Title of article :
Synthesis and structure of a complex of copper(I) with L-cysteine and chloride ions containing Cu12S6 nanoclusters
Author/Authors :
Gizatullin, Amir A. M. Butlerov Chemistry Institute - Kazan Federal University, Russian Federation , Becker, Jonathan Institute of Inorganic and Analytical Chemistry - Justus-Liebig University of Giessen, Germany , Islamov, Daut A. E. Arbuzov Institute of Organic and Physical Chemistry - FRC Kazan Scientific Center of RAS, Russian Federation , Serova, Nikita A. M. Butlerov Chemistry Institute - Kazan Federal University, Russian Federation , Schindler, Siegfried Institute of Inorganic and Analytical Chemistry - Justus-Liebig University of Giessen, Germany , Klimovitskii, Alexander A. M. Butlerov Chemistry Institute - Kazan Federal University, Russian Federation , Shtyrlin, Valery A. M. Butlerov Chemistry Institute - Kazan Federal University, Russian Federation
Abstract :
The title hydrated copper(I)–L-cysteine–chloride complex has a polymeric structure of composition {[Cu16(CysH2)6Cl16]·xH2O}n [CysH2 = HO2CCH(NH3+)CH2S− or C3H7NO2S], namely, poly[tetra-μ3-chlorido-deca-μ2-chlorido-dichloridohexakis(μ4-L-cysteinato)hexadecacopper] polyhydrate]. The copper atoms are linked by thiolate groups to form Cu12S6 nanoclusters that take the form of a tetrakis cuboctahedron, made up of a Cu12 cubo-octahedral subunit that is augmented by six sulfur atoms that are located symmetrically atop of each of the Cu4 square units of the Cu12 cubo-octahedron. The six S atoms thus form an octahedral subunit themselves. The exterior of the Cu12S6 sphere is decorated by chloride ions and trichlorocuprate units. Three chloride ions are coordinated in an irregular fashion to trigonal Cu3 subunits of the nanocluster, and four trigonal CuCl3 units are bonded via each of their chloride ions to a copper ion on the Cu12S6 sphere. The trigonal CuCl3 units are linked via Cu2Cl2 bridges covalently connected to equivalent units in neighboring nanoclusters. Four such connections are arranged in a tetrahedral fashion, thus creating an infinite diamond-like net of Cu12S6Cl4(CuCl3)4 nanoclusters. The network thus formed results in large channels occupied by solvent molecules that are mostly too ill-defined to model. The content of the voids, believed to be water molecules, was accounted for via reverse Fourier-transform methods using the SQUEEZE algorithm [Spek (2015[Spek, A. L. (2015). Acta Cryst. C71, 9-18.]). Acta Cryst. C71, 9–18]. The protonated amino groups of the cysteine ligands are directed away from the sphere, forming N—H⋯Cl hydrogen bonds with chloride-ion acceptors of their cluster. The protonated carboxy groups point outwards and presumably form O—H⋯O hydrogen bonds with the unresolved water molecules of the solvent channels. Disorder is observed in one of the two crystallographically unique [Cu16(CysH2)6Cl16] segments for three of the six cysteine anions.
Keywords :
crystal structure , cysteine , metal–organic framework , SQUEEZE procedure , cage structure , copper(I)
Journal title :
Acta Crystallographica Section E: Crystallographic Communications