Share Email Print

Proceedings Paper

Synthesis, optical, thermal, and redox properties of 2,3,9,10-tetrasubstituted- 6,13- dialkynylpentacenes
Author(s): John E. Anthony; Christopher R. Swartz; Chad A. Landis; Sean R. Parkin
Format Member Price Non-Member Price
PDF $14.40 $18.00
cover GOOD NEWS! Your organization subscribes to the SPIE Digital Library. You may be able to download this paper for free. Check Access

Paper Abstract

A series of 2,3,9,10-tetrasubstituted-6,13-dialkynylpentacenes was synthesized and their properties evaluated. Various alkynes with different substituents were chosen to explore the effects of substitution on acene properties. The addition of alkyl groups to the pentacene 2,3,9,10-positions showed significant effects on the absorption, emission, and redox properties versus the non-alkylated (R = H) materials. The acenes exhibited excellent solubility in numerous solvents, and HOMO energy levels matched well with the work function of gold, an important electrode material. Crystallographic characterization of the methoxymethylene derivative showed it to adopt a 1-dimensional π-stacked arrangement, with good overlap of the aromatic faces.

Paper Details

Date Published: 30 August 2005
PDF: 12 pages
Proc. SPIE 5940, Organic Field-Effect Transistors IV, 594002 (30 August 2005); doi: 10.1117/12.615939
Show Author Affiliations
John E. Anthony, Univ. of Kentucky (United States)
Christopher R. Swartz, Univ. of Kentucky (United States)
Chad A. Landis, Univ. of Kentucky (United States)
Sean R. Parkin, Univ. of Kentucky (United States)

Published in SPIE Proceedings Vol. 5940:
Organic Field-Effect Transistors IV
Zhenan Bao; David J. Gundlach, Editor(s)

© SPIE. Terms of Use
Back to Top