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LEWIS ACIDITY OF MESOPOROUS MOLECULAR SIEVESFOR ACYLATION REACTIONS

机译:介孔分子裂缝的路易斯酸度筛灵酰化反应

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The effect of the concentration of Lewis acid sites on the activity and selectivity ofdifferent molecular sieve catalysts was investigated in the Friedel-Crafts acylation offerrocene with acetic anhydride, toluene with isobutyryl chloride, and cyclohexene and1-methylcyclohexene with propionic anhydride. H-, Zn-, Fe-, Al- and La-forms ofmesoporous molecular sieves (AI)MCM-41 and (AI)SBA-15 were studied and comparedwith large-pore zeolites. No general relationship between the type of cation andconversion of substrate was found. In acylation of ferrocene the highest ferroceneconversions were reached over Zn- and H-forms while in toluene acylation Al-formswere the most active. The selectivities over mesoporous molecular sieves were lower (61— 89 %) compared with zeolites (82 — 98 %).
机译:用乙酸酐,用异丁烯酰氯,甲苯和环己烯和1-甲基环己烯,研究了路易斯分子筛催化剂的活性和选择性对多样子分子筛催化剂的活性和选择性的影响,用丙烯酸酐和环己烯和1-甲基环己烯。研究并与大孔沸石进行了倍多的分子筛(AI)MCM-41和(AI)SBA-15的H-,Zn-,Fe-,Al-and和La-as和La-形式。没有发现衬底阳离子和混合物类型之间的一般关系。在二茂铁的酰化中,在甲苯酰化Al-Formspspsh最活跃的情况下,在Zn和H形式中达到最高的铁核onversions。与沸石(82-98%)相比,在中孔分子筛上的选择性较低(61-89%)。

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