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Updated: May 7, 2026
Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
Published on: May 28, 2014
Distinct stepwise reduction of a nickel-nickel-bonded compound containing an α-diimine ligand: from perpendicular to
Qingsong Dong1, Xiao-Juan Yang, Shida Gong
1State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, CAS, Lanzhou 730000 (P.R. China).
Abstract:
A nickel-nickel-bonded complex, [{Ni(μ-L(.-))}2] (1; L=[(2,6-iPr2C6H3)NC(Me)]2), was synthesized from reduction of the LNiBr2 precursor by sodium metal. Further controllable reduction of 1 with 1.0, 2.0 and 3.0 equiv of Na, respectively, afforded the singly, doubly, and triply reduced compounds [Na(DME)3]·[{Ni(μ-L(.-))}2] (2; DME=1,2-dimethoxyethane), [Na(Et2O)]Na[(L(.-))Ni-NiL(2-)] (3), and [Na(Et2O)]2Na[L(2-)Ni-NiL(2-)] (4). Here L represents the neutral ligand, L(.-) denotes its radical monoanion, and L(2-) is the dianion. All of the four compounds feature a short Ni-Ni bond from 2.2957(6) to 2.4649(8) Å. Interestingly, they display two different structures: the perpendicular (1 and 2) and the coaxial (3 and 4) structure, in which the metal-metal bond axis is perpendicular to or collinear with the axes of the α-diimine ligands, respectively. The electronic structures, Ni-Ni bonding nature, and energetic comparisons of the two structure types were investigated by DFT computations.
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