Rubrenes: Planar and Twisted
✍ Scribed by Abhimanyu S. Paraskar; A. Ravikumar Reddy; Asit Patra; Yair H. Wijsboom; Ori Gidron; Linda J. W. Shimon; Gregory Leitus; Michael Bendikov
- Book ID
- 101834613
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 426 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0947-6539
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Surprisingly, despite its very high mobility in a single crystal, rubrene shows very low mobility in vacuum‐sublimed or solution‐processed organic thin‐film transistors. We synthesized several rubrene analogues with electron‐withdrawing and electron‐donating substituents and found that most of the substituted rubrenes are not planar in the solid state. Moreover, we conclude (based on experimental and calculated data) that even parent rubrene is not planar in solution and in thin films. This discovery explains why high mobility is reported in rubrene single crystals, but rubrene shows very low field‐effect mobility in thin films. The substituted rubrenes obtained in this work have significantly better solubility than parent rubrene and some even form films and not crystals after evaporation of the solvent. Thus, substituted rubrenes are promising materials for organic light‐emitting diode (OLED) applications.
📜 SIMILAR VOLUMES
Ab initio molecular-orbital calculations are used to examine the structure of the ethylene radiul ation. The results point to a twisted equilibrium geometry, in agreement with experiment Very large basis sets and highly correlated wavefunctions are necessary to describe even qualitatively the torsio