Shavaleev, Nail M.Eliseeva, Svetlana V.Scopelliti, RosarioBunzli, Jean-Claude G.2010-04-142010-04-14201010.1021/ic100129rhttps://infoscience.epfl.ch/handle/20.500.14299/49347WOS:000276556900049Sterically hindered N-aryl-benzimidazole pyridine-2-carboxylic acids (aryl = phenyl, 4-biphenyl, 2-naphthyl) readily form homoleptic, neutral, nine-coordinate europium complexes which display efficient sensitized luminescence in solid state and in dichloromethane solution with quantum yields reaching 59% and have monoexponential and nearly temperature-independent lifetimes as long as 2.7 ms. The ligand-centered absorption band with a maximum at 321-342 nm and intensity (50-56) x 10(3) M(-1)cm(-1) ensures efficient harvesting of excitation light by the complexes. Variation of N-aryl chromophore enhances the ligand absorption at 250-350 rim without changing its triplet state energy which amounts to (19.2-21.3) x 10(3) cm(-1). Photophysical properties of europium complexes benefit from adequate protection of the metal by the ligands against non-radiative deactivation and efficient ligand-to-metal energy transfer exceeding 70%. A correlation is observed between the sensitized luminescence quantum yields of europium and the ligand triplet state energy; in certain cases it points to the presence of a second-sphere quenching of Eu-III by co-crystallized water in the solid state.Bond-Valence ParametersIntramolecular Energy-TransferHighly LuminescentCoordination-ComplexesCyclometalated IridiumLanthanide ComplexesExcited-StatesQuantum YieldsLightPhosphorescenttext::journal::journal article::research article