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(Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate

To aid in the elucidation of catalytic reaction mechanism of palladacycles, we found that reaction of trifluoro­methane­sulfonic acid with a phosphapalladacycle resulted in elimination of the palladium and formation of the title phospholium salt, C(20)H(26)P(+)·CF(3)SO(3) (−). Selected geometrical p...

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Detalles Bibliográficos
Autores principales: Muller, Alfred, Holzapfel, Cedric W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588282/
https://www.ncbi.nlm.nih.gov/pubmed/23476408
http://dx.doi.org/10.1107/S1600536812049045
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author Muller, Alfred
Holzapfel, Cedric W.
author_facet Muller, Alfred
Holzapfel, Cedric W.
author_sort Muller, Alfred
collection PubMed
description To aid in the elucidation of catalytic reaction mechanism of palladacycles, we found that reaction of trifluoro­methane­sulfonic acid with a phosphapalladacycle resulted in elimination of the palladium and formation of the title phospholium salt, C(20)H(26)P(+)·CF(3)SO(3) (−). Selected geometrical parameters include P—biphenyl (av.) = 1.801 (3) Å and P—t-Bu (av.) = 1.858 (3) Å, and significant distortion of the tetra­hedral P-atom environment with biphen­yl—P—biphenyl = 93.93 (13)° and t-Bu—P—t-Bu = 118.82 (14)°. In the crystal, weak C—H⋯O inter­actions lead to channels along the c axis that are occupied by CF(3)SO(3) (−) anions.
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spelling pubmed-35882822013-03-08 (Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate Muller, Alfred Holzapfel, Cedric W. Acta Crystallogr Sect E Struct Rep Online Organic Papers To aid in the elucidation of catalytic reaction mechanism of palladacycles, we found that reaction of trifluoro­methane­sulfonic acid with a phosphapalladacycle resulted in elimination of the palladium and formation of the title phospholium salt, C(20)H(26)P(+)·CF(3)SO(3) (−). Selected geometrical parameters include P—biphenyl (av.) = 1.801 (3) Å and P—t-Bu (av.) = 1.858 (3) Å, and significant distortion of the tetra­hedral P-atom environment with biphen­yl—P—biphenyl = 93.93 (13)° and t-Bu—P—t-Bu = 118.82 (14)°. In the crystal, weak C—H⋯O inter­actions lead to channels along the c axis that are occupied by CF(3)SO(3) (−) anions. International Union of Crystallography 2012-12-05 /pmc/articles/PMC3588282/ /pubmed/23476408 http://dx.doi.org/10.1107/S1600536812049045 Text en © Muller and Holzapfel 2013 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
Muller, Alfred
Holzapfel, Cedric W.
(Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate
title (Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate
title_full (Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate
title_fullStr (Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate
title_full_unstemmed (Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate
title_short (Biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate
title_sort (biphenyl-2,2′-di­yl)di-tert-butyl­phos­phonium trifluoro­methane­sulfonate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588282/
https://www.ncbi.nlm.nih.gov/pubmed/23476408
http://dx.doi.org/10.1107/S1600536812049045
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