Abstract
Six 1-halobenzoyl-4-(2-methoxyphenyl)piperazines have been prepared using carbodiimide-mediated coupling reactions between halobenzoic acids and N-(2-methoxyphenyl)piperazine. The molecules of 1-(4-fluorobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19FN2O2 (I), are linked into a chain of rings by a combination of C-H···O and C-H···π(arene) hydrogen bonds. 1-(4-Chloro-benzoyl)-4-(2-methoxyphenyl)piperazine, C18H19ClN2O2 (II), crystallizes in the space group Pca21 with Z' = 4 and it exhibits both pseudosymmetry and inversion twinning: a combination of six C-Six 1-halobenzoyl-4-(2-methoxyphenyl)piperazines have been prepared using carbodiimide-mediated coupling reactions between halobenzoic acids and N-(2-methoxyphenyl)piperazine. The molecules of 1-(4-fluorobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19FN2O2 (I), are linked into a chain of rings by a combination of C—H⋯O and C—H⋯π(arene) hydrogen bonds. 1-(4-Chlorobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19ClN2O2 (II), crystallizes in the space group Pca21 with Z′ = 4 and it exhibits both pseudosymmetry and inversion twinning: a combination of six C—H⋯O and two C—H⋯π(arene) hydrogen bonds generate a three-dimensional assembly. In 1-(4-bromobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19BrN2O2 (III), which also crystallizes in space group Pca21 but with Z′ = 2, the bromobenzoyl unit in one of the molecules is disordered. Pseudosymmetry and inversion twinning are again present, and a combination of three C—H⋯O and one C—H⋯π(arene) hydrogen bonds generate a two-dimensional assembly. A single C—H⋯O hydrogen bond links the molecules of 1-(4-iodobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19IN2O2 (IV), into simple chains but in the isomeric 3-iodobenzoyl analogue (V), which crystallizes in space group P212121 with Z′ = 2, a two-dimensional assembly is generated by a combination of four C—H⋯O and two C—H⋯π(arene) hydrogen bonds; pseudosymmetry and inversion twinning are again present. A single C—H⋯O hydrogen bond links the molecules of 1-(2-fluorobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19FN2O2 (VI), into simple chains. Comparisons are made with the structures of some related compounds.H center dot center dot center dot O and two C-H center dot center dot center dot pi(arene) hydrogen bonds generate a three-dimensional assembly. In 1-(4-bromobenzoyl)4-(2-methoxyphenyl)piperazine, C18H19BrN2O2 (III), which also crystallizes in space group Pca2(1) but with Z' = 2, the bromobenzoyl unit in one of the molecules is disordered. Pseudosymmetry and inversion twinning are again present, and a combination of three C-H···O and one C-H···π(arene) hydrogen bonds generate a two-dimensional assembly. A single C-H···O hydrogen bond links the molecules of 1-(4-iodobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19IN2O2 (IV), into simple chains but in the isomeric 3-iodobenzoyl analogue (V), which crystallizes in space group P212121 with Z' = 2, a two-dimensional assembly is generated by a combination of four C-H··· O and two C-H ···π(arene) hydrogen bonds; pseudosymmetry and inversion twinning are again present. A single C-H ···O hydrogen bond links the molecules of 1-(2-fluorobenzoyl)-4-(2-methoxyphenyl)piperazine, C18H19FN2O2 (VI), into simple chains. Comparisons are made with the structures of some related compounds.
Original language | English |
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Pages (from-to) | 5-13 |
Journal | Acta Crystallographica Section E Crystallographic Communications |
Volume | 77 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1 Jan 2021 |
Keywords
- Piperazines
- Synthesis
- Crystal structure
- Molecular conformation
- Disorder
- Pseudosymmetry
- Inversion twinning
- Hydrogen bonding
- Supramolecular assembly
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Six 1-halobenzoyl-4-(2-methoxyphenyl)piperazines having Z' values of one, two or four; disorder, pseudosymmetry, twinning and supramolecular assembly in one, two or three dimensions (dataset)
Glidewell, C. (Creator), Cambridge Crystallographic Data Centre, 2021
https://dx.doi.org/10.5517/ccdc.csd.cc26q1ss and 5 more links, https://dx.doi.org/10.5517/ccdc.csd.cc26q1rr, https://dx.doi.org/10.5517/ccdc.csd.cc26q1qq, https://dx.doi.org/10.5517/ccdc.csd.cc26q1pp, https://dx.doi.org/10.5517/ccdc.csd.cc26q1nn, https://dx.doi.org/10.5517/ccdc.csd.cc26q1mm (show fewer)
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