期刊文献+

微波辐射法合成喹喔啉铱(Ⅲ)配合物及其发光性质 被引量:2

Microwave-Assisted Synthesis and Photoluminescence of Iridium(Ⅲ) Quinoxaline Complex
下载PDF
导出
摘要 采用微波辐射加热方法,将2,3-二苯基喹喔啉(DPQ)与水合三氯化铱(IrCl3.H2O)反应,合成了一种新型三环喹喔啉铱配合物[Ir(DPQ)3],通过元素分析、1HNMR和质谱方法对配合物结构进行了表征,并初步研究了配合物的吸收光谱和荧光光谱。结果表明,配合物Ir(DPQ)3在387和458nm处存在单线态1MLCT和三线态3MLCT(金属到配体的电荷跃迁)的吸收;在634nm处有较强的金属配合物三线态的磷光发射。 Microwave-assisted synthesis of a novel cyclometalated iridium(Ⅲ ) quinoxaline complex with the formula Ir( DPQ)3 (DPQ = 2,3-diphenylquinoxaline ) was performed via the reaction of DPQ and iridium trichloride hydrate. The complex was characterized by elemental analysis, 1H NMR and mass spectrometry. The complex shows strong J MLCT ( singlet metal to ligand charge-transfer) absorption at 387 and 3 MLCT (triplet metal to ligand charge-transfer) absorption at 458 nm, respectively. The complex also shows strong photoluminescence at 634 nm at room temperature. These results suggest that the complex is a promising phosDhorescent material.
出处 《应用化学》 CAS CSCD 北大核心 2009年第7期863-865,共3页 Chinese Journal of Applied Chemistry
基金 辽宁省自然科学基金(20051023)资助项目
关键词 磷光材料 喹喔啉铱配合物 三线态 微波合成 phosphorescent material,iridium quinoxaline complex, triplet, microwave-assisted synthesis
  • 相关文献

参考文献13

  • 1Baldo M A,O'Brien D F,You Y,Shoustikov A,Thompson M E,Forrest S R. Nature[J] ,1998,395:151.
  • 2Takizawa S, Nishida J, Tsuzuki T, Tokito S, Yamashita Y. Inorg Chem [ J ] ,2007,46 (10) :4 308.
  • 3Pomestcheako I E, Luman C R, Hissler M, Ziessel R, Castellano F. Inorg Chem [ J ] ,2003,42 (5) : 1 394.
  • 4Gong X,Ostrowski J C,Bazan G C,Moses D,Heeger A J,Liu M S,Jen A K Y. Adv Mater[J] ,2003,15( 1 ) :45.
  • 5Adachi C, Kwong R C, Djurovich P, Adamovich V, Baldo M A, Thompson M E, Forrest S R. Appl Phys Lett[ J ] , 2001, 116:379.
  • 6Zhao Q,Liu S J,Shi M,Wang C M,Yu M X,Li L,Li F Y,Yi T,Huang C H. Inorg Chem[J] ,2006,45(16) :6 152.
  • 7Lamansky S, Djarovich P, Murphy D, Razzaq F A, Lee H E, Adachi C, Burrows P E, Forrest S R, Thompson M E. J Am Chem Soc[J] ,2001,123(18) :4 304.
  • 8Lo S C,Shipley C P,Bera R N,Harding R E,Cowley A R,Burn P L,Samuel I D W. Chem Mater[J] ,2006,18(21 ) :5 119.
  • 9Duan J P,Sun P P,Cheng C H. Adv Mater[J] ,2003,15(3) :224.
  • 10Takvorian A G,Combs A P. J Comb Chem[ J] ,2004,6(2) :171.

