Chiral photochemistry of achiral molecules

Umberto Raucci, Hayley Weir, Christoph Bannwarth, David M. Sanchez and Todd J. Martínez ()
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Umberto Raucci: Stanford University
Hayley Weir: Stanford University
Christoph Bannwarth: Stanford University
David M. Sanchez: Stanford University
Todd J. Martínez: Stanford University

Nature Communications, 2022, vol. 13, issue 1, 1-7

Abstract: Abstract Chirality is a molecular property governed by the topography of the potential energy surface (PES). Thermally achiral molecules interconvert rapidly when the interconversion barrier between the two enantiomers is comparable to or lower than the thermal energy, in contrast to thermally stable chiral configurations. In principle, a change in the PES topography on the excited electronic state may diminish interconversion, leading to electronically prochiral molecules that can be converted from achiral to chiral by electronic excitation. Here we report that this is the case for two prototypical examples – cis-stilbene and cis-stiff stilbene. Both systems exhibit unidirectional photoisomerization for each enantiomer as a result of their electronic prochirality. We simulate an experiment to demonstrate this effect in cis-stilbene based on its interaction with circularly polarized light. Our results highlight the drastic change in chiral behavior upon electronic excitation, opening up the possibility for asymmetric photochemistry from an effectively nonchiral starting point.

Date: 2022
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DOI: 10.1038/s41467-022-29662-1

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