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首页> 外文期刊>Journal of Fluorescence >Novel Stilbene-triazine Symmetrical Optical Brighteners:Synthesis and Applications
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Novel Stilbene-triazine Symmetrical Optical Brighteners:Synthesis and Applications

机译:新型二苯乙烯-三嗪对称荧光增白剂的合成与应用

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摘要

A series of new high light fastness, hot pressing fastness optical brighteners was efficiently synthesized by a three-step approach involving the successive replacement of the three chloro groups of 2,4,6-trichloro-1,3,5-triazine under different conditions of temperature and pH. Thus, 2,4,6-trichloro-1,3,5-triazine was treated with different anilines and the resulting dichlorotriazinyl intermediates (3a-I) were further condensed with 4,4-diaminostilbene-2,2′-disulfonic acid to afford bis-monochlorotriazine (5a-I) followed by nucleophilic substitution with ethanolamine to furnish the final hybrid brighteners (7a-I). All of the newly synthesized compounds were characterized by Fourier-Transform Infrared (FT-IR), UV-visible absorption, NMR spectroscopy and the elemental analyses. The synthesized optical brighteners were also assessed for their efficacy as fluorescent brightening agents.
机译:通过三步法有效合成了一系列新型的高耐光性,热压牢度荧光增白剂,该方法涉及在不同条件下连续置换2,4,6-三氯-1,3,5-三嗪的三个氯基团温度和pH值。因此,将2,4,6-三氯-1,3,5-三嗪用不同的苯胺处理,并将得到的二氯三嗪基中间体(3a-I)与4,4-二氨基sti-2,2'-二磺酸进一步缩合为得到双-单氯三嗪(5a-I),然后用乙醇胺进行亲核取代以提供最终的杂化增白剂(7a-I)。所有新合成的化合物均通过傅里叶变换红外(FT-IR),紫外可见吸收,NMR光谱和元素分析进行​​了表征。还评估了合成的荧光增白剂作为荧光增白剂的功效。

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