A group of scientists, led by Professor Joost Reek from the University of Amsterdam’s Van ‘t Hoff Institute for Molecular Sciences (HIMS), has developed a new approach in enhancing catalytic performance. In the current issue of Nature Chemistry they present functionalized, self-assembled nanospheres that enable highly efficient catalytic conversion by acting as “nanocentrators.”
The research, which is part of UvA’s research priority area Sustainable Chemistry, was funded through Joost Reek’s ERC Advanced Grant in “Nature Inspired Transition Metal Catalysis.”
The new catalytic nanosphere concept was inspired by the working principles of natural enzymes. These bind molecules in well-defined pockets close to their active sites, thus introducing a pre-organization that facilitates highly efficient transformations. The researchers mimic this enzymatic behavior in synthetic nanocontainers, which can contain very high local catalyst concentrations and further enhances the catalytic performance.
The new nanocontainers are formed by self-assembly: mixing 12 palladium metals and 24 so-called ditopic nitrogen ligands leads to formation of nano-sized spheres. The ligands are modified with guanidinium binding motifs so that the resulting nanocontainers are able to bind sulfonates and carboxylates in their interior. Sulfonate guests are thereby bound much more strongly than carboxylates because of so-called cooperative binding (employing multiple binding sites). The researchers use this to firmly fix the sulfonated gold-based catalyst, while the remaining binding sites are available for the pre-organisation of the carboxylate moieties that are to be converted (the substrates).
The working principles of this “nanoconcentrator” system were established using a gold-catalyzed cyclization reaction (shown above). The local high concentration of the metal catalyst combined with the pre-organization of the substrate resulted in dramatically enhanced reaction rates in comparison to common systems where the catalyst and the reactants are not pre-organized but just both dissolved in a solvent. Reaction rates usually increase with catalyst and substrate concentration; however this is generally limited by solubility issues or unfavorable catalyst/reactant ratios. This issue has now been solved by taking advantage of local concentrations in the self-assembled nanoconcentrator.
Since many existing metal catalysts are utilized with sulfonate groups (generally to make them water soluble), the presented nanoconcentrator system potentially provides a widely applicable general strategy to many different reactions. Furthermore, the researchers established that the encapsulated sulfonate-containing gold catalysts did not (or only slowly) convert neutral (acid) substrates. This provides a starting point for the development of more complex catalyst systems with substrate-selective catalysis and base-triggered on/off switching.
Release Date: January 12, 2016
Source: University of Amsterdam