Issue 57, 2021
From the journal:

Chemical Communications

Pyrrole-bridged quinones: π-electronic systems that modulate electronic structures by tautomerism and deprotonation†

Shinya Sugiuraa  and  Hiromitsu Maeda ORCID logo *a  

* Corresponding authors

a Department of Applied Chemistry, College of Life Sciences, Ritsumeikan University, Kusatsu 525-8577, Japan
E-mail: maedahir@ph.ritsumei.ac.jp

Abstract

A new series of π-extended quinone derivatives containing a pyrrole bridge exhibited NH/OH-type tautomerization and anion binding along with deprotonation that induced near-infrared absorption and ion-pairing assemblies.

Graphical abstract: Pyrrole-bridged quinones: π-electronic systems that modulate electronic structures by tautomerism and deprotonation

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/D1CC02691G
Article type
Communication
Submitted
22 May 2021
Accepted
17 Jun 2021
First published
18 Jun 2021

Chem. Commun., 2021,57, 6983-6986

Permissions

Request permissions

Pyrrole-bridged quinones: π-electronic systems that modulate electronic structures by tautomerism and deprotonation

S. Sugiura and H. Maeda, Chem. Commun., 2021, 57, 6983 DOI: 10.1039/D1CC02691G

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