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Bioinspired Dinuclear Copper Complexes for Oxygen Activation

dc.contributor.advisorMeyer, Franc Prof. Dr.
dc.contributor.authorDzemski, Martin Alfred
dc.date.accessioned2022-12-06T16:11:10Z
dc.date.available2023-09-28T00:50:11Z
dc.date.issued2022-12-06
dc.identifier.urihttp://resolver.sub.uni-goettingen.de/purl?ediss-11858/14394
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-9599
dc.format.extent178 Seitende
dc.language.isoengde
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540de
dc.titleBioinspired Dinuclear Copper Complexes for Oxygen Activationde
dc.typedoctoralThesisde
dc.contributor.refereeMeyer, Franc Prof. Dr.
dc.date.examination2022-09-29de
dc.description.abstractengThis thesis explores new bioinspired bimetallic copper complexes for the activation of dioxygen. Therefore, two novel TACN/pyrazolate ligand scaffolds with reduced steric hindrance were introduced and successfully established. The important primary reactive dioxygen adducts, such as the peroxido, hydroperoxido and superoxido species of the corresponding dinuclear copper complexes, were synthesized and studied by UV/vis spectroscopy. Moreover, the decomposition of the µ-1,2-peroxo dicopper(II) complexes were studied at different temperatures. These experiments allowed the determination of the activation energies for the decomposition reactions. Additionally, the interaction of the new cupric peroxides with Lewis acids like lithium and calcium ions were investigated by UV/vis titration experiments. Reactivity studies were also performed with the reactive oxygen adducts. Initial results regarding the oxygen reduction reaction are presented and discussed in this work.de
dc.contributor.coRefereeSiewert, Inke Prof. Dr.
dc.subject.engtransition metal complexde
dc.subject.engbimetallic complexde
dc.subject.engoxygen activationde
dc.subject.engcopper complexesde
dc.subject.engcoordination chemistryde
dc.subject.engdinuclear complexde
dc.subject.enguv/vis spectroscopyde
dc.subject.engresonance raman spectroscopyde
dc.identifier.urnurn:nbn:de:gbv:7-ediss-14394-9
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullChemie  (PPN62138352X)de
dc.description.embargoed2023-09-28de
dc.identifier.ppn1826746617
dc.notes.confirmationsentConfirmation sent 2022-12-07T06:15:01de


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