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Stabilities of C3-C5 alkoxide species inside H-FER zeolite : a hybrid QM/MM study

Adsorption (π-complex formation) and chemisorption (alkoxide formation) of ethene, propene, 1-butene, and 1-pentene, as well as of isobutene and 2-methyl-1-butene, in zeolite H-FER are examined by a hybrid quantum mechanics/molecular mechanics (QM/MM) method that takes van der Waals (dispersion) int...

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Bibliographic Details
Published in:Journal of catalysis 2005-04, Vol.231 (2), p.393-404
Main Authors: NIEMINEN, Ville, SIERKA, Marek, MURZIN, Dmitry Yu, SAUER, Joachim
Format: Article
Language:English
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Summary:Adsorption (π-complex formation) and chemisorption (alkoxide formation) of ethene, propene, 1-butene, and 1-pentene, as well as of isobutene and 2-methyl-1-butene, in zeolite H-FER are examined by a hybrid quantum mechanics/molecular mechanics (QM/MM) method that takes van der Waals (dispersion) interactions into account. The predicted heats of adsorption (36, 51, 45, 64, 41, 47 kJ/mol, respectively) fall into energy ranges inferred from experimental values for alkanes in H-zeolites. Vibrational frequencies are calculated for adsorbed butenes and butyl alkoxide species and compared with observed spectra for adsorbed 1-butene and isobutene. Primary and secondary alkoxide species are found to be significantly more stable than the adsorption complexes with chemisorption energies between 137 and 205 kJ/mol. The stability increases with the length of the alkyl chain. Geometrical constrictions close to the active site result in reduced stabilities of bulky alkoxide isomers. The tert-butyl and 1,1-dimethylpropyl species are less stable (chemisorption energies of 62 and 78 kJ/mol, respectively) or even nonexistent at sterically hindered framework positions. The implications of relatively stable alkoxide intermediates for hydrocarbon transformation reactions over H-zeolites are discussed.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2005.01.035