Novel Chiral Self-Assembled Nano-Fluorescence Materials with AIE Characteristics for Specific Enantioselective Recognition of L-Lysine

• Published in: International journal of molecular sciences Vol. 25; no. 19; p. 10666
• Main Authors: Wang, Peng, Wang, Rong, Sun, Yue, Hu, Yu, Song, Kaiyue, Sun, Xiaoxia
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.10.2024; MDPI
• Subjects: aggregation-induced emission (AIE); Amino acids; Biosensors; Catalysis; Chemical properties; chiral nano-fluorescence; Enantiomers; enantioselective recognition; Ethanol; Fluorescence; Fluorescent Dyes - chemistry; Identification and classification; Lysine; Lysine - chemistry; Materials; Nanomaterials; Nanostructures - chemistry; Optics; Scientific imaging; self-assembled; Solvents; Spectrometry, Fluorescence - methods; Stereoisomerism; Water; China; lysine; enantioselective recognition; self-assembled; aggregation-induced emission (AIE); chiral nano-fluorescence
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms251910666

In this paper, two aggregation-induced emission (AIE) chiral fluorescent materials, S-1 and S-2, were synthesized. The two materials are based on BINOL and H -BINOL backbones, respectively, and large electron-absorbing groups are attached to the chiral backbones through the Knoevenagel reaction. At the same time, the CD signals of these two chiral fluorescent materials are gradually weakened (f gradually increases) as they continue to aggregate. However, S-2 underwent a flip-flop from a negative to positive chiral CD signal at f ≥ 90. And both materials also showed significant enantioselective recognition of lysine, demonstrating their potential as novel chiral fluorescent probes. Among them, the enantioselective fluorescence enhancement ratios (ef) of S-1 and S-2 for lysine were 10.0 and 10.3, respectively, while different degrees of blue shifts were produced by the ICT mechanism during the recognition process. In addition, the self-assembled morphology of the two nanomaterials is different; S-1 comprises hollow-core vesicles that are more likely to aggregate to form larger self-assembled vesicles, whereas S-2 is a solid block structure. When L/D-lysine was added alone, the morphology of S-1 was more distinctly different compared to S-2. With the addition of L-lysine, S-1 was dispersed and regularly spherical, whereas with the addition of D-lysine, S-1 itself remained in the form of aggregated large vesicles. This suggests that both S-1 and S-2 are important in the fields of chiral optics, chiral recognition, and nanoscale self-assembly.