe(TDFSPP) was superior to the results obtained in homogeneous conditions but the opposite effect was observed for the Fe(TCFSPP), indicating that instead of the structural similarity of both iron porphyrins (second generation porphyrins), the immobilization way produced different catalysts. The best catalytic activity of the Fe(TDFSPP)/Si-3-APTS (65%) compared to Fe(TCFSPP)/Si-3-APTS (33%) can be explained by the easy access of the oxidant and the substrate to the catalytic sites in the former. A schematic representation for the immobilization and a mechanism for the oxidation reaction have been presented. (c) 2005 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.molcata.2005.08.019
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