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

• Published in: Journal of catalysis Vol. 261; no. 1; pp. 75 - 87
• Main Authors: Gascon, Jorge, Aktay, Ugur, Hernandez-Alonso, Maria D., van Klink, Gerard P.M., Kapteijn, Freek
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Inc 2009; Elsevier; Elsevier BV
• Subjects: Base-catalyzed reactions; Catalysis; Catalysts; Chemistry; Colloidal state and disperse state; Exact sciences and technology; Functional organic sites; General and physical chemistry; Heterogeneous catalysis; IRMOF-3; Knoevenagel condensation; Metal-organic frameworks; Metals; MIL-53; MOF; Organic chemistry; Porous materials; Surface physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Functional organic sites; Heterogeneous catalysis; MOF; Knoevenagel condensation; MIL-53; Base-catalyzed reactions; IRMOF-3; Metal-organic frameworks; Basic site; Amino group; Selectivity; Solid; Aniline; Reaction mechanism; Diffusion; Base reaction; Catalytic reaction; Pore structure; Benzaldehyde; Topology; Aldehyde; Infrared spectrometry; Adsorption; Homogeneous catalysis; Benzenic compound; Alkalinity; Catalyst
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2008.11.010

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-3 DEF exhibits 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 p K a 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. Metal organic frameworks (MOFs) with non-coordinated amino groups are shown to be stable solid basic catalysts. 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.