Dodds, C.A. and Lehmann, M.A. and Ojo, J.F. and Reglinski, J. and Spicer, M.D. (2004) Cobalt half-sandwich, sandwich, and mixed sandwich complexes with soft tripodal ligands. Inorganic Chemistry, 43 (16). pp. 4927-4934. ISSN 0020-1669Full text not available in this repository. (Request a copy from the Strathclyde author)
Reaction of sodium hydrotris(methimazolyl)borate (NaTmMe) with cobalt halides leads to the formation of paramagnetic pseudotetrahedral [Co(Tm-Me)X] (X = Cl, Br, I), of which the bromide has been crystallographically characterized. Mass spectrometry reveals the presence of higher molecular weight fragments [Co(Tm-Me)(2)](+) and [Co-2(Tm-Me)(2)X](+) in solution. Aerial oxidation in donor solvents (e.g. MeCN) leads to formation of the [Co(Tm-Me)(2)](+) cation, which has been crystallographically characterized as the BF4-, ClO4-, Br-, and I-, salts. Attempts to prepare the mixed sandwich complex, [Co(Cp)(Tm-Me)](+), resulted in ligand decomposition to yield [Co(mtH)(3)I]I (mtH = 1-methylimidazole-2-thione), but with the more electron donating methylcyclopentadienyl (Cp-Me) ligand, [Co(Cp-Me)(Tm-Me)]I was isolated and characterized. Electrochemical measurements reveal that the cobalt(III) Tm-Me complexes are consistently more difficult to reduce than their Tp and Cp congeners.
|Keywords:||ORGANOMETALLIC CHEMISTRY, TRANSITION-METALS, CYCLOPENTADIENYL, NICKEL(II), FIELD, IRON, TM, Chemistry, Physical and Theoretical Chemistry, Inorganic Chemistry|
|Subjects:||Science > Chemistry|
|Department:||Faculty of Science > Pure and Applied Chemistry
|Depositing user:||Mr Derek Boyle|
|Date Deposited:||20 Mar 2006|
|Last modified:||22 Mar 2017 09:19|