化学
对映体
拉曼光谱
对映选择合成
分子
组合化学
氨基酸
有机化学
催化作用
生物化学
物理
光学
作者
Zhipeng Zhang,Kecen Chen,Kai Tang,Kai Chen,Ruili Li,Xiaotong Sun,Yuyang Hu,Qi Liu,Miao Chen,Hua Yang,Xiaoqing Chen
标识
DOI:10.1021/acs.analchem.2c04839
摘要
Due to low optical activity and structural simplicity, synchronous chiral discrimination and identification of aliphatic amino acids (AAs) are still challenging yet demanding. Herein, we developed a novel surface-enhanced Raman spectroscopy (SERS)-based chiral discrimination-sensing platform for aliphatic AAs, in which l- and d-enantiomers are able to discriminately bind with quinine to generate distinct differences in the SERS vibrational modes. Meanwhile, the plasmonic sub-nanometer gaps supported by the rigid quinine enable the maximization of SERS signal enhancement to reveal feeble signals, allowing for simultaneously acquiring the structural specificity and enantioselectivity of aliphatic amino acid enantiomers in a single SERS spectrum. Different kinds of chiral aliphatic AAs were successfully identified by using this sensing platform, demonstrating its potential and practicality in recognizing chiral aliphatic molecules.
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