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Synthesis, supramolecular structures and luminescent properties of quinacridone derivatives bearing carbazole groups

Synthesis, supramolecular structures and luminescent properties of quinacridone derivatives bearing carbazole groups
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摘要 The syntheses of three carbazyl-containing quinacridone derivatives, N,N’-di((N-carbazyl)-n-butyl) quinacridone (DCBQA), N,N’-di((N-carbazyl)-n-hexyl)quinacridone (DCHQA) and N,N’-di((N-carbazyl)-n-octyl)quinacridone (DCOQA), are reported, and the photoluminescent (PL) characteristics are pre- sented. The single crystal X-ray structures of DCBQA, DCHQA and DCOQA are investigated. The crystal of DCBQA is characterized by intermolecular π…π interactions between quinacridone cores and carbazole moieties resulting in the formation of DCBQA molecule layer, in which every quinacridone core is surrounded by four carbazole groups. In DCHQA crystal, molecules assemble into two kinds of oriented columns based on intermolecular π…π interactions between quinacridone cores. The DCOQA crystal displays intermolecular CH…π and hydrogen bonding interactions feature. In DCOQA solid, every quinacridone core is sandwiched by two alkyl chains from two adjacent DCOQA molecules and simultaneously linked together with two other quinacridone cores by hydrogen bonding interactions. The PL spectra of the three compounds in solution exhibit concentration-dependent properties and their PL quantum causes decrease with the increasing concentration. The syntheses of three carbazyl-containing quinacridone derivatives, N,N'-di((N-carbazyl)-n-butyl) quinacridone (DCBQA), N,N'-di((N-carbazyl)-n-hexyl)quinacridone (DCHQA) and N,N'-di((N-carbazyl)-n-octyl)quinacridone (DCOQA), are reported, and the photoluminescent (PL) characteristics are presented. The single crystal X-ray structures of DCBQA, DCHQA and DCOQA are investigated. The crystal of DCBQA is characterized by intermolecular TT TT interactions between quinacridone cores and carbazole moieties resulting in the formation of DCBQA molecule layer, in which every quinacridone core is surrounded by four carbazole groups. In DCHQA crystal, molecules assemble into two kinds of oriented columns based on intermolecular TT TT interactions between quinacridone cores. The DCOQA crystal displays intermolecular CH TT and hydrogen bonding interactions feature. In DCOQA solid, every quinacridone core is sandwiched by two alkyl chains from two adjacent DCOQA molecules and simultaneously linked together,with two other quinacridone cores by hydrogen bonding interactions. The PL spectra of the three compounds in solution exhibit concentration-dependent properties and their PL quantum causes decrease with the increasing concentration.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2009年第10期1677-1684,共8页
基金 Supported by the National Natural Science Foundation of China (Grant Nos. 50773027 and 5073302) National High Technology Research and Development Program of China (Grant No. 2006AA03A162)
关键词 吖啶酮衍生物 超分子结构 发光性能 合成 咔唑 氢键相互作用 喹吖啶酮 浓度依赖性 supramolecular chemistry quinacridone carbazole luminescence
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参考文献10

  • 1Lee E C,Kim D K,Jurecka P, et al.Understanding of assembly phenomena by aromatic-aromatic interactions: benzene dimmer and the substituted systems[].Journal of Physical Chemistry A.2007
  • 2Koren A B,Curtis M D,Kampf J W.Crystal engineering of conju- gated oligomers and the spectral signature of π stacking in conjugated oligomers and polymers[].Chemistry of Materials.2000
  • 3Harder S.Can CH/pi bonding be classified as hydrogen bonding? A systematic investigation of CH-C(pi) bonding to cyclopentadienyl anions[].Chemistry A European Journal.1999
  • 4Shi J,Tang C W.Doped organic electroluminescent devices with improved stability[].Applied Physics.1997
  • 5Steiner T.The hydrogen bond in the solid state[].Angewandte Chemie International Edition.2002
  • 6Hiramoto M,,Kawase S,Yokoyama M.Photoinduced hole injection multiplication in p-type quinacridone pigment films[].Japanese Journal of Applied Physics.1996
  • 7Shichiri T,Suezaki M,Inoue T.Three-layer organic solar cell[].Chemistry Letters.1992
  • 8Nakahara H,Kitahara K,Nishi H, et al.Orientation control of quina-cridone derivatives with long alkyl chains in Langmuir-Blodgett films[].Chemistry Letters.1992
  • 9Hiroo Nakahara and Kiyoshige FukudaMasaaki Ikeda,Kiyoshi Kitahara and Hisao Nishi.Langmuir-Blodgett films of polyheterocyclic compounds with long alkyl chains[].Thin Solid films.1992
  • 10Shaheen S E,Kippelen B,Peyghambarian N,et al.Energy and charge transfer in organic-light emitting diodes:A solu- ble quinacridone study[].Journal of Applied Physics.1999

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