Step-Wise Changes in the Excited State Lifetime of [Eu(D2O)9]3+ and [Eu(DOTA)(D2O)]- as a Function of the Number of Inner-Sphere O-H Oscillators

Lanthanide luminescence is dominated by quenching from high-energy oscillators in the chemical environment. The rate of non-radiative energy transfer to a single H2O molecule coordinated to a Eu3+ ion exceeds the usual rates of emission by an order of magnitude. We know these rates, but the details of these energy transfer processes are yet to be established. In this work, we study the quenching rates of [Eu(D2O)9]3+ and [Eu(DOTA)(D2O)]- in H2O/D2O mixtures by sequentially exchanging the deuterons with protons. Flash freezing the solutions allows us to identify species with varying D/H content in solution and thus to quantify the energy transfer processes to individual OH-oscillators. This is not possible in solution due to fast exchange in the ensembles present at room temperature. We conclude that the energy transfer processes is accurately described, predicted, and simulated using a step-wise addition of the rates of each quenching O-H oscillator. These document the sequential increase in the rate of the energy transfer processes in the quenching lanthanide luminescence, and further provides a methodology to identify isotopic impurities in deuterated lanthanide systems in solution.