Ultrafast radiation chemistry of glycine in aqueous solution

Investigating the ultrafast dynamics of primary biological compounds is crucial for gaining insights into radiation damage. We computationally investigate the ionization-induced dynamics of glycine in an aqueous solution. By employing fewest-switches-surface hopping simulations, we specifically address ionization in different orbital levels of the glycine molecule as well as in water molecules in its solvation shell. Upon ionization, glycine undergoes rapid fragmentation on the Cα-C bond, resulting in the formation of CO2 and the methylamine (+H3NH2C⋅) radical. Our analysis shows that the solvation shell has little effect on the fragmentation dynamics. When ionized in water, or a deeper valence orbital of glycine, the system first relaxes to the ground state, involving the transfer of the valence hole between water and glycine. The associated redox reaction exemplifies the oxidizing power of H2O⋅+.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-02-24
DOI
https://doi.org/10.1063/5.0316290
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Ultrafast radiation chemistry of glycine in aqueous solution

Anthony Ferté, Mathilde Goullieux, Robin Santra, Ana Martínez Gutiérrez et al.
The Journal of Chemical Physics
Spectroscopy and Quantum Chemical Studies
article

Ultrafast radiation chemistry of glycine in aqueous solution

Anthony Ferté, Mathilde Goullieux, Robin Santra, Ana Martínez Gutiérrez, Ludger Inhester
article en

Abstract

Investigating the ultrafast dynamics of primary biological compounds is crucial for gaining insights into radiation damage. We computationally investigate the ionization-induced dynamics of glycine in an aqueous solution. By employing fewest-switches-surface hopping simulations, we specifically address ionization in different orbital levels of the glycine molecule as well as in water molecules in its solvation shell. Upon ionization, glycine undergoes rapid fragmentation on the Cα-C bond, resulting in the formation of CO2 and the methylamine (+H3NH2C⋅) radical. Our analysis shows that the solvation shell has little effect on the fragmentation dynamics. When ionized in water, or a deeper valence orbital of glycine, the system first relaxes to the ground state, involving the transfer of the valence hole between water and glycine. The associated redox reaction exemplifies the oxidizing power of H2O⋅+.

The Journal of Chemical PhysicsVol. 164(8)
Universität Hamburg (DE), Deutsches Elektronen-Synchrotron DESY (DE), Instituto de Ciencia de Materiales de Madrid (ES), Center for Free-Electron Laser Science (DE), Max Planck Institute for the Structure and Dynamics of Matter (DE)
Clean water and sanitation
Openalex Percentile: Top 44%
Spectroscopy and Quantum Chemical Studies
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