In the title compound, C(22)H(19)N(2) (+)·ClO(4) (-), the three pendant aromatic rings are twisted from the plane of the imidazolium ring by dihedral angles of 17.3 (2), 65.7 (2) and 3.4 (2)°. In the crystal structure, N-H⋯O and N-H⋯(O,O) hydrogen bonds link the ions, forming a ribbon-like structure along the a axis.

In the title salt, C(9)H(9)N(2) (+)·Br(-), the ethynyl groups are nearly anti-parallel to each other [the angle between the two ethynyl groups is179.7 (2)°]. No classical hydrogen bonds or π-π inter-actions are observed. The mol-ecules are linked by C-H⋯Br hydrogen bonds. The bromide anions are involved in inter-actions with three H atoms.

In the title mol-ecular salt, C(9)H(9)N(2) (+)·C(2)HO(4) (-), the dihedral angle between the aromatic rings of the cation is 17.5 (3)° and the dihedral angle between the -CO(2)H and -CO(2) groups of the anion is 38.6 (2)°. In the crystal, the components inter-act by way of O-H⋯O and N-H⋯O hydrogen bonds.

The title compound, C(7)H(8)N(2)O(4), crystallizes as a zwitterion, with mol-ecules organized into mol-ecular sheets via carbox-yl-carboxyl-ate and N(+)-H⋯carboxyl-ate contacts. These sheets are constructed from translationally related mol-ecules that further link to neighboring motifs via π-stacking [centroid-centroid distance 3.504 (3) Å] and weak C-H⋯O contacts.

In the title compound, C(19)H(22)N(3)O(+)·Br(-), the imidazole ring is approximately coplanar with the pyridine ring [dihedral angle = 0.88 (13)°] and nearly perpendicular to the benzene ring [dihedral angle = 81.70 (13)°]. O-H⋯Br and C-H⋯Br hydrogen bonding helps to stabilize the crystal structure.

This study focuses on the synthesis and characterization of the inclusion complex of β-Cyclodextrin (β-CD) with dicationic ionic liquid, 3,3'-(1,4-Phenylenebis [methylene]) bis(1-methyl-1H-imidazol-3-ium) di(bromide) (PhenmimBr). The inclusion complex was prepared at room temperature utilizing conventional kneading technique. Proton ((1)H) NMR and 2D ((1)H-(1)H) COSY NMR were the primary charac...

The title compound, bis-[2,2'-dimethyl-3,3'-(butane-1,4-di-yl)diimidazol-1-ium] β-octa-molybdate(VI), (C(12)H(20)N(4))(2)[Mo(8)O(26)], was produced by hydro-thermal reaction of an acidified aqueous solution of Na(2)MoO(4) and 1,4-bis-(2-methyl-1H-imidazol-1-yl)butane (hereafter L). The structure of the title compound consists of the β-octa-molybdate anions having a center of symmetry, and proto...

2-(Alkyl-1-yl)-1H-imidazol-5(4H)-ones 5a-n were synthesized via nucleophilic substitution of the methylsulfanyl group of the corresponding 2-(methylthio)-1H-imidazol-5(4H)-ones 3a-c with suitably substituted secondary amines. The starting 2-thioxo- imidazolidin-4-ones 2a,2b were prepared by condensation of thiohydantoin and benzo[b]-thiophene-3-carbaldehyde or benzofuran-3-carbaldehyde under mi...