ArticleThe journal of physical chemistry. A2025
Response of a General Restricted Open-Shell Hartree-Fock Wave Function. I: Formalism, Analytic Gradients, and Electric and Magnetic Response Properties.
Article in The journal of physical chemistry. A, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
In this work, the formal development and implementation of a general restricted open-shell Hartree-Fock (g-ROHF) response theory is presented. The theory enables analytic computation of electric and magnetic response properties for arbitrarily complex open-shell configurations. In contrast to traditional ROHF methods, which are typically restricted to high-spin cases, the g-ROHF formulation supports general-spin couplings and orbital degeneracies while preserving the spin purity. A new set of vector-coupling coefficients is introduced that allows for the calculation of a proper spin density from a g-ROHF wave function. Analytic nuclear derivatives, along with the electric and magnetic orbital Hessians, are derived in a unified framework. Special attention is given to the treatment of SCF instabilities and the projection of unphysical modes from the response space. An efficient AO-driven implementation is described and validated across a broad range of open-shell systems, including small molecules, transition-metal complexes, and metal-radical assemblies. Specifically, the method is applied to the calculation of g-tensors and hyperfine couplings (including spin-orbit coupling corrections) in experimentally well-characterized systems such as mixed-valence manganese(III/IV) dimers and the metal-radical complex Fe(GMA)(pyridine)
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