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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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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. |
format | Online Article Text |
id | pubmed-3588282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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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