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Glucose Binding Drives Reconfiguration of a Dynamic Library of Urea‐Containing Metal–Organic Assemblies

2020; Wiley; Volume: 60; Issue: 9 Linguagem: Inglês

10.1002/anie.202014568

1521-3773

Dong Yang, Larissa K. S. von Krbek, Le Yu, Tanya K. Ronson, John D. Thoburn, John P. Carpenter, Jake L. Greenfield, Duncan J. Howe, Biao Wu, Jonathan R. Nitschke,

Supramolecular Self-Assembly in Materials

A bis-urea-functionalized ditopic subcomponent assembled with 2-formylpyridine and FeII , resulting in a dynamic library of metal-organic assemblies: an irregular FeII4 L6 structure and three FeII2 L3 stereoisomers: left- and right-handed helicates and a meso-structure. This library reconfigured in response to the addition of monosaccharide derivatives, which served as guests for specific library members, and the rate of saccharide mutarotation was also enhanced by the library. The (P) enantiomer of the FeII2 L3 helical structure bound β-D-glucose selectively over α-D-glucose. As a consequence, the library collapsed into the (P)-FeII2 L3 helicate following glucose addition. The α-D-glucose was likewise transformed into the β-D-anomer during equilibration and binding. Thus, β-D-glucose and (P)-3 amplified each other in the product mixture, as metal-organic and saccharide libraries geared together into a single equilibrating system.