<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>65(Pt 3)</volume><submitter>Zhang LF</submitter><pubmed_abstract>The title salt, poly[aqua-?(3)-oxalurato-potassium(I)], [K(C(3)H(3)N(2)O(4))(H(2)O)](n), which was obtained from a water solution of oxaluric acid and KOH at room temperature, crystallizes as potassium and oxalurate ions along with a water mol-ecule. The K(+) cation lies on a crystallographic twofold rotation axis (site symmetry 2, Wyckoff position f), and the water and oxalurate mol-ecules are located within different mirror planes (site symmetry m, Wyckoff position g). The K(+) cation is eight-coordinated by six O atoms of six oxalurate ligands and two O atoms from two water mol-ecules in a distorted square-anti-prismatic geometry. All of the eight coordinated O atoms are in a monodentate bridging mode, with alternate bridged K?K distances of 3.5575?(12) and 3.3738?(12)?Å. The oxalurate ligand shows a ?(3)-bridging coordination mode, which links the K(+) cation into a three-dimensional network. The oxalurate ligands and the water mol-ecules are involved in inter- and intra-molecular N-H?O, and O-H?O hydrogen bonds, which stabilize the network.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>m308-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2968634</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Potassium oxalurate monohydrate.</pubmed_title><pmcid>PMC2968634</pmcid><pubmed_authors>Zhang LF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Potassium oxalurate monohydrate.</name><description>The title salt, poly[aqua-?(3)-oxalurato-potassium(I)], [K(C(3)H(3)N(2)O(4))(H(2)O)](n), which was obtained from a water solution of oxaluric acid and KOH at room temperature, crystallizes as potassium and oxalurate ions along with a water mol-ecule. The K(+) cation lies on a crystallographic twofold rotation axis (site symmetry 2, Wyckoff position f), and the water and oxalurate mol-ecules are located within different mirror planes (site symmetry m, Wyckoff position g). The K(+) cation is eight-coordinated by six O atoms of six oxalurate ligands and two O atoms from two water mol-ecules in a distorted square-anti-prismatic geometry. All of the eight coordinated O atoms are in a monodentate bridging mode, with alternate bridged K?K distances of 3.5575?(12) and 3.3738?(12)?Å. The oxalurate ligand shows a ?(3)-bridging coordination mode, which links the K(+) cation into a three-dimensional network. The oxalurate ligands and the water mol-ecules are involved in inter- and intra-molecular N-H?O, and O-H?O hydrogen bonds, which stabilize the network.</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Feb</publication><modification>2021-02-28T08:30:08Z</modification><creation>2019-03-27T00:00:07Z</creation></dates><accession>S-EPMC2968634</accession><cross_references><pubmed>21582086</pubmed><doi>10.1107/S1600536809005637</doi></cross_references></HashMap>