Issue 34, 2019

Synthesis and electrochromic behavior of a multi-electron redox-active N-heteroheptacenequinone

Abstract

We report a novel N-heteroheptacenequinone derivative (C6OAHCQ) as a large π-conjugated framework. C6OAHCQ shows good electron-accepting behaviour owing to eight electron-deficient imino-N atoms and two carbonyl moieties and excellent solubility in common organic solvents. When a potential between 0 and −2.20 V is applied, C6OAHCQ is able to accept four electrons, which is more than fullerene C60 (three electrons) could accept in this voltage range. Moreover, a solution of C6OAHCQ and nBu4NPF6 in CH2Cl2 exhibits a clearly reversible brown-to-green colour change, suggesting that C6OAHCQ has potential as an electrochromic material.

Graphical abstract: Synthesis and electrochromic behavior of a multi-electron redox-active N-heteroheptacenequinone

Supplementary files

Article information

Article type
Paper
Submitted
10 Jun 2019
Accepted
02 Jul 2019
First published
03 Jul 2019

Org. Biomol. Chem., 2019,17, 7884-7890

Synthesis and electrochromic behavior of a multi-electron redox-active N-heteroheptacenequinone

K. Isoda, M. Matsuzaka, T. Sugaya, T. Yasuda and M. Tadokoro, Org. Biomol. Chem., 2019, 17, 7884 DOI: 10.1039/C9OB01323G

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