Publication: Oligoindenopyrenes: A new class of polycyclic aromatics
| dc.bibliographiccitation.firstpage | 9080 | |
| dc.bibliographiccitation.issue | 24 | |
| dc.bibliographiccitation.journal | The Journal of Organic Chemistry | |
| dc.bibliographiccitation.lastpage | 9087 | |
| dc.bibliographiccitation.volume | 71 | |
| dc.contributor.author | Wegner, Hermann A. | |
| dc.contributor.author | Reisch, Helge | |
| dc.contributor.author | Rauch, Karsten | |
| dc.contributor.author | Demeter, Attila | |
| dc.contributor.author | Zachariasse, Klaas A. | |
| dc.contributor.author | de Meijere, Armin | |
| dc.contributor.author | Scott, Lawrence T. | |
| dc.date.accessioned | 2018-11-07T08:57:00Z | |
| dc.date.available | 2018-11-07T08:57:00Z | |
| dc.date.issued | 2006 | |
| dc.description.abstract | A new class of polycyclic aromatic hydrocarbons-oligoindenopyrenes-has been synthesized featuring a Pd-catalyzed Suzuki-Heck coupling cascade. The oligoindenopyrenes are robust, highly colored substructures of C-70 and have properties that might prove useful in new organic materials or devices. After excitation, the tetraindenopyrene derivative 3d undergoes efficient deactivation ( 99%) by internal conversion to the ground state. The small fluorescence quantum yield ( 0.004) is in accordance with the short ( 0.6 ns) fluorescence decay time. | |
| dc.identifier.doi | 10.1021/jo0613939 | |
| dc.identifier.isi | 000242123900012 | |
| dc.identifier.pmid | 17109533 | |
| dc.identifier.uri | https://resolver.sub.uni-goettingen.de/purl?gro-2/23280 | |
| dc.notes.status | zu prüfen | |
| dc.notes.submitter | Najko | |
| dc.publisher | Amer Chemical Soc | |
| dc.relation.issn | 0022-3263 | |
| dc.title | Oligoindenopyrenes: A new class of polycyclic aromatics | |
| dc.type | journal_article | |
| dc.type.internalPublication | yes | |
| dc.type.peerReviewed | yes | |
| dc.type.status | published | |
| dspace.entity.type | Publication |