Issue 99, 2015

Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations

Abstract

A nitro-substituted dipyrrolylphenol was synthesized as a precursor of a π-electronic anion, whose phenolate (phenoxide) moiety upon deprotonation was stabilized by the hydrogen-bond-donating pyrrole NH, thus forming solid-state ion pairs with various cationic species.

Graphical abstract: Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations

Supplementary files

Article information

Article type
Communication
Submitted
07 sept. 2015
Accepted
12 oct. 2015
First published
14 oct. 2015

Chem. Commun., 2015,51, 17572-17575

Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations

H. Maeda, A. Fukui, R. Yamakado and N. Yasuda, Chem. Commun., 2015, 51, 17572 DOI: 10.1039/C5CC07493B

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