Hexyl-substituted oligothiophenes with a central tetrafluorophenylene unit: crystal engineering of planar structures for p-type organic semiconductors
Chemical Communications2005Iss. 11, pp. 1465–1465
Citations Over TimeTop 10% of 2005 papers
Abstract
Rigidification has been achieved in thiophene-tetrafluorophenylene architectures through strong S...F and H...F intramolecular interactions; the resulting materials are promising candidates for p-type organic field effect transistors.
Related Papers
- → Electronic and Crystal Engineering of Acenes for Solution‐Processible Self‐Assembling Organic Semiconductors(2006)131 cited
- → 2,6-Dialkylbenzo[1,2-b:4,5-b′]dithiophenes (Cn-BDTs) as Soluble Organic Semiconductors for Solution-processed Organic Field-effect Transistors(2008)37 cited
- → Nitroaromatics as n-type organic semiconductors for field effect transistors(2020)21 cited
- → Charge carrier mobilities in organic semiconductors: crystal engineering and the importance of molecular contacts(2015)28 cited