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

Scott L Cockroft; Christopher A Hunter

doi:10.1039/b902351h

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

Research output: Contribution to journal › Article › peer-review

Abstract / Description of output

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 alpha/beta H-bond constants.

Original language	English
Pages (from-to)	3961-3963
Number of pages	3
Journal	Chemical Communications
Volume	2009
Issue number	26
DOIs	https://doi.org/10.1039/b902351h
Publication status	Published - 2009

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10.1039/b902351h

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http://pubs.rsc.org/en/Content/ArticleLanding/2009/CC/b902351h

Cite this

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title = "Desolvation and substituent effects in edge-to-face aromatic interactions",

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 alpha/beta H-bond constants.",

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

Abstract / Description of output

Access to Document

Other files and links

Fingerprint

How much do dispersion interactions contribute to molecular recognition in solution?

Seeing Through Solvent Effects using Molecular Balances

Lecture at AstraZeneca Alderley Park

Lecture at Eisai Pharmaceuticals

Cite this

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

Abstract / Description of output

Access to Document

Other files and links

Fingerprint

Projects

How much do dispersion interactions contribute to molecular recognition in solution?

Research output

Seeing Through Solvent Effects using Molecular Balances

Activities

Lecture at AstraZeneca Alderley Park

Lecture at Eisai Pharmaceuticals

Cite this