ABSTRACT Salen‐type Schiff‐base ligands (H 2 L) were synthesized through the condensation reaction between 1,2‐diphenylethane‐1,2‐diamine and o‐vanillin. Three novel luminescent Zn‐Ln complexes, ZnL 2 Ln (Ln = Gd, Tb, Eu), were successfully prepared by reacting the zinc complex (ZnL) with LnCl 3 . Subsequent treatment of ZnL 2 Ln with dibenzoylmethane yielded three dinuclear derivatives, β‐ZnLLn (Ln = Gd, Tb, Eu). All complexes were comprehensively characterized by single‐crystal X‐ray diffraction and FT‐IR spectroscopy. Structural analyses revealed that complexes 1–3 adopt trinuclear Zn‐Ln‐Zn architectures, whereas complexes 4–6 exhibit dinuclear Zn‐Ln configurations. Solid‐state photoluminescence measurements demonstrated quantum yields of 27.94% (ZnL), 0.90% (ZnL 2 Eu), 1.82% (ZnL 2 Tb), 1.05% (ZnL 2 Gd), 0.65% (β‐ZnLEu), 1.16% (β‐ZnLTb), and 0.70% (β‐ZnLGd), indicating their potential as advanced fluorescent rare‐earth materials. The LED devices based on complexes β‐ZnLEu and β‐ZnLTb exhibit stronger emission intensities compared to those based on complexes ZnL 2 Eu and ZnL 2 Tb. The obtained complexes were fabricated in LED; the CIE chromaticity coordinates of complexes β‐ZnLEu and β‐ZnLTb are (0.344, 0.316) and (0.347, 0.323), respectively, which are very close to the standard white light coordinates (0.33, 0.33).
Ye et al. (Wed,) studied this question.
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