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• W2112514319 abstract "The concepts of confinement- and molecular recognition-driven chemical reactivity of cation-exchanged zeolites is illustrated by our recent results from periodic and cluster density functional theory (DFT) calculations. The reactivity of alkali-earth- and alkaline-exchanged low-silica zeolites for selective photo-oxidation of alkenes with molecular oxygen and for N2O4 disproportionation is shown to be mainly due to the specific arrangement and the size of the cations in the zeolite cage. An attempt is made to separate the effects of basicity of the framework, the Lewis acidity of the extra-framework cations and the electrostatic field in the zeolite cage as well as its geometrical properties for the respective reactions. The importance of the favorable adsorption fashion of the reagents controlled by noncovalent interactions with the microporous matrix is shown. The role of the weak interactions with the zeolite walls and the factors, which determine the preference for a particular adsorption mode, are discussed by the example of light alkanes adsorption to Mg- and Ca-exchanged faujasites. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010" @default.
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• W2112514319 date "2010-01-01" @default.
• W2112514319 modified "2023-10-16" @default.
• W2112514319 title "Molecular recognition in cation-exchanged zeolites" @default.
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• W2112514319 doi "https://doi.org/10.1002/qua.22251" @default.
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