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新型二甲基硅双醛腙类化合物的合成与表征

Synthesis and characterization of novel dimethylsilane dialdehyde hydrazones
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摘要 由二(4′-甲酰肼基苯基)-二甲基硅烷与苯甲醛、4-乙氧基苯甲醛和4-己氧基苯甲醛为原料经缩合反应合成了一系列含有Si的双醛腙类化合物。通过红外、核磁和飞行时间质谱确定其结构;通过紫外、荧光、热重以及差示扫描量热对化合物的性能进行表征。测试结果表明其最大吸收波长在305~320nm之间,溶液中荧光发射波长处于378~423nm之间,固态时荧光发射波长处于387~441nm之间,荧光量子产率在0.38~0.44之间。在热稳定性方面,其热分解温度均大于300℃,熔点在210℃以上,且玻璃态转化温度在139~200℃之间,具有良好的热稳定性。 4,4′-(dimethylsilanediyl)di(benzohydrazide)and benzaldehyde,4-ethoxy benzaldehyde,4-hexyloxy benzaldehyde as starting materials were used to synthesize a series of silicon-linked dialdehyde hydrazone compounds by the condensation reaction.The compounds were characterized by FT-IR,NMR,TOF,UV-Vis,fluorescence spectroscopy,TGA and DSC.The photophysical properties of target compounds showed that the maximum absorption wavelengths ranged from-305 nm to 320 nm,the maximum emission wavelengths in DMF were between 378 nm and 423 nm,the maximum emission wavelengths in solid state were at about 387-441nm,the fluorescence quantum yields were from 0.38 to 0.44.The thermal decomposition temperature of compounds were more than 300℃ and their melting points were all above 210℃ and their glass transition temperature were between 139 and 200℃ which showed that their thermal stability were good.
出处 《化工新型材料》 CAS CSCD 北大核心 2017年第2期98-100,共3页 New Chemical Materials
基金 国家自然科学基金(21442004) 吉林省科技厅自然科学基金(20101548)
关键词 双醛腙 合成 荧光 silicon dialdehyde hydrazone synthesis fluorescence
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  • 1Kim J.S.,Quang D.T..Chem.Rev.[J],2007,107(9):3799-3780. 被引量:1
  • 2Que E.L.,Domaille D.W.,Chang C.J..Chem.Rev.[J],2008,108(5):1517-1549. 被引量:1
  • 3Avirah R.R.,Jyothish K.,Ramaiah D..J.Org.Chem.[J],2008,73(1):274-279. 被引量:1
  • 4Zeng L.,Miller E.W.,Pralle A.,Isacoff E.Y.,Chang C.J..J.Am.Chem.Soc.[J],2006,128(1):10-11. 被引量:1
  • 5Sukhdeep K.,Subodh K..Tetrahedron Lett.[J],2004,45(26):5081-5085. 被引量:1
  • 6Kumar S.,Singha P.,Kaura S..Tetrahedron[J],2007,63(19):11724-11732. 被引量:1
  • 7Liang F.,Hu J.X.,Zhang L.D.,Hu Y.F.,Hu H.W..J.Heterocyclic Chem.[J],2001,38(4):853-857. 被引量:1
  • 8Sippl W..Bioorg.Med.Chem.[J],2002,10:3741-3755. 被引量:1
  • 9Sayah B.,Pelloux-Leon N.,Vallee Y..J.Org.Chem.[J],2000,65:2824-2826. 被引量:1
  • 10Hu J.X.,Jiang X.,He T.,Hu Y.F.,Hu H.W..J.Chem.Soc.,Perkin Trans.1[J],2001,15:1820-1825. 被引量:1

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