Spectroscopic characterization and room-temperature structure of bis(4-aminopyridinium) dichromate

Abstract

Crystals of bis(4-aminopyridinium) dichromate (C5H7N2)2[Cr2O7] (1) were isolated via slow solvent evaporation and characterized by energy dispersive spectroscopy (EDS), infrared (IR) and ultratviolet-visible (UV-Vis) spectroscopy, and single crystal X-ray diffraction. The room-temperature (RT; 298 K) phase of 1 crystallizes in the monoclinic space group P21/m. Its asymmetric unit consists of two crystallographically independent 4-aminopyridinium cations (A and B) and two halves of symmetry-independent dichromate anions (A and B). Cations and anions are linked with the aid of several moderate N–H⋯O hydrogen bonds and weak C–H⋯O interactions resulting in a three-dimensional supramolecular network. The crystal structure is further stabilized by extensive π–π stacking interactions between adjacent pyridine rings. A comparison of the structure of the RT phase of 1 and that of the low temperature (LT; 150 K) phase is described.