0000000000400405
AUTHOR
James A. Rego
Synthesis and Characterization of Fluorescent, Low-Symmetry Triphenylene Discotic Liquid Crystals: Tailoring of Mesomorphic and Optical Properties
A series of monofunctionalized triphenylene-based discotic liquid crystals were synthesized starting from 2-hydroxy-3,6,7,10,11-pentakis(pentyloxy)triphenylene. These compounds are unique in that they possess a single electron-withdrawing group (and consequently a large dipole moment) connected directly to the polyaromatic core. All of the new liquid crystals show a significantly broader range of mesogenicity relative to the parent compound 2,3,6,7,10,11-hexakis(pentyloxy)triphenylene. Moreover, some of the new mesogens exhibit a more ordered mesophase relative to the hexagonal columnar phase (Dh) at lower temperatures. Monofunctionalization of the triphenylene core has a dramatic effect on…
Synthesis of New Functionalized Discotic Liquid Crystals for Photoconducting Aplications
Abstract The columnar structure of discotic liquid crystals has been shown to be well suited for electronic transport parallel to the columnar axis. To tailor the processibility and mesophase behavior of such materials, several hydroxytriphenylene derivatives were synthesized. These hydroxytriphenylenes can be converted into oligomers, networks or polymers. Further, they can be reduced to arenes which posses reactive sites for classical aromatic substitutions. A number of mixed tail triphenylene derivatives and fluorescent, low symmetry triphenylene discotic liquid crystals were synthesized and characterized.