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α-蒎烯衍生物发光配体的合成及性能研究

Synthesis and Properties of α-Pinene Novel Electroluminescence Materials
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摘要 以α-蒎烯为原料,制备3种新型有机发光材料。由α-蒎烯合成桃金娘烯醛后,分别与邻氨基苯酚、邻苯二胺、邻氨基苯硫酚缩合得到3种α-蒎烯衍生物的发光配体,即:(1-苯并噁唑)-α-蒎烯,(1-苯并咪唑)-α-蒎烯,(1-苯并噻唑)α--蒎烯。以四氢呋喃为溶剂,对它们的光谱性能进行了测试。1-(苯并噁唑)-α-蒎烯的最大吸收峰为466nm,最大发射波长为441 nm,呈黄色光;1-(苯并咪唑)-α-蒎烯的最大吸收峰为299 nm,最大发射波长为384 nm,呈蓝绿色光;1-(苯并噻唑)-α-蒎烯的最大吸收峰为302 nm,最大发射波长为368 nm,呈蓝绿色光,可作为发光材料应用于有机电致发光器件中。 Three novel organic electroluminescence materials,i.e.,1-benzoxazolyl-α-pinene,1-benzimidazolyl-α-pinene,and 1-benzothiazolyl-α-pinene,were synthesized by the oxidation of α-pinene to myrtenic aldehyde,followed by the condensation with 2-aminophenol,1,2-phenylenediamine,and 2-aminothiophenol,respectively.The results indicated that 1-benzoxazolyl-α-pinene gave a strong yellow emission with a peak at 441nm and its UV-visible spectrum peak was at 466nm,1-benzimidazolyl-α-pinene emitted a strong blue-green fluorence with a peak at 384nm and the maximum UV-visible wavelength was at 299nm,and 1-benzothiazolyl-α-pinene showed a strong blue-green light with emission peak at 302nm and its UV-visible spectrum peak was at 368nm,which made them luminescent materials in OLEDs.
出处 《化工技术与开发》 CAS 2009年第4期4-6,共3页 Technology & Development of Chemical Industry
基金 广西教育厅科研项目(006706003) 广西研究生教育创新人才联合培养基地项目 桂林工学院科研启动费资助项目
关键词 Α-蒎烯 苯并噁唑 苯并咪唑 苯并噻唑 α-pinene benzothiazole benzoxazole benzimidazole
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  • 1Z. L. Shen, P. E. Burrow, V. Bulovic, S. R. Forrest and M. E. Thompson.Three-Color, Tunable, Organic Light - Emitting Devices [ J ]. Science, 1997,276: 2009- 2011.
  • 2J.D.Slinker, A.A.Gorodetsky, M.S.Lowry, J.J.Wang, S. Parker, R. Rohl, S. Bemhard and G.G. MaUiaras. Efficient Yellow Electroluminescence from a Single Layer of a Cyclometalated Iridium Complex [ J ]. J.Am. Chem.Soc, 2004, 126 : 2763-2767.
  • 3S.C. Lo, E.B. Namdas, P.L.Burn and I.D.W.Samuel. Synthesis and Propetties of Highly Efficient Electrolumi- nescent Green Phosphorescent Iridium Cored Eendrimers [J ]. Macromolecules, 2003,36: 9721-9730.
  • 4M. A. Baldo and D. F. O'Brien. High Efficient Phosphorescent Emission from Organic Electmluminescent Devices[J ]. Nature, 1998,395 : 151-154.
  • 5D. F. O' Brien, M. A. Baldo and M. E. Thopson. High-efficency Organic Electrophosphorescent Device with Ir(ppy)3[J]. Appl. Phys. Lett,2000, 77:904- 907.
  • 6S. Lamansky, P.Djurovich, D. Murphy, F. A. Razzaq, H. E. Lee, C. Adachi, P.E. Burrows, S.R. Forrest and M.E.Thompson. Highly Phosphorescent Bis-Cyclometalated Iridium Complexes: Synthesis, Photophysical Characterization, and Use in Organic Light Emitting Diodes [J]. J. Am. Chem. Soc, 2001,123:4304-4312.
  • 7J.C.Ostrowski,M.R.Robimson,A.J.heeger and G.C.Bazan.Amorphous Iridium Complexes for Electrophosphorescent Light Emitting Devices [J]. Chem. Commun, 2002,784-785.
  • 8T.Tsuzuki, N.Shirasawa, T.Suzuki and S.Tokito. Color Tunable Organic Light-Emitting Diodes Using Pentafluorophenyl- Substituted Iridium Complexes [J]. Adv. Mater, 2003,15(17) : 1455-1458.
  • 9I. R. Laskar and T.M. Chen. Tuning of Wavelengths: Synthesis and Photophysical Studies of Iridium Complexes and Their Applications in Organic Light Emitting Devices [J ]. Chem. Mater,2004,16:111-117.
  • 10H.Z.Xie, M.W.Liu, Q.Y.Wang, X.H.Zhang, C.S.Li, L.S.Huang, S.T.Li,P.F.Teng, H.L.K wong, H.Zhang and C. M. Che. Reduction of Self- Quenching Effect in Organic Electrophosphoresoence Emitting Devices via the Use of Sterically Hindered Spacers in Phosphorescence Molecules [J]. Adv.Mater,2001, 13(16): 1245-1248.

二级参考文献32

  • 1丁国华,荆淑萍,许兆武,徐仲玉,田禾,高佳,马东阁.橙红色磷光铱配合物的合成及其性能[J].应用化学,2005,22(5):502-506. 被引量:3
  • 2Baldo M A,Lamansky S,Burrows P E, et al. Appl Phys Lett[J] ,1999,75:4.
  • 3Jason D,Slinker,Alon A, et al. J Am Chem Soc[J] ,2004,126:2 763.
  • 4Lo S C,Namdas E B,Burn P L, et al. Macromolecules[J] ,2003,36:9 721.
  • 5Baldo M A,O'Brien D F,You Y, et al. Nature[J] ,1998,395:151.
  • 6Adachi C,Baldo M A,Thompson M E, et al. J Appl Phys[J] ,2001,90:5 048.
  • 7Lamamsky S,Djurovich P,Thompson M E, et al. JAm Chem Soc[J] ,2001,123:4 304.
  • 8Ostrowski J C,Robinson M R,Heeger A, et al. Chem Commun[J] ,2002:784.
  • 9Tsuzuki N,Shirasowa T,Suzuki, et al. Adv Mater[J] ,2003,15:1 455.
  • 10Andrade B W D,Thompson M E,Forrest S R, et al. Adv Mater[J] ,2002,14:147.

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