Abstract

We report the synthesis and characterization of several salan-type CuII complexes. Suitable crystals suitable for X-ray diffraction were obtained for several of the CuII complexes, including a “half-salen” compound, revealing square-planar coordination environments common to d9 species. The CuII–salan complexes are tested as catalysts in sulfoxidation, alkene oxidation, and oxidative naphthol coupling. At room temperature the compounds exhibit low to moderate catalytic activity in sulfoxidations and alkene oxidations, but no activity in oxidative naphthol coupling. The saturated coordination environments around the Cu centers probably are the main reason for the lower catalytic activities compared to the Ti- and V-salan analogs. Spectroscopic and mass spectrometry studies revealed that the CuII–salan complexes decompose, in the presence of H2O2, significantly faster at 40 °C than at room temperature. The catalytic activity observed is probably due to the CuII–salan degradation products, observed in the mass spectrometry studies, and not to the original CuII–salan precursors.

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