Experimental and theoretical investigations of the [Ln(β-dik)(NO3)2(phen)2]⋅H2O luminescent complexes

• Autor(a) principal: Santos, Paulo R.S.
• Data de Publicação: 2020
• Outros Autores: Pereira, Dariston K.S., Costa, Israel F., Silva, Iran F., Brito, Hermi F., Faustino, Wagner M., Carneiro Neto, Albano N., Moura, Renaldo T., Araujo, Maria H., Diniz, Renata, Malta, Oscar L., Teotonio, Ercules E.S.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10773/37191

In this work, the coordination compounds presenting the formulas [Eu(acac)(NO3)2 (phen)2]⋅H2O (Eu1) and [Eu(bzac)(NO3)2(phen)2]⋅H2O (Eu2), acac: acetylacetonate, bzac: benzoylacetonate and, phen: 1,10-phenantroline, were successfully synthesized and some spectroscopic properties were investigated by theoretical and experimental methods. These compounds were characterized via elemental analysis, FTIR spectroscopy and thermogravimetric analysis (TGA). The X-ray diffraction data revealed that the compound Eu1 crystallizes in the monoclinic space group P2/n. Spectroscopic data showed that ligand-to-metal charge transfer states (LMCT) in the [Eu(β-dik)(NO3)2(phen)2]⋅H2O complexes (β-dik: acac or bzac) are redshift as compared with [Eu(β-dik)3(phen)] complexes. These data showed that LMCT states play the most important role on the luminescence quenching in the complexes Eu1 and Eu2, which only exhibit high luminescence intensities at low temperatures. Furthermore, the role of changes in the chemical environment on the intensity parameters Ωλ (λ = 2 and 4) have been investigated from the theoretical point of view for the complexes Eu1 to Eu2, and from these to tris β–dik complexes. Interestingly, the theoretical intensity parameters ratio Ω2/Ω4 calculated are in a good agreement with those experimental ones.