Synthetic Models of the Inactive Copper(II)−Tyrosinate and Active Copper(II)−Tyrosyl Radical Forms of Galactose and Glyoxal Oxidases

Abstract

A series of CuII and ZnII complexes with new ligands having either one or two substituted phenolates appended to the 1,4,7-triazacyclononane frame were prepared and characterized by optical absorption, EPR, NMR, and/or resonance Raman spectroscopy, cyclic voltammetry, and, in eight cases, X-ray crystallography. Features of the active site geometries of the CuII−tyrosinate forms of galactose and glyoxal oxidases (GAO and GLO) were modeled by these complexes, including the binding of a redox-active phenolate and an exogenous ligand (Cl-, CH3CO2 -, or CH3CN) in a cis-equatorial position of a square pyramidal metal ion. The role of the unique ortho S−C covalent bond between a cysteine (C228) and the equatorial tyrosinate (Y272) in the proteins was probed through an examination of the optical absorption and electrochemical properties of sets of similar complexes comprised of phenolate ligands with differing ortho substituents, including thioether groups. The o-alkylthio unit influences the PhO- → CuII LMCT transition and the MII−phenolate/MII−phenoxyl radical redox potential, but to a relatively small degree. Electrochemical and chemical one-electron oxidations of the CuII and ZnII complexes of ligands having tert-butyl protecting groups on the phenolates yielded new species that were identified as novel MII−phenoxyl radical compounds analogous to the active CuII−tyrosyl radical forms of GAO and GLO. The MII−phenoxyl radical species were characterized by optical absorption, EPR, and resonance Raman spectroscopy, as well as by their stoichiometry of formation and chemical reduction. Notable features of the CuII−phenoxyl radical compounds that are similar to their protein counterparts include EPR silence indicative of magnetic coupling between the CuII ion and the bound radical, a band with λmax ≈ 410 nm (ε ≈ 3900 M-1 cm-1) in UV−vis spectra diagnostic for the phenoxyl radical, and a feature attributable to the phenoxyl radical C−O vibration (ν7a) in resonance Raman spectra. Similar Raman spectra and electrochemical behavior for the ZnII analogs, as well as an isotropic signal at g = 2.00 in their X-band EPR spectra, further corroborate the formulations of the MII−phenoxyl radical species.

Sulfanyl stabilization of copper-bonded phenoxyls in model complexes and galactose oxidase

“…Discussion Models of GO generally use ortho-sulfanylphenols to provide faithful structural correspondence to the covalent bond between Cys228 and the ortho position of Tyr272 (12,(17)(18)(19)(20)(21)(22)(23)(24)(25)(26). The results herein show that para-sulfanyl substituents have electrochemical and spectroscopic effects comparable to those at ortho position, while allowing variation in the steric demands of the alkylsulfanyl group with minimal potential changes in the copper coordination geometry.…”

“…12,[17][18][19][20][21][22][23][24][25][26]. The para positioning of sulfanyl substituents in 1 R2 is designed purposefully to assure minimal copper coordination changes by preserving the sterically abutting ortho-t-butyl substituents (R 3 , Fig.…”

Conformational studies of Zn-Ligand-Hexose diastereomers using ion mobility measurements and density functional theory calculations

“…Where several structures of a given diastereomer are listed, only hydrogen bonding interactions have been changed, however, the monosaccharide, coordinating groups, and coordination geometry of the complexes are as shown (see Figure 7 for the structures that met the search criteria). a Error ϭ ͉E (B3LYP/6 -31ϩG*//B3LYP/6 -31ϩG*) Ϫ E (B3LYP/6 -31ϩG*//ONIOM) ͉ investigation of Zn(II) and Cu(II) complexes [38]. All Zn-coordinating bond lengths were between 1.98 -2.19 Å.…”

(N-Benzyl-bis-N′,N″-salicylidene)-cis-1,3,5-triaminocyclohexane copper(ii): a novel catalyst for the aerobic oxidation of benzyl alcohol

“…16 In this case, both the Zn II and Cu II complexes undergo analogous oxidation chemistry; the system also incorporates the same di-tert-butyl substitution pattern around the phenolate ring. Stack and coworkers also observed similar behaviour from a binapthyl salentype N 2 O 2 -donor Cu II complex.…”