Fiche publication
Date publication
août 2025
Journal
Journal of the American Chemical Society
Auteurs
Membres identifiés du Cancéropôle Est :
Dr CHARBONNIERE Loïc
Tous les auteurs :
Godec L, Knighton RC, Hamon N, Thor W, Wong KL, Tripier R, Charbonnière LJ
Lien Pubmed
Résumé
We report the synthesis of a tritopic ligand, , composed of two strongly binding lanthanide (Ln) sites using tris-functionalized triazacyclononane (tacn) scaffolds bridged by a weaker Ln binding triethylene glycol chain. Coordination chemistry of Ln (Ln = Eu, Tb, Yb, Lu) was investigated by using NMR and photoluminescent spectroscopies. The first two Ln ions are coordinated by the tacn scaffolds to form [Ln] and [Ln] species, followed by tri- and tetranuclear complexes, [Ln(Ln)] and [Ln(Ln)]. The third and fourth exomacrocyclic binding events occur at the polyethylene glycol binding site, buttressed by a synergistic interaction of the phosphonate arms, confirmed by DFT modeling. [Ln] (Ln = Tb, Eu, Yb, and Lu) homobimetallic complexes were prepared, and characterized and their spectroscopic properties determined in HO and DO. Titration of the [Yb] dinuclear complex by Tb salts in DO confirmed the formation of the tri- and tetranuclear species. Upon excitation into the F ← F absorption band of Yb at 980 nm, a cooperative sensitization upconversion process is evidenced, displaying visible Tb emission bands. Heating resulted in Ln scrambling in the tacn coordination sites, increasing the UC efficiency by ca. 10. The most efficient emitter for UC is the tetranuclear [TbYb(TbYb)], with one of each Ln species in the tacn scaffolds and one of each Ln species coordinated by the polyethylene glycol chain. Optimization on the pD led to an overall 9.0 × 10 UC quantum yield (λ = 980 nm, = 10.8 W·cm). The same experiment was repeated in water, affording UC at the molecular level.
Référence
J Am Chem Soc. 2025 08 13;:
