Sensitised lanthanide luminescence using a Ru polypyridyl functionalised dipicolinic acid chelate.

A visible light absorbing [RuII(tpy)2]2+-type chromophore appended with a dipicolinic acid LnIII chelator has been prepared and complexed with several differing lanthanide cations to form the corresponding heterobimetallic d-f assemblies. The subseqent solution speciation analysed by 1H NMR spectroscopy revealed an unexpected decrease in the LnIII chelate complex stability, in particular for the 1 : 3 complex, when compared to the parent dipicolinic acid. As a result, the desired Ln(ML)3 complexes could not be isolated, and the 1 : 1 LnIII-ML complexes were instead characterised and investigated using steady state absorption and emission spectroscopy.

Enhanced Near-Infrared Emission from Eight-Coordinate vs Nine-Coordinate Yb Complexes Using 2-(5-Methylpyridin-2-yl)-8-hydroxyquinoline.

Enhanced near-infrared (NIR) luminescence from two structurally related heterobinuclear NaYb eight-cooridnate and heterobinuclear YbNa eight-coordinate (CN = 8) complexes is reported and compared to a nine-coordinate (CN = 9) homoleptic complex. For the heteroleptic complex, [Yb(MPQ)(acac)], the Yb cation is coordinated to two tridentate 2-(5-methylpyridin-2-yl)-8-quinolinate (MPQ) anions, with a bidentate acetylacetonate (acac) anion completing the coordination sphere. Instead, the heterobinuclear [NaYb(MPQ)] complex comprises a total of four anionic MPQ ligands, two of which exhibit κ-coordination to the Yb cation.

Quantitative Sensitization Efficiencies in NIR-Emissive Homoleptic Ln(III) Complexes Using 2-(5-Methylpyridin-2-yl)-8-hydroxyquinoline.

A series of isostructural lanthanide complexes [Ln(MPQ)] (Ln = Nd, Gd, Er, Yb, Lu) using a monoanionic tridentate methylpyridyl-substituted 8-hydroxyquinoline ligand (MPHQ = 2-(5-methylpyridin-2-yl)-8-hydroxyquinoline) have been prepared and characterized using elemental analysis (CHN), single-crystal X-ray diffraction (XRD), and H NMR spectroscopy. This ligand forms homoleptic charge-neutral lanthanide complexes with three coordinated ligands arranged in an "up-up-down" fashion around the metal center. The photophysical properties of the Nd, Er, and Yb complexes were investigated using absorption and emission spectroscopy, with the latter species displaying efficient sensitization in the Near Infra-Red (NIR) region and a photoluminescence quantum yield (PLQY) as high as 1.

Structure and efficient luminescence upconversion of Ln(iii) aromatic N-oxide coordination polymers.

A series of lanthanide-based coordination polymers {[Yb1-xErx(4,4'-bpdo)3(H2O)2](CF3SO3)3}∞ were synthesised by solvent diffusion techniques, where 4,4'-bpdo = 4,4'-bipyridine-N,N'-dioxide, and using differing mole fractions of Yb(iii) and Er(iii) which were systematically varied (x = 0, 0.05, 0.20, 0.