Cargando…

Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate

The title compound, C(19)H(34)N(+)·C(10)H(7)O(4)S(−), is a charge-control agent used for toners in electrophotography. In the crystal structure, centrosymmetric anions associate through O—H⋯O hydrogen bonds formed between the O—H group of one anion and the sulfonate O atom of a neighbor. The compone...

Descripción completa

Detalles Bibliográficos
Autores principales: Uta, Kazuya, Mizuguchi, Jin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968190/
https://www.ncbi.nlm.nih.gov/pubmed/21581925
http://dx.doi.org/10.1107/S1600536809000178
_version_ 1782189800364703744
author Uta, Kazuya
Mizuguchi, Jin
author_facet Uta, Kazuya
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 used for toners in electrophotography. In the crystal structure, centrosymmetric anions associate through O—H⋯O hydrogen bonds formed between the O—H group of one anion and the sulfonate O atom of a neighbor. The components of the dimer are offset with respect to each other so that the separation between the two parallel naphthalene skeletons is about 1.6 Å. The ethyl residues of two of the butyl groups are disordered and were modelled over two postions (site occupancies = 0.33/0.67 and 0.34/0.66).
format Text
id pubmed-2968190
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29681902010-12-30 Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate Uta, Kazuya 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 used for toners in electrophotography. In the crystal structure, centrosymmetric anions associate through O—H⋯O hydrogen bonds formed between the O—H group of one anion and the sulfonate O atom of a neighbor. The components of the dimer are offset with respect to each other so that the separation between the two parallel naphthalene skeletons is about 1.6 Å. The ethyl residues of two of the butyl groups are disordered and were modelled over two postions (site occupancies = 0.33/0.67 and 0.34/0.66). International Union of Crystallography 2009-01-17 /pmc/articles/PMC2968190/ /pubmed/21581925 http://dx.doi.org/10.1107/S1600536809000178 Text en © Uta and Mizuguchi 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
Mizuguchi, Jin
Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate
title Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate
title_full Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate
title_fullStr Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate
title_full_unstemmed Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate
title_short Benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate
title_sort benzyl­tributyl­ammonium 4-hydroxy­naphthalene-2-sulfonate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968190/
https://www.ncbi.nlm.nih.gov/pubmed/21581925
http://dx.doi.org/10.1107/S1600536809000178
work_keys_str_mv AT utakazuya benzyltributylammonium4hydroxynaphthalene2sulfonate
AT mizuguchijin benzyltributylammonium4hydroxynaphthalene2sulfonate