Synthesis of Bifluorenylidene- and Cycloocta[1,2,3-jk:6,5,4-j'k']difluorene-Extended Tetrathiafulvalenes – Novel Multi-Redox Systems

Herein, we present the synthesis of a novel 9,9’-bifluorenylidene-extended tetrathiafulvalene (TTF) as an E/Z isomeric mixture that was found to readily undergo an oxidative dimerization to furnish a TTF vinylogue with the two dithiafulvene units connected to an eight-membered ring fused to a bifluorenylidene core. This compound exhibited multi-redox behavior and was found to take six charge states under cyclic voltammetry conditions: -2, -1, 0, +1, +2, +3. The dication corresponds to a cycloocta[1,2,3-jk:6,5,4-j’k’]difluorene with two appended 1,3-dithiolium rings.