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基于1,2-二轴阻转异构体的手性分子开关的发散合成

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

作者信息

Han Tian-Jiao, Yang Qiu-Le, Hu Jiaen, Wang Min-Can, Mei Guang-Jian

机构信息

College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.

Pingyuan Laboratory (Zhengzhou University), Zhengzhou 450001, China.

出版信息

JACS Au. 2024 Oct 14;4(11):4445-4454. doi: 10.1021/jacsau.4c00777. eCollection 2024 Nov 25.

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.

摘要

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手性光分子开关的开发,目前是一个充满活力的科技前沿领域。在此,我们报道了一种基于1,2-二轴阻转异构体的实用人工动态系统。有机催化的平行动力学拆分允许从相同的外消旋单轴底物出发,发散合成两组具有邻位C-C和N-N轴的立体异构体。通过简单地改变单一催化剂的构型,可以得到所有四种立体异构体。共价解锁/锁定和热异构化过程的连续进行,能够实现所有四种阻转异构状态之间的顺序切换,并伴有电子圆二色性信号反转,提供了一个多态手性光分子开关的实例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/261d/11600187/9bb7282262b3/au4c00777_0001.jpg

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