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Sythesis of a novel unsymmetrical photochromic diarylethene compound bearing indole unit

机译:带有吲哚单元的新型不对称光致变色二芳基乙烯化合物的合成

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A novel unsymmetrical diarylethene derivative bearing both indole and thiophene moieties, in which 1,3-dithiolpentane group was substituted at the meta-positions of the terminal phenyl ring, was synthesized. At the same time, its photochromic properties and fluorescence switch were investigated in detail. The results showed that this compound exhibited reversible photochromism, undergoing reversible cyclization and cycloreversion reactions upon alternating irradiation with UV and visible light both in solution and in PMMA film, and its absorption maxima were observed at 584 nm in hexane and at 607 nm in PMMA amorphous film, respectively, upon irradiation with 297 nm UV light. The fluorescence intensity of diarylethene decreased dramatically along with the photochromism from open-ring isomer to closed-ring isomer upon irradiation with 297 nm UV light in PMMA. In hexane solution, the open-ring isomer of the diarylethene 1 exhibited relatively strong fluorescence at 426 nm when excited at 350 nm. This new photochromic system also exhibited remarkable optical storage character.
机译:合成了同时带有吲哚和噻吩部分的新型不对称二芳基乙烯衍生物,其中在末端苯环的间位取代了1,3-二硫代戊烷基。同时,对其光致变色性质和荧光开关进行了详细研究。结果表明,该化合物在溶液和PMMA膜中交替照射紫外线和可见光后,表现出可逆的光致变色,并经历可逆的环化和环还原反应,在己烷中584 nm和在PMMA非晶态中的607 nm处观察到其最大吸收。分别在297 nm的紫外线下照射。在PMMA中用297 nm紫外光照射时,二芳基乙烯的荧光强度随开环异构体到闭环异构体的光致变色而显着降低。在己烷溶液中,当在350 nm激发时,二芳基乙烯1的开环异构体在426 nm处显示出较强的荧光。这种新的光致变色系统还表现出卓越的光学存储特性。

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