Related Experiment Video
Updated: Jul 16, 2025

Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers
Published on: August 18, 2017
Precise Detection, Control and Synthesis of Chiral Compounds at Single-Molecule Resolution
Chen Yang1, Weilin Hu1, Xuefeng Guo2,3
1Beijing National Laboratory for Molecular Sciences, National Biomedical Imaging Center, College of Chemistry and Molecular Engineering, Peking University, 292 Chengfu Road, Haidian District, Beijing, 100871, People's Republic of China.
This study introduces a universal strategy for chirality detection and control using external symmetry breaking. Single-molecule junctions enable precise, event-resolved synthesis and detection of chiral molecules.
Area of Science:
- Molecular Chirality
- Asymmetric Synthesis
- Single-Molecule Electronics
Background:
- Chirality is crucial in biological processes, necessitating accurate detection and preparation of homochiral compounds.
- Current methods for chiral recognition and synthesis are often inefficient due to molecular disorder and custom reagent requirements.
Discussion:
- A universal strategy is proposed using external symmetry breaking to align molecular frames with stimuli.
- Explores the interplay between molecular chirality, electron spin, and photon polarization for symmetry breaking.
- Single-molecule junctions are presented as a platform for single-event chirality detection and synthesis.
Key Insights:
- External stimuli-induced molecular alignment offers a universal approach to chirality control.
- Single-molecule junctions provide high-resolution detection and synthesis capabilities.
- CMOS-compatible interfaces facilitate external symmetry breaking for practical applications.
Outlook:
- This approach promises more efficient and accurate methods for chirality detection and asymmetric synthesis.
- Interdisciplinary collaboration is key to advancing applications in chemistry, physics, and engineering.
- Potential for integration into advanced materials and devices for chiral analysis and production.
Related Concept Videos
Chirality in Nature
Molecules with Multiple Chiral Centers
Chirality
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Prochirality
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
Racemic Mixtures and the Resolution of Enantiomers

