Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate

The title compound, C(19)H(34)N(+)·C(10)H(7)O(4)S(−), is a charge-control agent for toners used in electrophotography. Inter­moleclar O—H⋯O hydrogen bonding between the OH group of one anion and the sulfonate O atom of a neighboring anion leads to the formation of one-dimensional chains along the b...

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Detalles Bibliográficos
Autores principales: Uta, Kazuya, Sato, Yohei, Mizuguchi, Jin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968198/
https://www.ncbi.nlm.nih.gov/pubmed/21581924
http://dx.doi.org/10.1107/S1600536809001329
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author Uta, Kazuya
Sato, Yohei
Mizuguchi, Jin
author_facet Uta, Kazuya
Sato, Yohei
Mizuguchi, Jin
author_sort Uta, Kazuya
collection PubMed
description The title compound, C(19)H(34)N(+)·C(10)H(7)O(4)S(−), is a charge-control agent for toners used in electrophotography. Inter­moleclar O—H⋯O hydrogen bonding between the OH group of one anion and the sulfonate O atom of a neighboring anion leads to the formation of one-dimensional chains along the b axis. In addition, C—H⋯O hydrogen bonds are observed. One of the n-butyl chains of the cation is disordered over two sites in a 0.88:0.12 ratio.
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spelling pubmed-29681982010-12-30 Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate Uta, Kazuya Sato, Yohei Mizuguchi, Jin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(19)H(34)N(+)·C(10)H(7)O(4)S(−), is a charge-control agent for toners used in electrophotography. Inter­moleclar O—H⋯O hydrogen bonding between the OH group of one anion and the sulfonate O atom of a neighboring anion leads to the formation of one-dimensional chains along the b axis. In addition, C—H⋯O hydrogen bonds are observed. One of the n-butyl chains of the cation is disordered over two sites in a 0.88:0.12 ratio. International Union of Crystallography 2009-01-17 /pmc/articles/PMC2968198/ /pubmed/21581924 http://dx.doi.org/10.1107/S1600536809001329 Text en © Uta et al. 2009 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
Uta, Kazuya
Sato, Yohei
Mizuguchi, Jin
Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate
title Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate
title_full Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate
title_fullStr Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate
title_full_unstemmed Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate
title_short Benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate
title_sort benzyl­tributyl­ammonium 6-hydroxy­naphthalene-2-sulfonate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968198/
https://www.ncbi.nlm.nih.gov/pubmed/21581924
http://dx.doi.org/10.1107/S1600536809001329
work_keys_str_mv AT utakazuya benzyltributylammonium6hydroxynaphthalene2sulfonate
AT satoyohei benzyltributylammonium6hydroxynaphthalene2sulfonate
AT mizuguchijin benzyltributylammonium6hydroxynaphthalene2sulfonate

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