Electrophilic Modulation of the Superoxide Anion Radical Scavenging Ability of Copper(II) Complexes with 4-Methyl Imidazole

Three Cu(II) coordination compounds with 4-methyl imidazole were obtained, such as [Cu(C4H6N2)(4)(NO3)(2)], [Cu(C4H6N2)(4)Br-2], and [Cu(C4H6N2)(4)Cl-2]. Crystallographic studies confirmed their structural similarity with Cu(II) in the active site of endogenous copper-zinc superoxide dismutase (CuZn-SOD). The superoxide anion radical (O-2(center dot-)) scavenging activity was evaluated by the non-enzymatic experimental assay and followed the trend [Cu(C4H6N2)(4)(NO3)(2)] > [Cu(C4H6N2)(4)Br-2] > [Cu(C4H6N2)(4)Cl-2]. The density functional theory and the hard and soft acids and bases principle showed the importance of the electron-deficient character of Cu(II) in the chemical reactivity of the coordination compounds; Cu(II) is the softest site in the molecule and it is preferred for the nucleophilic and radical attacks of the soft O-2(center dot-). A simple rule was obtained: the electron-deficient character of Cu(II) is the key index for the O-2(center dot-) scavenging activity and is modulated by the electron-releasing counteranion effect on the coordination compound.

Automated summary

Experimental evaluation showed that the scavenging activity of three copper coordination compounds on superoxide anion radicals followed the order [Cu(C4H6N2)4(NO3)2] > [Cu(C4H6N2)4Br2] > [Cu(C4H6N2)4Cl2]. The electron-deficient character of Cu(II) was identified as the key index for this scavenging activity, which is modulated by the electron-releasing effect of the counteranion on the coordination compound.