Zinc Carboxylate Cluster Formation in Conjugated Metallomacrocycles: Evidence for Templation

A new [3 + 3] Schiff base macrocycle incorporating three N2O2 salphen-type binding sites and peripheral neopentyloxy
substituents has been prepared. The incorporation of Zn2+ ions into this and related conjugated Schiff base
macrocycles has been studied by NMR spectroscopy, mass spectrometry, and X-ray diffraction. When reacted with
7 equiv of zinc acetate, the macrocycles template the formation of heptanuclear complexes. Two tetranuclear Zn2+
complexes that are plausible intermediates in the assembly of the heptanuclear complexes have been isolated and
structurally characterized. These reactive intermediates are promising substrates for the synthesis of polynuclear,
mixed-metal clusters. We also demonstrate that this chemistry may be generalized to other bridging carboxylate
ligands, such as methacrylate.