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Capturing the Antiaromatic #6094C68 Carbon Cage in the Radio-Frequency Furnace

Authors

  • Dr. Konstantin Yu. Amsharov,

    1. Max Planck Institute for Solid State Research, Heisenbergstrasse 1, 70569 Stuttgart (Germany), Fax: (+49) 711-689-1502
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  • Karolin Ziegler,

    1. Max Planck Institute for Solid State Research, Heisenbergstrasse 1, 70569 Stuttgart (Germany), Fax: (+49) 711-689-1502
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  • Andreas Mueller,

    1. Max Planck Institute for Solid State Research, Heisenbergstrasse 1, 70569 Stuttgart (Germany), Fax: (+49) 711-689-1502
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  • Prof. Martin Jansen

    Corresponding author
    1. Max Planck Institute for Solid State Research, Heisenbergstrasse 1, 70569 Stuttgart (Germany), Fax: (+49) 711-689-1502
    • Max Planck Institute for Solid State Research, Heisenbergstrasse 1, 70569 Stuttgart (Germany), Fax: (+49) 711-689-1502
    Search for more papers by this author

Abstract

Although all fullerenes do not satisfy the classical aromaticity condition, as a result of their nonplanar nature, they experience effective stabilization due to extensive cyclic π-electron delocalization and exhibit pronounced “spherical aromaticity”. This feature has raised the question of the opposite phenomenon, that is, the existence of antiaromatic carbon cages. Here the first experimental evidence of the existence of antiaromatic fullerenes is reported. The elusive #6094C68 was effectively captured as C68Cl8 by in situ chlorination in the gas phase during radio-frequency synthesis. The chlorinated cage was separated by means of multistage HPLC, and its connectivity unambiguously determined by single-crystal X-ray analysis. Halogen-stripped pristine #6094C68 was monitored by mass spectrometry of the chlorinated C68Cl8 cage. Quantum chemical calculations reveal the highly antiaromatic character of #6094C68, in accordance with all geometric, energetic, and magnetic criteria of aromaticity. Chlorine addition leads to substantial stabilization of the cage owing to aromatization in the resulting C68Cl8, which explains its high abundance in the primary fullerene soot. This work provides new insights into the process of fullerene formation and better understanding of aromaticity phenomena in general.

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