Issue 39, 2021

BN-Substituted coronene diimide donor–acceptor–donor triads: photophysical, (spectro)-electrochemical studies and Lewis behavior

Abstract

Boron/nitrogen substituted polyaromatic hydrocarbons (PAHs) are unique materials, with similar molecular structures to their carbon/carbon analogs, but different electronic properties. We report how these may be tuned by substitution at the B and/or N atoms: the BN-PAH analogues we investigated are BN-substituted coronene diimide (BNCDI) acceptors, combined with electron-rich (hetero)arene substituents (donors) on the boron atoms at either side of the BNCDI, resulting in donor–acceptor–donor (DAD) triads. In comparison to the all-carbon coronene diimide, the implementation of two BN units led to a bathochromic shift of absorption/emission (44 nm) and luminescence quantum yields close to unity. The uniqueness of the BN-based DAD motif became clear as the substitution effect of the (hetero)arene substituents was investigated. The strong electron-donating triphenylamine motif had a minor influence on the absorption behavior but showed strongly solvent-dependent luminescence properties. This could be attributed to an intramolecular photoinduced electron transfer (PeT) process which was supported by a Rehm–Weller analysis and density functional theory computations. This process was not observed for the other substituents. Moreover, we probed the influence of the aryl substituent on the B–N bond itself by using (spectro)electrochemistry and analyzed the Lewis behavior of the BN unit. The species that formed showed strong absorptions across the whole UV/vis/NIR region.

Graphical abstract: BN-Substituted coronene diimide donor–acceptor–donor triads: photophysical, (spectro)-electrochemical studies and Lewis behavior

Supplementary files

Article information

Article type
Paper
Submitted
29 Jun 2021
Accepted
03 Sep 2021
First published
15 Sep 2021

J. Mater. Chem. C, 2021,9, 13926-13934

BN-Substituted coronene diimide donor–acceptor–donor triads: photophysical, (spectro)-electrochemical studies and Lewis behavior

J. Hoffmann, D. Jacquemin, M. Hissler and A. Staubitz, J. Mater. Chem. C, 2021, 9, 13926 DOI: 10.1039/D1TC03034E

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