MODELS OF THE MANGANESE CATALASE ENZYMES - DINUCLEAR MANGANESE(III) COMPLEXES WITH THE [MN2(MU-O)(MU-O2CR)2]2- PREPARATION AND PROPERTIES OF [MN2O(O2CR)2X2(BPY)2] (X = C1-, N3-, H2O)( CORE AND TERMINAL MONODENTATE LIGANDS )

Procedures are reported that allow access to dinuclear Mn(III) complex es possessing the [Mn2O(mu-O2CR)2]2+ core. The complexes have the gene ral formulation [Mn2O(O2CR)2X2(bpy)2] (X = Cl-, N3-, H2O; bpy = 2,2'-b ipyridine) and are potential models of the Mn catalase enzymes. Treatm ent of MnCl2/bpy/acetic acid reaction mixtures in MeCN with NBun4MnO4 in MeCN leads to subsequent isolation of [Mn2O(OAc)2Cl2(bpy)2].AcOH.H2 O(1). Analogous reactions allow the preparation of [Mn2O(O2CPh)2Cl2(bp y)2].2H2O (2) and [Mn2O(O2CEt)2Cl2(bpy)2].3EtCO2H.H2O (3). In the pres ence of N3-, the complex [Mn2O(O2CPh)2(N3)2(bpy)2] (5) is obtained; us e of AcO- and a greater MnO4- amount yields [Mn2O2(N3)4(bpy)2] (6). Co mplex 1 can also be prepared from a reaction in which a solution of Cl 2 in MeCN is employed as the oxidizing agent instead of NBun4MnO4. If, however, aqueous HOAc is employed as the reaction medium, oxidation w ith an excess of C12 leads to [Mn2O(OAC)2(H2O)2(bpy)2](ClO4)2 (7). The three Mn2 units are extremely similar and differ only in the identity of the terminal ligands X (Cl-, N3-, or H2O). They each contain a tri ply-bridged [Mn2(mu-O)(mu-O2CR)2]2+ core with chelating bpy and termin al X groups completing near-octahedral geometry at each Mn atom. In ea ch case, the X group and an oxygen atom from a bridging RCO2- group li e on a Jahn-Teller elongation axis (high-spin d4 Mn(III)). Complexes 1 , 2, 3, and 5 have been studied by cyclic voltammetry in DMF; they eac h display a quasi-reversible oxidation at -0.4 V (1, 2, and 3) and 0.1 8 V (5) vs ferrocene, assigned to the 2Mn(III)/Mn(III)Mn(IV) couple. V ariable-temperature solid-state magnetic susceptibilities of 1 and 5 w ere measured in the temperature range 5.0 to ca. 330 K. The effective magnetic moment per Mn2III (mu(eff)) for 1 decreases gradually from 6. 33 mu(B) at 327.7 K to 5.85 mu(B) at 100 K and then more steeply to 2. 09, mu(B) at 5.0 K. For 5, mu(eff) increases steadily from 6.96 mu(B) at 320 K to a maximum of 8.12 mu(B) at 30 K and then decreases to 7.45 mu(B) at 5.0 K. The data were fit to a model that included an isotrop ic Heisenberg exchange interaction, an isotropic Zeeman interaction, a nd axial zero-field splitting terms for both ions. For complex 1, a go od fit was found with J = -4.1 cm-1, g = 1.88, D1 = D2 = -0.07 cm-1, a nd 0.8% by weight of a paramagnetic S = 2 impurity. For complex 5, the corresponding values are J = +8.8 cm-1, g = 1.86 and D1 = D2 = 0.3 cm -1; the quality of the fit is less than that for 1, and this was concl uded to be due to the presence of intermolecular exchange interactions propagated by the intermolecular hydrogen-bonding network observed in the crystal structure of 5-MeCN-4H2O. Thus, 5 is ferromagnetically co upled and has an S = 4 ground state. The J values for all available co mplexes containing the [Mn2O(O2CR)2]2+ core are compared, and a ration alization is suggested for the differences between 1/7 (negative J) an d 5 (positive J). The relevance of these results to Mn catalase are di scussed as well as to the observed difference in sign of the J values for deoxyhemerythrin (negative J) versus deoxy-N3--hemerythrin (positi ve J).