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Heterometallic Europium(III)–Lutetium(III) Terephthalates as Bright Luminescent Antenna MOFs

A new series of luminescent heterometallic europium(III)–lutetium(III) terephthalate metal–organic frameworks, namely (Eu(x)Lu(1−x))(2)bdc(3)·nH(2)O, was synthesized using a direct reaction in a water solution. At the Eu(3+) concentration of 1–40 at %, the MOFs were formed as a binary mixture of the...

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Detalles Bibliográficos
Autores principales: Nosov, Viktor G., Kupryakov, Arkady S., Kolesnikov, Ilya E., Vidyakina, Aleksandra A., Tumkin, Ilya I., Kolesnik, Stefaniia S., Ryazantsev, Mikhail N., Bogachev, Nikita A., Skripkin, Mikhail Yu., Mereshchenko, Andrey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505590/
https://www.ncbi.nlm.nih.gov/pubmed/36144501
http://dx.doi.org/10.3390/molecules27185763
Descripción
Sumario:A new series of luminescent heterometallic europium(III)–lutetium(III) terephthalate metal–organic frameworks, namely (Eu(x)Lu(1−x))(2)bdc(3)·nH(2)O, was synthesized using a direct reaction in a water solution. At the Eu(3+) concentration of 1–40 at %, the MOFs were formed as a binary mixture of the (Eu(x)Lu(1−x))(2)bdc(3) and (Eu(x)Lu(1−x))(2)bdc(3)·4H(2)O crystalline phases, where the Ln(2)bdc(3)·4H(2)O crystalline phase was enriched by europium(III) ions. At an Eu(3+) concentration of more than 40 at %, only one crystalline phase was formed: (Eu(x)Lu(1−x))(2)bdc(3)·4H(2)O. All MOFs containing Eu(3+) exhibited sensitization of bright Eu(3+)-centered luminescence upon the 280 nm excitation into a (1)ππ* excited state of the terephthalate ion. The fine structure of the emission spectra of Eu(3+ 5)D(0)-(7)F(J) (J = 0–4) significantly depended on the Eu(3+) concentration. The luminescence quantum yield of Eu(3+) was significantly larger for Eu-Lu terephthalates containing a low concentration of Eu(3+) due to the absence of Eu-Eu energy migration and the presence of the Ln(2)bdc(3) crystalline phase with a significantly smaller nonradiative decay rate compared to the Ln(2)bdc(3)·4H(2)O.