Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate

The ionic title compound, C(12)H(28)P(+)·C(18)HBF(15)O(−), was obtained by the stoichiometric reaction of (t)Bu(3)P, B(C(6)F(5))(3) and water in toluene. A weak P—H⋯O hydrogen bond is observed in the crystal structure.

Detalles Bibliográficos
Autores principales: Klahn, Marcus, Spannenberg, Anke, Rosenthal, Uwe
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/PMC3344648/
https://www.ncbi.nlm.nih.gov/pubmed/22590410
http://dx.doi.org/10.1107/S1600536812018144
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author Klahn, Marcus
Spannenberg, Anke
Rosenthal, Uwe
author_facet Klahn, Marcus
Spannenberg, Anke
Rosenthal, Uwe
author_sort Klahn, Marcus
collection PubMed
description The ionic title compound, C(12)H(28)P(+)·C(18)HBF(15)O(−), was obtained by the stoichiometric reaction of (t)Bu(3)P, B(C(6)F(5))(3) and water in toluene. A weak P—H⋯O hydrogen bond is observed in the crystal structure.
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spelling pubmed-33446482012-05-15 Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate Klahn, Marcus Spannenberg, Anke Rosenthal, Uwe Acta Crystallogr Sect E Struct Rep Online Organic Papers The ionic title compound, C(12)H(28)P(+)·C(18)HBF(15)O(−), was obtained by the stoichiometric reaction of (t)Bu(3)P, B(C(6)F(5))(3) and water in toluene. A weak P—H⋯O hydrogen bond is observed in the crystal structure. International Union of Crystallography 2012-04-28 /pmc/articles/PMC3344648/ /pubmed/22590410 http://dx.doi.org/10.1107/S1600536812018144 Text en © Klahn 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
Klahn, Marcus
Spannenberg, Anke
Rosenthal, Uwe
Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate
title Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate
title_full Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate
title_fullStr Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate
title_full_unstemmed Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate
title_short Tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate
title_sort tri-tert-butyl­phospho­nium hy­droxy­tris­(penta­fluoro­phen­yl)borate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344648/
https://www.ncbi.nlm.nih.gov/pubmed/22590410
http://dx.doi.org/10.1107/S1600536812018144
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