Schmidt, RuedigerRuedigerSchmidtGoettling, SilkeSilkeGoettlingLeusser, DirkDirkLeusserStalke, DietmarDietmarStalkeKrause, Ana-MariaAna-MariaKrauseWuerthner, FrankFrankWuerthner2018-11-072018-11-072006https://resolver.sub.uni-goettingen.de/purl?gro-2/45402Acene derivatives 3, 5, 7 and 9 bearing two trimethoxyphenylethynyl substituents have been synthesized. The optical properties of these acenes have been investigated by UV/Vis and fluorescence spectroscopy and their eletrochemical properties have been elucidated by cyclic voltammetry (CV). X-Ray analysis of the anthracene and tetracene derivatives 3 and 5 has revealed a 1-D pi-stacking in crystals of 3 and 5. In contrast to their parent hydrocarbons, the present disubstituted acenes are highly soluble in different solvents. Spin-coating has afforded amorphous thin films that exhibit field effect mobility. Best performance has been achieved for the OTFTs prepared from the pentacene derivative 7 with a field effect mobility of 1.9 x 10(-5) cm(2) V-1 s(-1) and an on/off ratio of 10(3).Highly soluble acenes as semiconductors for thin film transistorsjournal_article10.1039/b607172d000240637600006