Abstract

The alternative coordination sites of 3-(3,5-dimethyl-pyrazol-4-yl)pentane-2,4-dione (H2acacPz) differ with respect to Pearson hardness. The softer, heterocyclic moiety was used as N donor toward Zn(II) and Ag(I); it yielded a tetrahedral, neutral Zn complex in the former and a monocationic, linear bis(ligand) Ag complex in the latter case. After deprotonation with silver benzoate, the pyrazolyl ring may act as a monoanionic N,N′-bridge between neighboring cations in a hexanuclear Ag aggregate; in addition to ligand-supported Ag···Ag distances of ca. 3.2 A, these aggregates feature ligand-unsupported argentophilic interactions of ca. 2.9 A. With stronger bases and in the presence of oxophilic Mg cations, the harder hydroxyketone part of the H2acacPz ligand may be deprotonated to a chelating acetylacetonate. The resulting bis(ligand) Mg complex has been used as starting compound for a bimetallic derivative: the ditopic ligand allows coordinating cadmium acetate to its dangling N donor site, thus, bridging ...

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