Probing Triplet State Properties of Organic Chromophores via Design and Synthesis of Os(II)-Diketonate Complexes: The Triplet State Intramolecular Charge Transfer

We report the probe of specific triplet state properties of organic chromophores that are otherwise inaccessible
in low viscous solution. The prototypical example demonstrated here is [Os(CO)3(Cl)(NDP)] (1) ((NDP)H =
2-naphthyl-7-dimethylanilino-1,3-propanedione), which, upon electronic excitation, undergoes intramolecular
charge transfer in both S1 and T1 manifolds of NDP. The dipolar changes in S1 and T1 monitored via the
solvatochromism for both fluorescence and phosphorescence were deduced to be 18.0 and 11.9 D, respectively.
The appreciable difference in the dipolar change can be qualitatively rationalized by different extents of
charge-transfer character between S1 and T1 states. The results led to the probe of other reactions in triplet
manifold feasible.