Publikation: Substituent effects on triplet yields in aminoanthraquinones : radiationless deactivation via intermolecular and intramolecular hydrogen bonding
Dateien
Datum
Autor:innen
Herausgeber:innen
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
URI (zitierfähiger Link)
DOI (zitierfähiger Link)
Internationale Patentnummer
Link zur Lizenz
Angaben zur Forschungsförderung
Projekt
Open Access-Veröffentlichung
Sammlungen
Core Facility der Universität Konstanz
Titel in einer weiteren Sprache
Publikationstyp
Publikationsstatus
Erschienen in
Zusammenfassung
The dependence of the triplet quantum yields of monosubstituted and disubstituted aminoanthraquinones on the number of substituents and on their position was studied. Using fluorescence lifetimes, fluorescence quantum yields and triplet quantum yields, the rate constants of the intersystem crossing into the triplet state and of the internal conversion into the ground state were evaluated. For monosubstituted aminoanthraquinones the individual contributions of various mechanisms to the internal conversion have been estimated. In quenching the excited singlet state, intermolecular hydrogen bonding to the solvent is more efficient by an order of magnitude than intramolecular hydrogen bonding.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
RITTER, J., Hans-Ulrich BORST, T. LINDNER, Manfred HAUSER, Stefan BROSIG, Karl BREDERECK, Ulrich STEINER, Dietmar KÜHN, J. KELEMEN, Horst E. A. KRAMER, 1988. Substituent effects on triplet yields in aminoanthraquinones : radiationless deactivation via intermolecular and intramolecular hydrogen bonding. In: Journal of Photochemistry and Photobiology A. 1988, 41(2), pp. 227-244. ISSN 1010-6030. Available under: doi: 10.1016/1010-6030(88)80040-6BibTex
@article{Ritter1988Subst-9611, year={1988}, doi={10.1016/1010-6030(88)80040-6}, title={Substituent effects on triplet yields in aminoanthraquinones : radiationless deactivation via intermolecular and intramolecular hydrogen bonding}, number={2}, volume={41}, issn={1010-6030}, journal={Journal of Photochemistry and Photobiology A}, pages={227--244}, author={Ritter, J. and Borst, Hans-Ulrich and Lindner, T. and Hauser, Manfred and Brosig, Stefan and Bredereck, Karl and Steiner, Ulrich and Kühn, Dietmar and Kelemen, J. and Kramer, Horst E. A.} }
RDF
<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/9611"> <dc:rights>Attribution-NonCommercial-NoDerivs 2.0 Generic</dc:rights> <dc:creator>Lindner, T.</dc:creator> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/9611/1/Substituent_effects_on_triplet_yields_in_aminoanthraquinones.pdf"/> <dc:contributor>Lindner, T.</dc:contributor> <dc:format>application/pdf</dc:format> <dc:creator>Hauser, Manfred</dc:creator> <dc:creator>Brosig, Stefan</dc:creator> <dc:contributor>Kramer, Horst E. A.</dc:contributor> <dc:creator>Kramer, Horst E. A.</dc:creator> <dc:creator>Kühn, Dietmar</dc:creator> <dc:contributor>Kühn, Dietmar</dc:contributor> <dcterms:abstract xml:lang="eng">The dependence of the triplet quantum yields of monosubstituted and disubstituted aminoanthraquinones on the number of substituents and on their position was studied. Using fluorescence lifetimes, fluorescence quantum yields and triplet quantum yields, the rate constants of the intersystem crossing into the triplet state and of the internal conversion into the ground state were evaluated. For monosubstituted aminoanthraquinones the individual contributions of various mechanisms to the internal conversion have been estimated. In quenching the excited singlet state, intermolecular hydrogen bonding to the solvent is more efficient by an order of magnitude than intramolecular hydrogen bonding.</dcterms:abstract> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T18:13:09Z</dcterms:available> <dcterms:issued>1988</dcterms:issued> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/9611/1/Substituent_effects_on_triplet_yields_in_aminoanthraquinones.pdf"/> <dc:contributor>Brosig, Stefan</dc:contributor> <dc:contributor>Borst, Hans-Ulrich</dc:contributor> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/9611"/> <dc:creator>Borst, Hans-Ulrich</dc:creator> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dcterms:title>Substituent effects on triplet yields in aminoanthraquinones : radiationless deactivation via intermolecular and intramolecular hydrogen bonding</dcterms:title> <dc:contributor>Ritter, J.</dc:contributor> <dc:creator>Bredereck, Karl</dc:creator> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T18:13:09Z</dc:date> <dc:contributor>Hauser, Manfred</dc:contributor> <dc:contributor>Kelemen, J.</dc:contributor> <dcterms:bibliographicCitation>First publ. in: Journal of Photochemistry and Photobiology A, 41 (1988), 2, pp. 227-244</dcterms:bibliographicCitation> <dc:contributor>Steiner, Ulrich</dc:contributor> <dc:creator>Steiner, Ulrich</dc:creator> <dcterms:rights rdf:resource="http://creativecommons.org/licenses/by-nc-nd/2.0/"/> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dc:language>eng</dc:language> <dc:creator>Ritter, J.</dc:creator> <dc:contributor>Bredereck, Karl</dc:contributor> <dc:creator>Kelemen, J.</dc:creator> </rdf:Description> </rdf:RDF>