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Supramolecular interactions between catalytic species allow rational control over reaction kinetics

Teunissen, A.J.P.; Paffen, T.F.E.; Filot, I.A.W.; Lanting, M.D.; van der Haas, R.J.C.; de Greef, T.F.A.; Meijer, E.W.

Journal article 2019 Open access
6 Citations Scopus
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Yes Open access Gold OA

Abstract

The adaptivity of biological reaction networks largely arises through non-covalent regulation of catalysts' activity. Such type of catalyst control is still nascent in synthetic chemical networks and thereby hampers their ability to display life-like behavior. Here, we report a bio-inspired system in which non-covalent interactions between two complementary phase-transfer catalysts are used to regulate reaction kinetics. While one catalyst gives bimolecular kinetics, the second displays autoinductive feedback, resulting in sigmoidal kinetics. When both catalysts are combined, the interactions between them allow rational control over the shape of the kinetic curves. Computational models are used to gain insight into the structure, interplay, and activity of each catalytic species, and the scope of the system is examined by optimizing the linearity of the kinetic curves. Combined, our findings highlight the effectiveness of regulating reaction kinetics using non-covalent catalyst interactions, but also emphasize the risk for unforeseen catalytic contributions in complex systems and the necessity to combine detailed experiments with kinetic modelling.

Abstract from OpenAlex , checked 2026-06-29.

Citation

Teunissen, A.J.P.; Paffen, T.F.E.; Filot, I.A.W.; Lanting, M.D.; van der Haas, R.J.C.; de Greef, T.F.A.; Meijer, E.W. Supramolecular interactions between catalytic species allow rational control over reaction kinetics. Chem. Sci. 2019, 10, 9115-9124. 10.1039/C9SC02357G

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Citation markers are read from Scopus when configured, with public DOI metadata as fallback, and cached locally. They can differ from Pure counts shown on institutional portals. Checked 2026-07-09 via Scopus.