Issue 20, 2011
From the journal:

Chemical Communications

Donor-extended tripodal pyrroles: encapsulation, metallation, and H-bonded tautomers†‡

John S. Hart,a   Fraser J. Whitea  and  Jason B. Love*a  

* Corresponding authors

a EaStCHEM School of Chemistry, University of Edinburgh, Joseph Black Building, The King's Buildings, West Mains Road, Edinburgh EH9 3JJ, UK
E-mail: jason.love@ed.ac.uk
Fax: +44 (0)131 6504743

Abstract

A tripodal iminopyrrole provides an environment suited to the encapsulation of water through hydrogen-bonding, and the formation of metal complexes by deprotonation and imine–pyrrole tautomerisation.

Graphical abstract: Donor-extended tripodal pyrroles: encapsulation, metallation, and H-bonded tautomers

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1CC11378J
Article type
Communication
Submitted
09 mars 2011
Accepted
01 avr. 2011
First published
18 avr. 2011

Chem. Commun., 2011,47, 5711-5713

Permissions

Request permissions

Donor-extended tripodal pyrroles: encapsulation, metallation, and H-bonded tautomers

J. S. Hart, F. J. White and J. B. Love, Chem. Commun., 2011, 47, 5711 DOI: 10.1039/C1CC11378J

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