Solubilizing alkyl chains play a crucial role in the design of semiconducting polymers because they define the materials solubility and processability as well as both the crystallinity and solid-state microstructure. In this paper, we present a scarcely explored design approach by attaching the alkyl side chains on one side (cis-) or on both sides (trans-) of the conjugated backbone. We further investigate the effects of this structural modification on the solid-state properties of the polymers and on the charge-carrier mobilities in organic thin-film transistors.

The field of organic electronics is entering its commercial phase. The recent market introduction of the first prototypes based on organic transistors fabricated from solution is set to augment the existing market presence of organic light-emitting diode applications. Organic photovoltaic products are not far behind. In this article, we provide a brief overview of these devices, with our main focus being organic transistor applications. In particular, we examine some of the key performance requirements for working devices. We also review some of the important advances in semiconductor design and device fabrication techniques and discuss some of the technical challenges that remain in the optimization of next-generation products.

Until recently, the synthesis of polythiophenes using Suzuki chemistry has proven difficult because of the ready protodeborylation of thiophene boronates. However, we now report that the new generation of bulky, electron-rich Pd(0)-phosphane catalysts are effective and reliable for the preparation of regioregular polyalkylthiophenes using Suzuki coupling. Moreover, the monomers can be prepared in high yield by Ir-catalysed borylation, without the need for strong organolithium bases, making this potentially a highly functional group-tolerant approach to polyalkylthiophene derivatives. Perfluoroalkylthiophenes also undergo this reaction.

The ability of a poly(phenylene ethynylene) conjugated polyelectrolyte to detect a small molecule quencher in the solid state was assessed by coating the polymer onto a plastic-backed, non-fluorescent, silica-gel TLC plate. The efficiency of the emission quenching process was quantified by noting the resulting loss of emission with increasing quencher concentration, in accordance with the Stern-Volmer relation. The emission quenching induced by the addition of the analyte occurred with Stern-Volmer constants in the range of 103 M−1.

Organic thin film transistor (OTFT) gas sensors fabricated with an array of different active materials are monitored for shifts in performance characteristics during continuous operation over many days in both inert and ambient environments. We analyze the different patterns of degradation behavior observed in different materials and discuss approaches to decoupling a device's sensor response from its stress response.