Trupp Leandro, Bruttomesso Andrea C, Vardé Mariana, Eliseeva Svetlana V, Ramírez Javier A, Petoud Stéphane, Barja Beatriz C
Departamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Int. Güiraldes 2160, Ciudad Universitaria, Buenos Aires, 1428, Argentina.
Instituto de Química Física de los Materiales, Medio Ambiente y Energía, (INQUIMAE), CONICET-Universidad de Buenos Aires, Int. Güiraldes 2160, Ciudad Universitaria, Buenos Aires, 1428, Argentina.
Chemistry. 2020 Dec 15;26(70):16900-16909. doi: 10.1002/chem.202003524. Epub 2020 Nov 12.
Herein, the synthesis and characterization of the first family of multipodal ligands with a Tröger's base framework designed for the preparation of luminescent lanthanide(III) complexes are reported. Eight ligands were designed and synthesized using different strategies, including alkylation reactions, amide couplings, and Ugi multicomponent reactions. All the ligands bear carboxylate groups for the coordination of the lanthanide(III) ions, with the lanthanide(III)-sensitizing units consisting of the Tröger's base framework itself or attached benzamides. Upon irradiation of the chromophoric ligands, green terbium(III) emission was efficiently generated, whereas europium(III) emission was negligible. The geometry and substitution pattern of the ligands allow control of the stoichiometry of the species formed and the Tb luminescence sensitization efficiency, showing that para-substitution patterns are more efficient than meta substitution for the formation of coordination compounds with lower Tb /ligand ratio. We propose that the species formed are self-assembled 2:2 or 2:4 metallosupramolecular structures.
本文报道了首个设计用于制备发光镧系(III)配合物的具有特罗格碱骨架的多齿配体家族的合成与表征。使用不同策略设计并合成了八个配体,包括烷基化反应、酰胺偶联反应和乌吉多组分反应。所有配体都带有羧酸根基团用于镧系(III)离子的配位,镧系(III)敏化单元由特罗格碱骨架本身或连接的苯甲酰胺组成。在照射发色配体时,有效地产生了绿色铽(III)发射,而铕(III)发射可忽略不计。配体的几何形状和取代模式允许控制所形成物种的化学计量比和铽发光敏化效率,表明对位取代模式在形成具有较低铽/配体比的配位化合物方面比间位取代更有效。我们提出所形成的物种是自组装的2:2或2:4金属超分子结构。