Dimeric Copper(I) Complex with a Disulfonamide-Bridged Core.

Abstract

Pyridine-2-yl-sulfonyl-quinolin-8-yl-amide (psq) has produced the first sulfonamidato-bridged dicopper(I) complex, {Cu[κ4-(μ-κN:κN-psq)]}2 containing the rhombic Cu(I)2N2 core. The single crystal X-ray structure of this complex shows that two anionic psq ligands straddle the metal atoms via bridging sulfonamide N atoms to give a Cu···Cu distance of 2.9593(8) Å. When it is dissolved in chloroform [Cu(psq)]2 activates C-Cl bonds as demonstrated through the rapid formation of [CuCl(psq)]2. While the solid orange compound is stable for weeks under N2. Acetonitrile solutions of [Cu(psq)]2 are rapidly oxidized in air. A 1D-carbonato-bridged coordination polymer, {Cu2[κ4-(μ-κO:κN-psq)]2[μ3-CO3][H2O]}, and the bis-homoleptic complex [Cu(κ3-psq)(κ2-psq)] are concurrently isolated in high yield without evidence of ligand oxidation with H2O2 detected as a side product. This implicit O2 activation was harnessed in the oxidation of phenol substrates. 2,6-Di-tert-butylphenol is catalytically converted to the coupled dione product with 100% yield. If a para-blocked phenol is used, the reaction become stoichiometric and an O2-derived hydroperoxide group is installed into the ortho position. In contrast, nitrophenol is not oxidized and the result is metal-based oxidation and isolation of [Cu(OC6H4NO2)(psq)]2. This is rationalized by this more acidic phenol acting as a proton donor, rather than a H atom donor to a putative O2 adduct.