Cargando…

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...

Descripción completa

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
_version_ 1782240167988297728
author Trella, Thomas
Frank, Walter
author_facet Trella, Thomas
Frank, Walter
author_sort Trella, Thomas
collection PubMed
description 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.
format Online
Article
Text
id pubmed-3414175
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-34141752012-08-17 Hexaaqua­aluminium(III) tris­(methane­sulfonate) Trella, Thomas Frank, Walter Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers 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. International Union of Crystallography 2012-07-28 /pmc/articles/PMC3414175/ /pubmed/22904782 http://dx.doi.org/10.1107/S1600536812033235 Text en © Trella and Frank 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Metal-Organic Papers
Trella, Thomas
Frank, Walter
Hexaaqua­aluminium(III) tris­(methane­sulfonate)
title Hexaaqua­aluminium(III) tris­(methane­sulfonate)
title_full Hexaaqua­aluminium(III) tris­(methane­sulfonate)
title_fullStr Hexaaqua­aluminium(III) tris­(methane­sulfonate)
title_full_unstemmed Hexaaqua­aluminium(III) tris­(methane­sulfonate)
title_short Hexaaqua­aluminium(III) tris­(methane­sulfonate)
title_sort hexaaqua­aluminium(iii) tris­(methane­sulfonate)
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414175/
https://www.ncbi.nlm.nih.gov/pubmed/22904782
http://dx.doi.org/10.1107/S1600536812033235
work_keys_str_mv AT trellathomas hexaaquaaluminiumiiitrismethanesulfonate
AT frankwalter hexaaquaaluminiumiiitrismethanesulfonate