Linked and Mercury-Bridged Nido-Carboranes. High-Yield Synthesis of mu, mu' - ((CH3)2C2B4H5)2Hg, Conversion to 5,5'-((CH3)2C2B4H5)2, Cleavage, and Oxidative Addition of Benzene. Synthesis of mu, mu'-(B5H8)2Hg.

Abstract

The nido-carborane anion (2,3-(CH3)2C2B4H5)(-) reacts readily with anhydrous HgCl2 in THF at room temperature, producing the bis(carboranyl) mercury(II) complex mu,mu'-((CH3)2C2B4H5)2Hg in which the metal is bound to two carborane ligands via B-Hg-B three-center, two-electron bridge bonds. On heating at 180 deg. in benzene, this compound quantitatively expels free mercury and forms the B-B linked nido-carborane 5,5'-((CH3)2C2B4H5)2 as a single pure isomer. Air oxidation of the linked carborane in benzene solution results in cleavage of the carborane-carborane B-B bond and oxidative addition of benzene to give 4-C6H5-2,3-(CH3)2C2B4H5, an apparently air-stable derivative of nido-2,3-C2B4H8. Similar treatment of the linked carborane in C6D6 gives the corresponding hexadeuterated carborane product. The reaction of B5H8 - ion with HgCl2 in THF produces mu,mu-(B5H8)2Hg, a stable solid in which mercury is evidently bridge-bonded to two pentaborane ligands. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 1979
Accession Number
ADA070777

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  • Narayan S. Hosmane
  • Russell N. Grimes

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  • University of Virginia

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