Yongbo Wang, Jinxuan Yang, Wencai Wang, Yanting Jia, Shaojie Wang
Chiral recognition is fundamentally pivotal in biomedicine, yet simultaneous discrimination of enantiomers of multiple structurally analogous molecules remains a key challenge. Herein, multicolor achiral carbon dots (CDs) (B-CDs, G-CDs, and Y-CDs) were successfully synthesized and employed for chiral recognition and quantitative detection of basic amino acid (Lys, His, and Arg) enantiomers. Systematic characterizations verified that the as-prepared CDs possessed abundant surface functional groups, thereby endowing them with unique optical properties. B-CDs, G-CDs, and Y-CDs exhibited selective fluorescence enhancement, concentration-dependent emission blue shift, and ratiometric fluorescence responses toward l-Lys with detection limits of 0.37 μM, 64.3 nM, and 0.57 μM, respectively. By integrating RGB/Lab color models with smartphone-assisted imaging, a convenient colorimetric method was established for visual recognition and rapid quantitative detection of l-lys. Furthermore, a three-channel fluorescent sensor array based on the three CDs was constructed, realizing 100% accurate discrimination of three basic amino acids and their six enantiomers. Chiral recognition mechanism studies revealed that differential binding affinities and stereochemical matching between CDs and l-Lys accounted for the chiral selectivity. Finally, the proposed sensing system is successfully validated in complex biological matrices with satisfactory recoveries (94.73% to 112.90%) and strong anti-interference capacity. Therefore, this achiral CD-based fluorescent platform enables efficient chiral recognition and quantification of basic amino acid enantiomers, offering significant potential for advanced chiral analysis.