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Metal-organic compounds that feature magnetic bistability have been proposed as bits for magnetic storage, but progress has been slow. Four-coordinate cobalt(II) complexes feature high inversion barriers of the magnetic moment, but they lack magnetic bistability. Developing radical-bridged polynuclear systems is a promising strategy to encounter this; however detailed investigations of such species are scarce. We report an air-stable radical-bridged dinuclear cobalt(II) complex, studied by a combination of magnetometry and spectroscopy. Fits of the data give D = -113 cm for the zero-field splitting (ZFS) and J = 390 cm for the metal-radical exchange. Ab initio investigations reveal first-order spin-orbit coupling of the quasi-degenerate and d orbitals to be at the heart of the large ZFS. The corresponding transitions are spectroscopically observed, as are transitions related to the exchange coupling. Finally, signatures of spin-phonon coupling are observed and theoretically analyzed. Furthermore, we demonstrate that the spectral features are not predominantly spin excitations, but largely vibrational in character.
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http://dx.doi.org/10.1038/s41467-025-57210-0 | DOI Listing |
Chemistry
July 2025
Department of Chemistry and Biomolecular Sciences, University of Ottawa, 10 Marie Curie, Ottawa, Ontario, K1N 6N5, Canada.
Exchange coupling is essential in defining the magnetic behavior of polymetallic lanthanide-based (Ln) single-molecule magnets (SMMs), where, thanks to the unpaired electron(s), radical ligands show promise as magnetic bridges between the paramagnetic metal centers. Combining high-performance lanthanide metallocene [Cp*₂Ln] (Cp* = pentamethylcyclopentadienyl) units with the 3,6-bis(2-pyrimidyl)-1,2,4,5-tetrazine radical ligand (bmtz) yielded two new radical-bridged dinuclear lanthanide metallocenes, [(Cp*₂Ln)₂(bmtz)](BPh)·Solvent (Ln = Gd (1), Solvent = THF; Dy (2), Solvent = toluene). The strong magnetic exchange coupling of J = -12.
View Article and Find Full Text PDFNat Commun
March 2025
Institute of Physical Chemistry, University of Stuttgart, Stuttgart, Germany.
Metal-organic compounds that feature magnetic bistability have been proposed as bits for magnetic storage, but progress has been slow. Four-coordinate cobalt(II) complexes feature high inversion barriers of the magnetic moment, but they lack magnetic bistability. Developing radical-bridged polynuclear systems is a promising strategy to encounter this; however detailed investigations of such species are scarce.
View Article and Find Full Text PDFJACS Au
September 2024
Institut für Anorganische Chemie and International Center for Advanced Studies of Energy Conversion, Georg-August-Universität Göttingen, Tammannstraße 4, 37077 Göttingen, Germany.
Photolysis of a platinum(II) azide complex in the presence of styrenes enables C=C double bond cleavage upon dissociative olefin imination to aldimido (Pt-N=CHPh) and formimido (Pt-N=CH) complexes as the main products. Spectroscopic and quantum chemical examinations support a mechanism that commences with the decay of the metallonitrene photoproduct (Pt-N) via bimolecular coupling and nitrogen loss as N. The resulting platinum(I) complex initiates a radical chain mechanism via a dinuclear radical-bridged species (Pt-CHCHPhN-Pt) as a direct precursor to C-C scission.
View Article and Find Full Text PDFChemistry
December 2024
Department of Chemistry, Indian Institute of Science Education and Research Bhopal, Address IISER Bhopal, Bhopal, Madhya Pradesh, 462066, India.
A well-judged combination of a high axial ligand field and a bridging radical ligand in a dinuclear lanthanide complex provides a single-molecule magnet with a higher effective energy barrier for magnetic relaxation and blocking temperature compared to its non-radical analog due to significant magnetic exchange coupling between radical and Ln(III) ions. In this work, we report two chloranilate (CA) bridged dinuclear dysprosium complexes, [{(bbpen)Dy(μ-CA)Dy(bbpen)}] (1Dy) and [{(bbpen)Dy(μ-CA⋅)Dy(bbpen)}{CoCp}] (2Dy), where 2Dy is the radical bridged Dy-complex obtained via the chemical reduction of bridging CA moiety (Hbbpen=N,N'-bis(2-hydroxybenzyl)-N,N'-bis(2-methylpyridyl)ethylenediamine). The presence of high electronegative phenoxide moiety enhances the axial anisotropy of pseudo-square antiprismatic Dy(III) ions.
View Article and Find Full Text PDFInorg Chem
May 2024
Department of Chemistry, Michigan State University (MSU), 578 South Shaw Lane, East Lansing, Michigan 48824, United States.
Ancillary ligand scaffolds that sufficiently stabilize a metal ion to allow its coordination to an open-shell ligand are scarce, yet their development is essential for next-generation spin-based materials with topical applications in quantum information science. To this end, a synthetic challenge must be met: devising molecules that enable the binding of a redox-active ligand through facile displacement and clean removal of a weakly coordinating anion. Here, we probe the accessibility of unprecedented radical-containing rare-earth guanidinate complexes by combining our recently discovered yttrium tetraphenylborate complex [{(MeSi)NC(NPr)}Y][(μ-η-Ph)(BPh)] with the redox-active ligands 2,2'-bipyridine (bpy) and 2,2'-bis(benzimidazole) (Bbim), respectively, under reductive conditions.
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