Tetrathiafulvalene Vinylogue-Fluorene Co-oligomers: Synthesis, Properties, and Supramoleclar Interactions with Carbon Nanotubes.

Abstract

A series of bis(dithiafulvenyl)-end-capped fluorene derivatives was prepared and subjected to a one-pot iodine-promoted oxidative polymerization to yield π-conjugated co-oligomers containing tetrathiafulvalene vinylogue and fluorene repeat units. The resulting π-oligomers were characterized to take either acyclic or cyclic molecular structures, depending on the π-conjugation length of the monomer used for the polymerization. Electronic and electrochemical redox properties were examined by UV-vis spectroscopic and cyclic voltammetric analyses, while the supramolecular interactions of the π-oligomers with single-walled carbon nanotubes were investigated by UV-vis-NIR and Raman spectroscopy.