Ligand Binding, Conformational and Spectroscopic Properties, and Biomimetic Monooxygenase Activity by the Trinuclear Copper–PHI Complex Derived fromL-Histidine

The trinuclear copper(II) complex derived from the octadentate N-donor ligand PHI [piperazine-1,4-bis(4-{N-[1-acetoxy-3-(1-methyl-1H-imidazol-4-yl)]-2-propyl}-N-(1-methyl- 1H-imidazol-2-ylmethyl)aminobutyl)] contains two equivalent Cu-A centers bound by tridentate arms and a Cu-B center bound by a central didentate residue. The conformational and ligand binding properties of the complex were extensively studied by various spectroscopic techniques (UV/Vis, CD, NMR, EPR) to probe its behavior in solution. Studies on the binding properties of the complex performed with the azide anion as a probe showed that the ligand preferably binds to the Cu-A centers of the complex and only weakly to the Cu-B center. The EPR spectra showed the existence of a strong coupling between one of the two Cu-A centers and the Cu-B center, which appears to be mediated by a hydroxido-bridging ligand. Further information about metal binding was obtained by analyzing the NMR spectra of the trinuclear Zn-3(II)-PHI complex, which serves as an analogue of the extremely oxygen sensitive Cu-3(I)-PHI complex. The latter complex does not form a stable dioxygen adduct at low temperature, but exhibits an interesting monooxygenase activity. This was studied at low temperature using p-chlorophenolate as a substrate; the formation of 4-chlorocatechol in sizeable yield indicates that some of the very reactive CunO2 intermediate should be involved. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).