摘要
Enantiorecognition of tyrosine (Tyr) enantiomers is realized via chiral ligand exchange technology combined with electrochemistry. A natural polymer, sodium alginate (SA), is electrodeposited on a glassy carbon electrode (GCE) and adopted as the chiral selector to form a diastereoisomeric ternary complex of [(SA)Zn(II)(L-Tyr)] or [(SA)Zn(II)(D-Tyr)] in the presence of Zn(II). Due to the difference in steric hindrance during the formation of these two complexes, the chiral selector preferentially recognizes D-Tyr. The electrochemical enantiorecognition of Tyr enantiomers is characterized by cyclic voltammetry and electrochemical impedance spectroscopy (EIS), and the parameters affecting the recognition efficiency are also investigated.
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