A Spin Frustrated Hourglass <b>{Gd</b> _<b>9</b> <b>}</b> Molecular Nanomagnet with Unusual Magnetocaloric Properties

We report a highly symmetric <b>{Gd</b>_<b>9</b><b>}</b> molecular nanocage with the formula [Gd₉(BA)₁₆(OH)₁₀]Cl·3(C₂H₅OH)·4(H₂O), which crystallizes in the cubic space group <i>Pn</i>3̅<i>n</i>. The structure features two crystallographically distinct Gd³⁺ ions, forming highly regular triangular Gd³⁺ arrangements leading to a geometrically frustrated magnetic network. Magnetization measurements at 2 K reveal a broad plateau between 1.5 and 4 T, while zero-field heat capacity shows a Schottky anomaly centered at 0.6 K─indicative of low-lying excited states and competing magnetic interactions. The magnetocaloric effect, evaluated through both direct and indirect methods, exhibits a re-entrant profile in the isentropic curves, pointing to a nontrivial evolution of magnetic entropy under applied fields. To probe the origin of this behavior, we employed the finite-temperature Lanczos method on a model spin Hamiltonian. The results reveal that the antiferromagnetic exchange between Gd³⁺ ions, combined with the frustration inherent to the <b>{Gd</b>_<b>9</b><b>}</b> geometry, leads to a degenerate ground state. An external field lifts this degeneracy, producing a regime with a sharply reduced density of states between 1.5 and 4 K, which underlies the unconventional magnetocaloric response. The <b>{Gd</b>_<b>9</b><b>}</b> cage thus represents a rare example of a spin-frustrated arrangement arising from competing antiferromagnetic interactions between the Gd³⁺. These findings demonstrate how frustrated topologies and tunable low-energy excitations can be exploited to modulate the magnetothermal properties, with potential implications for cryogenic magnetic cooling technologies.