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100 1 _ |a Stüber, Alexander
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245 _ _ |a Variable Coordination of Peroxide in a Dinuclear Copper Mono‐Oxygenase Model Complex Supported by a Pyridazine‐Bridged Ligand
260 _ _ |a Weinheim
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520 _ _ |a 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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700 1 _ |a Jurgeleit, Ramona
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700 1 _ |a Berger, Kira
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700 1 _ |a Grimm-Lebsanft, Benjamin
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700 1 _ |a Buchenau, Sören
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700 1 _ |a Senft, Laura
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700 1 _ |a Näther, Christian
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700 1 _ |a Ivanović-Burmazović, Ivana
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700 1 _ |a Rübhausen, Michael
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700 1 _ |a Naumova, Maria
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700 1 _ |a Tuczek, Felix
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773 _ _ |a 10.1002/ejic.202500286
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