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Synthesis and Structure of Pb[C2O5] - An Inorganic Pyrocarbonate Salt

MetadataDetails
Publication Date2022-06-22
JournalInorganic Chemistry
AuthorsDominik Spahr, Jannes Kƶnig, Lkhamsuren Bayarjargal, Rita Luchitskaia, Victor Milman
InstitutionsDassault SystĆØmes (United Kingdom), Goethe University Frankfurt
Citations28

We have synthesized Pb[C<sub>2</sub>O<sub>5</sub>], an inorganic pyrocarbonate salt, in a laser-heated diamond anvil cell (LH-DAC) at 30 GPa by heating a Pb[CO<sub>3</sub>] + CO<sub>2</sub> mixture to ā‰ˆ2000(200) K. Inorganic pyrocarbonates contain isolated [C<sub>2</sub>O<sub>5</sub>]<sup>2-</sup> groups without functional groups attached. The [C<sub>2</sub>O<sub>5</sub>]<sup>2-</sup> groups consist of two oxygen-sharing [CO<sub>3</sub>]<sup>3-</sup> groups. Pb[C<sub>2</sub>O<sub>5</sub>] was characterized by synchrotron-based single-crystal structure refinement, Raman spectroscopy, and density functional theory calculations. Pb[C<sub>2</sub>O<sub>5</sub>] is isostructural to Sr[C<sub>2</sub>O<sub>5</sub>] and crystallizes in the monoclinic space group <i>P</i>2<sub>1</sub>/<i>c</i> with <i>Z</i> = 4. The synthesis of Pb[C<sub>2</sub>O<sub>5</sub>] demonstrates that, just like in other carbonates, cation substitution is possible and that therefore inorganic pyrocarbonates are a novel family of carbonates, in addition to the established sp<sup>2</sup> and sp<sup>3</sup> carbonates.