Atom-centered electric multipole moments dynamically generated from QM/MM MD simulations

Atom-centered electric multipole moments can be extremely useful in chemistry, as they enable the systematic mapping of a complex electrostatic problem to a simpler model. However, since they do not correspond to physical observables, there is no unique way to define them. In this study, we present an extension of the dynamically generated RESP charges (D-RESP) method, referred to as xDRESP, where atom-centered multipoles are computed from mixed quantum mechanics/molecular mechanics molecular dynamics simulations. We compare the ability of xDRESP charges to reproduce the electrostatic potential, as well as molecular multipoles, against the performance of fixed point-charge models commonly used in force fields. Moreover, we highlight cases where xDRESP atomic multipoles can provide valuable information about chemical systems, such as indicating when polarization plays a significant role, and chemical reactions in which xDRESP atomic multipoles can be used as an on-the-fly analysis tool to track changes in electron density.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-03-04
DOI
https://doi.org/10.1063/5.0312012
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
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article

Atom-centered electric multipole moments dynamically generated from QM/MM MD simulations

Jógvan Magnus Haugaard Olsen, Andrej Antalík, Andrea Levy, Ursula Rothlisberger
The Journal of Chemical Physics
Advanced Chemical Physics Studies
article

Atom-centered electric multipole moments dynamically generated from QM/MM MD simulations

Jógvan Magnus Haugaard Olsen, Andrej Antalík, Andrea Levy, Ursula Rothlisberger
article en

Abstract

Atom-centered electric multipole moments can be extremely useful in chemistry, as they enable the systematic mapping of a complex electrostatic problem to a simpler model. However, since they do not correspond to physical observables, there is no unique way to define them. In this study, we present an extension of the dynamically generated RESP charges (D-RESP) method, referred to as xDRESP, where atom-centered multipoles are computed from mixed quantum mechanics/molecular mechanics molecular dynamics simulations. We compare the ability of xDRESP charges to reproduce the electrostatic potential, as well as molecular multipoles, against the performance of fixed point-charge models commonly used in force fields. Moreover, we highlight cases where xDRESP atomic multipoles can provide valuable information about chemical systems, such as indicating when polarization plays a significant role, and chemical reactions in which xDRESP atomic multipoles can be used as an on-the-fly analysis tool to track changes in electron density.

The Journal of Chemical PhysicsVol. 164(9)
École Polytechnique Fédérale de Lausanne (CH), Technical University of Denmark (DK)
Openalex Percentile: Top 34%
Advanced Chemical Physics Studies
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