Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Red-green Emitting And Superparamagnetic Nanomarkers Containing Fe3o4 Functionalized With Calixarene And Rare Earth Complexes
Author: Khan L.U.
Brito H.F.
Holsa J.
Pirota K.R.
Muraca D.
Felinto M.C.F.C.
Teotonio E.E.S.
Malta O.L.
Abstract: The design of bifunctional magnetic luminescent nanomaterials containing Fe3O4 functionalized with rare earth ion complexes of calixarene and β-diketonate ligands is reported. Their preparation is accessible through a facile one-pot method. These novel Fe3O4@calix-Eu(TTA) (TTA = thenoyltrifluoroacetonate) and Fe3O4@calix-Tb(ACAC) (ACAC = acetylacetonate) magnetic luminescent nanomaterials show interesting superparamagnetic and photonic properties. The magnetic properties (M-H and ZFC/FC measurements) at temperatures of 5 and 300 K were explored to investigate the extent of coating and the crystallinity effect on the saturation magnetization values and blocking temperatures. Even though magnetite is a strong luminescence quencher, the coating of the Fe3O4 nanoparticles with synthetically functionalized rare earth complexes has overcome this difficulty. The intramolecular energy transfer from the T1 excited triplet states of TTA and ACAC ligands to the emitting levels of Eu3+ and Tb3+ in the nanomaterials and emission efficiencies are presented and discussed, as well as the structural conclusions from the values of the 4f-4f intensity parameters in the case of the Eu3+ ion. These novel nanomaterials may act as the emitting layer for the red and green light for magnetic light-converting molecular devices (MLCMDs).
Editor: American Chemical Society
Citation: Inorganic Chemistry. American Chemical Society, v. 53, n. 24, p. 12902 - 12910, 2014.
Rights: fechado
Identifier DOI: 10.1021/ic5018856
Date Issue: 2014
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
2-s2.0-84920200824.pdf4.11 MBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.