Conformational effects on the dynamics of internal conversion in boron dipyrromethene dyes in solution

Hedley, G. J. , Ruseckas, A., Harriman, A. and Samuel, I. D.W. (2011) Conformational effects on the dynamics of internal conversion in boron dipyrromethene dyes in solution. Angewandte Chemie (International Edition), 50(29), pp. 6634-6637. (doi: 10.1002/anie.201101219) (PMID:21671319)

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Abstract

Internal conversion between the S2 and S1 excited singlet states is rapid in the target dyes (see picture) but shows a clear sensitivity to rotational flexibility of the meso‐phenyl ring. Steric crowding by methyl groups at the 4,7‐positions leads to a curved S2 potential‐energy surface punctured with nonlocal pinholes coupled to the S1 surface. Removal of these groups flattens the potential‐energy surface, promoting barrierless crossing to the S1 surface.

Item Type:Articles
Additional Information:Funding: Engineering and Physical Sciences Research Council EP/E062636/1.
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Hedley, Dr Gordon
Authors: Hedley, G. J., Ruseckas, A., Harriman, A., and Samuel, I. D.W.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Angewandte Chemie (International Edition)
Publisher:Wiley
ISSN:1433-7851
ISSN (Online):1521-3773
Published Online:10 June 2011

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