二级参考文献10

  • 1张国林 刘泽华 郭海清 啜玉涛 甄常刮 邹德春.高等学校化学学报,2004,25:397-397.
  • 2Brown, A. R. Pichler, K. Greenham, N. C. Chem. Phys. Lett. 1993, 210, 61.
  • 3Baldo, M. A. O'Brien, D. F. You, Y. Shoustikov, A. Thompson, M. E. Forrest, S. R. Nature 1998, 395, 151.
  • 4Baldo, M. A. Thompson, M. E. Forrest, S. R. Nature 2000,403, 750.
  • 5Pomestcheako, I. E. Luman, C. R. Hissler, M. Ziessel, R.Castellano, F. N. Inorg. Chem. 2003, 42, 1394.
  • 6Chen, X. W. Liao, J. L. Liang, Y. M. Ahmed, M. O. Tseng, H. E. Chen, S. A. J. Am. Chem. Soc. 2003, 125, 636.
  • 7Lamansky, S. Djarovich, P. Murphy, D. Razzaq, F. A. Kwong, R. Tsyba, I. Bortz, M. Mui, B. Bau, R. Thompson, M. E. J. Am. Chem. Soc. 2001, 123, 4304.
  • 8Duan, J. P. Sun, P. P. Cheng, C. H. Adv. Mater. 2003, 15,224.
  • 9Ohta, A. Masano, S. Iwakura, S. Tamura, A. Watahiki, H. Tsutsui, M. Akita, Y. Watanabe, T. J. Heterocycl. Chem. 1982, 19, 465.
  • 10张国林,潘献华,阚锦晴,张景辉,李永舫.导电复合材料葡萄糖氧化酶传感器的研究[J].物理化学学报,2003,19(6):533-537. 被引量:12

共引文献12

同被引文献34

  • 1张国林,郭海清,啜玉涛,邹德春.一种新型红色三线态喹喔啉铱(Ⅲ)配合物的合成及发光性质[J].化学学报,2005,63(2):143-147. 被引量:13
  • 2HE W, MEYERS M R , HANNEY B , et al. Potent qui- noxaline2Based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: the synthesis and biological activities of RPR127963 an orally bioavailable inhibitor[ J ]. Bioorg Med Chem Lett ,2003,13:3097 - 3100.
  • 3KIMY B , KIMY H , PARKJY, KIM S K. Synthesis and biological activity of new quinoxaline antibiotics of echi- nomycin analogues [ J ]. Bioorg Med Chem Lett , 2004, (14) :541 -544.
  • 4L INDSL EY C W, ZHAO Z , L EISTER W H , et al. AI- losteric Akt (PKB) inhibitors : discovery and SAR of isozyme selective inhibitors [ J ]. Bioorg Med Chem Lett , 2005, (15) :761 -764.
  • 5KIM J H , JAUNG J Y. The synthesis and optical proper- ties of meso2substituted porphyrins bearing quinoxaline de- rivatives [ J ] . Dyes andPigments ,2008, (77) :474 - 477.
  • 6DAIL EYS , FEAST WJ , PEACE R J , et al. Synthesis and device eharaeterisation of side2ehain polymer electron transport materials for organic semiconductor applications [ J ]. J Mater Chem ,2001, ( 11 ) :2238 - 2243.
  • 7Baldo MA, O'Brien DF, You Y, Shoustikov A, Sibley S, Thompson ME, Forrest SR. Highly efficient phosphorescent emission from electroluminescent devices. Nature,1998,395:151-153.
  • 8Adachi C, Baldo MA, Forrest SR, Thompson ME, Kwong RC. High-efficiency red electrophosphorescence devices. Appl Phys Lett,2001,78:1622-1624.
  • 9Xiao LX, Cheng ZJ, Qu B, Qu B, Luo JX, Kong S, Gong QH. Recent progresses on materials for electrophosphorescent organic lightemitting devices. Adv Mater,2011,23:926-952.
  • 10Tsuboyama A, Iwawaki H, Furugori M, Mukaide T, Jamatani J, Igawa S, Moriyama T, Miura S, Takiguchi T, Okada S, Hoshino M, Ueno K.Homoleptic cyclometalated iridium complexes with highly efficient red phosphorescence and application to organic light-emitting diode. J Am Chem Soc,2003,125:12971-12979.

引证文献2

二级引证文献1

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