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New heteronuclear Zn2Ln2 clusters [Zn2L2Ln2(hfac)6] (Ln = Eu (1), Tb (2) and Dy (3)) have been synthesized based on a flexible Schiff base (H2L = N,N′-bis(salicylidene)-3,6-dioxa-1,8-diaminooctane) and β-diketonate ligand (hfac = hexafluoroacetylacetonate). The structures of the isomorphous complexes 1–3 were determined by single-crystal X-ray crystallography. Photophysical studies indicate that the short intramolecular distance of Zn…Ln allows energy transfer from the Zn2L2-based sensitizers to the Eu(iii) and Tb(iii) centres; the lanthanide luminescence is indeed “lighted up” by the excitation of the zinc complex. More interestingly, white light emission was realized by codoping Eu(iii) ion into the Dy(iii) complex for the first time. [ABSTRACT FROM AUTHOR]

Three dinuclear lanthanide complexes are achieved by using H2salen or H2salen/acac ligands (H2salen = N,N′-ethylenebis(salicylideneimine), acac = acetylacetonate). They are homodinuclear [Er2(salen)3] (1), [Yb2(salen)2(acac)2] (2), and heterodinuclear geometrical [ErYb(salen)2(acac)2] (3). The structures of complexes were determined by single crystal X-ray crystallographic studies and their photophysical properties were investigated. The homonuclear Yb2 complex exhibits characteristic metal-centered NIR emission. The geometric ErYb isomer exhibits ‘dual emissions’ from both erbium(iii) and ytterbium(iii) ions. There was no detectable photoluminescence in the Er2 complex, not only in solid state but also in solvent. [ABSTRACT FROM AUTHOR]