Synthesis and Characterization of 14-Vertex Carboranes

Abstract

Twelve new 14-vertex <i>closo</i>-carboranes, including CAd (carbon atoms adjacent), CAp (carbon atoms apart), and cage B-substituted species, were synthesized and structurally characterized via either a [13 + 1] or a [12 + 2] polyhedral expansion protocol. Treatment of various 13-vertex <i>nido</i>-carborane dianionic salts with HBBr<sub>2</sub> gave the corresponding 14-vertex carboranes. Mono-B-substituted 14-vertex carboranes 1-R-2,3-(CH<sub>2</sub>)<sub>3</sub>-2,3-C<sub>2</sub>B<sub>12</sub>H<sub>11</sub> (R = Ph, Cl, Br, I) were prepared from the reaction of <i>nido</i>-[8,9-(CH<sub>2</sub>)<sub>3</sub>-2,3-C<sub>2</sub>B<sub>11</sub>H<sub>11</sub>]<sup>2–</sup> with the dihaloborane reagents RBX<sub>2</sub>. CAd 14-vertex <i>closo</i>-carboranes were also synthesized by treatment of 12-vertex <i>arachno</i>-carborane tetraanionic salts with HBBr<sub>2</sub> reagent. These new 14-vertex <i>closo</i>-carboranes were fully characterized by <sup>1</sup>H, <sup>13</sup>C, and <sup>11</sup>B NMR spectroscopy as well as high-resolution mass spectrometry. Their structures were further confirmed by single-crystal X-ray analyses

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The Francis Crick Institute

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Last time updated on 12/02/2018

This paper was published in The Francis Crick Institute.

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