Abstract
The reaction of closo-exo-5,6-[(m-H)2Li(TMEDA)]-1-Li(TMEDA)-2,4-(SiMe3)2-2,4-C2B4H4 with CoCl2 in a molar ratio of 1:1 in a solvent mixt. of dry benzene and n-hexane at 0° and then at room temp. produces, in 92\% yield, deep green crystals of a paramagnetic, half-sandwich Co(II) carborane, closo-1-(TMEDA)-1-Co-2,4-(SiMe3)2-2,4-C2B4H4 (I), which does not undergo disproportionation to give the corresponding Co(III) species and elemental cobalt. Unlike the cases of main-group metallacarboranes, the coordination of the metal in I with the Lewis base TMEDA does not produce a distortion of the metallacarborane. Thus, I exhibits an almost undistorted \dqcarbons apart\dq pentagonal-bipyramidal geometry, which was confirmed by a single-crystal x-ray diffraction study. [on SciFinder(R)]
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