Issue 42, 2023

ortho O-Annulated azabenzannulated perylenediimide and bisazacoronenediimide

Abstract

The development of new n-type organic semiconductors is crucial to the development of organic electronics. The introduction of heteroatoms into polycyclic aromatic hydrocarbons (PAHs) or nanographenes has been demonstrated to be a compelling strategy to tune their optoelectronic, coordination, magnetic and self-assembly properties, in order to adapt them to specific organic electronic devices. Perylenediimide (PDI) derivatives have been an interesting hetero-doping platform for the design of new functional electron-deficient structures, but rarely has oxygen been introduced into their π-conjugated scaffold. In this study, we present the preparation of Bisazacoronenediimide (BACD) derivatives annulated by the insertion of oxygen in their ortho position. These compounds exhibit high planarity and their properties are highly sensitive to the extension of their π-system. Their optoelectronic properties and performance in preliminary organic electronics studies are reported. This work shows that the ortho O-annulation of BACDs is a promising route to explore for the discovery of future new high-performance rylene diimide dyes.

Graphical abstract: ortho O-Annulated azabenzannulated perylenediimide and bisazacoronenediimide

Supplementary files

Article information

Article type
Paper
Submitted
06 jul 2023
Accepted
22 set 2023
First published
25 set 2023

J. Mater. Chem. C, 2023,11, 14631-14640

ortho O-Annulated azabenzannulated perylenediimide and bisazacoronenediimide

A. H. G. David, D. Shymon, H. Melville, L. Accou, A. Gapin, M. Allain, O. Alévêque, M. Force, A. Grosjean, P. Hudhomme, L. Le Bras and A. Goujon, J. Mater. Chem. C, 2023, 11, 14631 DOI: 10.1039/D3TC02376A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements