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

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.

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Publication Details

Journal
Chemical Science
Published
2024-12-06
DOI
https://doi.org/10.1039/d4sc07150f
Citations
3
Primary Topic
Nanomaterials for catalytic reactions
Type
article
Field-Weighted Citation Impact
0.75

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article

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

Carola Rando, Vladimír Šindelář, Petr Kulhánek, Jan Sokolov et al.
3 citations
Chemical Science
Nanomaterials for catalytic reactions
0.75
article

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

Carola Rando, Vladimír Šindelář, Petr Kulhánek, Jan Sokolov, Surbhi Grewal
article en
3 citations

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.

Chemical ScienceVol. 16(3)
Masaryk University (CZ)
European Commission, Ministerstvo Školství, Mládeže a Tělovýchovy, Grantová Agentura České Republiky, Horizon 2020 Framework Programme, RECETOX Přírodovědecké Fakulty Masarykovy Univerzity
Openalex Percentile: Top 31%
Nanomaterials for catalytic reactions
0.75
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