• 文献标题:   An electrochemical sensor employing ?-cyclodextrin chiral cross-linked metal organic framework and graphene oxide for chiral enantiomer recognition
  • 文献类型:   Article
  • 作  者:   SUN XZ, FU ZB, ZHANG M, FU H, LIN CH, KUANG JJ, ZHANG HY, HU P
  • 作者关键词:   ?cyclodextrin, cross linked mof, graphene oxide, electrochemical sensor, chiral recognition, mandelic acid
  • 出版物名称:   MICROCHEMICAL JOURNAL
  • ISSN:   0026-265X EI 1095-9149
  • 通讯作者地址:  
  • 被引频次:   6
  • DOI:   10.1016/j.microc.2022.108074 EA NOV 2022
  • 出版年:   2022

▎ 摘  要

Chirality is a universal feature of nature, and the effective differentiation of chiral molecules is still a challenge. Here we propose a method for recognizing chiral molecules based on an electrochemical detection method. We use beta-cyclodextrin as an organic ligand and coordinate it with K ions to form a metal-organic framework (MOF), then we use diphenyl carbonate to connect MOFs to obtain chiral Cross-Linked MOF (CLMOF). This CLMOF is different from the cyclodextrin MOFs reported in previous literature in that it can maintain a stable structure in the aqueous environment. CLMOF and graphene oxide (GO) are jointly modified on the glassy carbon electrode (GCE) surface to build a GO-CLMOF/GCE electrochemical sensor which is used for the chiral recognition of the enantiomers of mandelic acid (MA). The DL enantiomers of MA exhibit different electrochemical behaviors on the GO-CLMOF/GCE sensor. Their peak current ratio (IL/ID) reaches 1.8, and the peak potential difference Delta E (ED-EL) is 96 mV. It shows good linearity in the range of 0.5-30 mM. The detection limits of D-MA and L-MA are 0.15 mM and 0.09 mM, respectively. The method was successfully applied to the detection of DL-MA enantiomer of unknown concentration in urine. The recognition of DL enantiomers on the electrode surface is possible because DL-MA forms diastereomers with CLMOF. The electrochemical sensor made of CLMOF and GO is simple to prepare and has excellent selectivity for DL enantiomers of MA, and provides a possible idea for the identification and quantification of chiral isomers.