Chemistry - A European Journal · 2016 · 42 citations · 36 references
Improving our comprehension of diverse CO<sub>2</sub> activation pathways is of vital importance for the widespread future utilization of this abundant greenhouse gas. CO<sub>2</sub> activation by uranium(III) complexes is now relatively well understood, with oxo/carbonate formation predominating as CO<sub>2</sub> is readily reduced to CO, but isolated thorium(III) CO<sub>2</sub> activation is unprecedented. We show that the thorium(III) complex, [Th(Cp'')<sub>3</sub> ] (1, Cp''={C<sub>5</sub> H<sub>3</sub> (SiMe<sub>3</sub> )<sub>2</sub> -1,3}), reacts with CO<sub>2</sub> to give the mixed oxalate-carboxylate thorium(IV) complex [{Th(Cp'')<sub>2</sub> [κ<sup>2</sup> -O<sub>2</sub> C{C<sub>5</sub> H<sub>3</sub> -3,3'-(SiMe<sub>3</sub> )<sub>2</sub> }]}<sub>2</sub> (μ-κ<sup>2</sup> :κ<sup>2</sup> -C<sub>2</sub> O<sub>4</sub> )] (3). The concomitant formation of oxalate and carboxylate is unique for CO<sub>2</sub> activation, as in previous examples either reduction or insertion is favored to yield a single product. Therefore, thorium(III) CO<sub>2</sub> activation can differ from better understood uranium(III) chemistry.
36
Using carbon dioxide as a building block in organic synthesis
Qiang Liu, Lipeng Wu, Ralf Jackstell et al. · Nature Communications · 2015 · 2.1K citations · Full text
Carbon Dioxide, Carbon Sequestration, Chemical Engineering +13
Uranium-mediated electrocatalytic dihydrogen production from water
Dominik P. Halter, Frank W. Heinemann, Julien Bachmann et al. · Nature · 2016 · 189 citations