Self-Assembly of Triple-Stranded Lanthanide Molecular Quasi-Lantern Containing 2,2′-Bipyridine Receptor: Luminescence Sensing and Magnetic Property

High Resolution Image Download MS PowerPoint Slide Ln 2 L 3 -type supramolecular architectures have received significant attention recently due to their unique magnetism and optical properties. Herein, we report the triple-stranded Ln 2 L 3 -type lanthanide molecular quasi-lanterns, which are fabricated by the deprotonation self-assembly of a linear ligand featuring a β-diketone chelating claw and 2,2′-bipyridine (bpy) moiety with lanthanide ions (Ln = Eu 3+ and Dy 3+ ). The crystal structure analysis indicates that Eu 3+ and Dy 3+ ions are all coordinated by eight oxygen donors but in different coordination geometries. The eight oxygen donors in Eu 2 L 3 and Dy 2 L 3 are arranged in a square antiprism and triangular dodecahedron geometry, respectively. Taking into account the fact that the bpy moiety has a strong coordination affinity for transition metal ions, luminescence sensing toward Cu 2+ ions has been demonstrated with Eu 2 L 3, bearing a detection of limit as low as 2.84 ppb. The luminescence sensing behavior of Eu 2 L 3 is ascribed to the formation host–guest complex between Eu 2 L 3 and Cu 2+ ions with a 1:2 binding ratio. Dynamic AC susceptibility measurements for Dy 2 L 3 reveal the relaxation of magnetization in it. This work provides a potential way for design and fabrication of lanthanide-based molecular materials with functions endowed by the ligands.