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A series of coordination complexes, where a heavy chalcogen (Se, Te) acts as the acceptor site, using a variety of electron rich Lewis bases (phosphine, imine, N-heterocyclic carbene), have been synthesized and comprehensively characterized. Each derivative is a representative example of a E-->Ch coordinative bond, characterizing an efficient E-E bond forming methodology and a systematic investigation into the coordination chemistry of the chalcogens. The complexes are susceptible to classic ligand exchange reactions, verifying the dative E-->Ch bonding motif.
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Dutton et al. (2009) studied this question.
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