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Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand
James P Durrant1, Jinkui Tang2, Akseli Mansikkamäki3
1Department of Chemistry, School of Life Sciences, University of Sussex, Brighton, BN1 9QR, UK. R.Layfield@sussex.ac.uk and School of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Abstract:
Intact transfer of the cyclobutadienyl ligand [C4(SiMe3)4]2- to yttrium and dysprosium (M) produces the half-sandwich complexes [M{η4-C4(SiMe3)4}(BH4)2(THF)]- as coordination polymers with bridging sodium or potassium ions. The dysprosium versions are single-molecule magnets (SMMs) with energy barriers of 371(7) and 357(4) cm-1, respectively. The pristine cyclobutadienyl ligands provide a strong axial crystal field that enhances the SMM properties relative to related cyclopentadienyl compounds.
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