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一种可溶喹吖啶酮衍生物LB膜的光谱特性 被引量:1

Spectral Properties of a Novel Soluble Quinacridone Derivative Langmuir-blodgett Films
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摘要 采用表面压-分子面积(π-A)等温曲线、紫外-可见吸收谱和荧光光谱的方法研究了一种喹吖啶酮衍生物材料LB膜的制备及其光谱特性。实验表明,这种喹吖啶酮衍生物能够在水面上形成稳定的单分子膜,它与花生酸(AA)混合后不仅可以形成很好的单分子膜,而且可以较好的转移到固体基片上制备成LB膜多层膜。这种喹吖啶酮衍生物LB膜的紫外-可见吸收谱的吸收峰位较稀溶液发生了红移,这是由极性溶剂分子与其相互作用的结果。其溶液有很强的荧光效应,但LB膜没有荧光现象,原因是在LB膜中QACl6的浓度过高发生“自我猝息”而失光。它在溶液和LB膜中都是以单体的形式存在。 Spectral properties of a novel soluble quinaeridone derivative (QAC16) Langmuir- Blodgett (LB) films were investigated by using the surface pressure- molecule area (π-A) isotherm line, UV - visible absorption spectra and fluorescence spectra method. The experimental results demonstrated that novel soluble quinacridone derivative could form well stable monolayer on subphase surface. The mixed QAC16/arachidic acid not only could form well stable monolayer, but also could be transferred to solid substrate and deposited LB multilayers. The peak wavelength of UV - visible absorption spectra in LB film were red- shifted from the solution absorption spectra due to QAC16 molecule and polarity solvent molecule interaction. The solution of QAC16 have higher fluorescence quantum field. However, the LB films of QAC16 have very lower fluorescence quantum field, because of the higher concentration in LB films, Which lead to fluorescence quenching. QAC16 molecules are monomer formation in both dilute solution and Langmuir- Blodgett films.
出处 《光散射学报》 2006年第2期168-172,共5页 The Journal of Light Scattering
基金 国家高技术研究发展计划(863计划 编号:2004AA32G090) 山东省自然科学基金项目(编号:Y2003A02)
关键词 喹吖啶酮衍生物 Langmuir—Blodgett膜 紫外-可见吸收光谱 荧光光谱 Quinaeridone derivative Langmuir- Blodgett films UV- visible absorption spectra Fluorescence spectra
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参考文献7

  • 1Zasadzinski J A,Viswanathan R,Madsen L.et al.Langmuir-Blodgett films[J].Science.1994,263:1726-1733.
  • 2Roberts G.,Langmuir-Blodgett Films[M].Plenum Press.New York:1990,20-35.
  • 3董声雄.LB累积层膜的气体传质研究[J].福州大学学报(自然科学版),1993,21(1):88-92. 被引量:2
  • 4Labana S S,Labana L L.Quinacridones[J].Chem.Reviews,1967,67:1-18.
  • 5Jabbour G E,Kawabe Y,Shaneen S E,et al.Highly efficient and bright organic electroluminescent devices with an aluminum cathode[J].App.Phys.Lett.,1997,71:1762-1764.
  • 6Tomide M,Kusabayashi S,Yokoyama M,.Organic solar cell fabricationusing quinacridone pigment[J].Chem.Lett.,1987,16:609-612.
  • 7Pei-Hua Liu,He Tian,Chen-Pin Chang,Luminescence properties of novel soluble quinacridones[J].J.Photochemistry and Photobiology A:Chemistry,2000,137:99-104.

二级参考文献1

  • 1[日]中垣正幸 编,许景文,严忠.膜学入门[M]上海科学技术文献出版社,1984.

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同被引文献18

  • 1张慧东,张萍,孙迎辉,叶开其,张晶莹,王悦.喹吖啶酮衍生物/介孔分子筛MCM-41组装体的金属离子传感性能研究[J].高等学校化学学报,2006,27(3):506-509. 被引量:4
  • 2时东霞,季威,贺晓波,高利,程志海,杜世萱,庞世瑾,高鸿钧.通过不同烷基链取代调控喹吖啶酮分子在Ag(110)表面上的自组织结构[J].物理,2007,36(1):11-14. 被引量:1
  • 3高学喜,王文军,刘云龙,毛德伟,陶绪泉,李淑红,李云.两种偶氮苯化合物LB膜的光谱与非线性光学特性[J].中国激光,2007,34(9):1276-1281. 被引量:5
  • 4W.Herbst,K.Hunger.Industrial Organic Pigments(3rdedition)[M].Weinheim:Wiley-VCH,2004.
  • 5Julius Jackson,Westfield.Particle Size Reduction ofQuinacridone and Phthalocyanine Pigments[P].US Patent:3030370,1962.
  • 6Herman Gerson,F.John,C.Vincent.Preparation ofQuinacridone Pigments[P].US Patent:3257405,1966.
  • 7S.S.Labana,L.L.Labana.Quinacridones[J].Chem.Rev.,1967,67(1):1~18.
  • 8Kaiqi Ye,Jia Wang,Hui Sun et al..Supramolecular structuresand assembly and luminescent properties of quinacridonederivatives[J].J.Phys.Chem.B,2005,109(16):8008~8016.
  • 9S.E.Shaheen,B.Kippelen,N.Peyghambarian et al..Energyand charge transfer in organic light-emitting diodes:a solublequinacridone study[J].J.Appl.Phys.,1999,85(11):80~98.
  • 10Takeo Wakimoto,Yoshinobu Yonemoto,Jun Funaki et al..Stability characteristics of quinacridone and coumarin molecules asguest dopants in the organic LEDs[J].Synthetic Metals,1997,91(1-3):15~19.

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