Impact of Truncation on Optoelectronic Properties of Azaborole Helicenes.
azaboroles
circularly polarized organic light-emitting diodes (CP-OLEDs)
fluorescence
helicenes
phosphorescence
Journal
Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783
Informations de publication
Date de publication:
14 Dec 2023
14 Dec 2023
Historique:
received:
29
08
2023
pubmed:
31
8
2023
medline:
31
8
2023
entrez:
31
8
2023
Statut:
ppublish
Résumé
Herein, we report configurationally stable singly-truncated (ST) and structurally flexible doubly-truncated (DT) helically chiral compounds derived from azabora[7]helicenes by a hypothetical removal of a single or two C=C double bonds. The singly-truncated constitutional isomers were synthesized from either benzoisoquinoline (BIQ) or phenantherene building blocks and the corresponding biaryls in excellent yields to give azabora[5]helicenes with a pendant phenyl ring at a sterically hindered position. These systems highlight the electronic impact of the nitrogen donor substitution position. The compounds with a disrupted BIQ moiety (STN) possess remarkable photoluminescence quantum yields of up to 0.53 in the solid state and a blue emission in solution with dissymmetry factors of up to ca. 3×10
Identifiants
pubmed: 37651165
doi: 10.1002/chem.202302808
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202302808Subventions
Organisme : Deutsche Forschungsgemeinschaft
ID : NO 1459/1-1
Organisme : Deutsche Forschungsgemeinschaft
ID : 444286426
Organisme : Deutsche Forschungsgemeinschaft
ID : RTG 2591
Organisme : Hector Fellow Academy
Informations de copyright
© 2023 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.
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