Molten ligand synthesis method and luminescence study of Re3+ complexes with adipate

dc.contributor.authorASSUNÇAO, I.P.
dc.contributor.authorBRITO, H.F.
dc.contributor.authorFELINTO, M.C.F.C.
dc.contributor.authorMALTA, O.L.
dc.coverageInternacionalpt_BR
dc.creator.eventoBRAZILIAN MEETING ON INORGANIC CHEMISTRY, 18thpt_BR
dc.date.accessioned2017-05-10T12:57:24Z
dc.date.available2017-05-10T12:57:24Z
dc.date.eventoSeptember 25-30, 2016pt_BR
dc.description.abstractThe rare earth ions (RE3+) luminescent compounds have attracted much interest in the last few years, due to their intrinsic spectroscopic behavior and commercial applications in different areas such as: organic light-emitting diodes (OLEDs), optical markers, catalyses1,2 etc. This work presents the molten ligand synthesis method of RE3+ complexes, characterization and luminescent properties of the [RE2(ADP)3(DPSE)3] compound where RE: Eu3+ and Tb3+; ADP: adipic acid (hexanedioic acid) and DPSE: diphenyl sulfone. The lanthanides complexes were synthetized by molten ligand solid state method that, to the best of our knowloedge, it is unreported in the literature for this compounds, using the rare earth chloride and the ADP and DPSE ligands, which have the advantage of present low melting points at around 96 and 152 ºC, respectively. The characterization of the complexes were carried out via elemental analysis (CHN), thermal analysis (TG/DTG), x-ray diffraction by the powder method (XPD) and infrared spectroscopy with Fourier transform (FTIR). The infrared absorption spectra indicate that the ligand-metal interaction is via chelate-bridging and their XPD patterns suggest high crystallinity and that the complexes present isomorphic character. The principal photoluminescence properties were determined based on the emission spectra of the Eu3+ and Tb3+ complexes, presenting a strong intense red and green emission colors, under UV excitation at 394 and 378 nm, respectively. Moreover, the spectra show narrow emission bands characteristic of the 5D0→7F0-4 transitions of the Eu3+ and the 5D4→7F6-0 transitions of Tb3+ ion. The absence of the broad emission band from the triplet states (T1) of the organic ligands in the spectral range from 400 to 600 nm is also consistent with an efficient ligand-to-metal intramolecular energy transfer to the emitting levels of Eu3+ and Tb3+ in the complexes. The emission quantum efficiency of 5D0 level and the 4f−4f experimental intensity parameters of the Eu3+ ion will be discussed.pt_BR
dc.event.siglaBMICpt_BR
dc.identifier.citationASSUNÇAO, I.P.; BRITO, H.F.; FELINTO, M.C.F.C.; MALTA, O.L. Molten ligand synthesis method and luminescence study of Re3+ complexes with adipate. In: BRAZILIAN MEETING ON INORGANIC CHEMISTRY, 18th, September 25-30, 2016, São Pedro, SP. <b>Abstract...</b> Disponível em: http://repositorio.ipen.br/handle/123456789/27433.
dc.identifier.orcidhttps://orcid.org/0000-0001-7028-0878
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/27433
dc.local.eventoSão Pedro, SPpt_BR
dc.rightsopenAccesspt_BR
dc.titleMolten ligand synthesis method and luminescence study of Re3+ complexes with adipatept_BR
dc.typeResumo de eventos científicospt_BR
dspace.entity.typePublication
ipen.autorISRAEL P ASSUNçãO
ipen.autorMARIA CLAUDIA FRANCA DA CUNHA FELINTO
ipen.autorHERMI FELINTO DE BRITO
ipen.codigoautor15750
ipen.codigoautor1103
ipen.codigoautor3651
ipen.contributor.ipenauthorISRAEL P ASSUNçãO
ipen.contributor.ipenauthorMARIA CLAUDIA FRANCA DA CUNHA FELINTO
ipen.contributor.ipenauthorHERMI FELINTO DE BRITO
ipen.date.recebimento17-05pt_BR
ipen.event.datapadronizada2016pt_BR
ipen.identifier.ipendoc23732pt_BR
ipen.notas.internasAbstractpt_BR
ipen.type.genreResumo
relation.isAuthorOfPublication56e651b7-08d7-45de-ac45-4f5e8bd6280c
relation.isAuthorOfPublication1333caab-4e1b-4dd8-83b4-3f2013c0ce22
relation.isAuthorOfPublicationd5cd2f04-1d13-4c0d-a260-228b39274c42
relation.isAuthorOfPublication.latestForDiscovery56e651b7-08d7-45de-ac45-4f5e8bd6280c
sigepi.autor.atividadeBRITO, H.F.:3651:750:Npt_BR
sigepi.autor.atividadeFELINTO, M.C.F.C.:1103:750:Npt_BR
sigepi.autor.atividadeASSUNÇAO, I.P.:15750:750:S

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