Neil S. Oxtoby

TL;DR: In this paper, the authors report on mobilities up to 3.6 cm 2 /V s in organic field effect transistors (OFETs) with solution-processed dithiophene- and dibenzo-tetrathiafulvalene (DT- and DB-TTF) single crystals as active materials.

TL;DR: In this article, a series of growth experiments, from vapour or from solution, in films and in the bulk phase, describing the variety of transformations which occur among the different phases and their mixing, also at a micrometric scale.

TL;DR: It is demonstrated that an ionic tetrathiafulvalene (TTF) semiconductor can be directed from a macroscopic liquid solution and selectively deposited onto predefined nanoscale regions of a 1 cm(2) silicon chip with an accuracy of 40 nm.

TL;DR: In this article, a novel synthesis to prepare DT-TTF was described, which involves the coupling of a 1,3-dithiol-2-one and a 1.5-Dithiophene-tetrathiafulvalene.

TL;DR: In this paper, a method for obtaining derivatives of dichalcogenophene-tetrachalcogeneofulvalene and to the use thereof, said method comprising a coupling reaction using at least one ketone (III), which may be identical or different, in the presence of a coupling agent (II) in order to produce a derivative having general formula (I).