<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>60(12)</volume><submitter>Freccero R</submitter><funding>Max-Planck-Gesellschaft</funding><pubmed_abstract>The monogermanide LuGe is obtained via high-pressure high-temperature synthesis (5-15 GPa, 1023-1423 K). The crystal structure is solved from single-crystal X-ray diffraction data (structure type FeB, space group Pnma, a=7.660(2) Å, b=3.875(1) Å, and c=5.715(2) Å, R&lt;sub>F&lt;/sub> =0.036 for 206 symmetry independent reflections). The analysis of chemical bonding applying quantum-chemical techniques in position space was performed. It revealed-beside the expected 2c-Ge-Ge bonds in the germanium polyanion-rather unexpected four-atomic bonds between lutetium atoms indicating the formation of a polycation by the excess electrons in the system Lu&lt;sup>3+&lt;/sup> (2b)Ge&lt;sup>2-&lt;/sup> ×1 e&lt;sup>-&lt;/sup> . Despite the reduced VEC of 3.5, lutetium monogermanide is following the extended 8-N rule with the trend to form lutetium-lutetium bonds utilizing the electrons left after satisfying the bonding needs in the anionic Ge-Ge zigzag chain.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>6457-6461</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7986909</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>"Excess" electrons in LuGe.</pubmed_title><pmcid>PMC7986909</pmcid><pubmed_authors>Wagner FR</pubmed_authors><pubmed_authors>Schnelle W</pubmed_authors><pubmed_authors>Schmidt M</pubmed_authors><pubmed_authors>Schwarz U</pubmed_authors><pubmed_authors>Grin Y</pubmed_authors><pubmed_authors>Prots Y</pubmed_authors><pubmed_authors>Freccero R</pubmed_authors><pubmed_authors>Hubner JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>"Excess" electrons in LuGe.</name><description>The monogermanide LuGe is obtained via high-pressure high-temperature synthesis (5-15 GPa, 1023-1423 K). The crystal structure is solved from single-crystal X-ray diffraction data (structure type FeB, space group Pnma, a=7.660(2) Å, b=3.875(1) Å, and c=5.715(2) Å, R&lt;sub>F&lt;/sub> =0.036 for 206 symmetry independent reflections). The analysis of chemical bonding applying quantum-chemical techniques in position space was performed. It revealed-beside the expected 2c-Ge-Ge bonds in the germanium polyanion-rather unexpected four-atomic bonds between lutetium atoms indicating the formation of a polycation by the excess electrons in the system Lu&lt;sup>3+&lt;/sup> (2b)Ge&lt;sup>2-&lt;/sup> ×1 e&lt;sup>-&lt;/sup> . Despite the reduced VEC of 3.5, lutetium monogermanide is following the extended 8-N rule with the trend to form lutetium-lutetium bonds utilizing the electrons left after satisfying the bonding needs in the anionic Ge-Ge zigzag chain.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-04T20:35:46.888Z</modification><creation>2025-04-04T20:35:46.888Z</creation></dates><accession>S-EPMC7986909</accession><cross_references><pubmed>33236821</pubmed><doi>10.1002/anie.202014284</doi></cross_references></HashMap>