13 September 2007 Crystal design for organic semiconductors: the effects of substitution on crystal packing
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Proceedings Volume 6658, Organic Field-Effect Transistors VI; 66580L (2007); doi: 10.1117/12.731158
Event: Photonic Devices + Applications, 2007, San Diego, California, United States
Abstract
Electronic devices based on organic materials have been an area of intense research for the past several years. Pentacene, an oligoacene, is regarded as a benchmark due to its high charge carrier mobility. However it has poor solubilty, unoptimized π-overlap and is highly unstable. We have successfully demonstrated that peri-functionalization with trialkylsilyl ethynyl groups enhances the π-stacking, solubility and stability of pentacene and related compounds. TIPS pentacene exhibits both two dimensional (2D) π-stacking and good solubilty in common organic solvents. However changing the solubilizing groups or functionalizing the acene core results in a disruption of the desired 2D π-stacking. Molecules with one dimensional (1D) π-stacking have poorer mobility than those with 2D π-stacking and hence larger solubilizing groups are required to change the π-stacking to 2D. The emphasis of this paper is to show how small changes in substitution can disrupt π-stacking in these molecules and how one can achieve the desired π-stacking by careful selection of solubilzing groups.
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John E. Anthony, Balaji Purushothaman, "Crystal design for organic semiconductors: the effects of substitution on crystal packing", Proc. SPIE 6658, Organic Field-Effect Transistors VI, 66580L (13 September 2007); doi: 10.1117/12.731158; http://dx.doi.org/10.1117/12.731158
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KEYWORDS
Molecules

Crystals

Silicon

Chemical species

Selenium

Field effect transistors

Molecular interactions

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