2006Chemistry of MaterialsOpen access

H-Bond-Stabilized Triphenylene-Based Columnar Discotic Liquid Crystals

I. Paraschiv, Marcel Giesbers, Barend van Lagen, Ferdinand C. Grozema, Ruben D. Abellón, Laurens D. A. Siebbeles, Antonius T. M. Marcelis, Han Zuilhof, Ernst J. R. Sudhölter

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Abstract

A 1,3,5-benzenetrisamide with three pending hexaalkoxytriphenylene groups has been synthesized as an example of an interesting class of intermolecular H-bond-stabilized columnar discotic liquid crystalline materials. The material forms a plastic hexagonal discotic phase that does not crystallize on cooling from the isotropic phase, even after annealing for a few days at room temperature. X-ray and computational studies provide a detailed model for the organization of this material. The charge carrier mobility, 0.12 cm 2 V - 1 s - 1 at 180 °C, is the highest ever reported for liquid crystalline triphenylene systems, and even increases with temperature. The factors responsible for this behavior are discussed.

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What this paper is about

A 1,3,5-benzenetrisamide with three pending hexaalkoxytriphenylene groups has been synthesized as an example of an interesting class of intermolecular H-bond-stabilized columnar discotic liquid crystalline materials. The material forms a plastic hexagonal discotic phase that does not crystallize on cooling from the isotropic phase, even after annealing for a few days at room temperature. X-ray and computational studies provide a detailed model for the organization of this material. The charge carrier mobility, 0.12 cm 2 V - 1 s - 1 at 180 °C, is the highest ever reported for liquid crystalline triphenylene systems, and even increases with temperature. The factors responsible for this behavior are discussed.

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Available abstract

A 1,3,5-benzenetrisamide with three pending hexaalkoxytriphenylene groups has been synthesized as an example of an interesting class of intermolecular H-bond-stabilized columnar discotic liquid crystalline materials. The material forms a plastic hexagonal discotic phase that does not crystallize on cooling from the isotropic phase, even after annealing for a few days at room temperature. X-ray and computational studies provide a detailed model for the organization of this material. The charge carrier mobility, 0.12 cm 2 V - 1 s - 1 at 180 °C, is the highest ever reported for liquid crystalline triphenylene systems, and even increases with temperature. The factors responsible for this behavior are discussed.

Key concepts: Triphenylene, Discotic liquid crystal, Columnar phase, Materials science, Crystallography, Annealing (glass), Phase (matter), Intermolecular force

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