Abstract
Rigid and soluble electron donor–acceptor conjugates (3 and 11) that combine π-extended tetrathiafulvalene (exTTF) as an electron donor and C60 as an electron acceptor have been synthesized using oligo-vinylfluorene (oFV) linkers to connect the electroactive entities. Fluorescence and transient absorption measurements confirm that light-induced excitation induces charge-transfer reactions over distances of 28 A in THF. The incorporation of vinylene spacers into oligofluorene molecular wires has been shown both experimentally and theoretically to improve the charge-transfer features significantly to give a β value of 0.075 ± 0.001 A−1. Enhanced π-conjugation caused by higher orbital overlap is responsible for this trend.
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