Excited State Properties of Lanthanide(III) Complexes with a Nonadentate Bispidine Ligand

Eu^III , Tb^III , Gd^III and Yb^III complexes of the nonadentate bispidine derivative L² (bispidine=3,7-diazabicyclo[3.3.1]nonane) were successfully synthesized and their emission properties studied. The X-ray crystallography reveals full encapsulation by the nonadentate ligand L² that enforces to all Ln^III cations a common highly symmetrical capped square antiprismatic (CSAPR) coordination geometry (pseudo C_4v symmetry). The well-resolved identical emission spectra in solid state and in solution confirm equal structures in both media. As therefore expected, this results in long-lived excited states and high emission quantum yields ([Eu^III L² ]⁺ , H₂ O, 298 K, τ=1.51 ms, ϕ=0.35; [Tb^III L² ]⁺ , H₂ O, 298 K, τ=1.95 ms, ϕ=0.68). Together with the very high kinetic and thermodynamic stabilities, these complexes are a possible basis for interesting biological probes.