Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
66429 | Journal of Molecular Catalysis A: Chemical | 2011 | 8 Pages |
A highly porous metal–organic framework (IRMOF-8) was synthesized by a solvothermal method, and used as an efficient heterogeneous catalyst for the Friedel–Crafts acylation reaction. The solid catalyst was characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), atomic absorption spectrophotometry (AAS), and nitrogen physisorption measurements. High conversions were achieved in the presence of a catalytic amount of the IRMOF-8 (1–5 mol%) without the need for an inert atmosphere. The solid catalyst could be facilely separated from the reaction mixture by simple centrifugation, and could be reused without a significant degradation in catalytic activity. No contribution from homogeneous catalysis of active acid species leaching into the reaction solution was detected.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (128 K)Download as PowerPoint slideHighlights► IRMOF-8 was synthesized and characterized. ► IRMOF-8 was used as catalyst for the Friedel–Crafts acylation reaction. ► High conversions were achieved using catalytic amounts of the IRMOF-8. ► The catalyst could be reused.