Issue 7, 2022

Polycyclic aromatic hydrocarbon-based organic semiconductors: ring-closing synthesis and optoelectronic properties

Abstract

Polycyclic aromatic hydrocarbons (PAHs) as a typical class of organic semiconductors demonstrate unique optical, electrical, magnetic and other interesting properties due to their extended conjugation and diverse structures. Ring-closing reactions are very significant for the synthesis of PAHs with various structures and optoelectronic properties, which endow them great potential for applications in organic electronics. The aim of this article is to present a concise summary on the recent advances on the ring-closing reactions for the synthesis of organic semiconductors, with a discussion on their applicable conditions, followed by their attractive applications in organic field-effect transistors (especially chiral transistors and biradicaloid-based transistors), organic solar cells, etc. Finally, a short conclusion and perspective are given on the further development of new ring-closing reactions toward novel PAH materials with promising applications.

Graphical abstract: Polycyclic aromatic hydrocarbon-based organic semiconductors: ring-closing synthesis and optoelectronic properties

Article information

Article type
Review Article
Submitted
11 Oct 2021
Accepted
25 Nov 2021
First published
27 Nov 2021

J. Mater. Chem. C, 2022,10, 2411-2430

Polycyclic aromatic hydrocarbon-based organic semiconductors: ring-closing synthesis and optoelectronic properties

Q. Li, Y. Zhang, Z. Xie, Y. Zhen, W. Hu and H. Dong, J. Mater. Chem. C, 2022, 10, 2411 DOI: 10.1039/D1TC04866J

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