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.
Authors
- Jin‐Feng Hu (ORCID: https://orcid.org/0000-0002-0367-1454)
- Tian‐Jiao Han
- Guang‐Jian Mei (ORCID: https://orcid.org/0000-0002-8248-2327)
- Qingxiang Yang (ORCID: https://orcid.org/0000-0002-2988-4933)
- Min‐Can Wang (ORCID: https://orcid.org/0000-0002-3817-3607)
Institutions
- Zhengzhou University (CN)
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
Funders
- National Natural Science Foundation of China