Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-1541
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dc.contributor.authorTonhauser, Christoph
dc.date.accessioned2015-01-28T09:28:40Z
dc.date.available2015-01-28T10:28:40Z
dc.date.issued2015
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/1543-
dc.description.abstractThe thesis can be divided in four parts and summarized as follows:(i) The investigation and development of a continuous flow synthesis procedure affording end-functional polymers by anionic polymerization and subsequent termination in one reaction step and on a multigram scale was carried out. Furthermore, the implementation of not only a single hydroxyl but multiple orthogonal functionalities at the chain terminus was achieved by utilizing individually designed, functional epoxide-based end-capping reagents.(ii) In an additional step, the respective polymers were used as macroinitiators to prepare in-chain functionalized block copolymers and star polymers bearing intriguing novel structural and material properties. Thus, the second part of this thesis presents the utilization of end-functional polymers as precursors for the synthesis of amphiphilic complex and in some cases unprecedented macromolecular architectures, such as miktoarm star polymers based on poly(vinyl pyridine), poly(vinyl ferrocene) and PEO.(iii) Based on these structures, the third part of this thesis represents a detailed investigation of the preparation of stimuli-responsive ultrathin polymer films, using amphiphilic junction point-reactive block copolymers. The single functionality at the block interface can be employed as anchor group for the covalent attachment on surfaces. Furthermore, the change of surface properties was studied by applying different external stimuli.(iv) An additional topic related to the oxyanionic polymerizations carried out in the context of this thesis was the investigation of viscoelastic properties of different hyperbranched polyethers, inspired by the recent and intense research activities in the field of biomedical applications of multi-functional hyperbranched materials.en_GB
dc.language.isoeng
dc.rightsInCopyrightde_DE
dc.rights.urihttps://rightsstatements.org/vocab/InC/1.0/
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleFrom anionic polymerization in continuous flow to macromolecular architectures and stimuli-responsive surfacesen_GB
dc.typeDissertationde_DE
dc.identifier.urnurn:nbn:de:hebis:77-39702
dc.identifier.doihttp://doi.org/10.25358/openscience-1541-
jgu.type.dinitypedoctoralThesis
jgu.type.versionOriginal worken_GB
jgu.type.resourceText
jgu.organisation.departmentFB 08 Physik, Mathematik u. Informatik-
jgu.organisation.departmentFB 10 Biologie-
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.-
jgu.organisation.departmentFB 04 Medizin-
jgu.organisation.year2012
jgu.organisation.number2700-
jgu.organisation.number7950-
jgu.organisation.number7970-
jgu.organisation.number7940-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.organisation.placeMainz-
jgu.subject.ddccode540
opus.date.accessioned2015-01-28T09:28:40Z
opus.date.modified2015-01-28T09:29:03Z
opus.date.available2015-01-28T10:28:40
opus.subject.otherPolymerisation, Mikroreaktor, anionische Polymerisationde_DE
opus.subject.otherPolymerization, microreactor, anionic polymerisationen_GB
opus.organisation.stringFB 10: Biologie: FB 10: Biologiede_DE
opus.identifier.opusid3970
opus.institute.number1000
opus.institute.number0900
opus.institute.number0400
opus.institute.number0800
opus.metadataonlyfalse
opus.type.contenttypeDissertationde_DE
opus.type.contenttypeDissertationen_GB
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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