Tuning artificial oxidase catalysis by cavity modification
Previously, the ketone-bridged α-cyclodextrin derivative 6<sup>A</sup>,6<sup>D</sup>-di-<i>O</i>-propan-2-on-1,3-diyl α-cyclodextrin-6<sup>A</sup>,6<sup>D</sup>-dicarboxylate (2) was shown to be a potent artificial oxidase. In this work, a new isomer of this compound 6<sup>A</sup>,6<sup>D</sup>-di-<i>O</i>-propan-2-on-1,3-diyl 3<sup>A</sup>,3<sup>D</sup>-diepi-α-cyclodextrin-6<sup>A</sup>,6<sup>D</sup>-dicarboxylate 12 was synthesized and its catalytic properties were investigated and compared to those of 2. The catalyst 12 was also an excellent artificial enzyme exhibiting <i>k</i><sub>cat</sub> values 0.2 to 1.1 times and <i>K</i><sub>m</sub> values 0.1 to 4 times higher than those of 2. The reduced cavity size and the formation of a hydrogen bond are the primary factors affecting the catalytic performance.
Authors
- Mikael Bols (ORCID: https://orcid.org/0000-0002-6561-6952)
- Mingzhe Ren
Institutions
- University of Copenhagen (DK)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5ob01574j
- Primary Topic
- Enzyme Catalysis and Immobilization
- Type
- article
- Field-Weighted Citation Impact
- 0.00