Issue 8, 2013

Revisiting zethrene: synthesis, reactivity and semiconductor properties

Abstract

Zethrene, a unique polycyclic aromatic hydrocarbon with formally fixed C–C double bonds, is predicted to have interesting properties and potential applications as an optical and electronic material. Here we report a novel synthesis of zethrene with improved yield, which presumably involves dinaphtho[10]-annulene as an unstable intermediate. With this convenient access to zethrene, we used zethrene as a p-type semiconductor in thin film transistors for the first time. It is found that Diels–Alder addition to the bay region of zethrene leads to new derivatives of benzo[pqr]naphtho[8,1,2-bcd]perylene, which behave as n-type organic semiconductors.

Graphical abstract: Revisiting zethrene: synthesis, reactivity and semiconductor properties

Supplementary files

Article information

Article type
Edge Article
Submitted
29 Apr 2013
Accepted
07 Jun 2013
First published
07 Jun 2013

Chem. Sci., 2013,4, 3294-3297

Revisiting zethrene: synthesis, reactivity and semiconductor properties

L. Shan, Z. Liang, X. Xu, Q. Tang and Q. Miao, Chem. Sci., 2013, 4, 3294 DOI: 10.1039/C3SC51158H

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