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A New Design Strategy for Organic Optoelectronic Materials by Lateral Boryl Substitution
Article first published online: 14 DEC 2007
DOI: 10.1002/anie.200703722
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Elbing, M. and Bazan, G. (2008), A New Design Strategy for Organic Optoelectronic Materials by Lateral Boryl Substitution. Angewandte Chemie International Edition, 47: 834–838. doi: 10.1002/anie.200703722
Publication History
- Issue published online: 11 JAN 2008
- Article first published online: 14 DEC 2007
- Abstract
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Keywords:
- boron;
- conjugation;
- fluorescence;
- molecular design;
- organic electronics
Graphical Abstract
Lateral thinking: Molecular solids with tunable color and excellent emission efficiencies or increased electron affinities have been obtained by lateral boryl substitution on a π-delocalized framework (see picture, D=donor group, B=boryl group). This approach gives rise to a new design principle for organic optoelectronic materials.