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Synthesis and Lewis Acidity of Fluorinated Triaryl Borates: data

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posted on 2024-10-30, 07:33 authored by Mashael Alharbi, Yara Van Ingen, Alberto Roldan, Tanja KaehlerTanja Kaehler
<p>A series of fluorinated triaryl borates B(OAr<sup>F</sup>)<sub>3</sub> (Ar<sup>F</sup> = 2-FC<sub>6</sub>H<sub>4</sub>, 3-FC<sub>6</sub>H<sub>4</sub>, 4-FC<sub>6</sub>H<sub>4</sub>, 2,4-F<sub>2</sub>C<sub>6</sub>H<sub>3</sub>, 3,5-F<sub>2</sub>C<sub>6</sub>H<sub>3</sub>, 2,3,4-F<sub>3</sub>C<sub>6</sub>H<sub>2</sub>, 2,4,6-F<sub>3</sub>C<sub>6</sub>H<sub>2</sub>, 3,4,5-F<sub>3</sub>C<sub>6</sub>H<sub>2</sub>) have been prepared and isolated from the reactions of the mono-, di-, or tri-fluorophenol with BCl<sub>3</sub>. The Lewis acidity of these borates has been determined by NMR spectroscopic and theoretical methods and compared to their well-established borane counterpart. The dataset includes experimental procedures and compound characterisation. <br></p><p>Reserch results based upon these data are published at https://doi.org/10.1039/D2DT04095F<br></p><p><br></p>

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From Organic to Inorganic Chemistry: Exploiting the Isolobal Analogy to Develop Main Group Catalysts

Engineering and Physical Sciences Research Council

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