Femtosecond Spectroscopy on a Dibenzophenazine‐Cored Macrocycle Exhibiting Thermally Activated Delayed Fluorescence

Abstract: The photophysics of a thermally activated delayed fluorescence (TADF) emitting macrocycle consisting of two dibenzo[a,j]phenazine acceptor moieties bridged by two N,N,N’,N’‐tetraphenylene‐1,4‐diamine donor units was scrutinized in solution by steady‐state and time‐resolved spectroscopy. The fluorescence lifetime of the compound proved to be strongly solvent‐dependent. It ranges from 6.3 ns in cyclohexane to 34 ps in dimethyl sulfoxide. In polar solvents the fluorescence decay is predominantly due to internal conversion. In non‐polar ones radiative decay and intersystem crossing contribute. Contrary to the behaviour in polymer matrices (S. Izumi et al., J. Am. Chem. Soc. 2020, 142, 1482) the excited state decay is not predominantly due to prompt and delayed fluorescence. The solvent‐dependent behaviour is analyzed with the aid of quantum chemical computations.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Femtosecond Spectroscopy on a Dibenzophenazine‐Cored Macrocycle Exhibiting Thermally Activated Delayed Fluorescence ; day:26 ; month:04 ; year:2023 ; extent:11
ChemistryOpen ; (26.04.2023) (gesamt 11)

Urheber
Thom, Kristoffer A.
Nolden, Oliver
Weingart, Oliver
Izumi, Saika
Minakata, Satoshi
Takeda, Youhei
Gilch, Peter

DOI
10.1002/open.202300026
URN
urn:nbn:de:101:1-2023042715043009294216
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:57 MESZ

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