4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate

In the crystal of the title hydrated mol­ecular salt, C(8)H(12)NO(+)·Cl(−)·H(2)O, the water mol­ecule makes two O—H⋯Cl hydrogen bonds, generating [010] zigzag chains of alternating water mol­ecules and chloride ions. The cation is bonded to the chain by an O—H⋯O hydrogen bond and two weak C—H⋯Cl int...

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Autores principales: Seethalakshmi, T., Manivannan, S., Dhanuskodi, S., Lynch, Daniel E., Thamotharan, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684923/
https://www.ncbi.nlm.nih.gov/pubmed/23795025
http://dx.doi.org/10.1107/S1600536813011616
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author Seethalakshmi, T.
Manivannan, S.
Dhanuskodi, S.
Lynch, Daniel E.
Thamotharan, S.
author_facet Seethalakshmi, T.
Manivannan, S.
Dhanuskodi, S.
Lynch, Daniel E.
Thamotharan, S.
author_sort Seethalakshmi, T.
collection PubMed
description In the crystal of the title hydrated mol­ecular salt, C(8)H(12)NO(+)·Cl(−)·H(2)O, the water mol­ecule makes two O—H⋯Cl hydrogen bonds, generating [010] zigzag chains of alternating water mol­ecules and chloride ions. The cation is bonded to the chain by an O—H⋯O hydrogen bond and two weak C—H⋯Cl inter­actions. Weak aromatic π–π stacking [centroid–centroid separation = 3.5175 (15) Å] occurs between the chains.
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spelling pubmed-36849232013-06-21 4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate Seethalakshmi, T. Manivannan, S. Dhanuskodi, S. Lynch, Daniel E. Thamotharan, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal of the title hydrated mol­ecular salt, C(8)H(12)NO(+)·Cl(−)·H(2)O, the water mol­ecule makes two O—H⋯Cl hydrogen bonds, generating [010] zigzag chains of alternating water mol­ecules and chloride ions. The cation is bonded to the chain by an O—H⋯O hydrogen bond and two weak C—H⋯Cl inter­actions. Weak aromatic π–π stacking [centroid–centroid separation = 3.5175 (15) Å] occurs between the chains. International Union of Crystallography 2013-05-04 /pmc/articles/PMC3684923/ /pubmed/23795025 http://dx.doi.org/10.1107/S1600536813011616 Text en © Seethalakshmi et al. 2013 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 Organic Papers
Seethalakshmi, T.
Manivannan, S.
Dhanuskodi, S.
Lynch, Daniel E.
Thamotharan, S.
4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate
title 4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate
title_full 4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate
title_fullStr 4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate
title_full_unstemmed 4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate
title_short 4-Hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate
title_sort 4-hy­droxy-1,2,6-tri­methyl­pyridinium chloride monohydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684923/
https://www.ncbi.nlm.nih.gov/pubmed/23795025
http://dx.doi.org/10.1107/S1600536813011616
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AT dhanuskodis 4hydroxy126trimethylpyridiniumchloridemonohydrate
AT lynchdaniele 4hydroxy126trimethylpyridiniumchloridemonohydrate
AT thamotharans 4hydroxy126trimethylpyridiniumchloridemonohydrate

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