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dc.contributor.authorBurguete, M. Isabel
dc.contributor.authorMartí-Centelles, Vicente
dc.contributor.authorGalindo, Francisco
dc.contributor.authorIzquierdo Arcusa, María Ángeles
dc.contributor.authorKumar, Krishna
dc.contributor.authorWhite, Andrew J. P.
dc.contributor.authorLuis, Santiago V.
dc.contributor.authorVilar, Ramón
dc.date.accessioned2013-04-25T11:09:07Z
dc.date.available2013-04-25T11:09:07Z
dc.date.issued2012
dc.identifier.issn0022-3263
dc.identifier.issn1520-6904
dc.identifier.urihttp://hdl.handle.net/10234/62226
dc.description.abstractTwo new pseudopeptidic molecules (one macrocyclic and one open chain) containing an acridine unit have been prepared. The fluorescence response of these receptors to a series of acids was measured in CHCl3. Receptors are selective to H2PO4– versus HSO4–, and an even higher selectivity is found over other anions such as Cl–, Br–, CH3COO–, and CF3COO–. We show that the macrocyclic receptor is more selective for H2PO4– than the related open chain receptor. The supramolecular interactions of triprotonated receptors with different anions have been modeled in silico and have been studied by different experimental techniques. Optimized geometries obtained by computational calculations agree well with experimental data, in particular fluorescence experiments, suggesting that the selective supramolecular interaction takes places through coordination of the anions to the triprotonated form of the receptor.ca_CA
dc.format.extent10 p.ca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.relation.isPartOfJournal of Organic Chemistry, 77, 1ca_CA
dc.rightsCopyright © 2011 American Chemical Societyca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectfluorescence experimentsca_CA
dc.subjectH2PO4ca_CA
dc.subjectacridineca_CA
dc.titleFluorescent Acridine-Based Receptors for H2PO4–ca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/jo202077v
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://pubs.acs.org/doi/abs/10.1021/jo202077vca_CA


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