A metal-free approach combining sulfoxide-directed metal-free C–H cross-couplings with tuneable heterocyclizations and dimerizations allows expedient access to important organic materials.

Inkjet printing of functional frequency selective surfaces (FSS) and radio frequency identification (RFID) tags on commercial paper substrates using silver nanoparticle inks sintered using low temperature thermal, plasma and photonic techniques is reported. Printed and sintered FSS devices demonstrate performances which achieve wireless communication requirements having a forward transmission scattering parameter, S₂₁, depth greater than −20 dB at 13 GHz. Printed and plasma sintered RFID tags on transfer paper, which are capable of being mounted on skin, improved read distances compared to previously reported single layer transfer RFID tags fabricated by conventional thermal sintering.

Organic field‐effect transistors (OFETs) have shown great promise for use as chemical sensors for applications that range from the monitoring of food spoilage to the determination of air quality and the diagnosis of disease. However, for these devices to be truly useful, they must deliver reliable and stable low‐voltage operation over extended timescales. An important element to address this challenge is the development of a high‐capacitance gate dielectric that delivers excellent insulation with robust chemical resistance against the solution processing of organic semiconductors (OSC). The development of a bilayer gate dielectric containing a high‐k fluoropolymer relaxor ferroelectric layer modified at the OSC/dielectric interface with a photo‐crosslinked chemically resistant low‐k methacrylate‐based copolymer buffer layer is reported. Bottom‐gate OFET chemical sensors using this bilayer dielectric operate at low‐voltage with exceptional operational stability. They deliver reliable sensing performance over multiple cycles of ammonia exposure (2 to 50 ppm) with an estimated limit‐of‐detection below 1 ppm.

A range of triphenylene and phthalocyanine‐based discotic liquid crystals (DLCs) can be aligned within micrometer‐scale channels formed from SU8 patterned on silicon or glass surfaces. The channels can be filled with the DLC in its isotropic phase using capillary action. Alignment occurs spontaneously as the sample is slowly cooled into the Col_h phase. Whilst all of these DLCs align with the columns perpendicular to the surface when they are ‘sandwiched’ between glass slides, in these channels, the DLC aligns with the column director parallel to the surface. It is also constrained to lie across the channels. The same alignment occurs when these DLCs are confined between SU8‐topped interdigitated gold electrodes where it gives the optimum orientation for electrode‐to‐electrode conduction. The quality of the alignment depends on the particular liquid crystal used and on the width of the channel. For the Col_r phase of octaoctylphthalocyanine there is additional epitaxial control over the orientation of the lattice such that the a/c face of the lattice is parallel to the surface. This is an important prerequisite for creating a bistable display device that switches by virtue of changing the direction of the tilt of the discs.