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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].

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The ionic title compound, C12H28P+·C18HBF15O, was obtained by the stoichiometric reaction of tBu3P, B(C6F5)3 and water in toluene. A weak P—H...O hydrogen bond is observed in the crystal structure.
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