Abstract
Understanding the chemical behavior of actinide elements is essential for the effective management and use of actinide materials. In this study, we report an unprecedented η2(side-on) coordination of U by a cyanide in a UCN cluster, which was stabilized inside a C82fullerene cage. UCN@Cs(6)-C82was successfully synthesized and fully characterized by mass spectrometry, single crystal X-ray crystallography, cyclic voltammetry, spectroscopy, and theoretical calculations. The bonding analysis demonstrates significant donation bonding between CN-and uranium, and covalent interactions between uranium and the carbon cage. These effects correlate with an observed elongated cyanide C-N bond, resulting in a rare case where the oxidation state of uranium shows ambiguity between U(III) and U(I). The discovery of this unprecedented triangular configuration of the uranium cyanide cluster provides a new insight in coordination chemistry and highlights the large variety of bonding situations that uranium can have.
| Original language | English |
|---|---|
| Pages (from-to) | 16226-16234 |
| Number of pages | 9 |
| Journal | Journal of the American Chemical Society |
| Volume | 143 |
| Issue number | 39 |
| DOIs | |
| State | Published - Oct 6 2021 |
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