The crystal structures of salts of N-(4-fluorophenyl)piperazine with four aromatic carboxylic acids and with picric acid

Autor: Chayanna Harish Chinthal, Hemmige S. Yathirajan, Channappa N. Kavitha, Sabine Foro, Christopher Glidewell
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 8, Pp 1179-1186 (2020)
Druh dokumentu: article
ISSN: 2056-9890
20569890
DOI: 10.1107/S2056989020008749
Popis: The structures are reported for five salts formed by reactions between N-(4-fluorophenyl)piperazine and aromatic acids. In 4-(4-fluorophenyl)piperazin-1-ium 2-fluorobenzoate monohydrate, C10H14FN2+·C7H4FO2−·H2O, (I), the components are linked by a combination of N—H...O and O—H...O hydrogen bonds to form a chain of alternating R46(12) and R66(16) rings. The ionic components of 4-(4-fluorophenyl)piperazin-1-ium 2-bromobenzoate 0.353-hydrate, C10H14FN2+·C7H4BrO2−·0.353H2O, (II), are linked by N—H...O hydrogen bonds to form a centrosymmetric four-ion aggregate containing an R44(12) motif, and these aggregates are linked into a molecular ladder by a single C—H...π(arene) hydrogen bond. 4-(4-Fluorophenyl)piperazin-1-ium 2-iodobenzoate, C10H14FN2+·C7H4IO2−, (III), crystallizes with Z′ = 2 in space group P\overline{1}: the four independent ions are linked by N—H...O hydrogen bonds to form a non-centrosymmetric aggregate again containing an R44(12) motif, and aggregates of this type are linked into a ribbon by a combination of C—H...O and C—H...π(arene) hydrogen bonds. The anion in 4-(4-fluorophenyl)piperazin-1-ium 2,4,6-trinitrophenolate, C10H14FN2+·C6H2N3O7−, (IV), shows clear evidence of extensive electronic delocalization from the phenolate O atom into the adjacent ring. The ions are linked by a combination of two-centre N—H...O and three-centre N—H...(O)2 hydrogen bonds to form centrosymmetric four-ion aggregates containing three types of ring. The ions in 4-(4-fluorophenyl)piperazin-1-ium 3,5-dinitrobenzoate, C10H14FN2+·C7H3N2O6−, (V), are again linked by N—H...O hydrogen bonds to form centrosymmetric R44(12) aggregates, which are themselves linked by a C—H...π(arene) hydrogen bond to form sheets, the stacking of which leads to the formation of narrow channels, containing disordered and/or mobile solvent entities. Comparisons are made with some related structures.
Databáze: Directory of Open Access Journals