Issue 45, 2024

Substituent tailoring anti-aromaticity and charge transport polarity of cyclopenta[hi]aceanthrylenes

Abstract

When the substituents of cyclopenta[hi]aceanthrylene change from trimethylsilyl to a cyano group, we observed reduced anti-aromaticity, decreased LUMO level from −2.49 to −3.59 eV, and inverted charge transport polarity from p type to n type, shedding light on the development of organic semiconductors based on cyclopenta-fused polycyclic aromatic hydrocarbons.

Graphical abstract: Substituent tailoring anti-aromaticity and charge transport polarity of cyclopenta[hi]aceanthrylenes

Supplementary files

Article information

Article type
Communication
Submitted
25 Aug 2024
Accepted
22 Oct 2024
First published
24 Oct 2024

J. Mater. Chem. C, 2024,12, 18238-18242

Substituent tailoring anti-aromaticity and charge transport polarity of cyclopenta[hi]aceanthrylenes

W. Chen, F. Sun, J. Guo, F. Qie, X. Jia, C. Shi and Y. Zhen, J. Mater. Chem. C, 2024, 12, 18238 DOI: 10.1039/D4TC03634D

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