Azulene-Fused Linearly π-Extended Polycyclic Aromatic Compounds: Synthesis, Photophysical Properties, and OFETs Applications
Authors:
- 15 September 2023
- journal article
- research article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 96 (9) , 1077-1081
Abstract
By introducing azulene into linearly π-extended polycyclic aromatic hydrocarbons, we found that the HOMO–LUMO gap can be narrowed comparable to [n]acenes while affording high stability against air under visible light. The fabricated OFET devices with one of the derivatives exihibited typical p-type behavior under ambient conditions.Keywords
This publication has 66 references indexed in Scilit:
- Integrated Materials Design of Organic Semiconductors for Field-Effect TransistorsJournal of the American Chemical Society, 2013
- Large N‐Heteroacenes: New Tricks for Very Old Dogs?Angewandte Chemie International Edition, 2013
- Semiconducting π-Conjugated Systems in Field-Effect Transistors: A Material Odyssey of Organic ElectronicsChemical Reviews, 2011
- Recent developments and perspectives in palladium-catalyzed cyanation of aryl halides: synthesis of benzonitrilesChemical Society Reviews, 2011
- The Rylene Colorant Family—Tailored Nanoemitters for Photonics Research and ApplicationsAngewandte Chemie International Edition, 2010
- Near‐Infrared Organic Compounds and Emerging ApplicationsChemistry – An Asian Journal, 2010
- Air-assisted High-performance Field-effect Transistor with Thin Films of PiceneJournal of the American Chemical Society, 2008
- Near‐Infrared Light‐Emitting Ambipolar Organic Field‐Effect TransistorsAdvanced Materials, 2007
- Direct Introduction of a Boryl Substituent into the 2‐Position of Azulene: Application of the Miyaura and Smith Methods to AzuleneEuropean Journal of Organic Chemistry, 2003
- An Improved Procedure for Aromatic CyanationSynthetic Communications, 1994