Potential-Induced Fine-Tuning of the Enantioaffinity of Chiral Metal Phases

被引:33
作者
Assavapanumat, Sunpet [1 ,2 ]
Yutthalekha, Thittaya [2 ]
Garrigue, Patrick [1 ]
Goudeau, Bertrand [1 ]
Lapeyre, Veronique [1 ]
Perro, Adeline [1 ]
Sojic, Neso [1 ]
Wattanakit, Chularat [2 ]
Kuhn, Alexander [1 ]
机构
[1] Univ Bordeaux, CNRS UMR 5255, Bordeaux INP, Site ENSCBP, Pessac, France
[2] Vidyasirimedhi Inst Sci & Engn VISTEC, Sch Energy Sci & Engn, Rayong, Thailand
基金
欧洲研究理事会;
关键词
electrochromatography; enantioselectivity; mesoporous metals; molecular imprinting; platinum; MOLECULARLY IMPRINTED POLYMERS; ENANTIOSELECTIVE RECOGNITION; AMINO-ACIDS; SEPARATION; ELECTROCHROMATOGRAPHY; ENANTIOMERS; FILM; ELECTROPHORESIS; NANOPARTICLES; SENSITIVITY;
D O I
10.1002/anie.201812057
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Concepts leading to single enantiomers of chiral molecules are of crucial importance for many applications, including pharmacology and biotechnology. Recently, mesoporous metal phases encoded with chiral information have been developed. Fine-tuning of the enantioaffinity of such structures by imposing an electric potential is proposed, which can influence the electrostatic interactions between the chiral metal and the target enantiomer. This allows the binding affinity between the chiral metal and the target enantiomer to be increased, and thus, the discrimination between two enantiomers to be improved. The concept is illustrated by generating chiral encoded metals in a microfluidic channel by reduction of a platinum salt in the presence of a liquid crystal and l-tryptophan as a chiral model template. After removal of the template molecules, the modified microchannel retains a pronounced chiral character. The chiral recognition efficiency of the microchannel can be fine-tuned by applying a suitable potential to the metal phase. This enables the separation of both components of a racemate flowing through the channel. The approach constitutes a promising and complementary strategy in the frame of chiral discrimination technologies.
引用
收藏
页码:3471 / 3475
页数:5
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