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首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Hydroxylation of cyclohexane with molecular oxygen catalyzed by highly efficient heterogeneous Mn(III) porphyrin catalysts prepared by special synthesis and immobilization method
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Hydroxylation of cyclohexane with molecular oxygen catalyzed by highly efficient heterogeneous Mn(III) porphyrin catalysts prepared by special synthesis and immobilization method

机译:特殊合成和固定化方法制备的高效多相锰(III)卟啉催化剂催化分子氧催化环己烷的羟化反应

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摘要

A novel method to synthesize and immobilize porphyrins as well as manganese porphyrins on crosslinked polystyrene (CPS) microspheres was designed. The chlo-romethyl groups of chloromethylated CPS microspheres (CMCPS microspheres) were first oxidized to aldehyde groups via Kornblum oxidation reaction, obtaining aldehyde group-functionalized microspheres, and then, the synchronous synthesis and immobilization of porphyrins on CPS microspheres were carried out via the Adler reaction between solid-liquid phases, obtaining three kinds of functional microspheres, on which phenyl porphyrin (PP), p-chlorophenyl porphyrin (CPP) and p-nitrophenyl porphyrin (NPP) were immobilized. Finally, three manganese porphyrin-immobilized microspheres, MnPP-CPS, MnCPP-CPS and MnNPP-CPS, were prepared, these solid catalysts were used in the catalytic hydroxylation reaction of cyclohexane with molecular oxygen as oxidant, and their catalytic performances were mainly investigated in this work. Some surprising experimental results were obtained. The prepared immobilized manganese porphyrin catalysts display amazing catalytic activity and selectivity, and Cyclohexane conversion can get up to 45 % and cyclo-hexanol selectivity in the reaction product can be up to 90-100 %.
机译:设计了一种在卟啉交联聚苯乙烯(CPS)微球上合成和固定卟啉和锰卟啉的新方法。首先通过Kornblum氧化反应将氯甲基化CPS微球(CMCPS微球)的​​氯甲基氧化为醛基,得到醛基官能化的微球,然后通过Adler进行卟啉的同步合成和固定化。固液相反应,得到三种功能性微球,分别固定了苯基卟啉(PP),对氯苯基卟啉(CPP)和对硝基苯基卟啉(NPP)。最后,制备了三种固定有锰卟啉的微球:MnPP-CPS,MnCPP-CPS和MnNPP-CPS,将这些固体催化剂用于以分子氧为氧化剂的环己烷催化羟基化反应,主要研究了它们的催化性能。这项工作。获得了一些令人惊讶的实验结果。制备的固定化锰卟啉催化剂表现出惊人的催化活性和选择性,环己烷转化率可达45%,反应产物中环己醇的选择性可达90-100%。

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