The low-field effect in radical pairs: A zero-field singlet–triplet basis picture

We present a new formulation of the low-field effect (LFE) in spin-correlated radical pairs based on a zero-field singlet-triplet basis for the isotropic spin Hamiltonian. The aim is to provide a description that is both formally rigorous and mechanistically transparent, especially in the regime of weak magnetic fields such as the geomagnetic field. For the standard model radical pair containing a single spin-12 nucleus, we show that the usual electron singlet-triplet basis obscures the distinct dynamical roles of the hyperfine and Zeeman interactions. In a zero-field S-T basis constructed from the angular-momentum structure of the zero-field Hamiltonian, by contrast, the mechanism separates cleanly: isotropic hyperfine coupling mixes singlet-doublet and triplet-doublet states, whereas the weak-field Zeeman interaction mixes triplet-quartet and triplet-doublet states without directly introducing an additional singlet-triplet coupling. The LFE is, therefore, revealed as a sequential process in which a weak field unlocks access from a triplet-only manifold to a singlet-accessible triplet manifold, from which hyperfine-driven singlet-triplet interconversion can occur. We then generalize this picture to radical pairs with arbitrary isotropic hyperfine structures by identifying maximal, interior, and, when present, minimal triplet-only manifolds in the zero-field spectrum. Finally, we introduce a practical blockwise triplet-only state recruitment measure for the triplet-only zero-field state space made singlet-accessible by a weak field and show how this quantity depends on hyperfine symmetry, including the effects of equivalent nuclei. The resulting framework provides both a simple physical picture of the LFE and a general route for estimating its structural upper bound for arbitrary radical pairs.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-06-16
DOI
https://doi.org/10.1063/5.0337201
Primary Topic
Magnetism in coordination complexes
Type
article
Field-Weighted Citation Impact
0.00

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article

The low-field effect in radical pairs: A zero-field singlet–triplet basis picture

Jonathan Woodward
The Journal of Chemical Physics
Magnetism in coordination complexes
article

The low-field effect in radical pairs: A zero-field singlet–triplet basis picture

Jonathan Woodward
article en

Abstract

We present a new formulation of the low-field effect (LFE) in spin-correlated radical pairs based on a zero-field singlet-triplet basis for the isotropic spin Hamiltonian. The aim is to provide a description that is both formally rigorous and mechanistically transparent, especially in the regime of weak magnetic fields such as the geomagnetic field. For the standard model radical pair containing a single spin-12 nucleus, we show that the usual electron singlet-triplet basis obscures the distinct dynamical roles of the hyperfine and Zeeman interactions. In a zero-field S-T basis constructed from the angular-momentum structure of the zero-field Hamiltonian, by contrast, the mechanism separates cleanly: isotropic hyperfine coupling mixes singlet-doublet and triplet-doublet states, whereas the weak-field Zeeman interaction mixes triplet-quartet and triplet-doublet states without directly introducing an additional singlet-triplet coupling. The LFE is, therefore, revealed as a sequential process in which a weak field unlocks access from a triplet-only manifold to a singlet-accessible triplet manifold, from which hyperfine-driven singlet-triplet interconversion can occur. We then generalize this picture to radical pairs with arbitrary isotropic hyperfine structures by identifying maximal, interior, and, when present, minimal triplet-only manifolds in the zero-field spectrum. Finally, we introduce a practical blockwise triplet-only state recruitment measure for the triplet-only zero-field state space made singlet-accessible by a weak field and show how this quantity depends on hyperfine symmetry, including the effects of equivalent nuclei. The resulting framework provides both a simple physical picture of the LFE and a general route for estimating its structural upper bound for arbitrary radical pairs.

The Journal of Chemical PhysicsVol. 164(23)
Tokyo University of the Arts (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 17%
Magnetism in coordination complexes
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