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首页> 外文期刊>RSC Advances >Synthesis and spectroscopic properties of propeller type 2,4,6-tri(anthracen-9-yl)-1,3,5-triazine
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Synthesis and spectroscopic properties of propeller type 2,4,6-tri(anthracen-9-yl)-1,3,5-triazine

机译:螺旋桨类型2,4,6-三(蒽-9-基)-1,3,5-三嗪的合成及光谱性质

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摘要

The novel propeller type compound, 2,4,6-tri(anthracen-9-yl)-1,3,5-triazine (TAT) with C3 symmetry was synthesized by using 9-anthryl lithium with 1,3,5-trichlorotriazine or 2-chloro-4,6-dimethoxy-1,3,5-triazine in the presence of palladium catalyst in 22-48% yield. Another two propeller-like compounds, 2-(anthracen-9-yl)-4,6-dimethoxy-1,3,5-triazine (3) and 2,4-di(anthracen-9-yl)-6-methoxy-1,3,5-triazine (4) were obtained at the same time. The propeller type structures of TAT, 3 and 4 were confirmed by crystal analysis and theoretical calculations. The intramolecular C-C bond rotations between the anthryl groups and the triazine units in molecules TAT, 3 and 4 were regarded as the key factor to understand their spectroscopic behaviors in fluid medium and rigid solution.
机译:新型螺旋桨型化合物2,4,6-三(蒽-9-基)-1,3,5-三嗪(TAT)是通过9-蒽锂与1,3,5-三氯三嗪合成的或在钯催化剂存在下2-氯-4,6-二甲氧基-1,3,5-三嗪的产率为22-48%。另外两种螺旋桨状化合物,2-(蒽-9-基)-4,6-二甲氧基-1,3,5-三嗪(3)和2,4-二(蒽-9-基)-6-甲氧基同时获得-1,3,5-三嗪(4)。通过晶体分析和理论计算确定了TAT,3和4的螺旋桨式结构。 TAT,3和4分子中蒽基和三嗪单元之间的分子内C-C键旋转被认为是了解它们在流体介质和刚性溶液中的光谱行为的关键因素。

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