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

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.

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Publication Details

Journal
JACS Au
Published
2024-10-14
DOI
https://doi.org/10.1021/jacsau.4c00777
Citations
17
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
4.25

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article

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

Jin‐Feng Hu, Tian‐Jiao Han, Guang‐Jian Mei, Qingxiang Yang et al.
17 citations
JACS Au
Axial and Atropisomeric Chirality Synthesis
4.25
article

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

Jin‐Feng Hu, Tian‐Jiao Han, Guang‐Jian Mei, Qingxiang Yang, Min‐Can Wang
article en
17 citations

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.

JACS AuVol. 4(11)
Zhengzhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 5%
Axial and Atropisomeric Chirality Synthesis
4.25
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