A new series of (diisopropylcarbamato)(oxido)zinc complexes were obtained by innovative synthetic approaches. (2) were synthesised by an identical reaction procedure involving protolysis of ZnEt 2 with iPr 2 NH/ CO 2 and followed by stoichiometric hydrolysis. Recrystallisation of the reaction product from nitrile solvents yielded the tetrazinc complex 1. Conversely, recrystallisation from alkane solvents yielded crystals of the octazinc complex 2. The two structural isomers were readily interconverted simply by recrystallisation from the appropriate solvent. Both complexes were structurally characterised by X-ray crystallogra-