| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1302331 | Inorganic Chemistry Communications | 2012 | 5 Pages |
With the binuclear Zn2L ([Zn2L(OAc)2(H2O)], 1) compound from the Salen-type Schiff-base ligand H2L (H2L: N,N′-bis(salicylidene)cyclohexane-1,2-diamine) with the flexible linker as the precursor, a series of hetero-trinuclear Zn2Ln complexes (Ln = Nd (2), Ln = Yb (3), Ln = Er (4) or Ln = Gd (5)) have been obtained by further reaction with Ln(OAc)3·6H2O. The result of their photophysical properties shows that the strong and characteristic NIR luminescence with emissive lifetimes in the ranges of microseconds for each of the complexes 2–4, has been sensitized from the excited state (1LC and 3LC) of the Salen-type Schiff-base ligand with the flexible linker. Especially, the almost planar arrangement of two energy donors of ZnL components around the Ln3 + ion for the larger conjugation effect, endowing the energy level's good match between the excited state (3LC) of the chromophore to the corresponding Ln3 + ion's exciting state, results in the enhancement of their NIR luminescence.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Hetero-trinuclear Zn2Ln arrayed complexes assembled from the precursor Zn2L ► Arrangement of energy donors around the Ln3 + ion ► Enhancement of near-infrared luminescent properties
