<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Errulat D</submitter><pubmed_abstract>Single-ion anisotropy is vital for the observation of Single-Molecule Magnet (SMM) properties (i.e., a slow dynamics of the magnetization) in lanthanide-based systems. In the case of europium, the occurrence of this phenomenon has been inhibited by the spin and orbital quantum numbers that give way to J = 0 in the trivalent state and the half-filled population of the 4f orbitals in the divalent state. Herein, by optimizing the local crystal field of a quasi-linear bis(silylamido) Eu&lt;sup>II&lt;/sup> complex, the [Eu&lt;sup>II&lt;/sup>(N{SiMePh&lt;sub>2&lt;/sub>}&lt;sub>2&lt;/sub>)&lt;sub>2&lt;/sub>] SMM is described, providing an example of a europium complex exhibiting slow relaxation of its magnetization. This behavior is dominated by a thermally activated (Orbach-like) mechanism, with an effective energy barrier of approximately 8 K, determined by bulk magnetometry and electron paramagnetic resonance. Ab initio calculations confirm second-order spin-orbit coupling effects lead to non-negligible axial magnetic anisotropy, splitting the ground state multiplet into four Kramers doublets, thereby allowing for the observation of an Orbach-like relaxation at low temperatures.</pubmed_abstract><journal>Nature communications</journal><pagination>3010</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11001981</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Slow magnetic relaxation in a europium(II) complex.</pubmed_title><pmcid>PMC11001981</pmcid><pubmed_authors>Rouzieres M</pubmed_authors><pubmed_authors>Hill S</pubmed_authors><pubmed_authors>Harriman KLM</pubmed_authors><pubmed_authors>Errulat D</pubmed_authors><pubmed_authors>van Tol J</pubmed_authors><pubmed_authors>Clerac R</pubmed_authors><pubmed_authors>Galico DA</pubmed_authors><pubmed_authors>Mansikkamaki A</pubmed_authors><pubmed_authors>Murugesu M</pubmed_authors><pubmed_authors>Salerno EV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Slow magnetic relaxation in a europium(II) complex.</name><description>Single-ion anisotropy is vital for the observation of Single-Molecule Magnet (SMM) properties (i.e., a slow dynamics of the magnetization) in lanthanide-based systems. In the case of europium, the occurrence of this phenomenon has been inhibited by the spin and orbital quantum numbers that give way to J = 0 in the trivalent state and the half-filled population of the 4f orbitals in the divalent state. Herein, by optimizing the local crystal field of a quasi-linear bis(silylamido) Eu&lt;sup>II&lt;/sup> complex, the [Eu&lt;sup>II&lt;/sup>(N{SiMePh&lt;sub>2&lt;/sub>}&lt;sub>2&lt;/sub>)&lt;sub>2&lt;/sub>] SMM is described, providing an example of a europium complex exhibiting slow relaxation of its magnetization. This behavior is dominated by a thermally activated (Orbach-like) mechanism, with an effective energy barrier of approximately 8 K, determined by bulk magnetometry and electron paramagnetic resonance. Ab initio calculations confirm second-order spin-orbit coupling effects lead to non-negligible axial magnetic anisotropy, splitting the ground state multiplet into four Kramers doublets, thereby allowing for the observation of an Orbach-like relaxation at low temperatures.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-04-05T15:07:39.915Z</modification><creation>2025-04-05T15:07:39.915Z</creation></dates><accession>S-EPMC11001981</accession><cross_references><pubmed>38589348</pubmed><doi>10.1038/s41467-024-46196-w</doi></cross_references></HashMap>