The nature of the interaction on two different catalysts (zeolite BEA and γ-alumina) of some aromatic substrates, 1,2-methylendioxybenzene, 1,2-ethylendioxybenzene, and 1,2-dimethoxybenzene, have been investigated by FT-IR spectroscopy. FT-IR data suggest that the adsorption of 1,2-methylendioxybenzene occurs through oxygen atoms and the molecule maintains the original puckered conformation, whereas the planar structure due to the absence of a fused ring in the case of 1,2- dimethoxybenzene and the twisted conformation of 1,2-ethylendioxybenzene cause an orientation of the molecules parallel to the catalyst surface, with the benzene ring directly interacting to it. The puckered conformation of MDB leads the benzene ring to be electron-deficient, then deactivated toward alkylation, such as confirmed by the obtained catalytic results, which show that MDB is totally not reactive using the investigated heterogeneous catalysts, while in the traditional homogeneous system shows a reactivity comparable to the other considered substrates.

FT-IR Investigation of Methoxy Substituted Benzenes Adsorbed on Solid Acid Catalysts

LUCARELLI, CARLO;
2012

Abstract

The nature of the interaction on two different catalysts (zeolite BEA and γ-alumina) of some aromatic substrates, 1,2-methylendioxybenzene, 1,2-ethylendioxybenzene, and 1,2-dimethoxybenzene, have been investigated by FT-IR spectroscopy. FT-IR data suggest that the adsorption of 1,2-methylendioxybenzene occurs through oxygen atoms and the molecule maintains the original puckered conformation, whereas the planar structure due to the absence of a fused ring in the case of 1,2- dimethoxybenzene and the twisted conformation of 1,2-ethylendioxybenzene cause an orientation of the molecules parallel to the catalyst surface, with the benzene ring directly interacting to it. The puckered conformation of MDB leads the benzene ring to be electron-deficient, then deactivated toward alkylation, such as confirmed by the obtained catalytic results, which show that MDB is totally not reactive using the investigated heterogeneous catalysts, while in the traditional homogeneous system shows a reactivity comparable to the other considered substrates.
Lucarelli, Carlo; Giugni, A.; Morosi, G.; Vaccari, A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/1790140
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