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dc.contributor.refereeAmsharov, Konstantin-
dc.contributor.refereeJux, Norbert-
dc.contributor.authorEl Alaoui, Nour-Eddine-
dc.date.accessioned2026-03-06T10:40:06Z-
dc.date.available2026-03-06T10:40:06Z-
dc.date.issued2026-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/124425-
dc.identifier.urihttp://dx.doi.org/10.25673/122480-
dc.description.abstractThis study investigates the synthesis of two distinct classes of macrocycles: non-fluorinated cyclo-para-phenylenes (CPPs) and fluorinated cyclo-meta-phenylenes (CMPSs). On-Surface Synthesis (CPPs): We synthesized quasi-planar, π-extended CPPs on Au(111). Characterization via STM/STS and DFT. Solution-Phase Synthesis (CMPs): We developed a modular route using selective ironmediated bromination to create fluorinated oligophenylene scaffolds. These precursors undergo nickel-mediated Yamamoto coupling to form fluorinated CMPsThis dualmethodology framework explores how curvature, fluorination, and electronic confinement interact within strained benzenoid architectures.eng
dc.format.extent1 Online-Ressource (iii, 147 Seiten)-
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc540-
dc.titleSpecific bromination of fluorinated oligophenylenes, towards cyclo-para- and cyclo-meta-phenyleneseng
dcterms.dateAccepted2026-01-28-
dcterms.typeHochschulschrift-
dc.typePhDThesis-
dc.identifier.urnurn:nbn:de:gbv:3:4-1981185920-1244251-
local.versionTypepublishedVersion-
local.publisher.universityOrInstitutionMartin-Luther-Universität Halle-Wittenberg-
local.subject.keywordsCycloparaphenylenes (CPP), Cyclometaphenylenes (CMP), On-surface synthesis, Fluorinated oligophenylenes, Scanning tunneling microscopy (STM), π-extension, Regioselective bromination, Yamamoto coupling, Electronic confinement, Macrocyclic strain-
local.openaccesstrue-
dc.identifier.ppn1963630009-
cbs.publication.displayformHalle, 2026-
local.publication.countryXA-DE-
cbs.sru.importDate2026-03-06T10:39:17Z-
local.accessrights.dnbfree-
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