Redox-controlled hybridization of helical foldamers
Résumé
Tetrathiafulvalene redox units were grafted at both extremities of an oligopyridine–dicarboxamide foldamer through a straightforward copper-catalyzed azide–alkyne cycloaddition. The present work demonstrates that the hybridization equilibrium of foldamers can be tuned through redox stimulations.
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