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    Probing Instantaneous Single-Molecule Chirality in the Planar Ground State of Formic Acid

    D. Tsitsonis1, M. Kircher1, N. M. Novikovskiy2, F. Trinter3, J. B. Williams4, K. Fehre1, L. Kaiser1, S. Eckart1, O. Kreuz5 et al.

    A. Senftleben2, Ph. V. Demekhin2,*, R. Berger5,†, T. Jahnke6,7,‡, M. S. Schöffler1,§, and R. Dörner1,∥

    • *Contact author: demekhin@physik.uni-kassel.de
    • †Contact author: robert.berger@uni-marburg.de
    • ‡Contact author: jahnke@atom.uni-frankfurt.de
    • §Contact author: schoeffler@atom.uni-frankfurt.de
    • ∥Contact author: doerner@atom.uni-frankfurt.de

    Phys. Rev. Lett. 136, 043001 – Published 30 January, 2026

    DOI: https://doi.org/10.1103/bvqj-pm3n

    Abstract

    We experimentally demonstrate that individual molecules of formic acid are chiral even when they are in the vibronic ground state, which has a planar equilibrium structure. We ionize the C 1s shell of the molecule and record the photoelectron in coincidence with positively charged fragments. This provides two consecutive measurements of the structure of one molecule, the first by photoelectron diffraction imaging and the second by Coulomb explosion imaging. We find that both measurements show the same handedness of the specific molecule. The phenomenon of being achiral on average but chiral at the level of individual molecules is general to prochiral molecules and is a consequence of the three-dimensional zero-point delocalization of the nuclei in the vibrational ground state.

    Physics Subject Headings (PhySH)

    Corrections

    24 February, 2026

    Correction: An incorrect version of Fig. 1 was used for publication and has now been replaced with the correct version.

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