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Hexaaqua­aluminium(III) tris­(methane­sulfonate)

The title compound, [Al(H(2)O)(6)](CH(3)SO(3))(3) (common name: aluminium methane­sulfonate hexa­hydrate), was crystallized from an aqueous solution prepared by the precipitation reaction of aluminium sulfate and barium methane­sulfonate. Its crystal structure is the first of the boron group methane...

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Detalles Bibliográficos
Autores principales: Trella, Thomas, Frank, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414175/
https://www.ncbi.nlm.nih.gov/pubmed/22904782
http://dx.doi.org/10.1107/S1600536812033235
Descripción
Sumario:The title compound, [Al(H(2)O)(6)](CH(3)SO(3))(3) (common name: aluminium methane­sulfonate hexa­hydrate), was crystallized from an aqueous solution prepared by the precipitation reaction of aluminium sulfate and barium methane­sulfonate. Its crystal structure is the first of the boron group methane­sulfonates to be determined. The characteristic building block is a centrosymmetric unit containing two hexa­aqua­aluminium cations that are connected to each other by two O atoms of the –SO(3) groups in an O—H⋯O⋯H—O sequence. Further O—H⋯O hydrogen bonding links these blocks in orthogonal directions – along [010] forming a double chain array, along [10-1] forming a layered arrangement of parallel chains and along [101] forming a three-dimensional network. As indicated by the O⋯O distances of 2.600 (3)–2.715 (3) Å, the hydrogen bonds are from medium–strong to strong. A further structural feature is the arrangement of two and four methyl groups, respectively, establishing ‘hydro­phobic islands’ of different size, all positioned in a layer-like region perpendicular to [101]. The only other building block within this region is one of the –SO(3) groups giving a local connection between the hydro­philic structural regions on both sides of the ‘hydro­phobic’ one. Thermal analysis indicates that a stepwise dehydration process starts at about 413 K and proceeds via the respective penta- and dihydrate until the compound completely decomposes at about 688 K.