1. Enantioselective fragmentation of an achiral molecule in a strong laser field
- Author
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L. Ph. H. Schmidt, Robert Berger, M. Weller, Markus Schöffler, Sebastian Eckart, Martin Pitzer, C. Janke, Alexander Hartung, Till Jahnke, D. Trabert, K. Fehre, S. Zeller, Jonas Rist, Maksim Kunitski, and Reinhard Dörner
- Subjects
inorganic chemicals ,High Energy Physics::Lattice ,010402 general chemistry ,01 natural sciences ,Condensed Matter::Materials Science ,Fragmentation (mass spectrometry) ,0103 physical sciences ,polycyclic compounds ,Physics::Atomic and Molecular Clusters ,Molecule ,heterocyclic compounds ,Physics::Chemical Physics ,010306 general physics ,Circular polarization ,Research Articles ,Physics ,Quantitative Biology::Biomolecules ,Multidisciplinary ,organic chemicals ,Enantioselective synthesis ,Coulomb explosion ,technology, industry, and agriculture ,SciAdv r-articles ,Helicity ,0104 chemical sciences ,Chemistry ,Chemical physics ,Enantiomer ,Chirality (chemistry) ,Research Article - Abstract
Prochiral formic acid has been enantioselectively driven to chiral fragmentation, leading to photoion circular dichroism in the molecular frame., Chirality is omnipresent in living nature. On the single molecule level, the response of a chiral species to a chiral probe depends on their respective handedness. A prominent example is the difference in the interaction of a chiral molecule with left or right circularly polarized light. In the present study, we show by Coulomb explosion imaging that circularly polarized light can also induce a chiral fragmentation of a planar and thus achiral molecule. The observed enantiomer strongly depends on the orientation of the molecule with respect to the light propagation direction and the helicity of the ionizing light. This finding might trigger new approaches to improve laser-driven enantioselective chemical synthesis.
- Published
- 2019