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dc.contributor.advisorDraper, Sylvia
dc.contributor.authorMc Goldrick, Niamh
dc.date.accessioned2017-06-01T14:37:18Z
dc.date.available2017-06-01T14:37:18Z
dc.date.issued2014
dc.identifier.citationNiamh Mc Goldrick, 'Developing 1,10-phenanthroline complexes towards their application as triplet sensitizers', [thesis], Trinity College (Dublin, Ireland). School of Chemistry, 2014, pp 258
dc.identifier.otherTHESIS 10369
dc.description.abstractSummary - Chapter 1: This chapter begins with a general introduction to polycyclic aromatic hydrocarbons, followed by a focused review of recent 3,8-substituted 1,10-phenanthroline systems reported in the literature. The chapter also describes the synthesis a series of 3,8-aryl acetylene 1,10-phenanthroline ligands via a sequence of Sonogashira cross-coupling and Diels-Alder cycloaddition reactions, and the issues surrounding the use of copper catalysts in cross-coupling reactions with 1,10-phenanthrolines. The characterisation and spectroscopic properties of the ligands are discussed. In addition, brief computational investigations of both the neutral and protonated pyrene functionalised 1,0-phenanthroline ligand are also presented.
dc.format1 volume
dc.language.isoen
dc.publisherTrinity College (Dublin, Ireland). School of Chemistry
dc.relation.isversionofhttp://stella.catalogue.tcd.ie/iii/encore/record/C__Rb15662419
dc.subjectChemistry, Ph.D.
dc.subjectPh.D. Trinity College Dublin
dc.titleDeveloping 1,10-phenanthroline complexes towards their application as triplet sensitizers
dc.typethesis
dc.type.supercollectionthesis_dissertations
dc.type.supercollectionrefereed_publications
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (Ph.D.)
dc.rights.ecaccessrightsopenAccess
dc.format.extentpaginationpp 258
dc.description.noteTARA (Trinity’s Access to Research Archive) has a robust takedown policy. Please contact us if you have any concerns: rssadmin@tcd.ie
dc.identifier.urihttp://hdl.handle.net/2262/80325


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