Anion-π interaction guided switchable TADF and low-temperature phosphorescence in phosphonium salts for multiplexed...

Anion-π⁺ interactions have gained continuous attention in diverse organic aggregates, as they can effectively alter emission behavior. Herein, the anion-π⁺ interaction is introduced to phosphonium salts, which exhibit tunable thermally activated delayed fluorescence and phosphorescence emission. Intriguingly, the emission spectra evolve from deep-blue to yellow emission by regulation of the anion-π⁺ interaction strength through varying the anions, such as BF₄ ^-, CF₃SO₃ ^-, PF₆ ^-, and NO₃, accompanied by adjustable luminescent decay times from milliseconds to several seconds. Notably, bright blue emission with a high photoluminescence quantum yield near 100% is achieved when substituting the iodide ions with larger counter anions. The phosphonium iodide with strong anion-π⁺ interaction and heavy atom effect shows a high inter-system crossing rate, which inhibits the direct and prompt fluorescence emission. The anion-π⁺ interaction and twisted structure strongly suppress π-π stacking and afford ultra-high photoluminescence yields. Furthermore, the participation of polar solvent molecules results in the solvation and bathochromic-shift phenomenon of the solid-state phosphonium iodide due to the ionic polarized host-guest structure. This work provides new insights into the anion-π⁺ interaction in luminescent phosphonium aggregates.