Bimetallic Complexes for Cooperative Polymerization Catalysis

Schütze, Mike

dc.contributor.advisor	Meyer, Franc Prof. Dr.
dc.contributor.author	Schütze, Mike
dc.date.accessioned	2018-09-07T08:36:52Z
dc.date.available	2018-09-07T08:36:52Z
dc.date.issued	2018-09-07
dc.identifier.uri	http://hdl.handle.net/11858/00-1735-0000-002E-E4A0-A
dc.identifier.uri	http://dx.doi.org/10.53846/goediss-7022
dc.language.iso	eng	de
dc.publisher	Niedersächsische Staats- und Universitätsbibliothek Göttingen	de
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc	540	de
dc.title	Bimetallic Complexes for Cooperative Polymerization Catalysis	de
dc.type	doctoralThesis	de
dc.contributor.referee	Meyer, Franc Prof. Dr.
dc.date.examination	2018-06-25
dc.description.abstracteng	This work contributed to the understanding of cooperativity in bi- and oligometallic complexes through three chapters. The first chapter on CO2/epoxide copolymerization led to the discovery of several promising novel catalysts. One in particular, with an ONO-pincer ligand, provided high polymerization activity and stereoselectivity. The self-assembled ONO-pincer type catalysts proved to be highly active. They serve as proof of concept to the field of CO2/epoxide copolymerization with their new design, coming along with a great potential for future applications, continuing several beneficial features of previously reported catalysts. In the second chapter, the interactions and mutual effects within a dinuclear complex holding an allylpalladium unit and a palladium dihalide unit in close proximity were investigated. New valuable insights into the interactions between the two fragments were gained by changing the substituents and ligands within the complex. The extent of interaction was represented by the allyl exchanges, investigated by kinetic studies through EXSY-NMR spectroscopy. Four model complexes were used for the investigations and to understand the cooperative effects of interest. In the last chapter, a dinuclear nickel complex was investigated for its applicability for the copolymerization of ethylene and MMA. The complex was found to be active for forming the homopolymers PMMA and PE. The complex, after activation with MAO, catalyzes the formation of PMMA with a TOF of 33 1/h (at 23°C) and provided a TOF of up to 19000 1/h (at 25°C and 10 bar ethylene pressure) for PE.	de
dc.contributor.coReferee	Vana, Philipp Prof. Dr.
dc.contributor.thirdReferee	Walter, Marc Prof. Dr.
dc.contributor.thirdReferee	Otte, Matthias Dr.
dc.contributor.thirdReferee	Das, Shoubhik Dr.
dc.contributor.thirdReferee	Demir, Selvan Prof. Dr.
dc.subject.eng	cooperativity	de
dc.subject.eng	catalysis	de
dc.subject.eng	polymerization	de
dc.subject.eng	copolymerization	de
dc.subject.eng	CO2 utilization	de
dc.subject.eng	CO2 epoxide copolymerization	de
dc.subject.eng	ONO-pincer	de
dc.subject.eng	kinetic studies	de
dc.subject.eng	EXSY-NMR spectroscopy	de
dc.subject.eng	dinuclear allylpalladium complexes	de
dc.subject.eng	CCU	de
dc.subject.eng	CCS	de
dc.subject.eng	green chemistry	de
dc.subject.eng	sustainable catalysis	de
dc.subject.eng	Cooperative Polymerization Catalysis	de
dc.identifier.urn	urn:nbn:de:gbv:7-11858/00-1735-0000-002E-E4A0-A-4
dc.affiliation.institute	Fakultät für Chemie	de
dc.subject.gokfull	Chemie (PPN62138352X)	de
dc.identifier.ppn	1030476128

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Fakultät für Chemie (inkl. GAUSS) [701]

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