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1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate
In the crystal structure of the title ionic compound (C(7)H(6)NS)[AuCl(4)]·C(4)H(8)O, the [AuCl(4)](−) anion shows a typical square-planar geometry. Numerous weak C—H⋯Cl hydrogen bonds between [AuCl(4)](−) and the 1,3-benzothiazolium units form layers comprised of 24-membered rings in which hydroge...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968643/ https://www.ncbi.nlm.nih.gov/pubmed/21582047 http://dx.doi.org/10.1107/S1600536809003572 |
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author | Hagos, Tesfamariam K. Nogai, Stefan D. Dobrzańska, Liliana Cronje, Stephanie Raubenheimer, Helgard G. |
author_facet | Hagos, Tesfamariam K. Nogai, Stefan D. Dobrzańska, Liliana Cronje, Stephanie Raubenheimer, Helgard G. |
author_sort | Hagos, Tesfamariam K. |
collection | PubMed |
description | In the crystal structure of the title ionic compound (C(7)H(6)NS)[AuCl(4)]·C(4)H(8)O, the [AuCl(4)](−) anion shows a typical square-planar geometry. Numerous weak C—H⋯Cl hydrogen bonds between [AuCl(4)](−) and the 1,3-benzothiazolium units form layers comprised of 24-membered rings in which hydrogen-bonded tetrahydrofuran (THF) solvent molecules are accommodated. C—H⋯Cl interactions between THF and [AuCl(4)](−) from adjacent layers result in bilayers. These are further stabilized by π–π interactions between the thiazole and benzene rings [centroid–centroid distance = 3.971 (3) Å], resulting in the formation of a three-dimensional supramolecular assembly. |
format | Text |
id | pubmed-2968643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29686432010-12-30 1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate Hagos, Tesfamariam K. Nogai, Stefan D. Dobrzańska, Liliana Cronje, Stephanie Raubenheimer, Helgard G. Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers In the crystal structure of the title ionic compound (C(7)H(6)NS)[AuCl(4)]·C(4)H(8)O, the [AuCl(4)](−) anion shows a typical square-planar geometry. Numerous weak C—H⋯Cl hydrogen bonds between [AuCl(4)](−) and the 1,3-benzothiazolium units form layers comprised of 24-membered rings in which hydrogen-bonded tetrahydrofuran (THF) solvent molecules are accommodated. C—H⋯Cl interactions between THF and [AuCl(4)](−) from adjacent layers result in bilayers. These are further stabilized by π–π interactions between the thiazole and benzene rings [centroid–centroid distance = 3.971 (3) Å], resulting in the formation of a three-dimensional supramolecular assembly. International Union of Crystallography 2009-02-06 /pmc/articles/PMC2968643/ /pubmed/21582047 http://dx.doi.org/10.1107/S1600536809003572 Text en © Hagos et al. 2009 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 Hagos, Tesfamariam K. Nogai, Stefan D. Dobrzańska, Liliana Cronje, Stephanie Raubenheimer, Helgard G. 1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate |
title | 1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate |
title_full | 1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate |
title_fullStr | 1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate |
title_full_unstemmed | 1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate |
title_short | 1,3-Benzothiazolium tetrachloridoaurate(III) tetrahydrofuran solvate |
title_sort | 1,3-benzothiazolium tetrachloridoaurate(iii) tetrahydrofuran solvate |
topic | Metal-Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968643/ https://www.ncbi.nlm.nih.gov/pubmed/21582047 http://dx.doi.org/10.1107/S1600536809003572 |
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