Low polydispersity regioregular polythiophenes with number average molecular weights ranging from 2 to 13 kDa were cast under the same conditions from solution to form a series of field effect transistors (FETs). Tapping mode AFM and grazing incidence small-angle X-ray scattering revealed that in all cases the polymers formed regular nanofibrillar morphologies with the width of nanofibrils proportional to the weight average contour length of polymer chains, indicating that conjugated backbones were oriented perpendicular to the nanofibril axes. FET charge carrier mobilities exhibited exponential dependence on nanofibril width, pointing to the decisive role of extended conjugated pathways in charge transport.

A simple method for the synthesis of end-functionalized regioregular poly(3-alkylthiophene)s is presented. Using a modified Grignard metathesis (GRIM) reaction, a series of polymers have been synthesized bearing functional groups on one or both ends of the polymer. This method has been demonstrated to work with a variety of different types of Grignard reagents (i.e., aryl, alkyl, allyl, vinyl, etc.). The reactivity of these depends on their nature, where allyl, ethynyl, and vinyl groups produced monofunctionalized polymers, and all others yielded difunctionalized polymers. The end group composition of the polymers was monitored by a combination of MALDI-TOF and 1H NMR and approaches 100% in most cases. By utilizing the proper protecting groups −OH, −CHO, and −NH2 groups have been incorporated onto the polymer ends. The main advantage of this method is that it allows for the in situ functionalization of regioregular polythiophene, generating a variety of end-capped polymers in one step. This approach is advantageous in comparison to previously reported methods because it is not only reliable but also highly versatile and highly efficient.

A facile one‐step synthetic method to functionalize regioregular polythiophene is described (see Figure). End‐group functionalization leads to a number of new uses for these polymers including end‐group‐driven self‐assembly onto surfaces and into conducting polymer networks, and their use as building blocks for the synthesis of block copolymers.

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