高级检索

    杨晓林, 高保娇, 黄建龙. 聚合物微球固载N-羟基邻苯二甲酰亚胺催化剂的制备及其催化氧化性能初探[J]. 功能高分子学报, 2014, 27(3).
    引用本文: 杨晓林, 高保娇, 黄建龙. 聚合物微球固载N-羟基邻苯二甲酰亚胺催化剂的制备及其催化氧化性能初探[J]. 功能高分子学报, 2014, 27(3).
    YANG Xiao lin, GAO Bao jiao, HUANG Jian long. Preparation of Immobilized N-hydroxyphthalimide Catalyst on Polymer Microspheres and Primarily Investigation of Its Catalytic Property in Oxidation Reaction[J]. Journal of Functional Polymers, 2014, 27(3).
    Citation: YANG Xiao lin, GAO Bao jiao, HUANG Jian long. Preparation of Immobilized N-hydroxyphthalimide Catalyst on Polymer Microspheres and Primarily Investigation of Its Catalytic Property in Oxidation Reaction[J]. Journal of Functional Polymers, 2014, 27(3).

    聚合物微球固载N-羟基邻苯二甲酰亚胺催化剂的制备及其催化氧化性能初探

    Preparation of Immobilized N-hydroxyphthalimide Catalyst on Polymer Microspheres and Primarily Investigation of Its Catalytic Property in Oxidation Reaction

    • 摘要: 首先采用悬浮聚合法,制备了甲基丙烯酸缩水甘油酯(GMA)和甲基丙烯酸甲酯(MMA)的交联聚合物微球(GMA/MMA),然后经过几步大分子反应在微球表面合成与固载了N-羟基邻苯二甲酰亚胺(NHPI),形成固载有NHPI的功能微球GMA/MMA-NHPI。采用红外光谱(FT-IR)及扫描电子显微镜(SEM)等方法对功能微球进行了表征。结果表明,以含环氧基团的GMA/MMA为载体,通过大分子反应可实现NHPI的合成与固载。GMA/MMA-NHPI与醋酸钴(Co(OAc)2)构成的共催化体系,在分子氧对环己烷和环己醇的氧化过程中,显示出良好的催化活性。

       

      Abstract: Crosslinked polymer microspheres of glycidyl methacrylate (GMA) and methyl methacrylate (MMA) were first prepared by suspension polymerization, obtaining the polymer microspheres GMA/MMA. Subsequently, N-hydroxyphthalimide (NHPI) was synthesized and immobilized on GMA/MMA microspheres, and the functionalized microspheres GMA/MMA NHPI were obtained through several polymer reaction steps. GMA/MMA-NHPI microspheres were characterized by infrared spectroscopy (FT-IR) and scanning electron microscope (SEM). Results show that the synthesis and immobilization of NHPI on GMA/MMA microspheres can be carried out smoothly. The compositional catalyst system of GMA/MMA-NHPI microspheres and Co(OAc)2 displays fine catalytic activity in the oxidation reactions of cyclohexane and cyclohexanol with molecular oxygen as oxygen source.

       

    /

    返回文章
    返回