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Updated: Feb 19, 2026

Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers
Published on: August 18, 2017
Chiral Imprinting in the Gas Phase
David W Pratt1, Brooks H Pate2
1University of Vermont, Department of Chemistry, Discovery Building, 82 University Place, Burlington, 05405, USA.
Scientists can now control molecular handedness. Using precise microwave pulses, they successfully altered the proportions of specific enantiomers in a large gas-phase molecule, a breakthrough in chiral chemistry.
Area of Science:
- Chirality and molecular symmetry
- Quantum control of molecular populations
- Gas-phase spectroscopy
Background:
- Enantiomers are non-superimposable mirror-image molecules with identical physical properties.
- Controlling enantiomeric populations is crucial for pharmaceuticals and materials science.
- Previous methods for enantiomeric separation or enrichment were often complex or inefficient.
Purpose of the Study:
- To demonstrate the selective manipulation of enantiomeric populations in large gas-phase molecules.
- To explore the use of resonant microwave fields for controlling molecular chirality.
- To establish a novel method for enantiomeric enhancement.
Main Methods:
- Application of phase- and polarization-controlled microwave pulse sequences.
- Targeting specific enantiomers of a chiral terpene in the gas phase.
- Monitoring changes in relative enantiomeric populations.
Main Results:
- Successful enhancement of one enantiomer's population over the other.
- Demonstration of precise control over molecular enantiomeric ratios.
- Validation of microwave-driven population transfer for chiral molecules.
Conclusions:
- Resonant microwave fields offer a viable pathway for controlling enantiomeric composition.
- This technique provides a new tool for enantioselective synthesis and separation.
- The findings open avenues for manipulating molecular chirality with high precision.
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