Phenolate and phenoxyl radical complexes of Co(II) and Co(III) |
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Authors: | Benisvy Laurent Bill Eckhard Blake Alexander J Collison David Davies E Stephen Garner C David Guindy Christina I McInnes Eric J L McArdle Graeme McMaster Jonathan Wilson Claire Wolowska Joanna |
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Institution: | School of Chemistry, The University of Nottingham, University Park, Nottingham, UK NG7 2RD. |
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Abstract: | The new phenol-imidazole pro-ligands (R)LH react with Co(BF(4))(2).6H(2)O in the presence of Et(3)N to form the corresponding Co(II)((R)L)(2)] compound (R = Ph (1), PhOMe (2), or Bz (3)). Also, (Bz)LH, reacts with Co(ii) in the presence of Et(3)N and H(2)O(2) to form Co(III)((Bz)L)(3)](4). The structures of 1.2.5MeCN, 2.2DMF, 3.4MeOH, and 4.4DMF have been determined by X-ray crystallography. 1, 2, and 3 each involve Co(II) bound to two N,O-bidentate ligands with a distorted tetrahedral coordination sphere; 4 involves Co(III) bound to three N,O-bidentate ligands in a mer-N(3)O(3) distorted octahedral geometry. Co(II)((R)L)(2)](R = Ph or PhOMe) undergo two, one-electron, oxidations. The products of the first oxidation, 1](+) and 2](+), have been synthesised by the chemical oxidation of 1 and 2, respectively; these cations, formulated as Co(II)((R)L*)((R)L)(2)](+), comprise one phenoxyl radical and one phenolate ligand bound to Co(II) and are the first phenoxyl radical ligand complexes of tetra-coordinated Co(II). 4 undergoes two, one-electron, ligand-based oxidations, the first of which produces 4](+), Co(III)((Bz)L*)((Bz)L)(2)](+). Unlike 1](+) and 2](+), product of the one-electron oxidation of Co(II)((Bz)L)(2)], 3](+), is unstable and decomposes to produce 4](+). These studies have demonstrated that the chemical properties of M(II)((R)L*)((R)L)(2)](+)(M = Co, Cu, Zn) are highly dependent on the nature of both the ligand and the metal centre. |
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