Magnetic exchange interactions in binuclear and tetranuclear iron(III) complexes described by spin‐flip DFT and Heisenberg effective Hamiltonians. Issue 3 (14th June 2022)

• Record Type: Journal Article
• Authors: Kotaru, Saikiran; Kähler, Sven; Alessio, Maristella; Krylov, Anna I.
• Is Part Of: Journal of computational chemistry. Volume 44:Issue 3(2023)
• Page Start: 367
• Page End: 380
• Publication Date: 2022-06-14
• Subjects: electronic structure calculations -- Heisenberg Hamiltonian -- magnetic exchange interactions -- single‐molecule magnets -- spin‐flip methods -- quantum chemistry; Chemistry -- Data processing -- Periodicals; 542.85
• DOI: 10.1002/jcc.26941
• Languages: English
• ISSNs: 0192-8651

Abstract

Abstract: Low‐energy spectra of single‐molecule magnets (SMMs) are often described by Heisenberg Hamiltonians. Within this formalism, exchange interactions between magnetic centers determine the ground‐state multiplicity and energy separation between the ground and excited states. In this contribution, we extract exchange coupling constants ( J ) for a set of iron (III) binuclear and tetranuclear complexes from all‐electron calculations using non‐collinear spin‐flip time‐dependent density functional theory (NC‐SF‐TDDFT). For 12 binuclear complexes with J ‐values ranging from −6 to −132 cm −1, our benchmark calculations using the short‐range hybrid ω PBEh functional and 6‐31G(d, p) basis set agree well with the experimentally derived values (mean absolute error of 4.7 cm −1 ). For the tetranuclear SMMs, the computed J constants are within 6 cm −1 from the experimentally derived values. We explore the range of applicability of the Heisenberg model by analyzing bonding patterns in these Fe(III) complexes using natural orbitals (NO), their occupations, and the number of effectively unpaired electrons. The results illustrate the efficiency of the spin‐flip protocol for computing the exchange couplings and the utility of the NO analysis in assessing the validity of effective spin Hamiltonians. Abstract : Exchange interactions in polynuclear Fe (III) compounds are derived from ab initio calculations based on a single spin‐flip (1SF) approach.