Abstract
The active site of the purple acid phosphatase enzyme has been successfully modeled by a series of heterodinuclear M(II)-Fe(III) [M = Zn, Ni, Co, and Cu] type complexes of an unsymmetrical [N6O] ligand that contained a bridging phenoxide moiety and one imidazoyl and three pyridyl moieties as the terminal N-binding sites. In particular, the hetero-dinuclear complexes, {L[MII(mu-OAc)(2)Fe-III]}( ClO4)(2) [M = Zn (3a), Ni (3b), Co (4a), and Cu (4b)], were obtained directly from the phenoxy-bridged ligand (HL), namely 2-{[bis(2-methylpyridyl) amino] methyl}-6-{[((1-methylimidazol- 2-yl) methyl)(2-pyridylmethyl) amino] methyl}-4-t-butylphenol (2), upon sequential addition of Fe(ClO4)(3)center dot XH2O and M(ClO4)(2)center dot 6H(2)O (M = Zn and Ni) or M(OAc)(2)center dot XH2O (M = Co and Cu), in a low-to-moderate (ca. 32-53%) yield. The temperature-dependent magnetic susceptibility measurements indicated weak antiferromagnetic coupling interactions occurring between the two metal centers in their high-spin states. All of the 3(a-b) and 4(a-b) complexes successfully carried out the hydrolysis of the bis(2,4-dinitrophenyl) phosphate (2,4-BDNPP) substrate in a mixed CH3CN/H2O (v/v 1:1) medium in the pH range of 5.5-10.5 at room temperature, thereby mimicking the functional activity of the native enzyme. The spectrophotometric titration suggested a monoaquated and dihydroxo species of the type {L[(H2O)M-II(mu-OH) Fe-III(OH)]}(2+) to be the catalytically active species for the phosphodiester hydrolysis reaction within the pH range of ca. 5.80-7.15. Last, the kinetic studies on the hydrolysis of the model substrate, 2,4-BDNPP, divulge a Michaelis-Menten-type behavior for all complexes.