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基于氟代苯并咪唑配体的绿光铱配合物的合成与表征 被引量:1

Synthesis and Characterization of a Green-Emitting Iridium Complex Based on Fluorinated Benzoimidazole Ligand
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摘要 基于一种氟代的配体2-(4'-氟苯基)-1-苯基-苯并咪唑,在高温(>200℃)条件下直接合成了经式绿光铱配合物mer-Ir(FPBI)3,并通过1H NMR和单晶X射线衍射分析确定了其经式构型。不同于以前报道的具有经式构型的铱配合物(<0.1),mer-Ir(FPBI)3在甲苯溶液中的光致发光量子效率高达0.46。应用该配合物制备了高效磷光有机电致发光器件,最大电流效率和外量子效率分别为38.5 cd/A和11.8%,色坐标为(0.29,0.58)。 On the basis of a fluorinated ligand, namely 2-( 4'-fluorophenyl )-1-phenyl-benzoimidazole, a green-emitting iridium complex mer-Ir(FPBI) 3 with meridional configuration has been successfully synthesized under a temperature higher than 200 ~C, which is confirmed by both 1H NMR and single crystal X-ray diffraction analysis. Different from previously-reported meridional iridium complexes ( 〈 0. 1 ) , noticeably, mer-Ir( FPBI )3 shows a photoluminescent quantum yield as high as 0. ,$6. Therefore, highly efficient phosphorescent organic light-emitting diodes (PhOLEDs) are realized by tuning the doping concentration of mer-Ir( FPBI )3 into 4, 4'-N, N'-diearbazolebiphenyl (CBP), revealing a maximum current efficiency of 38.5 ed/A(11. 8% ) with the corresponding Commission Internationale de L'Eelairage(CIE) coordinates of (0.29, 0.58).
出处 《应用化学》 CAS CSCD 北大核心 2014年第10期1177-1184,共8页 Chinese Journal of Applied Chemistry
基金 国家重点基础研究发展计划(973计划)(2009CB623601) 国家自然科学基金资助项目(21174144 21204084 51322308和91333205)~~
关键词 经式构型 铱配合物 光致发光量子效率 磷光有机电致发光器件 meridional configuration, iridium complex, photoluminescent quantum yield, phosphorescent organic light-emitting diodes
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参考文献16

  • 1Baldo M A,O′Brien D F,You Y,et al.Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices[J].Nature,1998,395(6698):151-154.
  • 2Fan C H,Sun P,Su T H,et al.Host and Dopant Materials for Idealized Deep-Red Organic Electrophosphorescence Devices[J].Adv Mater,2011,23(26):2981-2985.
  • 3Tanaka D,Sasabe H,Li Y J,et al.Ultra High Efficiency Green Organic Light-Emitting Devices[J].Jpn J Appl Phys,2007,46(1/3):L10-L12.
  • 4Su S J,Gonmori E,Sasabe H,et al.Highly Efficient Organic Blue-and White-Light-Emitting Devices Having a Carrier-and Exciton-Confining Structure for Reduced Efficiency Roll-Off[J].Adv Mater,2008,20(21):4189-4194.
  • 5Tamayo A B,Alleyne B D,Djurovich P I,et al.Synthesis and Characterization of Facial and Meridional Tris-Cyclometalated Iridium(Ⅲ) Complexes[J].J Am Chem Soc,2003,125(24):7377-7387.
  • 6Yang C H,Fang K H,Chen C H,et al.High Efficiency mer-Iridium Complexes for Organic Light-Emitting Diodes[J].Chem Commun,2004,(19):2232-2233.
  • 7Holmes R J,Forrest S R,Sajoto T,et al.Saturated Deep Blue Organic Electrophosphorescence Using a Fluorine-Free Emitter[J].Appl Phys Lett,2005,87(24):243507.
  • 8Ding J Q,Gao J,Cheng Y X,et al.Highly Efficient Green-Emitting Phosphorescent Iridium Dendrimers Based on Carbazole Dendrons[J].Adv Funct Mater,2006,16(4):575-581.
  • 9Fehnel E A.Friedlander Syntheses with o-Aminoaryl Ketones.Ⅰ.Acid-Catalyzed Condensations of o-Aminobenzophenone with Ketones[J].J Org Chem,1966,31(9):2899-2902.
  • 10Dedeian K,Djurovich P I,Garces F O,et al.A New Synthetic Route to the Preparation of a Series of Strong Photoreducing Agents:fac Tris-Ortho-Metalated Complexes of Iridium(Ⅲ) with Substituted 2-Phenylpyridines[J].Inorg Chem,1991,30(8):1685-1687.

二级参考文献18

  • 1Baldo M A,Lamansky S,Burrows P E, et al. Appl Phys Lett[J] ,1999,75:4.
  • 2Jason D,Slinker,Alon A, et al. J Am Chem Soc[J] ,2004,126:2 763.
  • 3Lo S C,Namdas E B,Burn P L, et al. Macromolecules[J] ,2003,36:9 721.
  • 4Baldo M A,O'Brien D F,You Y, et al. Nature[J] ,1998,395:151.
  • 5Adachi C,Baldo M A,Thompson M E, et al. J Appl Phys[J] ,2001,90:5 048.
  • 6Lamamsky S,Djurovich P,Thompson M E, et al. JAm Chem Soc[J] ,2001,123:4 304.
  • 7Ostrowski J C,Robinson M R,Heeger A, et al. Chem Commun[J] ,2002:784.
  • 8Tsuzuki N,Shirasowa T,Suzuki, et al. Adv Mater[J] ,2003,15:1 455.
  • 9Andrade B W D,Thompson M E,Forrest S R, et al. Adv Mater[J] ,2002,14:147.
  • 10Andrade B W D,Brooks J,Thompson M E, et al. Adv Mater[J] ,2002,14:1 032.

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