Ultrasound-promoted synthesis of a copper-iron-based catalyst for the microwave-assisted acyloxylation of 1,4-dioxane and cyclohexene

A copper-iron-based catalyst has been prepared by a low-temperature co-precipitation and sonication method. The use of high-energy ultrasound reduces the time required for the preparation process from one workweek to one day with respect to the catalysts obtained by conventional coprecipitation and...

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Published inOrganic & biomolecular chemistry Vol. 21; no. 3; pp. 59 - 599
Main Authors Macías-Benítez, Pablo, Sierra-Padilla, Alfonso, Yeste, M. Pilar, Palacios-Santander, José María, Cubillana-Aguilera, Laura, Gatica, José M, Vidal, Hilario, Guerra, Francisco M, Moreno-Dorado, F. Javier
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 18.01.2023
Royal Society of Chemistry
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Summary:A copper-iron-based catalyst has been prepared by a low-temperature co-precipitation and sonication method. The use of high-energy ultrasound reduces the time required for the preparation process from one workweek to one day with respect to the catalysts obtained by conventional coprecipitation and thermal treatment methods. The resulting material has been characterized at compositional, textural, structural, and chemical levels by ICP-AES, BET, SEM-EDS, XRD, TEM, and FTIR among other techniques. The material shows catalytic activity in the acyloxylation reaction of 1,4-dioxane and cyclohexene under microwave irradiation. In parallel with the optimized catalyst synthesis, the use of microwaves allowed for a substantial improvement in the outcome of the reaction in terms of cleanliness, yield, and time. A copper-iron-based catalyst has been prepared by a low-temperature co-precipitation and sonication method. The material shows catalytic activity in the acyloxylation reaction of 1,4-dioxane and cyclohexene under microwave irradiation.
Bibliography:Electronic supplementary information (ESI) available. See DOI
https://doi.org/10.1039/d2ob02117j
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1477-0520
1477-0539
DOI:10.1039/d2ob02117j