Selective oxidations of a dithiolate complex produce a mixed sulfonate/thiolate complex

Oxygenation or peroxidation of a planar, tetracoordinate, low-spin nickel(II) complex of a NS-donor ligand, (N,N′-dimethyl-N,N′-bis-(2-mecaptoethyl)-1, 3-propanediaminato) nickel(II), proceeds via the formation of a mixed sulfinate/thiolate complex and leads to the production of a novel dimeric complex containing both sulfonate and thiolate ligands. Thus, reaction proceeds via selective oxidation of the sulfinate sulfur atom, leaving the thiolate reduced. The novel sulfonate/thiolate complex has been isolated and characterized by electospray ionization mass spectrometry and single-crystal X-ray diffraction. Crystals form in the monoclinic space group P2/c with cell dimensions a = 8.4647(12) Å, b = 12.592(3) Å, and c = 12.531(2) Å, angles α = γ = 90° and β = 106.645(11)°, and Z = 2. The structure was refined to R = 5.20% and R = 12.86% [I > 2σ(I)]. The isolation of this mixed sulfonate/thiolate complex from oxidation of a mixed sulfinate/thiolate complex provides experimental evidence for the formation of a sulfonate ligand via a Ni-O-O-SOR intermediate, as suggested by recent density functional theory calculations. © 2006 American Chemical Society.