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Synthesis and structure of a complex of copper(I) with l-cysteine and chloride ions containing Cu(12)S(6) nanoclusters

The title hydrated copper(I)–l-cysteine–chloride complex has a polymeric structure of composition {[Cu(16)(CysH(2))(6)Cl(16)]·xH(2)O}(n) [CysH(2) = HO(2)CCH(NH(3) (+))CH(2)S(−) or C(3)H(7)NO(2)S], namely, poly[[tetra-μ(3)-chlorido-deca-μ(2)-chlorido-di­chlorido­hexa­kis­(μ(4)-l-cysteinato)hexa­deca­...

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Detalles Bibliográficos
Autores principales: Gizatullin, Amir, Becker, Jonathan, Islamov, Daut, Serov, Nikita, Schindler, Siegfried, Klimovitskii, Alexander, Shtyrlin, Valery
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025850/
https://www.ncbi.nlm.nih.gov/pubmed/33936751
http://dx.doi.org/10.1107/S2056989021002012
Descripción
Sumario:The title hydrated copper(I)–l-cysteine–chloride complex has a polymeric structure of composition {[Cu(16)(CysH(2))(6)Cl(16)]·xH(2)O}(n) [CysH(2) = HO(2)CCH(NH(3) (+))CH(2)S(−) or C(3)H(7)NO(2)S], namely, poly[[tetra-μ(3)-chlorido-deca-μ(2)-chlorido-di­chlorido­hexa­kis­(μ(4)-l-cysteinato)hexa­deca­copper] polyhydrate]. The copper atoms are linked by thiol­ate groups to form Cu(12)S(6) nanoclusters that take the form of a tetra­kis cubocta­hedron, made up of a Cu(12) cubo-octa­hedral subunit that is augmented by six sulfur atoms that are located symmetrically atop of each of the Cu(4) square units of the Cu(12) cubo-octa­hedron. The six S atoms thus form an octa­hedral subunit themselves. The exterior of the Cu(12)S(6) sphere is decorated by chloride ions and trichlorocuprate units. Three chloride ions are coordinated in an irregular fashion to trigonal Cu(3) subunits of the nanocluster, and four trigonal CuCl(3) units are bonded via each of their chloride ions to a copper ion on the Cu(12)S(6) sphere. The trigonal CuCl(3) units are linked via Cu(2)Cl(2) 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 Cu(12)S(6)Cl(4)(CuCl(3))(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 ▸). 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 [Cu(16)(CysH(2))(6)Cl(16)] segments for three of the six cysteine anions.