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Unconventional Carbene-Donor Ligands for the Development of new Catalysts

dc.contributor.advisorStalke, Dietmar Prof. Dr.
dc.contributor.authorReichmann, Sven Ole
dc.date.accessioned2016-11-01T09:17:57Z
dc.date.available2016-11-01T09:17:57Z
dc.date.issued2016-11-01
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-002B-7C59-C
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5950
dc.language.isoengde
dc.publisherNiedersächsische Staats- und Universitätsbibliothek Göttingende
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc540de
dc.titleUnconventional Carbene-Donor Ligands for the Development of new Catalystsde
dc.typedoctoralThesisde
dc.contributor.refereeStalke, Dietmar Prof. Dr.
dc.date.examination2016-10-13
dc.description.abstractengThe development of a new synthesis strategy towards unconventional carbene ligands is shown in this work. Our major aim was to establish a synthetic strategy that would enable the efficient palladium or nickel catalysed blocking of the C2-position of an NHC with aryl substituents. The C2 blocking of the NHC was performed with an aryl compound, such as a phenyl group, to gain more electronic stabilisation. With these compounds in hand further reactions towards mesoionic carbene (MIC) transition metal complexes have been done. All new prepared compounds were analysed and investigated focusing on their properties. Moreover, the catalytic activity of these complexes were compared to well-known NHC complexes, which are often used in a large variety of catalytic reactions (e.g. click chemistry).de
dc.contributor.coRefereeGhadwal, Rajendra PD Dr.
dc.subject.engCarbenede
dc.subject.engNHCde
dc.subject.engPalladium catalysed C-C couplingde
dc.subject.engNickel catalysed C-C couplingde
dc.subject.engMesoionic Carbenesde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-002B-7C59-C-9
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullChemie  (PPN62138352X)de
dc.identifier.ppn871602237


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