Organic letters

A road map to stable, soluble, easily crystallized pentacene derivatives

JE Anthony, DL Eaton, SR Parkin

Index: Anthony, John E.; Eaton, David L.; Parkin, Sean R. Organic Letters, 2002 , vol. 4, # 1 p. 15 - 18

Full Text: HTML

Citation Number: 543

Abstract

A series of 6, 13-disubstituted pentacenes, in which the substituents are functionalized ethyne units, were synthesized and analyzed by X-ray crystallography. The resulting pentacene derivatives were highly soluble and oxidatively stable and exhibited a significant amount of π-stacking in the crystal.

Related Articles:

The influence of side chains on the structures and properties of functionalized pentacenes

[Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E. Journal of Materials Chemistry, 2008 , vol. 18, # 17 p. 1961 - 1969]

3, 6-Dithiophen-2-yl-diketopyrrolo [3, 2-b] pyrrole (isoDPPT) as an Acceptor Building Block for Organic Opto-Electronics

[Djukic, Brandon; Perepichka, Dmitrii F. Chemical Communications, 2012 , vol. 48, # 53 p. 6651 - 6653]

More Articles...