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Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds

Borosulfates are oxoanionic compounds consisting of condensed sulfur‐ and boron‐centered tetrahedra. Hitherto, they were mostly achieved from solvothermal syntheses in SO(3)‐enriched sulfuric acid, or from reactions with the superacid H[B(HSO(4))(4)]. The crystal structures are very similar to those...

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Autores principales: Bruns, Jörn, Höppe, Henning A., Daub, Michael, Hillebrecht, Harald, Huppertz, Hubert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384169/
https://www.ncbi.nlm.nih.gov/pubmed/31943390
http://dx.doi.org/10.1002/chem.201905449
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author Bruns, Jörn
Höppe, Henning A.
Daub, Michael
Hillebrecht, Harald
Huppertz, Hubert
author_facet Bruns, Jörn
Höppe, Henning A.
Daub, Michael
Hillebrecht, Harald
Huppertz, Hubert
author_sort Bruns, Jörn
collection PubMed
description Borosulfates are oxoanionic compounds consisting of condensed sulfur‐ and boron‐centered tetrahedra. Hitherto, they were mostly achieved from solvothermal syntheses in SO(3)‐enriched sulfuric acid, or from reactions with the superacid H[B(HSO(4))(4)]. The crystal structures are very similar to those of the corresponding class of silicates and their substitution variants, especially regarding the typical structural motif of corner‐sharing tetrahedra. However, the borosulfates are supposed to be even more versatile, because (BO(3)) units might also be part of the anionic network. The following article deals with detailed reports on the different synthesis strategies, the crystal chemistry of borosulfates in comparison to silicates, and their hitherto identified properties.
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spelling pubmed-73841692020-07-28 Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds Bruns, Jörn Höppe, Henning A. Daub, Michael Hillebrecht, Harald Huppertz, Hubert Chemistry Reviews Borosulfates are oxoanionic compounds consisting of condensed sulfur‐ and boron‐centered tetrahedra. Hitherto, they were mostly achieved from solvothermal syntheses in SO(3)‐enriched sulfuric acid, or from reactions with the superacid H[B(HSO(4))(4)]. The crystal structures are very similar to those of the corresponding class of silicates and their substitution variants, especially regarding the typical structural motif of corner‐sharing tetrahedra. However, the borosulfates are supposed to be even more versatile, because (BO(3)) units might also be part of the anionic network. The following article deals with detailed reports on the different synthesis strategies, the crystal chemistry of borosulfates in comparison to silicates, and their hitherto identified properties. John Wiley and Sons Inc. 2020-05-04 2020-06-26 /pmc/articles/PMC7384169/ /pubmed/31943390 http://dx.doi.org/10.1002/chem.201905449 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Bruns, Jörn
Höppe, Henning A.
Daub, Michael
Hillebrecht, Harald
Huppertz, Hubert
Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds
title Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds
title_full Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds
title_fullStr Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds
title_full_unstemmed Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds
title_short Borosulfates—Synthesis and Structural Chemistry of Silicate Analogue Compounds
title_sort borosulfates—synthesis and structural chemistry of silicate analogue compounds
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384169/
https://www.ncbi.nlm.nih.gov/pubmed/31943390
http://dx.doi.org/10.1002/chem.201905449
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