Área Departamental de Engenharia Química, Instituto Superior de Engenharia de Lisboa, IPL, R. Conselheiro Emídio Navarro, 1959-007 Lisboa, Portugal.
Centro de Química Estrutural (CQE), Faculdade de Ciências, Universidade de Lisboa, 1749-016 Lisboa, Portugal.
Molecules. 2020 Dec 2;25(23):5682. doi: 10.3390/molecules25235682.
Attempts to optimize heterogeneous catalysis often lack quantitative comparative analysis. The use of kinetic modelling leads to rate () and relative sorption equilibrium constants (), which can be further rationalized using Quantitative Structure-Property Relationships (QSPR) based on Multiple Linear Regressions (MLR). Friedel-Crafts acylation using commercial and hierarchical BEA zeolites as heterogeneous catalysts, acetic anhydride as the acylating agent, and a set of seven substrates with different sizes and chemical functionalities were herein studied. Catalytic results were correlated with the physicochemical properties of substrates and catalysts. From this analysis, a robust set of equations was obtained allowing inferences about the dominant factors governing the processes. Not entirely surprising, the rate and sorption equilibrium constants were found to be explained in part by common factors but of opposite signs: higher and stronger adsorption forces increase reaction rates, but they also make the zeolite active sites less accessible to new reactant molecules. The most relevant parameters are related to the substrates' molecular size, which can be associated with different reaction steps, namely accessibility to micropores, diffusion capacity, and polarizability of molecules. The relatively large set of substrates used here reinforces previous findings and brings further insights into the factors that hamper/speed up Friedel-Crafts reactions in heterogeneous media.
优化多相催化的尝试往往缺乏定量比较分析。动力学建模的使用导致了速率常数 (k) 和相对吸附平衡常数 (Kads),这些常数可以使用基于多元线性回归 (MLR) 的定量构效关系 (QSPR) 进一步合理化。本文使用商业和分级 BEA 沸石作为多相催化剂,用乙酸酐作为酰化剂,对一组具有不同大小和化学官能团的七种底物进行了 Friedel-Crafts 酰化反应。对催化结果与底物和催化剂的物理化学性质进行了相关性分析。从该分析中,获得了一组稳健的方程,可以推断出控制这些过程的主要因素。毫不奇怪,发现速率和吸附平衡常数部分由共同因素解释,但符号相反:较高和较强的吸附力会增加反应速率,但也会使沸石活性位对新反应物分子的可及性降低。最相关的参数与底物的分子大小有关,这与不同的反应步骤有关,即微孔可及性、扩散能力和分子的极化率。这里使用的相对较大的底物集强化了以前的发现,并进一步深入了解了在多相介质中阻碍/加速 Friedel-Crafts 反应的因素。