Improving catalysis through nanoconcentrator systems

Functionalised self-assembled nanospheres enable highly efficient catalytic conversion

12 January 2016

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 functionalised, 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'.

Joost Reek, photo by Jan Willem Steenmeijer

Prof. Joost Reek.

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-organisation that facilitates highly efficient transformations. The researchers mimic this enzymatic behaviour in synthetic nanocontainers, which can contain very high local catalyst concentrations and further enhances the catalytic performance.

Self-assembly

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).

Schematic nanoconcentrator Joost Reek

Schematic representation of the working principle of the nanoconcentrator. The gold(I) catalysts (drawn in red) are located in the sphere. Once the substrate (in black) is deprotonated the anionic substrate (in green) enters the sphere to pre-organize close to the catalyst via hydrogen bonding to the guanidine-binding site (displayed in blue). After rapid conversion of the substrate, the neutral cyclic product leaves the sphere. Image: HIMS.

Enhanced reaction rates

The working principles of this 'nanoconcentrator' system were established using a gold-catalysed 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-organised 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.

Widely applicable strategy

Catalysis in nanospheres

Image: HIMS.

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.

Article:

Qi-Qiang Wang, Sergio Gonell, Stefan H. A. M. Leenders, Maximilian Dürr, Ivana Ivanović-Burmazović & Joost N. H. Reek: Self-assembled nanospheres with multiple endohedral binding sites pre-organize catalysts and substrates for highly efficient reactions Nature Chemistry (2016) AOP 12 January 2016 doi:10.1038/nchem.2425

Published by  HIMS