Abstract

New bis(amidinate) complexes of calcium, [2,6-Pri2C6H3NC(But)NC6H4OMe-2]2Ca(DME) (2), and divalent ytterbium, [2,6-Pri2C6H3NC(But)NC6H4OMe-2]2Yb (4), were synthesized by the transamination of the bis(amide) derivatives [(Me3Si)2N]2M(THF)2 (M = Ca, Yb) with two equivalents of amidine 2,6-Pri2C6H3N=C(But)N(H)C6H4OMe-2, in which one nitrogen atom bears an o-methoxyphenylene moiety capable of coordinating a metalion. An X-ray diffraction study showed that, despite very similar ionic radii of Ca2+ and Yb2+, the amidinate ligands in complexes 2 and 4 bind to these ions in different coordination modes. In the calcium complex, both ligands adopt a κ2-N, O-chelating coordination mode. In the divalent ytterbium compound, one ligand is chelating and binds to the metalion in a κ2-N, O-coordination mode, while the second ligand is coordinated via both the N and O (κ2) atoms and the arene ring of the 2,6-Pri2C6H3 moiety (η6-coordination mode).

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