| Home > Publications database > Variable Coordination of Peroxide in a Dinuclear Copper Mono‐Oxygenase Model Complex Supported by a Pyridazine‐Bridged Ligand |
| Journal Article | PUBDB-2025-04602 |
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2025
Wiley-VCH
Weinheim
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Please use a persistent id in citations: doi:10.1002/ejic.202500286 doi:10.3204/PUBDB-2025-04602
Abstract: Copper-oxygen intermediates play an important role in nature as active species of many copper-containing enzymes. However, copper-oxygen intermediates have a key function not only in nature, but also in industry, for example as catalysts. Herein a study on a dinuclear copper complex is presented based on the literature known ligand BPMPD. This ligand combines features of the previously investigated systems (octadentate N-donor, like the MO8 system and pyridine donors, like the bdpdz system). Oxygenation of the Cu(I)-complex with O$_2$ at low temperature leads to the formation of a μ-1,2-peroxo intermediate (Cu$_2$O$_2$), which is characterized with UV/Vis-, rRaman- and X-ray absorption spectroscopy (XAS), as well as by cryo-UHR-electrospray ionization mass spectrometry. The Cu$_2$O$_2$ species can be reversibly converted into a μ-1,1-hydroperoxo intermediate (Cu$_2$OOH) by a reaction with lutidinium triflate and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), which can be monitored by UV/Vis and XAS. Furthermore, the reactivity of the Cu$_2$O$_2$ species toward dihydroanthracene is investigated.
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