Abstract
We present a new time-resolved chemosensor for the detection of Ba2+ ions. Our sensor is based on
an iridium(III) compound with dual (fluorescent and phosphorescent) emission. The nature of the
luminescent response of the sensor depends on its state; specifically, the phosphorescent emission of
the free state at long wavelengths is strongly suppressed, while that of the Ba2+-chelated compound
is strongly enhanced. Furthermore, the residual phosphorescent emission of the free compound
decays with two short decay constants, τ 1
free ∼ 3.5 ns (88%) and τ 2
free ∼ 209 ns (12%), while the
chelated compound decays with two long decay constants, τ 1ch ∼ 429 ns (21%) and τ 2 ch ∼ 1128 ns
(76%). This exceptional behaviour, supported by quantum chemical calculations, allows a time-
based separation between the signal of the free and the chelated species. Among other applications,
our sensor could be the basis of a Ba2+ tagging detector for neutrinoless double beta decay searches
in xenon.