A new functionalization strategy for pentacene

Literature Information

Publication Date 2007-09-06
DOI 10.1039/B711296C
Impact Factor 6.222
Authors

John E. Anthony, Johannes Gierschner, Chad A. Landis, Sean R. Parkin, Jes B. Sherman, Ronald C. Bakus II


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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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