Publications by authors named "Valentina A Chudakova"

The reactivity of digallane (dpp-Bian)Ga-Ga(dpp-Bian) (1) (dpp-Bian = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene) toward acenaphthenequinone (AcQ), sulfur dioxide, and azobenzene was investigated. The reaction of 1 with AcQ in 1:1 molar ratio proceeds via two-electron reduction of AcQ to give (dpp-Bian)Ga(μ2-AcQ)Ga(dpp-Bian) (2), in which diolate [AcQ](2-) acts as "bracket" for the Ga-Ga bond. The interaction of 1 with AcQ in 1:2 molar ratio proceeds with an oxidation of the both dpp-Bian ligands as well as of the Ga-Ga bond to give (dpp-Bian)Ga(μ2-AcQ)2Ga(dpp-Bian) (3).

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The reactivity of digallane (dpp-Bian)Ga-Ga(dpp-Bian) (1), which consists of redox-active ligand 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene (dpp-Bian), has been studied. The reaction of 1 with I2 proceeds via one-electron oxidation of each of two dpp-Bian ligands to a radical-anionic state and affords complex (dpp-Bian)IGa-GaI(dpp-Bian) (2). Dissolution of complex 2 in pyridine (Py) gives monomeric compound (dpp-Bian)GaI(Py) (3) as a result of a solvent-induced intramolecular electron transfer from the metal-metal bond to the dpp-Bian ligands.

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The reduction of benzophenone with the magnesium complex [(2,6-iPr(2)C(6)H(3)-bian)Mg(thf)(3)] (1), containing the 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene dianion, affords the pinacolato complex [(2,6-iPr(2)C(6)H(3)-bian)Mg(thf)](2)[micro-O(2)C(2)Ph(4)].(C(6)H(6))(4) (2). The reaction of 1 with 9(10H)-anthracenone yields the 9-anthracenolato complex [(2,6-iPr(2)C(6)H(3)-bian)Mg(OC(14)H(9))(thf)(2)] (3).

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