A very short O-H⋯O hydrogen bond in the structure of clozapinium hydrogen bis-(3,5-di-nitro-benzoate)

• Published in: Acta crystallographica. Section E, Crystallographic communications Vol. 76; no. Pt 10; pp. 1629 - 1633
• Main Authors: Shaibah, Mohammed A E, Kavitha, Channappa N, Yathirajan, Hemmige S, Foro, Sabine, Glidewell, Christopher
• Format: Journal Article
• Language: English
• Published: England International Union of Crystallography 01.10.2020
• Subjects: Research Communications; very short hydrogen bonds; crystal structure; hydrogen bonding; clozapine; mol­ecular conformation; supra­molecular assembly
• ISSN: 2056-9890; 2056-9890
• DOI: 10.1107/S2056989020012268

In the title salt {systematic name: 4-[6-chloro-2,9-di-aza-tri-cyclo-[9.4.0.0 ]penta-deca-1(15),3(8),4,6,9,11,13-heptaen-10-yl]-1-methyl-piperazin-1-ium 3,5-di-nitro-benzoate-3,5-di-nitro-benzic acid (1/1)}, C H ClN ·C H N O ·C H N O , there is a very short, asymmetric, O-H⋯O hydrogen bond [O⋯O = 2.453 (3) Å] within the anion. The oxygen atoms of one of the nitro groups of the anion are disordered over two sets of sites having occupancies of 0.56 (3) and 0.44 (3). The fused tricyclic portion of the cation adopts a butterfly conformation, with a dihedral angle of 45.59 (6)° between the planes of the two aryl rings. In the crystal, a combination of O-H⋯O, N-H⋯O and C-H⋯O hydrogen bonds links the component species into a three-dimensional framework. Comparisons are made with the structures of some related compounds.