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Rate enhancements for the reduction of dioxygen by a Mn(II) complex were observed in the presence of redox-inactive group 2 metal ions. The rate changes were correlated with an increase in the Lewis acidity of the group 2 metal ions. These studies led to the isolation of heterobimetallic complexes containing Mn(III)-(μ-OH)-M(II) cores (M(II) = Ca(II), Ba(II)) in which the hydroxo oxygen atom is derived from O(2). This type of core structure has relevance to the oxygen-evolving complex within photosystem II.

journal of the american chemical society

The Effects of Redox-Inactive Metal Ions on the Activation of Dioxygen: Isolation and Characterization of a Heterobimetallic Complex Containing a Mn<sup>III</sup>–(μ-OH)–Ca<sup>II</sup> Core

The Effects of Redox-Inactive Metal Ions on the Activation of Dioxygen: Isolation and Characterization of a Heterobimetallic Complex Containing a MnIII–(μ-OH)–CaII Core

The Effects of Redox-Inactive Metal Ions on the Activation of Dioxygen: Isolation and Characterization of a Heterobimetallic Complex Containing a Mn^III–(μ-OH)–Ca^II Core