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3,5-二(2’-芳基-1’,3’,4’-噁二唑基)吡啶的合成与性质 被引量:1

Synthesis and properties of 3,5-bis(2'-phenyl-1',3',4'-oxadiazole) pyridine
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摘要 合成了3个3,5-二(2’-芳基-1’,3’,4’-噁二唑基)吡啶化合物,用1H-NMR、FT-IR、MS对其结构进行了表征。研究了它们的UV-Vis吸收光谱、荧光光谱和电化学性能,吸收光谱表明:在270~273nm出现最大吸收峰;荧光光谱表明:目标化合物的DMF溶液发射强的紫色荧光,在334~356nm出现最大发射峰;固体发射强的紫蓝色荧光,在376~402nm出现最大发射峰。电子亲和势为2.72~3.11eV,离子势为6.28~6.70eV,说明目标化合物的电子传输性能良好(PBD:EA=2.82eV)。 Three novel compounds of 3,5-bis(2'-phenyl-l',3' ,4'-oxadiazole) pyridine have been synthesized. The structures of these compounds were confirmed by 1H NMR,FT-IR and MS. their UV-Vis spectroscopy, as well as fluo- rescent spectroscopy and electrochemical properties were studied. UV-Vis spectroscopy results showed that the maximum absorptive wavdength of target compounds were detected at 270~273nm, Fluorescent spectroscopy results showed that they were found to emit strong purple fluorescence in DMF solution, the emissive maximum wavelength of target corn pounds were from 334 to 356nm; The solid of target compounds were found to emit strong purp].e and h!.ue fluorescence, the emissive maximum wavelength of target compounds were from 376nm to 402nm. The target compounds kept high affinity energy (2.72-3. lleV) and ionic potential (6.28-6.70eV), which indicated that they were potentially better mate- rials as the electron transfer (PBD2 EA=2, 82eV).
出处 《化工新型材料》 CAS CSCD 北大核心 2008年第9期29-30,36,共3页 New Chemical Materials
基金 国家自然科学基金(50568001) 江西省教育厅科技项目(2007291)
关键词 吡啶环 1 3 4-噁二唑 合成 性质 pyridine ring, 1,3,4 oxzdiazole, synthesis, property
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