Regulating charge transfer of copper(I) coordination compounds via conformation engineering for highly-efficient radioluminescence and 3D X-ray imaging

Abstract

Copper(I) coordination compounds have emerged as promising candidates for X-ray scintillators because of their superior X-ray absorption capacity and tunable radioluminescence. However, the strategy that realizes efficient radioluminescence by varying the competition between radiative ligand-related transitions and nonradiative cluster-centered charge transfer has yet to be clearly demonstrated. Here, via conformation engineering, a series of copper(I) iodide coordination clusters have been designed and synthesized, named as (POPy) 4 Cu 2 I 2 , (POPy) 4 Cu 4 I 4 -α and (POPy) 4 Cu 4 I 4 -β (POPy = 4-phenoxypyridine).Mechanistic studies reveal that the radioluminescence in isomeric Cu 4 I 4 clusters originates from triplet metal/halide-toligand charge transfer ( 3 M/XLCT) and cluster-centered ( 3 CC) excited states, respectively. The experimental results discloses that intramolecular charge transfer is desirable for radioluminescence as it can transfer excitons generated by absorbing radiation ionizations to ligands to form thermal electrons. Due to the large X-ray absorption cross-section of Cu 4 I 4 cube and efficient 3 M/XLCT emissions, the scintillation film fabricated by (POPy) 4 Cu 4 I 4 -α realizes a high resolution of 20.2 lp mm -1 , and further enables a 3D X-ray imaging demonstration. Our work makes the comprehensive comparison of the radioluminescence characteristics between 3 M/XLCT and 3 CC excited states in isostructural Cu 4 I 4 -based clusters, providing a template for enhancing scintillation properties through conformation engineering.