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A Supramolecular Strategy to Modulate the Photoluminescence of Metallofullerenes via Motion-Induced Phosphorescence
Jiayi Liang1,2,3, Shuming Bai1, Chunru Wang1
1Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Structural Chemistry of Unstable and Stable Species, CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Abstract:
Yttrium-based metallofullerenes have attracted much attention due to their typical photoluminescence properties with thermally activated delayed fluorescence (TADF) and phosphorescence, which have the potential for photofunctional materials. In this work, a supramolecular strategy to modulate the TADF and phosphorescence of metallofullerene Y3N@C80 with a molecular nanoring is reported. A supramolecular complex Y3N@C80⊂[9]CPPH was first constructed by Y3N@C80 and a molecular nanoring of [9]CPPH. Temperature-dependent photoluminescence measurements revealed that Y3N@C80⊂[9]CPPH retains the characteristic TADF band at 700 nm and phosphorescence-dominated band at 738 nm, respectively. However, Y3N@C80⊂[9]CPPH shows significantly amplified TADF emission as well as decreased phosphorescence compared to that of pristine Y3N@C80. This phenomenon can be ascribed to the existing dynamic motion of Y3N@C80 inside the nanocavity of molecular nanoring, which could result in nonradiative decay of triplet states and suppress the phosphorescence emission finally. Density functional theory calculations of Y3N@C80⊂[9]CPPH were employed to illustrate the structure and excited states. Thus, this host-guest interaction provides a new strategy for tuning the photoluminescence of metallofullerene optical materials via motion-induced phosphorescence modulation.
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