2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate
The title compound, C7H7N·B(C6F5)3·C6H14, was obtained by the stoichiometric reaction of 2-vinylpyridine and tris(pentafluorophenyl)borane in toluene. The formed adduct exhibits a restricted rotation along the B—N bond resulting in an asymmetry, which can be a...
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International Union of Crystallography
2012-04-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536812013153 |
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doaj-2b24df0eadcf41bcb73d2d889606091d2020-11-25T01:35:55ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-04-01684o1261o126110.1107/S16005368120131532-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvateMarcus KlahnAnke SpannenbergUwe RosenthalThe title compound, C7H7N·B(C6F5)3·C6H14, was obtained by the stoichiometric reaction of 2-vinylpyridine and tris(pentafluorophenyl)borane in toluene. The formed adduct exhibits a restricted rotation along the B—N bond resulting in an asymmetry, which can be also observed in the 19F NMR spectra. The B—N distance is equivalent to the distances found for 2-methylpyridine and 2-ethylpyridine B(C6F5)3 adducts. For the final refinement, the contributions of disordered solvent molecules were removed from the diffraction data with SQUEEZE in PLATON [van der Sluis & Spek (1990). Acta Cryst. A46, 194–201; Spek (2009). Acta Cryst. D65, 148–155].http://scripts.iucr.org/cgi-bin/paper?S1600536812013153 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marcus Klahn Anke Spannenberg Uwe Rosenthal |
spellingShingle |
Marcus Klahn Anke Spannenberg Uwe Rosenthal 2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate Acta Crystallographica Section E |
author_facet |
Marcus Klahn Anke Spannenberg Uwe Rosenthal |
author_sort |
Marcus Klahn |
title |
2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate |
title_short |
2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate |
title_full |
2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate |
title_fullStr |
2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate |
title_full_unstemmed |
2-Vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate |
title_sort |
2-vinylpyridine–tris(pentafluorophenyl)borane hexane monosolvate |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2012-04-01 |
description |
The title compound, C7H7N·B(C6F5)3·C6H14, was obtained by the stoichiometric reaction of 2-vinylpyridine and tris(pentafluorophenyl)borane in toluene. The formed adduct exhibits a restricted rotation along the B—N bond resulting in an asymmetry, which can be also observed in the 19F NMR spectra. The B—N distance is equivalent to the distances found for 2-methylpyridine and 2-ethylpyridine B(C6F5)3 adducts. For the final refinement, the contributions of disordered solvent molecules were removed from the diffraction data with SQUEEZE in PLATON [van der Sluis & Spek (1990). Acta Cryst. A46, 194–201; Spek (2009). Acta Cryst. D65, 148–155]. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536812013153 |
work_keys_str_mv |
AT marcusklahn 2vinylpyridineamp8211trispentafluorophenylboranehexanemonosolvate AT ankespannenberg 2vinylpyridineamp8211trispentafluorophenylboranehexanemonosolvate AT uwerosenthal 2vinylpyridineamp8211trispentafluorophenylboranehexanemonosolvate |
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1725065422781284352 |