Issue 21, 2005
From the journal:

Chemical Communications

Illumination of the 9-mesityl-10-methylacridinium ion does not give a long-lived photoredox state

Andrew C. Benniston,a   Anthony Harriman,*a   Peiyi Li,a   James P. Rostrona  and  Jan W. Verhoevenb  

* Corresponding authors

a Molecular Photonics Laboratory, School of Natural Sciences, Bedson Building, University of Newcastle, Newcastle upon Tyne, UK
E-mail: anthony.harriman@ncl.ac.uk
Fax: +44 (0)191 222 8660
Tel: +44 (0)191 444 8660

b Laboratory of Organic Chemistry (HIMS), University of Amsterdam, Nieuwe Achtergracht 129, Amsterdam, The Netherlands

Abstract

Photolysis of the 9-mesityl-10-methylacridinium cation in benzonitrile forms an acridinyl radical, detected by EPR and UV–visible spectroscopy, by way of a sacrificial process.

Graphical abstract: Illumination of the 9-mesityl-10-methylacridinium ion does not give a long-lived photoredox state

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Article information

DOI
https://doi.org/10.1039/B501262G
Article type
Communication
Submitted
27 Jan 2005
Accepted
17 Mar 2005
First published
08 Apr 2005

Chem. Commun., 2005, 2701-2703

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Illumination of the 9-mesityl-10-methylacridinium ion does not give a long-lived photoredox state

A. C. Benniston, A. Harriman, P. Li, J. P. Rostron and J. W. Verhoeven, Chem. Commun., 2005, 2701 DOI: 10.1039/B501262G

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