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dc.contributor.advisorO'Hagan, David
dc.contributor.authorSkibiński, Maciej
dc.coverage.spatial195en_US
dc.date.accessioned2015-07-28T14:43:43Z
dc.date.available2015-07-28T14:43:43Z
dc.date.issued2014-06-25
dc.identifier.urihttp://hdl.handle.net/10023/7058
dc.description.abstractOwing to its unique electronic properties, the CF₂ group has the potential to affect the conformation and polarity of molecules. The Introduction provides an overview of the conformational effects induced by the incorporation of fluorine into hydrocarbons, e.g. gauche effect, 1,3-C,F bond repulsion and angle deviation in organofluorine compounds. A summary of synthetic strategies for the introduction of the gem-difluoride motif into organic molecules is also presented. In order to explore the conformational impact of the CF₂ group in alicyclic hydrocarbon systems, cyclododecane was employed as the molecular framework. In 1,1,4,4- and 1,1,7,7- tetrafluorocyclododecanes, two CF₂ groups replaced CH₂ units within the square [3333] cyclododecane ring where the spacing enables the CF₂ groups to occupy adjacent or opposite corner locations. In the case of 1,1,6,6-tetrafluorocyclododecane, one of the CF₂ groups was forced to the edge position, which changes the ring conformation dramatically. Strategic incorporation of two CF₂ groups is shown to either stabilise or significantly alter the conformation of the cyclododecane framework, a revealing conformational preference of the CF₂ group to locate at the corner rather than the edge position of hydrocarbon rings. The study extends to larger cycloalkanes, rectangular [3434] cyclotetradecanes and square [4444] cyclohexadecanes. The target cycloalkanes bearing two CF₂ units were assembled through a novel synthetic route, employing ring-closing metathesis (RCM) as the key step. X-Ray structure analyses revealed that the CF₂ groups occupy exclusively corner locations of these rings too. The spacing between the CF₂ moieties dictates the overall ring conformations and offers a useful tool for controlling molecular arrangement. An accelerating role of the CF₂ group, relative to the CH₂ group, on the ring-closing metathesis of C5-substituted 1,8-nonadienes has also been studied. Remarkably, the CF₂ group exhibited a similar reaction rate to that observed for nonadienes bearing 1,3-dioxolane or dimethylmalonate groups. This effect was rationalised by the thermodynamic stability of the cycloheptene products, rather than a Thorpe-Ingold effect.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subjectGem-difluoromethylene groupen_US
dc.subjectGem-difluorination reactionsen_US
dc.subjectConformational effectsen_US
dc.subjectCycloalkanesen_US
dc.subjectRing-closing metathesisen_US
dc.subjectThorpe-Ingold effecten_US
dc.subject.lccQD412.F1S6
dc.subject.lcshFluorohydrocarbons--Conformationen_US
dc.subject.lcshFluorinationen_US
dc.subject.lcshCycloalkanesen_US
dc.subject.lcshMetathesis (Chemistry)en_US
dc.titleEffect of gem-difluorination on the conformation of selected hydrocarbon systemsen_US
dc.typeThesisen_US
dc.contributor.sponsorEuropean Research Council (ERC)en_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US


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