(2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)

In the crystal structure of the title compound, C(9)H(13)BO(2)·C(18)H(15)OP, there are O—H⋯O hydrogen bonds between the O atom of triphenyl­phosphine oxide and one hy­droxy group of the boronic acid. Boronic acid mol­ecules form inversion-related hydrogen-bonded dimers in an R (2) (2)(8) motif. The...

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Detalles Bibliográficos
Autores principales: Roşca, Sorin, Olaru, Marian, Raţ, Ciprian I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254394/
https://www.ncbi.nlm.nih.gov/pubmed/22259536
http://dx.doi.org/10.1107/S1600536811051609
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author Roşca, Sorin
Olaru, Marian
Raţ, Ciprian I.
author_facet Roşca, Sorin
Olaru, Marian
Raţ, Ciprian I.
author_sort Roşca, Sorin
collection PubMed
description In the crystal structure of the title compound, C(9)H(13)BO(2)·C(18)H(15)OP, there are O—H⋯O hydrogen bonds between the O atom of triphenyl­phosphine oxide and one hy­droxy group of the boronic acid. Boronic acid mol­ecules form inversion-related hydrogen-bonded dimers in an R (2) (2)(8) motif. The structure is consolidated by inter­molecular C—H⋯O bonds and C—H⋯π inter­actions.
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spelling pubmed-32543942012-01-18 (2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1) Roşca, Sorin Olaru, Marian Raţ, Ciprian I. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(9)H(13)BO(2)·C(18)H(15)OP, there are O—H⋯O hydrogen bonds between the O atom of triphenyl­phosphine oxide and one hy­droxy group of the boronic acid. Boronic acid mol­ecules form inversion-related hydrogen-bonded dimers in an R (2) (2)(8) motif. The structure is consolidated by inter­molecular C—H⋯O bonds and C—H⋯π inter­actions. International Union of Crystallography 2011-12-07 /pmc/articles/PMC3254394/ /pubmed/22259536 http://dx.doi.org/10.1107/S1600536811051609 Text en © Roşca 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
Roşca, Sorin
Olaru, Marian
Raţ, Ciprian I.
(2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)
title (2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)
title_full (2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)
title_fullStr (2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)
title_full_unstemmed (2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)
title_short (2,4,6-Trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)
title_sort (2,4,6-trimethyl­phen­yl)boronic acid–triphenyl­phosphine oxide (1/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254394/
https://www.ncbi.nlm.nih.gov/pubmed/22259536
http://dx.doi.org/10.1107/S1600536811051609
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