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<p>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 6<i>d</i>-orbital valence delocalization in these clusters. These <i>S</i> = 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 1<i>S</i><sup>1</sup> magic number, the valence delocalization enables exalted diamagnetism, which is aromaticity, via superatom ring currents.</p><p></p>

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Valence-delocalized trithorium nanocluster superatoms with open-shell exalted diamagnetism

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年4月11日

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  • John A. Seed,
  • Xinglan Deng,
  • Josef Tomeček,
  • Adam Brookfield,
  • David Collison,
  • Floriana Tuna,
  • Ashley J. Wooles,
  • George F. S. Whitehead,
  • Nikolas Kaltsoyannis,
  • Stephen T. Liddle

摘要

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.