首页> 外文期刊>Journal of Applied Polymer Science >Triphase catalysis: Hydroxylation of cyclo-octane by NaOCl catalyzed by coordinatively bound manganese(III) porphyrin to nitrogen-based polymer supports
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Triphase catalysis: Hydroxylation of cyclo-octane by NaOCl catalyzed by coordinatively bound manganese(III) porphyrin to nitrogen-based polymer supports

机译:三相催化:配位键合的锰(III)卟啉与氮基聚合物载体催化的NaOCl催化环辛烷的羟化反应

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摘要

The anionic manganese (III) porphyrin was immobilized onto crosslinked poly(benzylpicoline-co-styrene) resin through coordinate linkage. The immobilized metalloporphyrin was employed as a heterogeneous catalyst for the hydroxylation of cycle-octane by NaOCl. The observed reaction rates depend on experimental parameters such as stirring speed, substrate amount, temperature, and catalyst amount. The influence of different polymer-based axial ligands, particle size, and percent crosslinking of the polymer support was also discussed. The imidazole-based polymer supports show higher rate constant values than the pyridine-based supports. The catalyst shows significant decrease in catalytic activity on recycling. (C) 2000 John Wiley & Sons, Inc. [References: 23]
机译:通过配位键合将阴离子锰(III)卟啉固定在交联的聚(苄基甲基吡啶-共苯乙烯)树脂上。固定化的金属卟啉被用作非均相催化剂,用于NaOCl对环辛烷进行羟基化。观察到的反应速率取决于实验参数,例如搅拌速度,底物量,温度和催化剂量。还讨论了不同的基于聚合物的轴向配体,粒径和聚合物载体交联百分比的影响。基于咪唑的聚合物载体显示出比基于吡啶的载体更高的速率常数。该催化剂显示出再循环的催化活性显着降低。 (C)2000 John Wiley&Sons,Inc. [参考:23]

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