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Current interests in the chemistry of high-nuclearity transition- metal complexes draw from their utility in the emerging science of nanomaterials,[1] as models for the multimetal active sites of metal-storage proteins,[2] and as single molecule magnets (SMMs).[3,4] In addition, such super-sized molecules often show a variety of supramolecular interactions.[5] The self-assembly process of generating a high-nuclearity cluster from a mono- or dimeric precursor generally involves low-dentate organic ligands.
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Mukherjee et al. (2003) studied this question.
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