Synthesis, crystal structure and Hirshfeld surface analysis of the hybrid salt bis-(2-methyl-imidazo[1,5- a ]pyridin-2-ium) tetra-chlorido-manganate(II).
Olga Yu VassilyevaElena A BuvayloVolodymyr N KokozayBrian W SkeltonPublished in: Acta crystallographica. Section E, Crystallographic communications (2023)
The 0-D hybrid salt bis-(2-methyl-imidazo[1,5- a ]pyridin-2-ium) tetra-chlorido-manganate(II), (C 8 H 9 N 2 ) 2 [MnCl 4 ] or [ L ] 2 [MnCl 4 ], consists of discrete L + cations and tetra-chlorido-manganate(II) anions. The fused heterocyclic rings in the two crystallographically non-equivalent monovalent organic cations are almost coplanar; the bond lengths are as expected. The tetra-hedral MnCl 4 2- dianion is slightly distorted with the Mn-Cl bond lengths varying from 2.3577 (7) to 2.3777 (7) Å and the Cl-Mn-Cl angles falling in the range 105.81 (3)-115.23 (3)°. In the crystal, the compound demonstrates a pseudo-layered arrangement of separate organic and inorganic sheets alternating parallel to the bc plane. In the organic layer, pairs of centrosymmetrically related trans -oriented L + cations are π-stacked. Neighboring MnCl 4 2- dianions in the inorganic sheet show no connectivity, with the minimal Mn⋯Mn distance exceeding 7 Å. The Hirshfeld surface analysis revealed the prevalence of the non-conventional C-H⋯Cl-Mn hydrogen bonding in the crystal packing.