Magnetic Anisotropy and Spin Coupling in a Cobalt(II) Dimer with Bioinspired Bridges

Cobalt(II) metal complexes constitute a versatile platform for investigating how coordination geometry and spin–orbit coupling determine their magnetic properties. Although numerous cobalt(II) coordination complexes have been reported in recent literature, only a limited number exhibit comprehensive and quantitatively reliable magnetic characterization. In this work, we investigate the magnetic properties of the hexacoordinated cobalt dimer [Co2(μ-L1H)2(μ-H2O)2(H2O)4]4NO3·2H2O, where L1H denotes the adenine bridging ligand. The hexacoordinated environment stabilizes a high-spin S = 3/2 configuration for both Co(II) centers, resulting in strong spin–orbit coupling and significant zero-field splitting, described by axial (D) and rhombic (E) anisotropy parameters. Fits to magnetic susceptibility and magnetization data reveal antiferromagnetic coupling between the Co(II) ions, with a ratio of E/D ≈ 1/4 and D/kB = 89 K, evidencing pronounced magnetic anisotropy in the system. This behavior is further supported by anisotropic Landé factors gx = gy = 2.5 and gz = 2.4, consistent with easy-plane magnetic anisotropy.

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Publication Details

Journal
ACS Physical Chemistry Au
Published
2026-02-26
DOI
https://doi.org/10.1021/acsphyschemau.5c00134
Primary Topic
Magnetism in coordination complexes
Type
article
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article

Magnetic Anisotropy and Spin Coupling in a Cobalt(II) Dimer with Bioinspired Bridges

L. Ghivelder, Mariem Masmoudi, Clebson Cruz, Paula Brandão et al.
ACS Physical Chemistry Au
Magnetism in coordination complexes
article

Magnetic Anisotropy and Spin Coupling in a Cobalt(II) Dimer with Bioinspired Bridges

L. Ghivelder, Mariem Masmoudi, Clebson Cruz, Paula Brandão, Ana Clara das Neves, Mario Reis, Alan Almeida
article en

Abstract

Cobalt(II) metal complexes constitute a versatile platform for investigating how coordination geometry and spin–orbit coupling determine their magnetic properties. Although numerous cobalt(II) coordination complexes have been reported in recent literature, only a limited number exhibit comprehensive and quantitatively reliable magnetic characterization. In this work, we investigate the magnetic properties of the hexacoordinated cobalt dimer [Co2(μ-L1H)2(μ-H2O)2(H2O)4]4NO3·2H2O, where L1H denotes the adenine bridging ligand. The hexacoordinated environment stabilizes a high-spin S = 3/2 configuration for both Co(II) centers, resulting in strong spin–orbit coupling and significant zero-field splitting, described by axial (D) and rhombic (E) anisotropy parameters. Fits to magnetic susceptibility and magnetization data reveal antiferromagnetic coupling between the Co(II) ions, with a ratio of E/D ≈ 1/4 and D/kB = 89 K, evidencing pronounced magnetic anisotropy in the system. This behavior is further supported by anisotropic Landé factors gx = gy = 2.5 and gz = 2.4, consistent with easy-plane magnetic anisotropy.

ACS Physical Chemistry AuVol. 6(2)
Universidade Federal do Rio de Janeiro (BR), Universidade Federal Fluminense (BR), Universidade Federal do Oeste da Bahia (BR), Universidade do Estado do Rio de Janeiro (BR), Centro Regional de Derechos Humanos y Justicia de Género, Corporación Humanas (CL), University of Aveiro (PT), Universidade Federal do ABC (BR)
Openalex Percentile: Top 45%
Magnetism in coordination complexes
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