Crystal structure and Hirshfeld surface analysis of bis-(2,6-di-amino-pyridinium) tetra-chlorido-cobaltate(II). 2018

Oumaima Ben Moussa, and Hammouda Chebbi, and Mohamed Faouzi Zid
University of Tunis El Manar, Faculty of Sciences of Tunis, Laboratory of Materials, Crystal Chemistry and Applied Thermodynamics, 2092 El Manar II, Tunis, Tunisia.

In the title mol-ecular salt, (C5H8N3)2[CoCl4], the cations are protonated at their pyridine N atoms and the anion is an almost regular tetra-hedron. The crystal structure consists of alternating inorganic layers, built from tetra-chlorido-cobaltate anions, and organic layers formed by protonated cations of 2,6-di-amino-pyridinium. The crystal packing is governed by C/N-H⋯Cl hydrogen-bonding inter-actions between the organic and the inorganic ions and Cl⋯Cl inter-actions. Moreover, the cations show a π-π stacking inter-action [inter-centroid distance = 3.763 (2) Å]. The prevalence of these inter-actions is illustrated by an analysis of the three-dimensional Hirshfeld surface and by two-dimensional fingerprint plots.

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