Details
Zusammenfassung: <jats:p>The title bromide salt, [Cr{CO(NH<jats:sub>2</jats:sub>)<jats:sub>2</jats:sub>}<jats:sub>6</jats:sub>](Cr<jats:sub>2</jats:sub>O<jats:sub>7</jats:sub>)Br·H<jats:sub>2</jats:sub>O, is isotypic to the corresponding chloride salt. Within the complex cation, the Cr<jats:sup>III</jats:sup>atom is coordinated by six O atoms of six urea ligands, displaying a slightly distorted octahedral coordination environment. The Cr—O bond lengths involving the urea ligands are in the range 1.9534 (13)–1.9776 (12) Å. The Cr<jats:sub>2</jats:sub>O<jats:sub>7</jats:sub><jats:sup>2−</jats:sup>anion has a nearly staggered conformation, with a bridging angle of 130.26 (10)°. The individual components are arranged in rows extending parallel to [100]. The Br<jats:sup>−</jats:sup>anion links the complex cation, as well as the solvent water molecule, through N—H...Br and O—H...Br hydrogen-bonding interactions. The supramolecular architecture also includes N—H...O and O—H...O hydrogen bonding between urea N—H and water O—H donor groups and the O atoms of the Cr<jats:sub>2</jats:sub>O<jats:sub>7</jats:sub><jats:sup>2−</jats:sup>anion as acceptor atoms, leading to a three-dimensional network structure.</jats:p>
Umfang: 1336-1339
ISSN: 2056-9890
DOI: 10.1107/s2056989015019258