Cyclometalated Iridium(III) Complexes Containing Viologen‐Modified Phenylpyridine Ligands as Electroluminochromic Active Molecules for Information Display

Abstract Electroluminochromic (ELC) materials have garnered significant research interest because of their potential applications in lighting, displaying, and sensing. These materials exhibit reversible modulation of photoluminescence under low‐voltage stimuli. Here five phosphorescent iridium(III) complexes are reported featuring viologen‐substituted 2‐phenylpyridine (Vppy) ligands acting as electroactive components. Four of the complexes are bis‐cyclometalated and coordinated with either neutral bipyridine derivatives or negatively charged 2‐picolinate. The remaining complex is heteroleptic tris‐cyclometalated, containing one Vppy and two 2‐phenylquinoline ligands. Upon photoexcitation, the bis‐cyclometalated complexes exhibit orange to red phosphorescence originating from mixed triplet metal‐to‐ligand charge transfer ( 3 MLCT) and intraligand ( 3 IL) dπ(Ir)/π(Vppy) → π*(Vppy) state, whereas the tris‐cyclometalated complex is non‐emissive due to a low Ir(IV/III) oxidation potential favoring oxidative quenching by the viologen pendants. When the cationic viologens are electrochemically reduced to their neutral form, the bis‐cyclometalated complexes show a remarkable blue‐shift in their phosphorescence maxima due to increased energy levels of the Vppy molecular orbitals. In the case of the tris‐cyclometalated complex, reduction of the viologen groups interrupts the quenching process, leading to a luminescence turn‐on. These complexes are used to develop ELC devices, which exhibit reversible luminescence response in terms of color or on‐off switching under a low voltage of 2 V.