4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate

In the title mol­ecular salt, C(18)H(22)NO(+)·C(7)H(7)O(3)S(−), the dihedral angle between the aromatic rings in the cation is 10.00 (9)°; its alkyl side chain adopts an extended conformation. In the crystal, weak C—H⋯O and π–π [centroid–centroid distance = 3.7658 (17) Å] inter­actions link the comp...

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Detalles Bibliográficos
Autores principales: Kumar, M. Krishna, Margret, S. Mabel, Chakkaravarthi, G., Velmurugan, D., Kumar, R. Mohan
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/PMC3648242/
https://www.ncbi.nlm.nih.gov/pubmed/23723862
http://dx.doi.org/10.1107/S1600536813009616
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author Kumar, M. Krishna
Margret, S. Mabel
Chakkaravarthi, G.
Velmurugan, D.
Kumar, R. Mohan
author_facet Kumar, M. Krishna
Margret, S. Mabel
Chakkaravarthi, G.
Velmurugan, D.
Kumar, R. Mohan
author_sort Kumar, M. Krishna
collection PubMed
description In the title mol­ecular salt, C(18)H(22)NO(+)·C(7)H(7)O(3)S(−), the dihedral angle between the aromatic rings in the cation is 10.00 (9)°; its alkyl side chain adopts an extended conformation. In the crystal, weak C—H⋯O and π–π [centroid–centroid distance = 3.7658 (17) Å] inter­actions link the components, generating a three-dimensional network.
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spelling pubmed-36482422013-05-30 4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate Kumar, M. Krishna Margret, S. Mabel Chakkaravarthi, G. Velmurugan, D. Kumar, R. Mohan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecular salt, C(18)H(22)NO(+)·C(7)H(7)O(3)S(−), the dihedral angle between the aromatic rings in the cation is 10.00 (9)°; its alkyl side chain adopts an extended conformation. In the crystal, weak C—H⋯O and π–π [centroid–centroid distance = 3.7658 (17) Å] inter­actions link the components, generating a three-dimensional network. International Union of Crystallography 2013-04-13 /pmc/articles/PMC3648242/ /pubmed/23723862 http://dx.doi.org/10.1107/S1600536813009616 Text en © Kumar 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
Kumar, M. Krishna
Margret, S. Mabel
Chakkaravarthi, G.
Velmurugan, D.
Kumar, R. Mohan
4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate
title 4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate
title_full 4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate
title_fullStr 4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate
title_full_unstemmed 4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate
title_short 4-[2-(4-But­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate
title_sort 4-[2-(4-but­oxy­phen­yl)ethen­yl]-1-methyl­pyridinium tosylate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648242/
https://www.ncbi.nlm.nih.gov/pubmed/23723862
http://dx.doi.org/10.1107/S1600536813009616
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