Abstract
In the title compound, (C5H6N)[Fe(NCS) 4(C5H5N)2], the FeIII ion is coordinated by four thiocyanate N atoms and two pyridine N atoms in a trans arrangement, forming an FeN6 polyhedron with a slightly distorted octahedral geometry. Charge balance is achieved by one pyridinium cation bound to the complex anion via N - H⋯S hydrogen bonding. The asymmetric unit consists of one FeIII cation, four thiocyanate anions, two coordinated pyridine molecules and one pyridinium cation. The structure exhibits π-π interactions between pyridine rings [centroid-centroid distances = 3.7267 (2), 3.7811 (2) and 3.8924 (2) Å]. The N atom and a neighboring C atom of the pyridinium cation are statistically disordered with an occupancy ratio of 0.58 (2):0.42 (2). © Shylin et al. 2013.
Cite
CITATION STYLE
Shylin, S. I., Gural’Skiy, I. A., Haukka, M., Kapshuk, A. A., & Prisyazhnaya, E. V. (2013). Pyridinium bis(pyridine-κN)tetrakis(thiocyanato-κN)ferrate(III). Acta Crystallographica Section E: Structure Reports Online, 69(6). https://doi.org/10.1107/S1600536813011628
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.