A new functionalization strategy for pentacene |
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Authors: | Anthony John E Gierschner Johannes Landis Chad A Parkin Sean R Sherman Jes B Bakus Ii Ronald C |
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Affiliation: | Department of Chemistry, University of Kentucky, Lexington, KY 40506-0055, USA. anthony@uky.edu |
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Abstract: | Functionalization of the pro-cata positions of pentacene with groups held perpendicular to the aromatic plane, in this case through a rigid 1,3-dioxole unit, yields pentacene derivatives that are stable and soluble, and still maintain edge-to-face interactions in the solid state. |
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