Abstract
Hydroxido-bridged CuII6M double-cubane clusters (M = MnII, CoII) supported by D-penicillaminedisulfide were unexpectedly formed by treating a D-penicillaminato CuII2PtII2 complex with MBr2 in water. The clusters displayed heterogeneous electrocatalytic activities for water oxidation dependent on the central M shared by two CuII cubane units.
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