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离子液体中芳烃侧链分子氧催化氧化反应研究

Catalytic Oxidation of Alkylbenzenes with Molecular Oxygen in Ionic Liquids

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【作者】 刘耀华崔鹏孙靖杨帆汤杰

【Author】 LIU Yao-Hua 1,2, CUI Peng 1, SUN Jing 1, YANG Fan 1*, TANG Jie 1 (1. Department of Chemistry, East China Normal University, Shanghai 200062, China; 2. Department of Chemistry, Taiyuan Teacher′s College, Taiyuan 030002, China)

【机构】 华东师范大学化学系华东师范大学化学系 上海200062太原师范学院化学系太原030002上海200062

【摘要】 分别以离子液体[Hex-mim]BF4,[Bmim]BF4,[Bmim]PF6和[Omim]BF4为溶剂,Co(Ⅱ),Mn(Ⅱ)或Ni(Ⅱ)/NHPI(AIBN)为复合催化剂,考察了不同离子液体-催化剂体系中常压分子氧氧化芳烃侧链烷基的反应.在[Hex-mim]BF4中,Co(Ⅱ)或Mn(Ⅱ)/NHPI可有效地催化芳烃侧链烷基的分子氧氧化.在优化条件下,乙苯、正丙苯和正丁苯分别以高达90%,94%和93%的收率得到相应的芳香酮;甲苯和对位取代甲苯以32%~47%的收率被氧化为相应的芳香酸.离子液体及金属催化剂体系在减压下除水后,可循环使用.

【Abstract】 Using ionic liquid [Hex-mim]BF4, [Bmim]BF4, [Bmim]PF6, and [Omim]BF4 as the solvent, respectively, the oxidation of alkylbenzenes by molecular oxygen was investigated under atmospheric pressure with Co(Ⅱ), Mn(Ⅱ), or Ni(Ⅱ)/NHPI (or AIBN) as the catalysts. The [Hex-mim]BF4/Co 2+(or Mn 2+)/NHPI system was demonstrated efficient for the oxidation of alkylbenzene. Under the optimized condition, ethylbenzene, n-propylbenzene, and n-butylbenzene were oxidized to the corresponding aromatic ketone with yields up to 90%, 94%, and 93%, respectively, toluene and p-substituted toluene were oridized to benzoic acid and the corresponding p-substituted benzoic acid with yields of 32%~47%. The ionic liquid and metal catalyst could be reused by removing water from them under a reduced pressure.

【基金】 国家自然科学基金(批准号:20172016);上海市科委基础研究重点项目(批准号:04JC14032);上海市科技启明星计划(批准号:01QA14017)资助.
  • 【文献出处】 高等学校化学学报 ,Chemical Journal of Chinese Universities , 编辑部邮箱 ,2006年12期
  • 【分类号】O643.32
  • 【被引频次】30
  • 【下载频次】496
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