A family of CuI-based 1D polymers showing colorful short-lived TADF and phosphorescence induced by photo- and X-ray irradiation

Exploiting 2-(alkylsulfonyl)pyridines as 1,3-N,S-ligands, herein we have constructed 1D CuI-based coordination polymers (CPs) bearing unprecedented (CuI) n chains and possessing remarkable photophysical properties. At room temperature, these CPs show efficient TADF, phosphorescence or dual emission in the deep-blue to red range with outstandingly short decay times of 0.4-2.0 μs and good quantum performance. Owing to great structural diversity, the CPs demonstrate a variety of emissive mechanisms, spanning from TADF of 1 (M + X)LCT type to 3 CC and 3 (M + X)LCT phosphorescence. Moreover, the designed compounds emit strong X-ray radioluminescence with the quantum efficiency of up to an impressive 55% relative to all-inorganic BGO scintillators. The presented findings push the boundaries in designing TADF and triplet emitters with very short decay times. We present 1D CuI-based polymers exhibiting remarkable short-lived TADF and phosphorescence induced by photo- or X-ray irradiation.