The hydrogen-bond accepting ligand K[TpCO2Et,Me] was prepared and its complexes with divalent Ni, Co, Mn and Cu reveal a stabilization of penta- or hexa-coordinate metal aquo complexes of the general form [TpCO2Et,MeM(H2O)x] (x = 2 or 3) which are unprecedented for the alkyl substituted Tp analogs. These complexes make good structural models for many of the enzymes of the vicinal oxygen chelate superfamily.
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Hammes et al. (2001) studied this question.
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