4-Cyano-1-methyl­pyridinium iodide

In the crystal structure of the title compound, C(7)H(7)N(2) (+)·I(−), the cations form inversion-related dimers via weak pairwise C—H⋯N hydrogen bonds. In the dimers, the pyridinium rings are parallel to one another with their mean planes separated by a normal distance of ca 0.28 Å. Weak C—H⋯N inte...

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Detalles Bibliográficos
Autores principales: Kammer, Michael N., Koplitz, Lynn V., Mague, Joel T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414965/
https://www.ncbi.nlm.nih.gov/pubmed/22904952
http://dx.doi.org/10.1107/S1600536812032230
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author Kammer, Michael N.
Koplitz, Lynn V.
Mague, Joel T.
author_facet Kammer, Michael N.
Koplitz, Lynn V.
Mague, Joel T.
author_sort Kammer, Michael N.
collection PubMed
description In the crystal structure of the title compound, C(7)H(7)N(2) (+)·I(−), the cations form inversion-related dimers via weak pairwise C—H⋯N hydrogen bonds. In the dimers, the pyridinium rings are parallel to one another with their mean planes separated by a normal distance of ca 0.28 Å. Weak C—H⋯N inter­actions between adjacent dimers generate a layer lying parallel to (10-1). The remaining H atoms form C—H⋯I inter­actions, which link the layers into a three-dimensional structure.
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spelling pubmed-34149652012-08-17 4-Cyano-1-methyl­pyridinium iodide Kammer, Michael N. Koplitz, Lynn V. Mague, Joel T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(7)H(7)N(2) (+)·I(−), the cations form inversion-related dimers via weak pairwise C—H⋯N hydrogen bonds. In the dimers, the pyridinium rings are parallel to one another with their mean planes separated by a normal distance of ca 0.28 Å. Weak C—H⋯N inter­actions between adjacent dimers generate a layer lying parallel to (10-1). The remaining H atoms form C—H⋯I inter­actions, which link the layers into a three-dimensional structure. International Union of Crystallography 2012-07-21 /pmc/articles/PMC3414965/ /pubmed/22904952 http://dx.doi.org/10.1107/S1600536812032230 Text en © Kammer et al. 2012 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
Kammer, Michael N.
Koplitz, Lynn V.
Mague, Joel T.
4-Cyano-1-methyl­pyridinium iodide
title 4-Cyano-1-methyl­pyridinium iodide
title_full 4-Cyano-1-methyl­pyridinium iodide
title_fullStr 4-Cyano-1-methyl­pyridinium iodide
title_full_unstemmed 4-Cyano-1-methyl­pyridinium iodide
title_short 4-Cyano-1-methyl­pyridinium iodide
title_sort 4-cyano-1-methyl­pyridinium iodide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414965/
https://www.ncbi.nlm.nih.gov/pubmed/22904952
http://dx.doi.org/10.1107/S1600536812032230
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