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用于高对映选择性合成的手性印迹介孔铂电极的自组装单层保护

Self-assembled monolayer protection of chiral-imprinted mesoporous platinum electrodes for highly enantioselective synthesis.

作者信息

Butcha Sopon, Lapeyre Véronique, Wattanakit Chularat, Kuhn Alexander

机构信息

School of Molecular Science and Engineering, School of Energy Science and Engineering, Vidyasirimedhi Institute of Science and Technology 21210 Wangchan Rayong Thailand

University of Bordeaux, CNRS, Bordeaux INP, ISM UMR 5255, Site ENSCBP 16 Avenue Pey Berland 33607 Pessac France

出版信息

Chem Sci. 2022 Feb 7;13(8):2339-2346. doi: 10.1039/d2sc00056c. eCollection 2022 Feb 23.

Abstract

In modern chemistry, chiral (electro)catalysis is a powerful strategy to produce enantiomerically pure compounds (EPC). However, it still struggles with uncontrollable stereochemistry due to side reactions, eventually producing a racemic mixture. To overcome this important challenge, a well-controlled design of chiral catalyst materials is mandatory to produce enantiomers with acceptable purity. In this context, we propose the synergetic combination of two strategies, namely the elaboration of mesoporous Pt films, imprinted with chiral recognition sites, together with the spatially controlled formation of a self-assembled monolayer. Chiral imprinted metals have been previously suggested as electrode materials for enantioselective recognition, separation and synthesis. However, the outermost surface of such electrodes is lacking chiral information and thus leads to unspecific reactions. Functionalising selectively this part of the electrode with a monolayer of organosulfur ligands allows an almost total suppression of undesired side reactions and thus leads to a boost of enantiomeric excess to values of over 90% when using these surfaces in the frame of enantioselective electrosynthesis. In addition, this strategy also decreases the total reaction time by one order of magnitude. The study therefore opens up promising perspectives for the development of heterogeneous enantioselective electrocatalysis strategies.

摘要

在现代化学中,手性(电)催化是制备对映体纯化合物(EPC)的一种有效策略。然而,由于副反应,它在立体化学控制方面仍存在困难,最终会产生外消旋混合物。为了克服这一重大挑战,必须对手性催化剂材料进行精心设计,以制备出具有可接受纯度的对映体。在此背景下,我们提出将两种策略协同结合,即制备带有手性识别位点的介孔铂膜,以及在空间上控制自组装单分子层的形成。手性印迹金属此前已被提议用作对映体选择性识别、分离和合成的电极材料。然而,此类电极的最外表面缺乏手性信息,因此会导致非特异性反应。用有机硫配体单分子层选择性地对电极的这一部分进行功能化处理,几乎可以完全抑制不期望的副反应,从而在对映体选择性电合成框架下使用这些表面时,将对映体过量提高到90%以上的值。此外,该策略还将总反应时间缩短了一个数量级。因此,该研究为非均相对映体选择性电催化策略的发展开辟了广阔前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f869/8864712/e8c4eb6333e9/d2sc00056c-f1.jpg

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