期刊文献+
任意字段
题名或关键词
题名
关键词
文摘
作者
第一作者
机构
刊名
分类号
参考文献
作者简介
基金资助
栏目信息

含芘结构基元有机光电材料的设计合成及其性质 被引量：1

Synthesis and Properties of Pyrene Derivatives for Optoelectronic Applications
下载PDF
导出
摘要 本论文就是通过Suzuki耦合反应,来合成含有芘基元的化合物1-[4-(2,2-二苯乙烯基)苯基]芘和2,8-二(1-芘)-6,12-二氢-5,11-甲基二苯[b,f][1,5]二氮芳辛。我们合成的化合物具有高效的位阻,能有效的防止π键堆积,有较好的荧光性能,其发光在蓝绿光区(430～465 nm)。 The pyrene derivatives were designed and synthesized by Suzuki coupling reaction for optoelectronic applications.With the use of large steric hindrance groups to prevent π-π aggregation,the resulting materials showed good fluorescence properties,emitting in the blue-green region（430~465 nm）.
作者 李本韩 林金辉
机构地区 成都理工大学材料与化学化工学院
出处 《广州化工》 CAS 2013年第2期65-68,共4页 GuangZhou Chemical Industry
关键词 有机电致发光 含芘结构基元 π键堆积 蓝色荧光 organic electroluminescent elements contained pyrene structure π key accumulation blue fluorescence
分类号 O622.6 [理学—有机化学]
  • 相关文献

参考文献17

  • 1刘彭义,唐振方,孙汪典.有机发光器件的研究进展及应用前景(综述)[J].暨南大学学报（自然科学与医学版）,2002,23(1):66-73. 被引量：32
  • 2Liu P Y,Tang Z F,Sun W D. Research progress and application prospects of organic electro luminescent devices[J].School journal of Jinan University,2002,(02):66-43.
  • 3尹盛,刘陈,钟志有.有机电致发光材料的研发现状[J].化工新型材料,2003,31(1):1-4. 被引量：17
  • 4Yi S,Liu C,Zhong Z Y. An organic electroluminescent light emitting material research[J].New Chemical Materials,2003,(01):1-4.doi:10.3969/j.issn.1006-3536.2003.01.001.
  • 5Lindsay F,Marc C. The bright future of organic LEDs[J].IEEE Potentials,2003,(04):64-70.
  • 6Kim S,Chun D H. Efficiency of organic light emitting diodes depending on AI based cathodes[A].Nagoya IEEE Press,2003.
  • 7Sotoyama W,Sato H,Kinoshita M. Tera-substituted pyrenes:new class of blue emitter for organic light-emitting diodes[J].SID Digest,2003.1294-1297.
  • 8Oyamada T,Akiyama S,Yahiro M. Unusual photoluminescence characteristics of tetreaphenylpyrene(TPPy) in various aggregated morphologies[J].Chemical Physics Letters,2006.295-299.
  • 9Jia W L,Liu Q D. Diarylamino functionalized pyrene derivatives for use in blue OLEDs and complex formation[J].Materials Chemistry,2004.3344-3350.
  • 10Lai S L,Tong Q X,Chan M Y. Distinct electrolumineseent ProPerties of triphenylamine derivatives in blue organic light-emitting devices[J].Materials Chemistry,2011.1206-1211.

二级参考文献29

  • 1[2]Bailey N, Information Display, 2000, 3:12
  • 2[3]YangY, HeegerAJ. ApplPhysLett, 1994, 64 (10): 1245
  • 3[4]Hatalis, Miltiadis K, Society of Photo- Optical Instrumentation Engineers (SPIE Proceedings. Vol. 3057), Bellingham, WA
  • 4[5]Van Slyke S A, Chen C H, Tang C W. Appl Phys Lett 1996, 69:2160
  • 5[6]ChoongVE, ShiS, CurlessJetal. ApplPhysLett, 1999, 75: 172
  • 6[7]Sakakibara V, Okutsu S, Enokisa T et al. Appl Phys Lett, 1999, 74:2587
  • 7[8]Jian. g X Z, Liu S, Ma H et al. Appl Phys Lett, 2000, 76: 1813
  • 8[10]Tang C W, Vanslyke S A. Appl Phys Lett, 1987, 51: 913
  • 9[11]Gu G, Parthasarathy G, Forrest S R. Appl Phys Lett, 1999, 74:305
  • 10[12]ChaoCL, ChenSA. ApplPhysLett, 1998, 73:426

共引文献37

同被引文献15

  • 1ZHAO Z, CHEN S, LAM J W Y, et al. Creation of highly efficient solid emitter by decorating pyrene core with AIE-active tetraphenylethene peripheries [ J ]. Chew Commun ,2010,46 ( 13 ) :2221 - 2223.
  • 2FIGUEIRA-DUARTE T M, DEL ROSSO P G, TRATI'NIG R S, et al. Designed suppression of aggregation in polypyrene: Toward high-performance blue-light-emitting diodes [ J ]. Adv Mater, 2010,22 (9) :990 - 993.
  • 3CHAN K L, LIM J P F, YANG X, et al. A graphene oxide platform for the assay of biomolecules based on chemilumines- cence resonance energy transfer[ J]. Chem Commun,2012,48 (1):106- 108.
  • 4TONG Q X, LAI S L, LO M F, et a|. An efficient hole-transporting blue fluorophore 3,6-dipyrenyl-9-ethylcarbazole for un- doped organic light-emitting devices [ J ]. Synth Met, 2012,162 ( 5 -6 ) :415 -418.
  • 5LI Y ,WANG D ,WANG L, et al. Novel asymmetrical pyrene derivatives as light emitting materials: Synthesis and photo- physics[ J]. J Lumin,2012,132(4) :1010 - 1014.
  • 6FENG X, HU J Y,IWANAGA F, et al. Blue-emitting butterfly-shaped 1,3,5,9-tetraarylpyrenes : Synthesis, crystal struc- tures, and photophysical properties[ J ]. Org Lett ,2013,15 (6) : 1318 - 1321.
  • 7GRIMSDALE A C, CHAN K L, MARTIN R E, et al. Synthesis of light-emitting conjugated polymers for applications in electroluminescent devices [ J ]. Chem Rev,2009,109 ( 3 ) : 897 - 1091.
  • 8SHIMIZU M, TATSUMI H, MOCHIDA K, et ah Synthesis, crystal structure, and photophysieal properties of (1 E,3E,5E)- 1,3,4,6-tetraarylhexa-1,3,5-trienes:A new class of fluorophores exhibiting aggregation-induced emission[J]. Chem Asi- an J ,2009,4 ( 8 ) : 1289 - 1297.
  • 9LO M Y,ZHEN C G,LAUTERS M, et al. Organic-inorganic hybrids based on pyrene functionalized octavinylsilsesquiox- ane cores for application in OLEDs [ J ]. J Am Chem Soc, 2007,129 (18) :5808 -5809.
  • 10WU K C, KU P J, LIN C S, et al. The photophysical properties of dipyrenylbenzenes and their application as exceedingly efficient blue emitters for electroluminescent devices [ J ]. Adv Funct Mater ,2008,18 (1) :67 -75.

引证文献1

二级引证文献1

广州化工
2013年 第2期

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部