Issue 3, 2025

Reversing selectivity of bambusuril macrocycles toward inorganic anions by installing spacious substituents on their portals

Abstract

Two chiral bambusurils, which are diastereomers to each other, show remarkable differences in their binding affinity and selectivity toward inorganic anions as determined by isothermal titration calorimetry. These differences are explained by quantum-chemical calculations.

Graphical abstract: Reversing selectivity of bambusuril macrocycles toward inorganic anions by installing spacious substituents on their portals

Supplementary files

Article information

Article type
Edge Article
Submitted
21 Oct 2024
Accepted
06 Dec 2024
First published
06 Dec 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2025,16, 1288-1292

Reversing selectivity of bambusuril macrocycles toward inorganic anions by installing spacious substituents on their portals

C. Rando, S. Grewal, J. Sokolov, P. Kulhánek and V. Šindelář, Chem. Sci., 2025, 16, 1288 DOI: 10.1039/D4SC07150F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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