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AuthorMeckle, Manueldc.contributor.author
Date of accession2016-05-30T13:40:11Zdc.date.accessioned
Available in OPARU since2016-05-30T13:40:11Zdc.date.available
Year of creation2016dc.date.created
Date of first publication2016-05-30dc.date.issued
AbstractSeries of fully alpha-conjugated cyclooligothiophenes C[n3]Ts with n = 3, 4, 5, 6, 7, 8, and 9 have been synthesised via a platinum templated cyclisation method and caracterised. Comparison with other C[n]Ts with different cycle sizes and/or substitutional patterns gives insights into structure-properties relationships. An oxidative substituent coupling method based on tetraorganoborates was succesfully transfered to thiophene containing borates and the substituents were modified to offer selective thiophene-thiophene coupling.dc.description.abstract
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
LicenseStandarddc.rights
Link to license texthttps://oparu.uni-ulm.de/xmlui/license_v3dc.rights.uri
KeywordOxidative couplingdc.subject
Dewey Decimal GroupDDC 540 / Chemistry & allied sciencesdc.subject.ddc
LCSHMacrocycles (Chemistry)dc.subject.lcsh
LCSHThiophenesdc.subject.lcsh
LCSHConjugated oligomersdc.subject.lcsh
LCSHBorondc.subject.lcsh
LCSHChemical templatesdc.subject.lcsh
TitleSynthesis and properties of fully conjugated cyclo[n]thiophenes and investigation into a boron-templated aryl-coupling methoddc.title
Resource typeDissertationdc.type
Date of acceptance2016-04-27dcterms.dateAccepted
RefereeBäuerle, Peterdc.contributor.referee
RefereeStreb, Carstendc.contributor.referee
DOIhttp://dx.doi.org/10.18725/OPARU-3974dc.identifier.doi
PPN862797519dc.identifier.ppn
URNhttp://nbn-resolving.de/urn:nbn:de:bsz:289-oparu-4013-5dc.identifier.urn
GNDMakrocyclische Verbindungendc.subject.gnd
GNDThiophendc.subject.gnd
GNDOligomeredc.subject.gnd
GNDBordc.subject.gnd
GNDKopplung <Analytische Chemie>dc.subject.gnd
FacultyFakultät für Naturwissenschaftenuulm.affiliationGeneral
InstitutionInstitut für Organische Chemie II und Neue Materialienuulm.affiliationSpecific
InstitutionInstitut für Anorganische Chemie I (Materialien und Katalyse)uulm.affiliationSpecific
Shelfmark print versionW: W-H 14.690uulm.shelfmark
Grantor of degreeFakultät für Naturwissenschaftenuulm.thesisGrantor
DCMI TypeTextuulm.typeDCMI
DCMI TypeDatasetuulm.typeDCMI
TypeErstveröffentlichunguulm.veroeffentlichung
CategoryPublikationenuulm.category
University Bibliographyjauulm.unibibliographie


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