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Functional star-shaped tris(triazolyl)triazines: columnar liquid crystal, fluorescent, solvatofluorochromic and electrochemical properties

机译:功能性星形三(三唑基)三嗪:柱状液晶,荧光,溶剂氟致变色和电化学性质

摘要

Columnar liquid crystals with a C3 star-shaped heteroaromatic nitrogen-rich core, i.e. 2,4,6-tris(1′,2′,3′-triazol-4′-yl)-1,3,5-triazine (TTT), that show luminescence and solvatofluorochromism, and are also electron-acceptors are described. The core has been extended with polyalkoxybenzoyloxyphenyl groups situated at the 1 position of the 1,2,3-triazole rings to obtain molecules with three, six or nine n-decyloxy chains (series TB) or three, six or nine (S)-3,7-dimethyloctyloxy chains (series TB*). The preparation of the target compounds involved a copper-catalysed alkyne–azide cycloaddition (CuAAC) “click chemistry” procedure with a 1,3,5-triazine precursor and aromatic azides and this proved to be a versatile way to functionalise the periphery of the heteroaromatic core. Comparison of these compounds and those bearing polyalkoxyphenyl substituents (series T) has led to a deeper understanding of the self-assembly of the compounds with the TTT core. It was found that they self-organise into columnar mesophases, in which two molecules with a low-symmetry conformation occupy on average a columnar stratum. These molecules tend to adopt a polar conformation instead of the apolar C3 conformation and arrange in an antiparallel assembly. For some compounds the molecules in this arrangement have enough flexibility to tilt upon lowering temperature or by applying an electric field. Interestingly, the hexagonal columnar arrangement is preserved in a glassy state at room temperature. Furthermore, the mesophases show luminescence in the blue region of the visible spectrum depending on the peripheral substitution and molecular structure. We also report a novel property of TTT compounds (series T, TB and TB*) as they are able to act as solvatofluorochromic probes, a property that allowed us to estimate the overall polarity of the liquid crystalline medium. An aromatic azide precursor was also found to be mesomorphic and exhibited a monolayer SmA mesophase.
机译:具有C3星形杂芳族富氮核的柱状液晶,即2,4,6-tris(1',2',3'-三唑-4'-基)-1,3,5-三嗪(TTT) ),其显示出发光和溶剂氟致变色现象,并且也是电子受体。用位于1,2,3-三唑环1位的聚烷氧基苯甲酰氧基苯基扩大了核心,以获得具有三个,六个或九个正癸氧基链(TB系列)或三个,六个或九个(S)-的分子3,7-二甲基辛氧基链(TB *系列)。目标化合物的制备涉及铜催化的炔-叠氮化物环加成(CuAAC)“点击化学”步骤,以及1,3,5-三嗪前体和芳族叠氮化物的合成,这被证明是一种功能广泛的方法,可用于对化合物的外围进行功能化杂芳族核心。这些化合物与带有聚烷氧基苯基取代基的化合物(T系列)的比较使人们对具有TTT核的化合物的自组装有了更深入的了解。发现它们自组织成柱状中间相,其中两个具有低对称构象的分子平均占据柱状层。这些分子倾向于采用极性构型而不是非极性C3构型,并以反平行的方式排列。对于某些化合物,这种排列方式的分子具有足够的柔韧性,可以在降低温度或通过施加电场时倾斜。有趣的是,六方柱状排列在室温下保持玻璃态。此外,中间相取决于外围取代和分子结构而在可见光谱的蓝色区域显示发光。我们还报告了TTT化合物(T,TB和TB *系列)的新颖特性,因为它们能够用作溶剂型荧光致变色探针,该特性使我们能够估算液晶介质的整体极性。还发现芳族叠氮化物前体是同构的,并表现出单层SmA中间相。

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