Investigation of the structure and catalytic activity in olefin cyclopropanation of neutral and cationic dicopper complexes of 3,5-bis(pyridinylimino)benzoic acid.

Three neutral and one cationic copper(I) complexes with 3,5-bis(pyridinylimino)benzoic acid are
synthesized and characterized in solution and in the solid state by a variety of spectroscopic techniques and X-ray crystallography. The compounds are tested for their catalytic activity in olefin cyclopropanation reactions by means of ethyl diazoacetate
decomposition and prove to be moderately active with the ionic one being the most active and the most promising since for cyclohexene it reveals a considerable diastereoselectivity and a 90:10 exo:endo ratio of the final product.