Pyrrolodiazine derivatives as blue organic luminophores : synthesis and properties. Part 3
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
A fast, efficient, general and environmentally friendly method for preparation of highly fluorescent derivatives containing the pyrrolodiazine moiety using microwave (MW) irradiation, in liquid phase, is reported. Under MW irradiation the yields are much higher, sometimes substantially (by almost double) and, the amount of solvent used is at least 5-fold less. The pyrrolopyridazine (PP) derivatives are very intense blue emitters and have high quantum yields (up to 90%) while pyrrolophthalazine (PHP) compounds are still intense blue emitters but the quantum yield is negligible. A certain influence of the substituents concerning fluorescence was found, those ones at the 7 position being crucial for fluorescence. The number of the substituents from the pyrrolo ring seems not to play an important role in regard with the fluorescence but, with an increasing number of substituents a certain hypsochromic shift in the absorption spectra was found.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
ZBANCIOC, Gheorghita N., Thomas HUHN, Ulrich GROTH, Calin DELEANU, Ionel I. MANGALAGIU, 2010. Pyrrolodiazine derivatives as blue organic luminophores : synthesis and properties. Part 3. In: Tetrahedron. 2010, 66(24), pp. 4298-4306. ISSN 0040-4020. Available under: doi: 10.1016/j.tet.2010.04.050BibTex
@article{Zbancioc2010Pyrro-12585, year={2010}, doi={10.1016/j.tet.2010.04.050}, title={Pyrrolodiazine derivatives as blue organic luminophores : synthesis and properties. Part 3}, number={24}, volume={66}, issn={0040-4020}, journal={Tetrahedron}, pages={4298--4306}, author={Zbancioc, Gheorghita N. and Huhn, Thomas and Groth, Ulrich and Deleanu, Calin and Mangalagiu, Ionel I.} }
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/123456789/12585"> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-06-16T08:15:38Z</dcterms:available> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/12585/1/huhn.pdf"/> <dc:contributor>Zbancioc, Gheorghita N.</dc:contributor> <dc:contributor>Huhn, Thomas</dc:contributor> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/12585"/> <dc:contributor>Groth, Ulrich</dc:contributor> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/> <dcterms:issued>2010</dcterms:issued> <dc:creator>Deleanu, Calin</dc:creator> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:creator>Groth, Ulrich</dc:creator> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/12585/1/huhn.pdf"/> <dc:language>eng</dc:language> <dc:rights>terms-of-use</dc:rights> <dc:contributor>Mangalagiu, Ionel I.</dc:contributor> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-06-16T08:15:38Z</dc:date> <dc:contributor>Deleanu, Calin</dc:contributor> <dcterms:abstract xml:lang="eng">A fast, efficient, general and environmentally friendly method for preparation of highly fluorescent derivatives containing the pyrrolodiazine moiety using microwave (MW) irradiation, in liquid phase, is reported. Under MW irradiation the yields are much higher, sometimes substantially (by almost double) and, the amount of solvent used is at least 5-fold less. The pyrrolopyridazine (PP) derivatives are very intense blue emitters and have high quantum yields (up to 90%) while pyrrolophthalazine (PHP) compounds are still intense blue emitters but the quantum yield is negligible. A certain influence of the substituents concerning fluorescence was found, those ones at the 7 position being crucial for fluorescence. The number of the substituents from the pyrrolo ring seems not to play an important role in regard with the fluorescence but, with an increasing number of substituents a certain hypsochromic shift in the absorption spectra was found.</dcterms:abstract> <dc:creator>Huhn, Thomas</dc:creator> <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/> <dcterms:title>Pyrrolodiazine derivatives as blue organic luminophores : synthesis and properties. Part 3</dcterms:title> <dc:creator>Zbancioc, Gheorghita N.</dc:creator> <dc:creator>Mangalagiu, Ionel I.</dc:creator> <dcterms:bibliographicCitation>First publ. in: Tetrahedron 66 (2010), 24, pp. 4298-4306</dcterms:bibliographicCitation> </rdf:Description> </rdf:RDF>