A trivalent 4f complex with two bis-silylamide ligands displaying slow magnetic relaxation.

Autor: Errulat D; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada., Harriman KLM; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada., Gálico DA; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada., Kitos AA; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada., Mansikkamäki A; NMR Research Unit, University of Oulu, Oulu, Finland., Murugesu M; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada. m.murugesu@uottawa.ca.
Jazyk: angličtina
Zdroj: Nature chemistry [Nat Chem] 2023 Aug; Vol. 15 (8), pp. 1100-1107. Date of Electronic Publication: 2023 May 25.
DOI: 10.1038/s41557-023-01208-y
Abstrakt: The best-performing single-molecule magnets (SMMs) have historically relied on pseudoaxial ligands delocalized across several coordinated atoms. This coordination environment has been found to elicit strong magnetic anisotropy, but lanthanide-based SMMs with low coordination numbers have remained synthetically elusive species. Here we report a cationic 4f complex bearing only two bis-silylamide ligands, Yb(III)[{N(SiMePh 2 ) 2 } 2 ][Al{OC(CF 3 ) 3 } 4 ], which exhibits slow relaxation of its magnetization. The combination of the bulky silylamide ligands and weakly coordinating [Al{OC(CF 3 ) 3 } 4 ] - anion provides a sterically hindered environment that suitably stabilizes the pseudotrigonal geometry necessary to elicit strong ground-state magnetic anisotropy. The resolution of the m J states by luminescence spectroscopy is supported by ab initio calculations, which show a large ground-state splitting of approximately 1,850 cm -1 . These results provide a facile route to access a bis-silylamido Yb(III) complex, and further underline the desirability of axially coordinated ligands with well-localized charges for high-performing SMMs.
(© 2023. The Author(s), under exclusive licence to Springer Nature Limited.)
Databáze: MEDLINE
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