Synthesis of open-shell ladder π-systems by catalytic C–H annulation of diarylacetylenes† †Electronic supplementary information (ESI) available: Syntheses, NMR, UV-vis-nearIR absorption, CV and crystallographic table. CCDC 1421865 (1a), 1421866 (1b). For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5sc03391h

A new open-shell ladder-shaped π-system has been synthesized. A new open-shell ladder-shaped π-system has been synthesized. Pentaleno[1,2- b :4,5- b ′]difluorene derivatives, 8 fused ring systems bearing 5- and 6-membered rings, were constructed from alkynylfluorenone through a reaction sequence including Pd-catalyzed C–H/C–H annulation. X-ray crystallography and ESR spectroscopy revealed the open-shell character of these ladder-shaped molecules, which derives from their extended π-electron conjugation. Absorption peaks in the near IR region as well as narrow redox potentials observed by cyclic voltammetry indicated small optical and fundamental energy gaps of these fused ring systems.