Article ID Journal Published Year Pages File Type
5409066 Journal of Molecular Liquids 2017 11 Pages PDF
Abstract
Three novel triphenylene tetramers with triazole bridges, rigid aromatic Schiff-bases and hydrogen-bonding spacers were designed and synthesized in yield of 73-78%. Their structures were confirmed by IR, NMR and MS. Their mesomorphic properties were studied by polarizing optical microscopy, differential scanning calorimetry and X-ray diffraction. These novel triphenylene tetramers possessed the hexagonal columnar mesophase and exhibited excellent mesomorphic properties with melting points at 30-60 °C, which was first observed near room temperature for triphenylene tetramers. This study suggested that the mesomorphic properties of triphenylene oligomers could be tuned conveniently by the structures of spacers.
Related Topics
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
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