PHENOXYL-COPPER(II) COMPLEXES - MODELS FOR THE ACTIVE-SITE OF GALACTOSE-OXIDASE

The reaction of the macrocycles 1,4,7-tris t-butyl-2-hydroxy-benzyl)-1 ,4,7-triazacyclononane, (LH3)-H-1, or methoxy-2-hydroxy-benzyl)-1,4,7- triazacyclononane, (LH3)-H-2, with CU(ClO4)(2) . 6H(2)O in methanol (i n the presence of Et3N) affords the green complexes [Cu-II((LH)-H-1)] (1), [Cu-II((LH)-H-2)]. CH3OH (2) and (in the presence of HClO4) [Cu-I I((LH2)-H-1)](ClO4) (3) and [CUII((LH2)-H-2)] (ClO4) (4). The Cu-II io ns in these complexes are five-coordinate (square-base pyramidal), and each contains a dangling, uncoordinated pendent arm (phenol). Complex es 1 and 2 contain two equatorially coordinated phenolate ligands, whe reas in 3 and 4 one of these is protonated, affording a coordinated ph enol. Electrochemically, these complexes can be oxidized by one electr on, generating the phenoxyl-copper(II) species [Cu-II((LH)-H-1)](+.), [Cu((LH)-H-2)](+.), [Cu-II((LH2)-H-1)](2+.), and [Cu-II((LH2)-H-2)](2); all of which are EPR-silent. These species are excellent models for the active form of the enzyme galactose oxidase (GO). Their spectrosc opic features (UV-VIS, resonance Raman) are very similar to those repo rted for GO and unambiguously show that the complexes are phenoxyl-cop per(II) rather than phenolato-copper(III) species.