9,10-Disubstituted Octafluoroanthracene Derivatives via Palladium-Catalyzed Cross-Coupling

9,10-Dichlorooctafluoroanthracene (1) reacts with aryl boronic acids and terminal alkynes under palladium-catalyzed cross-coupling conditions to afford 9,10-diaryloctafluoroanthracenes (2a−e) and 9,10-dialkynyloctafluoroanthracenes (6a,b), respectively. Optical spectroscopy and cyclic voltammetry indicate that octafluoro-9,10-di(thiophen-2-yl)anthracene (2d) exhibits donor−acceptor character and a LUMO energy level of −3.27 eV relative to vacuum. A functionalized 5-bromothiophen-2-yl derivative (2e) was obtained in high yield by bromination of 2d with NBS. X-ray crystallographic analysis of octafluoro-9,10-bis[(trimethylsilyl)ethynyl]anthracene (6a) reveals a solid-state structure that mimics the packing of columnar liquid crystals, with a π stacking distance of 3.39 Å between the octafluoroanthracene cores. In addition, octafluoro-9,10-bis(mesitylethynyl)anthracene (6b) displays a LUMO energy level of −3.50 eV, which approaches the value of −3.65 eV measured for perfluoropentacene, making 9,10-dialkynyloctafluoroanthracenes a promising new class of n-type organic materials.