Dinuclear Dysprosium Compounds: The Importance of Rigid Bridges

We report the synthesis, structures and magnetic behaviour of two isostructural dinuclear Dy<sup>3+</sup> complexes where the metal ions of a previously reported monomeric building block are connected by a peroxide (O<sub>2</sub> <sup>2-</sup>) or a pair of fluoride (2×F<sup>-</sup>) bridges. The nature of the bridge determines the distance between the metal ion dipoles leading to a dipolar coupling in the peroxido bridged compound of only ca. 70 % of that in the bis-fluorido bridged dimer. The sign of the overall coupling between the metals is antiferromagnetic for the peroxido bridged compound and ferromagnetic for the bis-fluorido bridged complex. This in turn influences the magnetisation dynamics. We compare the relaxation characteristics of the dimers with those of the previously reported monomeric building block. The relaxation dynamics for the bis-fluorido system are very fast. On the other hand, comparing the properties of the monomer, the peroxido bridged sample and the corresponding Y-doped sample show that the relaxation properties via a Raman process have very similar parameters. We show that a second dysprosium is important for either tuning or detuning the Single Molecule Magnet (SMM) properties of a system.

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Publication Details

Journal
Chemistry - A European Journal
Published
2024-10-07
DOI
https://doi.org/10.1002/chem.202403002
Citations
10
Primary Topic
Magnetism in coordination complexes
Type
article
Field-Weighted Citation Impact
1.18

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article

Dinuclear Dysprosium Compounds: The Importance of Rigid Bridges

Annie K. Powell, Matteo Briganti, Thomas Ruppert, Mauro Perfetti et al.
10 citations
Chemistry - A European Journal
Magnetism in coordination complexes
1.18
article

Dinuclear Dysprosium Compounds: The Importance of Rigid Bridges

Annie K. Powell, Matteo Briganti, Thomas Ruppert, Mauro Perfetti, Christopher E. Anson, Jonas Braun, Jacques Ollivier, Niels Andreas Bonde, Thomas Bergfeldt, Rouven F. Pfleger, Stergios Piligkos, Jesper Bendix
article en
10 citations

Abstract

We report the synthesis, structures and magnetic behaviour of two isostructural dinuclear Dy<sup>3+</sup> complexes where the metal ions of a previously reported monomeric building block are connected by a peroxide (O<sub>2</sub> <sup>2-</sup>) or a pair of fluoride (2×F<sup>-</sup>) bridges. The nature of the bridge determines the distance between the metal ion dipoles leading to a dipolar coupling in the peroxido bridged compound of only ca. 70 % of that in the bis-fluorido bridged dimer. The sign of the overall coupling between the metals is antiferromagnetic for the peroxido bridged compound and ferromagnetic for the bis-fluorido bridged complex. This in turn influences the magnetisation dynamics. We compare the relaxation characteristics of the dimers with those of the previously reported monomeric building block. The relaxation dynamics for the bis-fluorido system are very fast. On the other hand, comparing the properties of the monomer, the peroxido bridged sample and the corresponding Y-doped sample show that the relaxation properties via a Raman process have very similar parameters. We show that a second dysprosium is important for either tuning or detuning the Single Molecule Magnet (SMM) properties of a system.

Chemistry - A European JournalVol. 31(7)
Karlsruhe Institute of Technology (DE), University of Copenhagen (DK), Institut Laue-Langevin (FR), University of Florence (IT)
European Commission, Helmholtz-Gemeinschaft, Deutsche Forschungsgemeinschaft, Università degli Studi di Firenze, Helmholtz Association, Fondazione Cassa di Risparmio di Firenze, Karlsruhe House of Young Scientists, HORIZON EUROPE European Research Council
Openalex Percentile: Top 23%
Magnetism in coordination complexes
1.18
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