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dc.rights.licenseopenen_US
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorHESS, Robin
dc.contributor.authorBRENET, Marius
dc.contributor.authorRAJAONARIVELO, Haingo
dc.contributor.authorGAUTHIER, Maxime
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorKOEHLER, Victor
dc.contributor.authorWAELES, Philip
dc.contributor.authorHUC, Ivan
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorFERRAND, Yann
dc.contributor.authorCOUTROT, Frédéric
dc.date.accessioned2025-02-11T15:20:21Z
dc.date.available2025-02-11T15:20:21Z
dc.date.issued2024-12-09
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/204798
dc.description.abstractEnAbstract The design of a dynamically assembled foldarotaxane was envisioned with the aim of operating as a two cascading trigger‐based molecular shuttle. Under acidic conditions, both the macrocycle and helix were localized around their respective best molecular stations because they are far enough from each other not to alter the stability of complexes. The pH‐dependent localization of the macrocycle along the encircled axle allowed us to modulate the association between the helical foldamer and its sites of interaction on the axle. Under kinetic control—at low concentration and room temperature—when the foldarotaxane supramolecular architecture is kinetically stable, the pH‐responsive translation of the macrocycle along the thread triggered the gliding of the helix away from its initial best station. At higher concentration—when helix assembly/disassembly process is accelerated—the system reached the equilibrium state. A new foldarotaxane isomer then appeared through the change of the relative position of the helix and macrocycle along the thread. In this isomer, the helix segregated the macrocycle away from its best station. The fine control of the kinetic and thermodynamic processes, combined with the control of pH, allowed the reciprocal segregation of the helix or the ring away from their respective best sites of interaction.
dc.description.sponsorshipDes FoldaRotaxanes pour la Synthèse généralisée de Molécules Entrelacées Improbablesen_US
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subject.enFoldamers
dc.subject.enFoldarotaxanes
dc.subject.enMolecular shuttles
dc.subject.enRotaxanes
dc.subject.enSelf-assembly
dc.title.enCascading Macrocycle and Helix Motions in a Foldarotaxane Molecular Shuttle
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/anie.202413977en_US
dc.subject.halChimie/Matériauxen_US
dc.identifier.pubmed39248768en_US
bordeaux.journalAngewandte Chemie International Editionen_US
bordeaux.pagee202413977en_US
bordeaux.volume63en_US
bordeaux.hal.laboratoriesCBMN : Chimie & de Biologie des Membranes & des Nano-objets - UMR 5248en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccCC BY-NC-NDen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.date=2024-12-09&rft.volume=63&rft.spage=e202413977&rft.epage=e202413977&rft.au=HESS,%20Robin&BRENET,%20Marius&RAJAONARIVELO,%20Haingo&GAUTHIER,%20Maxime&KOEHLER,%20Victor&rft.genre=article


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