What Singles out Aluminyl Anions? A Comparative Computational Study of the Carbon Dioxide Insertion Reaction in Gold–Aluminyl, −Gallyl, and −Indyl Complexes
| Autor: | Diego Sorbelli, Paola Belanzoni, Leonardo Belpassi |
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| Rok vydání: | 2022 |
| Předmět: | |
| Zdroj: | Inorganic Chemistry |
| ISSN: | 1520-510X 0020-1669 |
| Popis: | Anionic aluminum(I) anions (“aluminyls”) are the most recent discovery along Group 13 anions, and the understanding of the unconventional reactivity they are able to induce at a coordinated metal site is at an early stage. A striking example is the efficient insertion of carbon dioxide into the Au–Al bond of a gold–aluminyl complex. The reaction occurs via a cooperative mechanism, with the gold–aluminum bond being the actual nucleophile and the Al site also behaving as an electrophile. In the complex, the Au–Al bond has been shown to be mainly of an electron-sharing nature, with the two metal fragments displaying a diradical-like reactivity with CO2. In this work, the analogous reactivity with isostructural Au–X complexes (X = Al, Ga, and In) is computationally explored. We demonstrate that a kinetically and thermodynamically favorable reactivity with CO2 may only be expected for the gold–aluminyl complex. The Au–Al bond nature, which features the most (nonpolar) electron-sharing character among the Group 13 anions analyzed here, is responsible for its highest efficiency. The radical-like reactivity appears to be a key ingredient to stabilize the CO2 insertion product. This investigation elucidates the special role of Al in these hetero-binuclear compounds, providing new insights into the peculiar electronic structure of aluminyls, which may help for the rational control of their unprecedented reactivity toward carbon dioxide. The reactivity of gold−aluminyl, −gallyl, and −indyl complexes with carbon dioxide is predicted to be favorable only for gold−aluminyl complexes. The increased polarity of the Au−Ga and Au−In bonds makes these compounds weaker nucleophiles in a radical-like reaction mechanism. |
| Databáze: | OpenAIRE |
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