Benzyl­ethyl­dimethyl­ammonium bromide

The crystal structure of the title compound, C(11)H(18)N(+)·Br(−), has been determined as part of an ongoing study of the influence of the alkyl chain length on amphiphilic activity of quaternary ammonium salts. The title salt forms a three-dimensional network of ionic contacts through weak C—H⋯Br h...

Descripción completa

Detalles Bibliográficos
Autores principales: Hodorowicz, Maciej, Stadnicka, Katarzyna
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960757/
https://www.ncbi.nlm.nih.gov/pubmed/21201938
http://dx.doi.org/10.1107/S1600536808002481
_version_ 1782188817413832704
author Hodorowicz, Maciej
Stadnicka, Katarzyna
author_facet Hodorowicz, Maciej
Stadnicka, Katarzyna
author_sort Hodorowicz, Maciej
collection PubMed
description The crystal structure of the title compound, C(11)H(18)N(+)·Br(−), has been determined as part of an ongoing study of the influence of the alkyl chain length on amphiphilic activity of quaternary ammonium salts. The title salt forms a three-dimensional network of ionic contacts through weak C—H⋯Br hydrogen bonds, with donor–acceptor distances in the range 3.757 (2)–3.959 (2) Å, in which methyl groups serve as donors.
format Text
id pubmed-2960757
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29607572010-12-30 Benzyl­ethyl­dimethyl­ammonium bromide Hodorowicz, Maciej Stadnicka, Katarzyna Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure of the title compound, C(11)H(18)N(+)·Br(−), has been determined as part of an ongoing study of the influence of the alkyl chain length on amphiphilic activity of quaternary ammonium salts. The title salt forms a three-dimensional network of ionic contacts through weak C—H⋯Br hydrogen bonds, with donor–acceptor distances in the range 3.757 (2)–3.959 (2) Å, in which methyl groups serve as donors. International Union of Crystallography 2008-02-15 /pmc/articles/PMC2960757/ /pubmed/21201938 http://dx.doi.org/10.1107/S1600536808002481 Text en © Hodorowicz and Stadnicka 2008 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
Hodorowicz, Maciej
Stadnicka, Katarzyna
Benzyl­ethyl­dimethyl­ammonium bromide
title Benzyl­ethyl­dimethyl­ammonium bromide
title_full Benzyl­ethyl­dimethyl­ammonium bromide
title_fullStr Benzyl­ethyl­dimethyl­ammonium bromide
title_full_unstemmed Benzyl­ethyl­dimethyl­ammonium bromide
title_short Benzyl­ethyl­dimethyl­ammonium bromide
title_sort benzyl­ethyl­dimethyl­ammonium bromide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960757/
https://www.ncbi.nlm.nih.gov/pubmed/21201938
http://dx.doi.org/10.1107/S1600536808002481
work_keys_str_mv AT hodorowiczmaciej benzylethyldimethylammoniumbromide
AT stadnickakatarzyna benzylethyldimethylammoniumbromide

Ejemplares similares