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dc.contributor.authorDavid, Arthur H. G.
dc.contributor.authorCasares, Raquel
dc.contributor.authorCuerva Carvajal, Juan Manuel 
dc.contributor.authorGonzález Campaña, Araceli 
dc.contributor.authorBlanco Suárez, Víctor 
dc.date.accessioned2025-01-27T10:46:59Z
dc.date.available2025-01-27T10:46:59Z
dc.date.issued2019-10-22
dc.identifier.citationJ. Am. Chem. Soc. 2019, 141, 45, 18064–18074es_ES
dc.identifier.urihttps://hdl.handle.net/10481/100499
dc.description.abstractA rotaxane-based molecular shuttle has been synthesized in which the switching of the position of a fluorescent macrocycle on the thread turns “on” or “off” the circularly polarized luminescence (CPL) of the system while maintaining similar fluorescence profiles and quantum yields in both states. The chiroptical activity relies on the chiral information transfer from an ammonium salt incorporating D or L-phenylalanine residues as chiral stereogenic covalent units to an otherwise achiral crown ether macrocycle bearing a luminescent 2,2’-bipyrene unit when they interact through hydrogen bonding. Each enantiomeric thread induces CPL responses of opposite signs on the macrocycle. Upon addition of base, the switching of the position of the macrocycle to a triazolium group disables the chiral information transfer to the macrocycle, switching “off” the CPL response. The in situ switching upon several acid/base cycles is also demonstrated.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleA [2]Rotaxane-Based Circularly Polarized Luminescence Switches_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doihttps://doi.org/10.1021/jacs.9b07143
dc.type.hasVersionAMes_ES


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