酰化
烷基化
化学
催化作用
弗里德尔-克拉夫茨反应
甲苯
布朗斯特德-洛瑞酸碱理论
二甲苯
有机化学
磷钨酸
选择性
作者
Cristhian Castro,Jaime Primo,Avelino Corma
出处
期刊:Journal of Molecular Catalysis A-chemical
[Elsevier BV]
日期:1998-09-01
卷期号:134 (1-3): 215-222
被引量:59
标识
DOI:10.1016/s1381-1169(98)00038-7
摘要
Pure phosphotungstic acid (H3PW12O40), supported on SiO2 and in the form of Cesium salts have been studied as acid catalysts for the acylation of toluene, p-xylene and m-xylene with crotonic acid. Since crotonic acid can either alkylate and/or acylate the alkylaromatic compounds, it was specifically selected to study the influence of the catalyst on the selectivity for these two competing reactions. Analysis of products obtained when acylating with an α,β-unsaturated acid show that all the catalysts are more active for acylation than for alkylation. Heteropolyacids were found to be more active than zeolites H-Y and Beta, even when the activity per acid site was considered. In the case of heteropolyacids, their activity is directly related to the number of accessible Brönsted acid sites.
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