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Mixed Tb/Dy coordination ladders based on tetra(carboxymethyl)thiacalix[4]arene: a new avenue towards luminescent molecular nanomagnets

The macrocyclic ligand calix[4]arene (L1) and its sulphur-containing analogue thia[4]calixarene (L2) are promising precursors for functional molecular materials as they offer rational functionalization with various organic groups. Here, we present the first example of lanthanide-based coordination p...

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Detalles Bibliográficos
Autores principales: Ovsyannikov, A. S., Khariushin, I. V., Solovieva, S. E., Antipin, I. S., Komiya, H., Marets, N., Tanaka, H., Ohmagari, H., Hasegawa, M., Zakrzewski, J. J., Chorazy, S., Kyritsakas, N., Hosseini, M. W., Ferlay, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050570/
https://www.ncbi.nlm.nih.gov/pubmed/35496632
http://dx.doi.org/10.1039/d0ra01263g
Descripción
Sumario:The macrocyclic ligand calix[4]arene (L1) and its sulphur-containing analogue thia[4]calixarene (L2) are promising precursors for functional molecular materials as they offer rational functionalization with various organic groups. Here, we present the first example of lanthanide-based coordination polymers built from the macrocyclic thiacalix[4]arene backbone bearing four carboxylic moieties, namely, ligand H(4)L3. The combination of H(4)L3 with the Tb(3+) and Dy(3+) cations led to the formation of 1D ladder-type coordination polymers with the formula [Ln(III)HL3DMF(3)]·(DMF) (where DMF = dimethylformamide and Ln = Tb or Dy, denoted as HL3–Tb and HL3–Dy), which resulted from the coordination of the lanthanide cations with the partially deprotonated ligand HL3(3−) that behaved as a T-shape connector. The coordination sphere around the metal was completed by the coordinated DMF solvent molecules. By combining both Tb(3+) and Dy(3+) cations, isostructural heterobimetallic solid solutions HL3–Tb(1−)(x)Dy(x) were also prepared. HL3–Tb and HL3–Dy showed visible light photoluminescence originating from the f–f electronic transitions of pale green emissive Tb(3+) and pale yellow emissive Dy(3+) with efficient sensitization by the functionalized thia[4]calixarene ligand HL3. In the HL3–Tb(1−)(x)Dy(x) solid solutions, the Tb/Dy ratio governed both the emission colour as well as the emission quantum yield, which reached even 28% at room temperature for HL3–Tb. Moreover, HL3–Dy exhibited a slow magnetic relaxation effect related to the magnetic anisotropy of the dodecahedral Dy(3+) complexes, which were well isolated in the crystal lattice by expanded organic spacers.