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dc.contributor.advisorGrayson, David
dc.contributor.authorBradley, David
dc.date.accessioned2019-04-29T14:32:17Z
dc.date.available2019-04-29T14:32:17Z
dc.date.issued2005
dc.identifier.citationDavid Bradley, 'Synthesis of novel heteromacrocyclic compounds', [thesis], Trinity College (Dublin, Ireland). School of Chemistry, 2005, pp 167
dc.identifier.otherTHESIS 7939
dc.identifier.urihttp://hdl.handle.net/2262/86220
dc.description.abstractMacromolecular systems containing pyridine subunits have been the focus of much attention. The availability of the lone-pair electrons of the pyridine nitrogen atom makes these moieties particularly attractive as chelating units in supramolecular assemblies, novel catalysts, artificial enzymes, and transition metal ligands. In substituted pyridines, the availability of the lone-pair electrons is strongly influenced by the nature of the substituents on the pyridine ring. 4-Dimethylaminopyridine (DMAP) constitutes an electron-rich pyridine ring and has been widely used as an acylation catalyst. Macrocyclic systems containing pyridine or DMAP moieties may therefore be expected to display interesting catalytic and/or ion-binding properties.
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__Rb12731609
dc.subjectChemistry, Ph.D.
dc.subjectPh.D. Trinity College Dublin
dc.titleSynthesis of novel heteromacrocyclic compounds
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 167
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


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