Divergent Synthesis of Chiroptical Molecular Switches Based on 1,2-Diaxial Atropisomers

IF 8.5 Q1 CHEMISTRY, MULTIDISCIPLINARY
Tian-Jiao Han, Qiu-Le Yang, Jiaen Hu, Min-Can Wang and Guang-Jian Mei*, 
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引用次数: 0

Abstract

The development of chiroptical molecular switches for chiral sensing, data communication, optical displays, chiral logic gates, and asymmetric catalysis is currently a vibrant frontier of science and technology. Herein, we report a practical artificial dynamic system based on a 1,2-diaxial atropisomer. Organocatalytic parallel kinetic resolution allows the divergent synthesis of two sets of stereoisomers with vicinal C–C and N–N axes from the same racemic single-axis substrates. By simply varying the configuration of the single catalyst, all four stereoisomers are accessible. The successive conduction of covalent unlocking/locking and thermal-isomerization processes enables sequential switching between all four atropisomeric states with electronic circular dichroism signal reversal, providing an example of multistate chiroptical molecular switches.

基于 1,2-二轴异构体的光电分子开关的异构合成
开发用于手性传感、数据通信、光学显示、手性逻辑门和不对称催化的气光分子开关是当前充满活力的科技前沿。在此,我们报告了一种基于 1,2-二轴异构体的实用人工动态系统。通过有机催化平行动力学解析,可以从相同的外消旋单轴底物中合成两组具有邻接 C-C 轴和 N-N 轴的立体异构体。只需改变单一催化剂的构型,就能获得所有四种立体异构体。通过共价解锁/锁定和热异构化过程的连续进行,可以在所有四种异构体状态之间进行顺序切换,同时实现电子圆二色性信号反转,从而提供了一个多态气旋分子开关的实例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.10
自引率
0.00%
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审稿时长
10 weeks
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