4.7 Article

Observation of Room Temperature B-Cl Activation of the HCB11Cl11- Anion and Isolation of a Stable Anionic Carboranyl Phosphazide

Journal

INORGANIC CHEMISTRY
Volume 52, Issue 21, Pages 12308-12310

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ic402436w

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Funding

  1. UCR [52255-DNI3]
  2. ACS PRF [52255-DNI3]
  3. Pfizer

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The perchlorinated carba-closo-dodecaborate anion is typically inert toward B-Cl functionalization. We present here the observation of two competing reactions that occur with this anion at ambient temperature. When this molecule is treated with n-BuLi and subsequently reacted with tosyl azide, a cycloaddition occurs and results in chloride substitution at a B-Cl vertex. The competing and dominant pathway is a substitution reaction to form the azide N3CB11Cl11-. This rare anionic carboranyl azide reacts with PPh3 in FC6H5 to afford a stable anionic phosphazide. When dissolved in tetrahydrofuran, the phosphazide is in equilibrium with free PPh3 and N3CB11Cl11-. Both the triazole and phosphazide are characterized by single-crystal X-ray diffraction, NMR and IR spectroscopy, and high-resolution mass spectrometry.

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