Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/9599
Full metadata record
DC FieldValueLanguage
dc.contributor.authorLazarides, T.en
dc.contributor.authorAlamiry, M. A. H.en
dc.contributor.authorAdams, H.en
dc.contributor.authorPope, S. J. A.en
dc.contributor.authorFaulkner, S.en
dc.contributor.authorWeinstein, J. A.en
dc.contributor.authorWard, M. D.en
dc.date.accessioned2015-11-24T16:50:22Z-
dc.date.available2015-11-24T16:50:22Z-
dc.identifier.issn1477-9226-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9599-
dc.rightsDefault Licence-
dc.subjectphotoinduced energy-transferen
dc.subjectvisible-light sensitizationen
dc.subjectlanthanide complexesen
dc.subjectphotophysical propertiesen
dc.subjectexciplex formationen
dc.subjectenhanced emissionen
dc.subjectpolar mediaen
dc.subjecttransitionen
dc.subjectacceptoren
dc.subjectcationsen
dc.titleAnthracene as a sensitiser for near-infrared luminescence in complexes of Nd(III), Er(III) and Yb(III): an unexpected sensitisation mechanism based on electron transferen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1039/B700714k-
heal.identifier.secondary<Go to ISI>://000245379800005-
heal.identifier.secondaryhttp://pubs.rsc.org/en/content/articlepdf/2007/dt/b700714k-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2007-
heal.abstractThe ligand L-1, which contains a chelating 2-(2-pyridyl) benzimidazole (PB) unit with a pendant anthacenyl group An connected via a methylene spacer, (L-1 = PB-An), was used to prepare the 8-coordinate lanthanide(III) complexes [Ln(hfac)(3)(L-1)] ( Ln = Nd, Gd, Er, Yb) which have been structurally characterised and all have a square antiprismatic N2O6 coordination geometry. Whereas free L-1 displays typical anthracene-based fluorescence, this fluorescence is completely quenched in its complexes. The An group in L-1 acts as an antenna unit: in the complexes [ Ln( hfac) 3( L1)] ( Ln = Nd, Er, Yb) selective excitation of the anthracene results in sensitised near-infrared luminescence from the lanthanide centres with concomitant quenching of An fluorescence. Surprisingly, the anthracene fluorescence is also quenched even in the Gd( III) complex and in its Zn(II) adduct in which quenching via energy transfer to the metal centre is not possible. It is proposed that the quenching of anthracene fluorescence in coordinated L-1 arises due to intra-ligand photoinduced electron-transfer from the excited anthracene chromophore (1)An* to the coordinated PB unit generating a short-lived charge-separated state [An(.+) -PB.-] which collapses by back electron-transfer to give (3)An*. This electron-transfer step is only possible upon coordination of L-1 to the metal centre, which strongly increases the electron acceptor capability of the PB unit, such that (1)An* -> PB PET is endoergonic in free L-1 but exergonic in its complexes. Thus, rather than a conventional set of steps ((1)An* -> (3)An* -> Ln), the sensitization mechanism now includes (1)An* -> PB photoinduced electron transfer to generate charge-separated [An(.+) - PB.-], then back electron-transfer to generate (3)An* which finally sensitises the Ln(III) centre via energy transfer. The presence of (3)An* in L-1 and its complexes is confirmed by nanosecond transient absorption studies, which have also shown that the 3An* lifetime in the Nd( III) complex matches the rise time of Nd-centred near-infrared emission, confirming that the final step of the sequence is (3)An* -> Ln( III) energy-transfer.en
heal.publisherRoyal Society of Chemistryen
heal.journalNameDalton Transactionsen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

Files in This Item:
File Description SizeFormat 
Lazarides-2007-Anthracene as a sens.pdf241.94 kBAdobe PDFView/Open    Request a copy


This item is licensed under a Creative Commons License Creative Commons