Hydrogen Bonds under Electric Fields with Quantum Accuracy

Hydrogen bonds (H-bonds) are pivotal in various chemical and biological systems and exhibit complex behavior under external perturbations. This study investigates the structural, vibrational, and energetic properties of prototypical H-bonded dimers, water (H<sub>2</sub>O)<sub>2</sub>, hydrogen fluoride (HF)<sub>2</sub>, hydrogen sulfide (H<sub>2</sub>S)<sub>2</sub>, and ammonia (NH<sub>3</sub>)<sub>2</sub> - and the respective monomers under static and homogeneous electric fields (EFs) using the accurate explicitly correlated singles and doubles coupled cluster method (CCSD) for equilibrium geometries and harmonic vibrational frequencies and the perturbative triples CCSD(T) method for energies. As for the vibrational response of the H<sub>2</sub>O, HF, H<sub>2</sub>S, and NH<sub>3</sub> monomers, it turns out that dipole derivatives primarily govern the geometry relaxation. Perturbation theory including cubic anharmonicity can reproduce CCSD results on the vibrational Stark effect, except for NH<sub>3</sub>, where deviations arise due to its floppiness. The field-induced modifications in H-bond lengths, vibrational Stark effects, binding energies, and charge-transfer mechanisms in monomers and dimers are elucidated. Symmetry-adapted perturbation theory (SAPT) analysis on dimers reveals that electrostatics dominates the stabilization of H-bonds across all field strengths, while induction contributions increase significantly with stronger fields, particularly in systems with more polarizable atoms. Our results reveal a universal strengthening of intermolecular interactions at moderate to strong field intensities with significant variability among dimers due to inherent differences in molecular polarizability and charge distribution. Notably, a direct correlation is observed between the binding energies and the vibrational Stark effect of the stretching mode of the H-bond donor molecule, both in relation to the charge-transfer energy term, across all of the investigated dimers. All of these findings provide insights into the EF-driven modulation of H-bonds, highlighting implications for catalysis, hydrogen-based technologies, and biological processes.

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Publication Details

Journal
The Journal of Physical Chemistry A
Published
2025-04-29
DOI
https://doi.org/10.1021/acs.jpca.5c01095
Citations
7
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
8.73

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article

Hydrogen Bonds under Electric Fields with Quantum Accuracy

Franz Saija, Jing Xie, Sebastiano Trusso, Giuseppe Cassone et al.
7 citations
The Journal of Physical Chemistry A
Spectroscopy and Quantum Chemical Studies
8.73
article

Hydrogen Bonds under Electric Fields with Quantum Accuracy

Franz Saija, Jing Xie, Sebastiano Trusso, Giuseppe Cassone, Klaudia Mràzikovà, Matteo Tommasini, Alessandro Amadeo, Marco Francesco Torre
article en
7 citations

Abstract

Hydrogen bonds (H-bonds) are pivotal in various chemical and biological systems and exhibit complex behavior under external perturbations. This study investigates the structural, vibrational, and energetic properties of prototypical H-bonded dimers, water (H<sub>2</sub>O)<sub>2</sub>, hydrogen fluoride (HF)<sub>2</sub>, hydrogen sulfide (H<sub>2</sub>S)<sub>2</sub>, and ammonia (NH<sub>3</sub>)<sub>2</sub> - and the respective monomers under static and homogeneous electric fields (EFs) using the accurate explicitly correlated singles and doubles coupled cluster method (CCSD) for equilibrium geometries and harmonic vibrational frequencies and the perturbative triples CCSD(T) method for energies. As for the vibrational response of the H<sub>2</sub>O, HF, H<sub>2</sub>S, and NH<sub>3</sub> monomers, it turns out that dipole derivatives primarily govern the geometry relaxation. Perturbation theory including cubic anharmonicity can reproduce CCSD results on the vibrational Stark effect, except for NH<sub>3</sub>, where deviations arise due to its floppiness. The field-induced modifications in H-bond lengths, vibrational Stark effects, binding energies, and charge-transfer mechanisms in monomers and dimers are elucidated. Symmetry-adapted perturbation theory (SAPT) analysis on dimers reveals that electrostatics dominates the stabilization of H-bonds across all field strengths, while induction contributions increase significantly with stronger fields, particularly in systems with more polarizable atoms. Our results reveal a universal strengthening of intermolecular interactions at moderate to strong field intensities with significant variability among dimers due to inherent differences in molecular polarizability and charge distribution. Notably, a direct correlation is observed between the binding energies and the vibrational Stark effect of the stretching mode of the H-bond donor molecule, both in relation to the charge-transfer energy term, across all of the investigated dimers. All of these findings provide insights into the EF-driven modulation of H-bonds, highlighting implications for catalysis, hydrogen-based technologies, and biological processes.

The Journal of Physical Chemistry AVol. 129(18)
University of Messina (IT), Beijing Institute of Technology (CN), University of Perugia (IT), Czech Academy of Sciences, J. Heyrovský Institute of Physical Chemistry (CZ), Federal Research and Clinical Center of Physical-Chemical Medicine named after Y.M. Lopukhin (RU), Institute for Chemical and Physical Processes (IT), National Research Council (IT), Cipla (Belgium) (BE), Politecnico di Milano (IT)
Ministero dell'Ambiente e della Tutela del Territorio e del Mare, Ministero dell'Università e della Ricerca
Affordable and clean energy
Openalex Percentile: Top 2%
Spectroscopy and Quantum Chemical Studies
8.73
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