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Activation of Nitric Oxide and Dioxygen at Diferrous Complexes with Compartmental Pyrazolate Ligand Scaffolds

dc.contributor.advisorMeyer, Franc Prof. Dr.
dc.contributor.authorSchober, Anne
dc.date.accessioned2017-04-06T07:57:22Z
dc.date.available2017-08-17T22:50:06Z
dc.date.issued2017-04-06
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0023-3E09-E
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-6181
dc.language.isoengde
dc.publisherNiedersächsische Staats- und Universitätsbibliothek Göttingende
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc540de
dc.titleActivation of Nitric Oxide and Dioxygen at Diferrous Complexes with Compartmental Pyrazolate Ligand Scaffoldsde
dc.typedoctoralThesisde
dc.contributor.refereeMeyer, Franc Prof. Dr.
dc.date.examination2016-08-18
dc.description.abstractengThis work comprises the synthesis and characterization of novel pyrazolate-bridged bimetallic iron complexes with bis(pentadentate) ligand scaffolds and the activation of dioxygen and nitric oxide at their diferrous sites. It describes the development of two new bridging ligand systems providing two compartments with a fivefold coordination environment for each metal ion. Furthermore, properties of the obtained diferrous complexes were studied by a series of analytical techniques including x-ray diffraction, Mössbauer spectroscopy and temperature dependent UV/Vis spectroscopy. In particular a temperature dependent spin crossover was observed, both in solid state and solution. Small molecule activation was monitored by optical spectroscopy. Especially two diiron dinitrosyl congeners ([{Fe(NO)}<sup>7</sup>]<sub>2</sub> ) are presented and studied in detail as low molecular weight analogues for Flavodiiron proteins with different reaction pathways, one including the formation of nitrous oxide upon reduction.de
dc.contributor.coRefereeSiewert, Inke Dr.
dc.subject.engsmall molecule activationde
dc.subject.engnitric oxidede
dc.subject.engpyrazolate bridging ligandsde
dc.subject.engdiferrous complexesde
dc.subject.engspin crossoverde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-0023-3E09-E-3
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullChemie  (PPN62138352X)de
dc.description.embargoed2017-08-17
dc.identifier.ppn884010406


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