4-Cyano-1-methyl­pyridinium bromide

In the crystal of the title mol­ecular salt, C(7)H(7)N(2) (+)·Br(−), the cations form inversion dimers via weak pairwise C—H⋯N hydrogen bonds; their mean planes are separated by 0.292 (6) Å. Weak C—H⋯Br inter­actions involving all of the remaining H atoms tie the cations and anions together into set...

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Detalles Bibliográficos
Autores principales: Kammer, Michael N., Mague, Joel T., Koplitz, Lynn V.
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/PMC3414330/
https://www.ncbi.nlm.nih.gov/pubmed/22904863
http://dx.doi.org/10.1107/S1600536812030449
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author Kammer, Michael N.
Mague, Joel T.
Koplitz, Lynn V.
author_facet Kammer, Michael N.
Mague, Joel T.
Koplitz, Lynn V.
author_sort Kammer, Michael N.
collection PubMed
description In the crystal of the title mol­ecular salt, C(7)H(7)N(2) (+)·Br(−), the cations form inversion dimers via weak pairwise C—H⋯N hydrogen bonds; their mean planes are separated by 0.292 (6) Å. Weak C—H⋯Br inter­actions involving all of the remaining H atoms tie the cations and anions together into sets of inter­penetrating sheets. The title compound is isostructural with its iodide analogue.
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spelling pubmed-34143302012-08-17 4-Cyano-1-methyl­pyridinium bromide Kammer, Michael N. Mague, Joel T. Koplitz, Lynn V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal of the title mol­ecular salt, C(7)H(7)N(2) (+)·Br(−), the cations form inversion dimers via weak pairwise C—H⋯N hydrogen bonds; their mean planes are separated by 0.292 (6) Å. Weak C—H⋯Br inter­actions involving all of the remaining H atoms tie the cations and anions together into sets of inter­penetrating sheets. The title compound is isostructural with its iodide analogue. International Union of Crystallography 2012-07-10 /pmc/articles/PMC3414330/ /pubmed/22904863 http://dx.doi.org/10.1107/S1600536812030449 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.
Mague, Joel T.
Koplitz, Lynn V.
4-Cyano-1-methyl­pyridinium bromide
title 4-Cyano-1-methyl­pyridinium bromide
title_full 4-Cyano-1-methyl­pyridinium bromide
title_fullStr 4-Cyano-1-methyl­pyridinium bromide
title_full_unstemmed 4-Cyano-1-methyl­pyridinium bromide
title_short 4-Cyano-1-methyl­pyridinium bromide
title_sort 4-cyano-1-methyl­pyridinium bromide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414330/
https://www.ncbi.nlm.nih.gov/pubmed/22904863
http://dx.doi.org/10.1107/S1600536812030449
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