Evidence map›Paper›PMID 41071957›Full record

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.

Frank Neese

Abstract read
In one paragraph

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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

1 author.

Frank NeeseDepartment of Molecular Theory and Spectroscopy, Max Planck Institut für Kohlenforschung, Kaiser Wilhelm Platz 1, Mülheim an der Ruhr D-45470, Germany.ORCID 0000-0003-4691-0547

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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)

Identifiers

PMID41071957
PMCPMC12557359

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.