Fine Tuning of Emission Behavior, Self-Assembly, Anion Sensing, and Mitochondria Targeting of...

Compared to the many studies that focus on the development of novel molecular frameworks pertaining to functionalized fluorescent materials, there is lesser emphasis on side chains even though they have a significant impact on the properties and applications of fluorescent materials. In this study, a series of pyridinium-functionalized tetraphenylethene salts (TPEPy-1 to TPEPy-4) possessing different alkyl chains are synthesized, and the influence of chain length on their optical performance and applications is thoroughly investigated. By changing the alkyl chain, the fluorogens exhibit opposite emission behavior in aqueous media because of their distinct hydrophobic nature, and their solid-state emission can be fine-tuned from green to red owing to their distinct molecular configuration. In addition, by increasing the chain length, the microstructure of the self-assembled fluorogens converts from microplates to microrods with various emission colors. Moreover, TPEPy-1 exhibits dual-mode fluorescence "turn-on" response toward NO₃^- and ClO₄^- in aqueous media because the anions induce the self-assembly of fluorogens. Furthermore, the fluorogens display cellular uptake selectivity while the proper alkyl chain impels the fluorogens to penetrate the cell membrane and accumulate in the mitochondria with high specificity.