Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/10381
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dc.contributor.authorPina, João-
dc.contributor.authorMelo, J. Seixas de-
dc.contributor.authorPina, Fernando-
dc.contributor.authorLodeiro, Carlos-
dc.contributor.authorLima, J. C.-
dc.contributor.authorParola, A. Jorge-
dc.contributor.authorSoriano, Conxa-
dc.contributor.authorPaz Clares, M.-
dc.contributor.authorAlbelda, M. Teresa-
dc.date.accessioned2009-06-26T12:07:27Z-
dc.date.available2009-06-26T12:07:27Z-
dc.date.issued2005-10-17-
dc.identifier.citationInorganic Chemistry. 44:21 (2005) 7449-7458en_US
dc.identifier.issn0020-1669-
dc.identifier.urihttps://hdl.handle.net/10316/10381-
dc.description.abstractA new fluorescent macrocyclic structure (L1) bearing two naphthalene units at both ends of a cyclic polyaminic chain containing two phenanthroline units was investigated with potentiometric and fluorescence (steady-state and time-resolved) techniques. The fluorescence emission spectra show the simultaneous presence of three bands: a short wavelength emission band (naphthalene monomer), a middle emission band (phenanthroline emission), and a long-wavelength band. All three bands were found to be dependent on the protonation state of the macrocyclic unit (including the polyaminic and phenanthroline structures). The existence of the long-wavelength emission band is discussed and is shown to imply that a bending movement involving the two phenanthroline units leads to excimer formation. This is determined by comparison with the excimer emission formed by intermolecular association of 1,10-phenanthroline. With ligand L1, excimer formation occurs only at pH values above 4. At very acidic pH values, the protonation of the polyamine bridges is extensive leading to a rigidity of the system that precludes the bending movement. The interaction with metal cations Zn(II) and Cu(II) was also investigated. Excimer formation is, in these situations, increased with Zn(II) and decreased with Cu(II). The long-emission band is shown to present a different wavelength maximum, depending on the metal, which can be considered as a characteristic to validate the use of ligand L1 as a sensor for a given metal.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsopenAccesseng
dc.titleSpectroscopy and Coordination Chemistry of a New Bisnaphthalene−Bisphenanthroline Ligand Displaying a Sensing Ability for Metal Cationsen_US
dc.typearticleen_US
dc.identifier.doi10.1021/ic050733q-
uc.controloAutoridadeSim-
item.openairetypearticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-1848-1167-
crisitem.author.orcid0000-0001-9708-5079-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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