Issue 26, 2009
From the journal:

Chemical Communications

Desolvation and substituent effects in edge-to-face aromatic interactions†

Scott L. Cockroft*a  and  Christopher A. Hunter*b  

* Corresponding authors

a School of Chemistry, University of Edinburgh, The King’s Buildings, West Mains Road, Edinburgh, UK
E-mail: scott.cockroft@ed.ac.uk

b Department of Chemistry, University of Sheffield, Sheffield, UK
E-mail: c.hunter@shef.ac.uk
Fax: +44 (0)114 2229346

Abstract

Experimental measurements of aromatic edge-to-face interaction energies in both molecular torsion balances and supramolecular zipper complexes can be reliably estimated using a simple electrostatic solvation model and α/βH-bond constants.

Graphical abstract: Desolvation and substituent effects in edge-to-face aromatic interactions

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B902351H
Article type
Communication
Submitted
04 Feb 2009
Accepted
07 May 2009
First published
27 May 2009

Chem. Commun., 2009, 3961-3963

Permissions

Request permissions

Desolvation and substituent effects in edge-to-face aromatic interactions

S. L. Cockroft and C. A. Hunter, Chem. Commun., 2009, 3961 DOI: 10.1039/B902351H

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