Low clearing asymmetric BTBT mesogen with perfect ambipolar charge transport
Abstract
Two new asymmetrically substituted BTBT mesogens were successfully synthesised. These mesogens were designed to achieve low melting and clearing temperatures via the decoration with swallow-tailed chains containing peripheral siloxane units. The aromatic endgroups (phenyl and phthalonitrile) impact significantly on the bilayer smectic self-assembly. For both materials the aromatic units intercalate completely into double layers, but the phenyl derivative generates a SmC phase and the phthalonitrile derivative a SmA phase. The latter is a weak donor-acceptor system showing outstanding charge transport properties in the mesophase. It exhibits perfectly balanced ambipolar charge carrier mobility in the range of 10-2 cm2V-1s-1 resulting in the material extremely promising for organic electronic applications.
- This article is part of the themed collection: Honorary collection in memory of Professor Dr Helmut Ringsdorf