A magnetic metal organic framework material as a highly efficient and recyclable catalyst for synthesis of cyclohexenone derivatives
A magnetic metal–organic framework, γ-Fe2O3@SiO2/IRMOF-3, has been prepared and identified as an efficient heterogeneous catalyst for the synthesis of cyclohexenone derivatives by reaction of aldehyde and acetoacetanilide under solvent-free conditions. The magnetic COF catalyst can also be convenien...
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Published in | Journal of catalysis Vol. 387; pp. 39 - 46 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.07.2020
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Subjects | |
Online Access | Get full text |
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Summary: | A magnetic metal–organic framework, γ-Fe2O3@SiO2/IRMOF-3, has been prepared and identified as an efficient heterogeneous catalyst for the synthesis of cyclohexenone derivatives by reaction of aldehyde and acetoacetanilide under solvent-free conditions. The magnetic COF catalyst can also be conveniently recycled and recycled through additional external magnets without considerable loss of its catalytic activity.
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•Preparation of a magnetic metal–organic framework material.•The magnetic material exhibits high catalytic activity for the synthesis of cyclohexenone derivatives.•The catalyst is easy to magnetically separate and reuse.
A magnetic metal–organic framework, γ-Fe2O3@SiO2/IRMOF-3, has been prepared and characterized. This magnetically separable catalyst exhibited high catalytic activity for the synthesis of cyclohexenone derivatives by reaction of aldehyde and acetoacetanilide under solvent-free conditions. The protocol has several advantages in terms of superior efficiency, high yield, the short reaction time, mild and environmentally benign conditions. Magnetic COF catalyst can also be conveniently recycled and recycled through additional external magnets, showing greater interest in practical applications. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0021-9517 1090-2694 |
DOI: | 10.1016/j.jcat.2020.04.013 |