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Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate]

Ethane­sulfonic acid-based buffers like 2-[4-(2-hy­droxy­eth­yl)­piperazin-1-yl]ethane­sulfonic acid (HEPES) are commonly used in biological experiments because of their ability to act as non-coordinating ligands towards metal ions. However, recent work has shown that some of these buffers may in fa...

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Autores principales: Bilinovich, Stephanie M., Panzner, Matthew J., Youngs, Wiley J., Leeper, Thomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200587/
https://www.ncbi.nlm.nih.gov/pubmed/22058835
http://dx.doi.org/10.1107/S160053681103008X
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author Bilinovich, Stephanie M.
Panzner, Matthew J.
Youngs, Wiley J.
Leeper, Thomas C.
author_facet Bilinovich, Stephanie M.
Panzner, Matthew J.
Youngs, Wiley J.
Leeper, Thomas C.
author_sort Bilinovich, Stephanie M.
collection PubMed
description Ethane­sulfonic acid-based buffers like 2-[4-(2-hy­droxy­eth­yl)­piperazin-1-yl]ethane­sulfonic acid (HEPES) are commonly used in biological experiments because of their ability to act as non-coordinating ligands towards metal ions. However, recent work has shown that some of these buffers may in fact coordinate metal ions. The title complex, {[Ag(C(8)H(17)N(2)O(4)S)]·3H(2)O}(n), is a metal–organic framework formed from HEPES and a silver(I) ion. In this polymeric complex, each Ag atom is primarily coordinated by two N atoms in a distorted linear geometry. Weaker secondary bonding inter­actions from the hy­droxy and sulfate O atoms of HEPES complete a distorted seesaw geometry. The crystal structure is stabilized by O—H⋯O hydrogen-bonding interactions.
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spelling pubmed-32005872011-11-06 Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate] Bilinovich, Stephanie M. Panzner, Matthew J. Youngs, Wiley J. Leeper, Thomas C. Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers Ethane­sulfonic acid-based buffers like 2-[4-(2-hy­droxy­eth­yl)­piperazin-1-yl]ethane­sulfonic acid (HEPES) are commonly used in biological experiments because of their ability to act as non-coordinating ligands towards metal ions. However, recent work has shown that some of these buffers may in fact coordinate metal ions. The title complex, {[Ag(C(8)H(17)N(2)O(4)S)]·3H(2)O}(n), is a metal–organic framework formed from HEPES and a silver(I) ion. In this polymeric complex, each Ag atom is primarily coordinated by two N atoms in a distorted linear geometry. Weaker secondary bonding inter­actions from the hy­droxy and sulfate O atoms of HEPES complete a distorted seesaw geometry. The crystal structure is stabilized by O—H⋯O hydrogen-bonding interactions. International Union of Crystallography 2011-08-02 /pmc/articles/PMC3200587/ /pubmed/22058835 http://dx.doi.org/10.1107/S160053681103008X Text en © Bilinovich et al. 2011 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
Bilinovich, Stephanie M.
Panzner, Matthew J.
Youngs, Wiley J.
Leeper, Thomas C.
Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate]
title Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate]
title_full Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate]
title_fullStr Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate]
title_full_unstemmed Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate]
title_short Poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(I)] trihydrate]
title_sort poly[[{μ(3)-2-[4-(2-hy­droxy­eth­yl)piperazin-1-yl]ethane­sulfonato}­silver(i)] trihydrate]
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200587/
https://www.ncbi.nlm.nih.gov/pubmed/22058835
http://dx.doi.org/10.1107/S160053681103008X
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