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Updated: May 14, 2025

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Valence-delocalized trithorium nanocluster superatoms with open-shell exalted diamagnetism
John A Seed1,2, Xinglan Deng1,2, Josef Tomeček1,2
1Department of Chemistry, The University of Manchester, Manchester, UK.
None:
Quantum-confined nanoclusters can be described by the jellium model, which emphasizes closed-shell electron configurations, but an open-shell variation with jellium aromaticity has been proposed. Such clusters are termed superatoms because they behave like an atom, and they exhibit unusual properties. Superatoms feature metal-metal bonding; hence, since their discovery 40 years ago, superatoms have exclusively involved main group or transition metals, with actinides only considered computationally as dopants owing to actinide-actinide bonding being exceedingly rare. Here we report trithorium nanoclusters exhibiting three-centre-one-electron actinide-actinide bonding. Experimental and computational analysis demonstrates Robin-Day Class III 6d-orbital valence delocalization in these clusters. These S = 1/2 clusters are paramagnetic, but in external applied magnetic fields they exhibit exalted diamagnetism, evidencing actinide open-shell jellium aromaticity superatom character. Exalted diamagnetism is not normally associated with a single unpaired electron, but with a 1S1 magic number, the valence delocalization enables exalted diamagnetism, which is aromaticity, via superatom ring currents.
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