Pillar[5]arene‐Based Ion‐Pair Recognition for Encapsulation of a Stilbazolium‐Type Dye with Enhanced Photophysical Properties and Nonlinear Optical Activity

Constructing organic composite materials through molecular recognition has emerged as an important theme in materials science. Here we report an ion‐pair recognition system involving the use of a propoxylated pillar[5]arene ( PrP5 ) to modulate the solid‐state photophysical properties of dye trans ‐4’‐(dimethylamino)‐ N ‐methyl‐4‐stilbazolium hexafluorophosphate ( DMASP ). Single crystal X‐ray diffraction analysis reveals that the dye guest DMASP is encapsulated by PrP5 to form a 2 : 1 host−guest complex 2PrP5⸧DMASP in the crystalline state. The macrocyclic skeleton of PrP5 imposes restrictions on the intramolecular motions of the dye guest, leading to a significant enhancement of its fluorescence emission. Additionally, within the 2PrP5⸧DMASP complex crystal structure, DMASP molecules are found to display two possible opposite orientations in the one‐dimensional channels formed by PrP5 molecules. This arrangement is believed to alter the overall solid‐state packing structure of DMASP , thereby activating its nonlinear optical activity. This work not only reports a novel ion‐pair molecular recognition system based on pillararenes but also provides valuable insights into the modulation of the crystalline state photophysical properties of organic dyes via cocrystal engineering.