Issue 19, 2023

Dihydroindenofluorenes as building units in organic semiconductors for organic electronics

Abstract

This review aims to discuss organic semiconductors constructed on dihydroindenofluorene positional isomers, which are key molecular scaffolds in organic electronics. Bridged oligophenylenes are key organic semiconductors that have allowed the development of organic electronic technologies. Dihydroindenofluorenes (DHIFs) belong to the family of bridged oligophenylenes constructed on a terphenyl backbone. They have proven to be very promising building blocks for the construction of highly efficient organic semiconductors for all OE devices, namely organic light emitting diodes (OLEDs), phosphorescent OLEDs, organic field-effect transistors (OFETs), solar cells, etc.

Graphical abstract: Dihydroindenofluorenes as building units in organic semiconductors for organic electronics

Article information

Article type
Review Article
Submitted
13 Apr 2023
First published
13 Sep 2023
This article is Open Access
Creative Commons BY-NC license

Chem. Soc. Rev., 2023,52, 6754-6805

Dihydroindenofluorenes as building units in organic semiconductors for organic electronics

C. Poriel and J. Rault-Berthelot, Chem. Soc. Rev., 2023, 52, 6754 DOI: 10.1039/D1CS00993A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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