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Immobilized metalloporphyrins in mesoporous MCM-48 as efficient and selective heterogeneous catalysts for oxidation of cyclohexene

机译:固定在中孔MCM-48中的金属卟啉作为环己烯氧化的高效选择性多相催化剂

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摘要

Three metalloporphyrins, Mn(IH)TCIPPCl, Fe(in)TClPPCl, and Co(II)TClPP (TC1PP = 5,10,15,20-tetrakis(4-chlorophenyl)porphyrin), were synthesized and immobilized in MCM-48 channels. The designed heterogeneous catalysts were characterized by XRD, ICP, UV-Vis, FT-IR, N2 adsorption-desorption, and scanning electron microscopy. These investigations showed that successful encapsulation occurred and the framework of mesoporous MCM-48 was retained without any change after incorporation of the metalloporphyrins. The effect of the support on the resistance to pore blocking was studied by comparing MCM-48 with MCM-41. The catalytic activities of the newly synthesized catalysts were examined in the oxidation of cyclohexene with r-butyl hydroperoxide as oxidant. All results confirmed that the supported catalysts presented interesting advantages such as high selectivity to the allylic products and more resistance to pore blocking. The heterogeneous catalysts were reused for several times without significant loss of their catalytic activity.
机译:合成了三种金属卟啉Mn(IH)TCIPPC1,Fe(in)TC1PPCl和Co(II)TC1PP(TC1PP = 5,10,15,20-四(4-氯苯基)卟啉)并固定在MCM-48通道中。通过XRD,ICP,UV-Vis,FT-IR,N2吸附-脱附和扫描电子显微镜对所设计的多相催化剂进行了表征。这些研究表明,结合金属卟啉后,成功地进行了包封并且保留了中孔MCM-48的框架而没有任何改变。通过比较MCM-48和MCM-41,研究了载体对抗孔堵塞的作用。在以过氧化叔丁基为氧化剂的环己烯氧化反应中,研究了新合成的催化剂的催化活性。所有结果证实了载体上的催化剂具有令人感兴趣的优点,例如对烯丙基产物的高选择性和对孔堵塞的更大抵抗力。该非均相催化剂可重复使用几次,而不会显着降低其催化活性。

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