Crystal Structure of Copper Ammonium Oxalate Dihydrate, Cu(NH4)2(C2O4)2·2H2O

Publisher Website
Google Scholar
Abstract
The crystal structure of copper ammonium oxalate dihydrate (space group P1̄ ) has been derived from a refinement of the two‐dimensional (hk0) and (0kl) x‐ray data using the atomic coordinates of the isomorphous salt CuK2(C2O4)2·2H2O as the starting point of the analysis. In contrast to the chromium complexes of oxalic acid the C–C bonds in both the two nonequivalent oxalate ions in the unit cell are single bonds (1.58 and 1.61 Å) consistent with the conclusion of Jeffrey and Parry that the carboxyl groups of the oxalate ion are separated by a pure σ bond with little or no π conjugation across the molecule. Both the oxalate ions are slightly nonplanar. The copper ions occupy the special positions (0, 0, 0) and 0, ½, 0) and their coordination is of the distorted octahedral type with four nearest oxygen neighbors (≈2 Å) at the corners of a square and two more distant atoms along the octahedral bond direction. The environment of the NH4 + ions consists of eight nearest oxygen atoms at a mean distance of 3 Å.