欢迎登录材料期刊网

材料期刊网

高级检索

合成了含偶氮苯基元的对称双(噁)二唑衍生物Fn,利用IR、1 H NMR方法确认了其分子结构,用荧光光谱研究了偶氮苯基元对(噁)二唑衍生物光致发光特性的影响.F3、F6、F10的发射峰皆为双峰,分别位于348、356 nm和345、357 nm及345、357 nm,属于(噁)二唑基团的特征发射峰.偶氮苯基元的引入,对(噁)二唑衍生物Fn在溶液中的最大发射峰位影响较小,对发光强度影响较大,其发光强度大大降低.这主要是由于在光激发过程中偶氮苯基团与(噁)二唑基团间发生了分子内电子能量转移.

参考文献

[1] YU Lianhe.Studies on Synthesis,Photochromic Mechanism and Applications of Fulgides[J].Imaging Sci Photochem,1995,13(1):90-91 (in Chinese).于联合.俘精酸酐的合成、光致变色机理及应用研究[J].感光科学与光化学,1995,13(1):90-91.
[2] Navarrete-Vázquez G,Molina-Salinas G M,Duarte-Fajardo Z V,et al.Synthesis and Antimycobacterial Activity of 4-(5-Substituted-1,3,4-oxadiazol-2-yl) pyridines[J].Bioorg Med Chem,2007,15:5502-5508.
[3] Sriram D,Yogeeswari P,Madhu K.Synthesis and in Vitro and in Vivo Antimycobacterial Activity of Isonicotinoyl Hydrazones[J].Bioorg Med Chem Lett,2005,15:4502-4505.
[4] Liu J,Wang M,Li Y,et al.Photo-triggered Assembly/Disassembly of Macroscopically Ordered Monodomain Lamellar Structure in Side-chain Liquid Crystalline Polymer Containing Strong Polar Azobenzene Mesogens[J].Liq Cryst,2011,38(1):105-113.
[5] Adachi C,Tokito S,Tsutsui T,et al.Organic Electroluminescent Device with A Three-Layer Structure[J].Jpn J Appl Phys,1988,27 (3):713-715.
[6] Jung S O,Kim Y H,Kwon S K,et al.New Hole Blocking Material for Green-emitting Phosphorescent Organic Electroluminescent Devices[J].Org Electron,2007,8 (4):349-356.
[7] Xiao D.Single Standard Calibration for an Optical Oxygen Sensor Based on Luminescence Quenching of a Ruthenium Complex[J].Anal Chim Acta,2000,403:57-65.
[8] Song S Y,Jang M S,Shim H K.Highly Efficient Light-Emitting Polymers Composed of Both Hole and Electron Affinity Units in the Conjugated Main Chain[J].Macromolecules,1999,32(5):1482-1487.
[9] Jiang F,Ling; Y,Qu J Q,et al.Synthesis and Crystal Structure of A Novel Chiral 1-Methylpropargyl Ester Carrying Azobenzene Moiety[J].Chinese J Struct Chem,2010,29:146-150.
[10] Li M,Guo C W,Wu Y Q.Design and Characterization of Novel Supramolecular Liquid Crystals through Multiple Hydrogen Bonds[J].Liq Cryst,2002,29(8):1031-1037.
[11] Wang H T,Zhang F L,Li M,et al.Synthesis Liquid Crystalline Properties and Fluorescence of Polycatenar 1,3,4-Oxadiazole Derivatives[J].Liq Cryst,2008,35:905-912.
[12] Qiu H J,Li M,Chen X F.Synthesis and Properties of Two Series of H-Bonded and Non-H-Bonded Thermotropic Liquid Crystal Monomers[J].Liq Cryst,1998,25 (3):419-425.
[13] Zhang P,Xia B,Zhang Q,et al.New 1,3,4-Oxadiazole Containing Materials with the Effective Leading Substituents:The Electrochemical Properties,Optical Absorptions,and The Electronic Structures[J].Synth Met,2006,156:705-713.
[14] Speiser S.Photophysics and Mechanisms of Intramolecular Electronic Energy Transfer in Bichromophoric Molecular Systems:Solution and Supersonic Jet Studies[J].Chem Rev,1996,96 (6):1953-1976.
[15] Mu Z,Yang X,Wang Z,et al.Influence of Substituents on Two-Dimensional Ordering of Oligo (phenylene-ethynylene) s:A Scanning Tunneling Microscopy Study[J].Langrnuir,2004,20 (20):8892-8896.
[16] Tomiki Ikeda,Osumu Tsutsumi.Optical Switching and Image Storage by Means of Azobenzene Liquid-crystal Films[J].Science,1995,268:1873-1875.
[17] Luo J D,Qin J G,Hu K,et al.A Postfunctionalization Strategy to Develop PVK-Based Nonlinear Optical Polymers with a High Density of Chromophores and Improved Processability[J].Chem Mater,2001,13:927-931.
[18] Keshtov M L,Venidiktova O V,Barachevskii V A,et al.Synthesis and Photophysical Properties of Photochromic Phenylsubstituted Polyphenylenes with Main Chain Azobenzene Fragments[J].Synth Photophys Properties,2007,49 (2):288-295.
[19] Rasmussen P H,Ramanujam P S,Hvilsted S,et.al.A Remarkably Efficient Azobenzene Peptide for Holographic Information Storage[J].J Am Chem Soc,1999,121:4738-4743.
[20] ZHANG Haichao,PAN Caiyuan.Studies on Liquid Crystalline and Optical Response Behavior of Poly[X-(4'-methoxy-4-azophenyloxy) hexyl]methacrylate[J].Chem J Chinese Univ,1999,20(7):1152-1155(in Chinese).张海潮,潘才元.聚甲基丙烯酸-对-甲氧基偶氮苯氧己基酯的液晶及光响应行为[J].高等学校化学学报,1999,20(7):1152-1155.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%