Starting from an active O2H3-bridged bimetallic complex, a bridging coordination mode of both urea and carbamate—the substrate and its first hydrolytic product in urease activity—at a dinickel(II) centre relevant to the active site of the metalloenzyme has been characterised structurally.
F. Meyer, Chem. Commun., 1998, 1555 DOI: 10.1039/A802554A
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