Abstract

In this work, we have further developed the pyridyl-tetrazole ligand systems into bis-tetrazole systems, where the linker introduced to join these moieties was a flexible (CH2)3 backbone, with the intention of forming frameworks with potential voids. We synthesised three different pyridyl-tetrazoles linked via this flexible backbone through the pyridine ring and not the tetrazole rings. Two crystals of ligand 1 were solved by X-ray crystallography and showed interesting polymorphism. No crystals of the copper(II) complexes of the ligands could be obtained, suggesting that they were polymeric in nature.

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