Amino-based metal-organic frameworks as stable, highly active basic catalysts

by J. Gascon, U. Aktay, M.D. Hernandez-Alonso, G.P.M. Van Klink, F. Kapteijn
Year: 2009 ISSN: DOI: 10.1016/j.memsci.2009.05.006


J. Gascon, U. Aktay, M.D. Hernandez-Alonso, G.P.M. van Klink, F. Kapteijn, J. Catal. 261 (2009) 75-87, Amino-based metal-organic frameworks as stable, highly active basic catalysts


​​Metal-organic frameworks (MOFs) with non-coordinated amino groups, i.e. IRMOF-3 and amino-functionalized MIL-53, are stable solid basic catalysts in the Knoevenagel condensation of ethyl cyanoacetate and ethyl acetoacetate with benzaldehyde. IRMOF-3DEFexhibits activities that are at least as high as the most active solid basic catalysts reported, with a 100% selectivity to the condensation product. For IRMOF-3 samples the catalytic activity correlated with the accessibility of the basic sites. Diffusion limitations could be excluded for this most active catalyst. A new MOF based on the MIL-53 topology and non-coordinated amino groups has been synthesized and characterized. Although active its poor performance in the studied Knoevenagel condensations is attributed to strong adsorption and diffusion limitations in the 1-D pore structure of this framework. The performance of the IRMOF-3 catalysts demonstrates that the basicity of the aniline-like amino group is enhanced when incorporated inside the MOF structure, increasing the pKa of the basic catalyst and more active than aniline as homogeneous catalyst. The IRMOF-3 catalysts are stable under the studied reaction conditions, and could be reused without significant loss in activity. The catalytic performance of IRMOF-3 in various solvents suggests that this open, accessible and well-defined structure behaves more like homogeneous basic catalysts, in contrast to other solid basic catalysts. By means of DRIFTS, the reaction mechanism has been elucidated, showing spectroscopic evidence of benzaldimine intermediates.​


IRMOF-3 MIL-53 MOF Metal-organic frameworks Knoevenagel condensation Base-catalyzed reactions Functional organic sites Heterogeneous Catalysis