Synthesis, Characterisation and Electrical Properties of Supramolecular DNA-Templated Polymer Nanowires of 2,5-(Bis-2-thienyl)-pyrrole

Supramolecular polymer nanowires have been prepared by using DNA‐templating of 2,5‐(bis‐2‐thienyl)‐pyrrole (TPT) by oxidation with FeCl3 in a mixed aqueous/organic solvent system. Despite the reduced capacity for strong hydrogen bonding in polyTPT compared to other systems, such as polypyrrole, the templating proceeds well. FTIR spectroscopic studies confirm that the resulting material is not a simple mixture and that the two types of polymer interact. This is indicated by shifts in bands associated with both the phosphodiester backbone and the nucleobases. XPS studies further confirm the presence of DNA and TPT, as well as dopant Cl− ions. Molecular dynamics simulations on a [{dA24:dT24}/{TPT}4] model support these findings and indicate a non‐coplanar conformation for oligoTPT over much of the trajectory. AFM studies show that the resulting nanowires typically lie in the 7–8 nm diameter range and exhibit a smooth, continuous, morphology. Studies on the electrical properties of the prepared nanowires by using a combination of scanned conductance microscopy, conductive AFM and variable temperature two‐terminal I–V measurements show, that in contrast to similar DNA/polymer systems, the conductivity is markedly reduced compared to bulk material. The temperature dependence of the conductivity shows a simple Arrhenius behaviour consistent with the hopping models developed for redox polymers. Captivated and electric: Duplex DNA molecules act as effective templates for the formation of nanowires of the conducting polymer, poly‐[2,5‐(bis‐2‐thienyl)‐pyrrole] (see scheme). The resulting supramolecular polymer strands are typically 7–8 nm in diameter and are shown to be electrically conducting by a variety of techniques including variable‐temperature conductivity measurements on a fabricated two‐terminal device.