dc.contributor.author
Krappe, Alexander R.
dc.contributor.author
Mayer, Jacob C.
dc.contributor.author
Zhang, Wuai
dc.contributor.author
Filla, Lina M.
dc.contributor.author
Ligorio, Giovanni
dc.contributor.author
Hermerschmidt, Felix
dc.contributor.author
Eitelhuber, Larissa S.
dc.contributor.author
Güttler, Arne
dc.contributor.author
Weber, Manuela
dc.contributor.author
Paulus, Beate
dc.contributor.author
Resch-Genger, Ute
dc.contributor.author
List-Kratochvil, Emil J. W.
dc.contributor.author
Eigler, Siegfried
dc.date.accessioned
2025-06-27T11:10:17Z
dc.date.available
2025-06-27T11:10:17Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/47647
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-47365
dc.description.abstract
We report the synthesis of a fluorescent polycyclic aromatic hydrocarbon dye with a “symmetry-broken” core, derived from the related hexa-peri-benzocoronene (HBC) core with a fluoranthene subunit. The fluorophore is composed of a pure carbon skeleton without heteroatoms and exhibits remarkable photoluminescence properties with a photoluminescence quantum yield (PLQY) of up to 67% in toluene, exceeding that of the parent HBC by a factor of 30. The single crystal X-ray structure reveals the distorted polycyclic aromatic hydrocarbon structure, which is responsible for the optoelectronic properties, as supported by density functional theory calculations. We show that the new fluorescent dye can be readily used for the fabrication of organic light-emitting diodes (OLED) without extensive optimization, whereby solubility in a variety of solvents and successful film formation are decisive.
en
dc.format.extent
7 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
hydrocarbons
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften
dc.title
Highly Emissive Hexa-peri-benzocoronene-fluoranthene Hybrid as Easily Processable and Stable OLED Material
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e202500742
dcterms.bibliographicCitation.doi
10.1002/chem.202500742
dcterms.bibliographicCitation.journaltitle
Chemistry – A European Journal
dcterms.bibliographicCitation.number
30
dcterms.bibliographicCitation.volume
31
dcterms.bibliographicCitation.url
https://doi.org/10.1002/chem.202500742
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie

refubium.funding
DEAL Wiley
refubium.note.author
Gefördert aus Open-Access-Mitteln der Freien Universität Berlin.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1521-3765