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A new functionalization strategy for pentacene
Authors:Anthony John E  Gierschner Johannes  Landis Chad A  Parkin Sean R  Sherman Jes B  Bakus Ii Ronald C
Affiliation:Department of Chemistry, University of Kentucky, Lexington, KY 40506-0055, USA. anthony@uky.edu
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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