アイテム詳細

要旨

Instability of end-on superoxocopper(II) complexes, with respect to conversion to peroxo-bridged dicopper(II) complexes, has largely constrained their study to very low temperatures. This limits their kinetic capacity to oxidize substrates. In response, we have developed a series of bulky ligands, Ar₃-TMPA (Ar = tpb, dpb, dtbpb), and used them to support copper(I) complexes that react with O₂ to yield [Cu^II(η¹-O₂^•–)(Ar₃-TMPA)]⁺ species, which are stable against dimerization at all temperatures. Binding of O₂ saturates at subambient temperatures and can be reversed by warming. The onset of oxygenation for the Ar = tpb and dpb systems is observed at 25 °C, and all three [Cu^II(η¹-O₂^•–)(Ar₃-TMPA)]⁺ complexes are stable against self-decay at temperatures of ≤−20 °C. This provides a wide temperature window for study of these complexes, which was exploited by performing extensive reaction kinetics measurements for [Cu^II(η¹-O₂^•–)(tpb₃-TMPA)]⁺ using a broad range of O–H, N–H, and C–H bond substrates. This includes correlation of second order rate constants (k₂) versus oxidation potentials (E_ox) for a range of phenols, construction of Eyring plots, and temperature-dependent kinetic isotope effect (KIE) measurements. The data obtained indicate that reaction with all substrates proceeds via H atom transfer (HAT), reaction with the phenols proceeds with significant charge transfer, and full tunneling of both H and D atoms occurs in the case of 1,2-diphenylhydrazine and 4-methoxy-2,6-di-tert-butylphenol. Oxidation of C–H bonds proved to be kinetically challenging, and whereas [Cu^II(η¹-O₂^•–)(tpb₃-TMPA)]⁺ can oxidize moderately strong O–H and N–H bonds, it is only able to oxidize very weak C–H bonds.