Abstract
<h2>Summary</h2> Single-molecule magnets (SMMs) are molecules that can retain magnetic polarization in the absence of an external magnetic field and embody the ultimate size limit for spin-based information storage and processing. Multimetallic lanthanide complexes lacking magnetic exchange coupling enable fast relaxation pathways that attenuate the full potential of these species. Employment of diamagnetic heavy main group elements with diffuse orbitals may lead to unprecedented strong coupling. Herein, two bismuth-cluster-bridged lanthanide complexes, [K(THF)<sub>4</sub>]<sub>2</sub>[Cp∗<sub>2</sub>Ln<sub>2</sub>Bi<sub>6</sub>] (Cp∗ = pentamethylcyclopentadienyl; <b>1-Ln</b>, Ln = Tb, Dy), were synthesized via a solution organometallic approach. The neutral [Ln<sub>2</sub>Bi<sub>6</sub>] heterometallocubane core features lanthanide centers that are bridged by a rare Bi<sub>6</sub><sup>6−</sup> Zintl ion, which supports strong ferromagnetic interactions between lanthanides. This affords the rare observation of magnetic blocking and open hysteresis loops for superexchange-coupled SMMs comprising solely lanthanide ions. Both compounds constitute the first SMMs containing bismuth donors paving the way for promising synthetic targets for quantum computation.
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