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Carbon-based? MXene-based Composites For The Electrochemical Chiral Recognition Of Tryptophan Enantiomers

Posted on:2022-04-14Degree:MasterType:Thesis
Country:ChinaCandidate:J J LiuFull Text:PDF
GTID:2480306500957209Subject:Master of Engineering
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Chirality is widespread in nature.In general,different conformations of enantiomers have similar physical properties but exert different pharmacological activities and chemical properties in different chiral environments.Electrochemical chiral recognition is a new detection technique that has been developed in recent years.The construction of a simple,efficient chiral sensor is a practical guide for electrochemical chiral recognition and detection.This thesis is based on N,S-doped carbon dots(N,S-CDs),three-dimensional N-doped graphene multi-walled carbon nanotubes(NGM)and MXene as substrate materials to construct different chiral sensors for the electrochemical chiral recognition of Tryptophan(Trp)enantiomers.The main three components are as follows.1.Construction of electrochemical sensors(N,S-CDs@(S,S)-CIL/GCE)based on complexes of N,S-CDs and chiral ionic liquids((S,S)-CIL)for the recognition of Trp enantiomers.The combination of N,S-CDs and(S,S)-CIL under electrostatic action is not only beneficial to fully exposed the chiral sites of(S,S)-CIL,but also can effectively reduce the agglomeration of N,S-CDs.Based on the synergistic effect of(S,S)-CIL and N,S-CDs,the selectivity coefficient(I_L/I_D)of N,S-CDs@(S,S)-CIL/GCE for the Trp enantiomers was 2.12.The detection limits of N,S-CDs@(S,S)-CIL/GCE for L-Trp and D-Trp were 0.035?M and 0.084?M,respectively.At the same time,the water contact angle further demonstrated that N,S-CDs@(S,S)-CIL/GCE had a good affinity for L-Trp.2.To further improve the recognition effect,NGM was used as a substrate material.The electrochemical chiral sensor(NGM@(S,S)-CIL/GCE)was constructed by electrodeposition.NGM@(S,S)-CIL/GCE exhibits excellent electrochemical properties and higher enantioselectivity(I_L/I_D=2.26).At the same time,UV-visible spectra and water contact angles demonstrated that NGM@(S,S)-CIL/GCE has a higher affinity for L-Trp.The peak current of NGM@(S,S)-CIL/GCE was linearly related to the Trp enantiomers concentration in the range of 0.01 m M to 5 m M.The detection limits(LOD)of NGM@(S,S)-CIL/GCE for L-Trp and D-Trp were 0.024 m M and 0.055 m M,respectively.In addition,NGM@(S,S)-CIL/GCE can be used to detect L-Trp or D-Trp in real samples(human urine and human serum).The construction of NGM@(S,S)-CIL/GCE also provides an efficient and convenient strategy for chiral identification.3.In the previous two chapters,zero-dimensional materials(N,S-CDs)and three-dimensional materials(NGM)were used as substrate materials,small molecule chiral ionic liquids was used as chiral selective reagents.In the work of this chapter,we constructed a simple electrochemical chiral sensor(MXene@CS/GCE)using a two-dimensional material MXene as the base material and a natural macromolecular polysaccharide-chitosan(CS)as the chiral selection reagent.The enantioselectivity coefficient(I_L/I_D)of the MXene@CS/GCE chiral sensor was 3.14.In the range of Trp enantiomers concentrations from 1.5 m M to 3.5 m M,the peak currents of MXene@CS/GCE showed a linear relationship.The limits of detection(LOD)of MXene@CS/GCE for L-Trp and D-Trp were 0.029?M and 0.056?M,respectively.
Keywords/Search Tags:Carbon-based materials, Chiral ionic liquids, MXene, Chiral sensors, Electrochemical chiral recognition
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