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Synfacts 2009(6): 0624-0624  
DOI: 10.1055/s-0029-1216665
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag Stuttgart ˙ New York

Fully Fluorinated Pentaphenylborole

Contributor(s): Timothy M. Swager, Jeewoo Lim
C. Feng, W. E. Piers*, M. Parvez
University of Calgary, Canada
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Publikationsdatum:
25. Mai 2009 (online)

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Erratum zu diesem Artikel:

Fully Fluorinated PentaphenylboroleSynfacts 2009; 2009(08): 0938-0938
DOI: 10.1055/s-0029-1217598

Significance

The authors report a synthesis of perfluorinated pentaphenylborole (2). Perfluorination, along with the antiaromaticity of the borole ring makes 2 a potent Lewis acid and possible precursors to a variety of interesting materials and building blocks.