Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/86564

TítuloNew 2,6-Bis(5-phenyloxazolyl)pyridine ligands for luminescent LnIII complexes
Autor(es)Carvalho, André
Ferreira, Paula M. T.
Martins, J. A. R.
Palavras-chavepyridine-bis-(5-phenyloxazolyl) ligands
Lanthanides
luminescence
Data18-Nov-2022
EditoraMDPI
RevistaChemistry Proceedings
CitaçãoCarvalho, A.; Ferreira, P.M.T.; Martins, J.A. New 2,6-Bis(5-phenyloxazolyl)pyridine Ligands for Luminescent LnIII Complexes. Chem. Proc. 2022, 12, 56. https://doi.org/10.3390/ecsoc-26-13714
Resumo(s)Lanthanide (Ln(III)) luminescent complexes have been attracting interest for technological applications and molecular imaging. The luminescence of Ln(III)) ions is weak and depends on the use of light absorbing coordination ligands which sensitizes the lanthanide ion. A large variety of coordination ligands has been screened such as dipicolinates, oligo-pyridines, cyclen and crown ether derivatives, porphyrins, cryptands or calixarenes. In our research group we have developed an expeditious methodology to prepare bis(oxazolyl)pyridine ligands for LnIII from threonine and 2,6-pyridinedicarbonyl dichloride. In this work, two new pyridine-bis-oxazolyl ligands with an aromatic ring in position 5 of the oxazole ring were prepared from phenyl-serine and 2,6-pyridinedicarbonyl dichloride. The photophysical properties of compounds 1 and 2 were studied in acetonitrile and in Tris-HCl buffer (0.1 M, pH 7.1). These compounds were used for complexation with Eu(III) and/or Tb(III) ions and the photophysical properties of the complexes studied. Luminescence titrations with anhydrous EuCl3 and TbCl3 allowed the determination of the stoichiometry of the complexes and of the stability constants.
TipoArtigo em ata de conferência
URIhttps://hdl.handle.net/1822/86564
DOI10.3390/ecsoc-26-13714
e-ISSN2673-4583
Versão da editorahttps://www.mdpi.com/2673-4583/12/1/56
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:CDQuim - Comunicações e Proceedings

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