Zur Kurzanzeige

Electrochemical C-H Activations with 3d and 4d Transition Metal Catalysts

dc.contributor.advisorAckermann, Lutz Prof. Dr.
dc.contributor.authorMassignan, Leonardo
dc.date.accessioned2021-12-20T15:39:31Z
dc.date.available2021-12-27T00:50:08Z
dc.date.issued2021-12-20
dc.identifier.urihttp://hdl.handle.net/21.11130/00-1735-0000-0008-59CE-D
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-9013
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-9013
dc.language.isoengde
dc.publisherNiedersächsische Staats- und Universitätsbibliothek Göttingende
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc540de
dc.titleElectrochemical C-H Activations with 3d and 4d Transition Metal Catalystsde
dc.typedoctoralThesisde
dc.contributor.refereeAckermann, Lutz Prof. Dr.
dc.date.examination2021-12-02
dc.description.abstractengThe oxidative metal-catalyzed C–H activation of inert bonds is a powerful tool for the functionalization of complex molecules. This platform allowed the broadening of the organic chemists’ toolbox and improved the resource-economy of synthetic routes, avoiding prefunctionalizations of starting materials. Nevertheless, its applications were constrained by the use of stoichiometric oxidants, which limited the sustainability of this approach. In contrast, the use of electricity as environmental-friendly and versatile oxidant enhanced the sustainability of oxidative metal-catalyzed C–H activation and opened the way to the study of novel reactivities and selectivities. Within this thesis, electrochemical cobalt catalyzed and ruthenium catalyzed annulation reactions were initially studied. The electrochemical approach was then broadened to the C–H oxygenation reactions with ruthenium catalysis enabled by electrogenerated hypervalent iodine species and with rhodium catalysis. In addition, C–H arylation and C–H alkylation reaction by earth-abundant manganese as catalyst and electricity as sustainable oxidant was developed.de
dc.contributor.coRefereeBreder, Alexander Prof. Dr.
dc.contributor.thirdRefereeTietze, Lutz Prof. Dr. Dr. H.c.
dc.contributor.thirdRefereeAlcarazo, Manuel Prof. Dr.
dc.contributor.thirdRefereeJohn, Michael Dr.
dc.contributor.thirdRefereeJanßen-Müller, Daniel Dr.
dc.subject.engC–H Activationde
dc.subject.engTransition Metal Catalysisde
dc.subject.engElectrochemistryde
dc.subject.engRutheniumde
dc.subject.engRhodiumde
dc.subject.engManganesede
dc.subject.engCobaltde
dc.subject.engHypervalent iodinede
dc.identifier.urnurn:nbn:de:gbv:7-21.11130/00-1735-0000-0008-59CE-D-8
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullChemie  (PPN62138352X)de
dc.description.embargoed2021-12-27
dc.identifier.ppn1782630406


Dateien

Thumbnail

Das Dokument erscheint in:

Zur Kurzanzeige