Photoluminescence and electroluminescence by gallium(III) complexes of N-salicylidene-o-aminophenol and its derivatives

被引:25
作者
Kagkelari, Adamantia [2 ]
Bekiari, Vlasoula [3 ]
Stathatos, Elias [4 ]
Papaefstathiou, Giannis S. [5 ]
Raptopoulou, Catherine P. [6 ]
Zafiropoulos, Theodoros F. [2 ]
Lianos, Panagiotis [1 ]
机构
[1] Univ Patras, Dept Engn Sci, Patras 26500, Greece
[2] Univ Patras, Dept Chem, Patras 26500, Greece
[3] Technol Educ Inst Messolonghi, Dept Fisheries & Aquaculture, Mesolongion 30200, Greece
[4] Technol Educ Inst Patras, Dept Elect Engn, Patras 26334, Greece
[5] Univ Athens, Dept Chem, Inorgan Chem Lab, Zografos 15771, Greece
[6] NCSR Demokritos, Inst Mat Sci, Aghia Paraskevi 15310, Greece
关键词
N-salicylidene-o-aminophenol; Gallium complexes; Photoluminescence; Electroluminescence; Organic LED; AROMATIC SCHIFF-BASE; FLUORESCENCE PROPERTIES; METAL-COMPLEXES; ALUMINUM; FLUORIMETRY; DIODES;
D O I
10.1016/j.jlumin.2008.12.017
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
N-salicylidene-o-aminophenol and two of its derivatives bearing either an electron-donating methyl group or an electron-withdrawing Br group were used as ligands for the synthesis of three Ga(III) complexes. The complexes involved the participation of one acetylacetonate and one ethanol or methanol molecule. The geometry of the dianion of the Schiff base in the complexes is planar while photoluminescence data showed that photoluminescence intensity was extensively increased upon complex formation. Complexes emitted ligand-centered luminescence by ligand-centered excitation. Substituent groups broadly modified emission maximum. These substitutions can be exploited to tune light emission by the complex. All three complexes were used for the construction of electroluminescence devices and all emitted electroluminescence. Both photoluminescence and electroluminescence emission was enhanced in the case of substituted Schiff bases. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:578 / 583
页数:6
相关论文
共 19 条
[1]   SUBSTITUENT-GROUP EFFECTS ON THE FLUORESCENCE OF ALUMINUM-SCHIFF BASE COMPLEXES AND THEIR APPLICATION TO THE DETERMINATION OF ALUMINUM [J].
AOKI, I ;
MATSUNAGA, T ;
WATANABE, K .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1989, 62 (07) :2369-2374
[2]   N-(2-HYDROXYPHENYL)SALICYLALDIMINE [J].
ELERMAN, Y ;
ELMALI, A ;
ATAKOL, O ;
SVOBODA, I .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1995, 51 :2344-2346
[3]   THE STRUCTURE AND CHARACTERISTICS OF THE FLUORESCENT METAL CHELATES OF ORTHO,ORTHO-'-DIHYDROXYAZO COMPOUNDS [J].
FREEMAN, DC ;
WHITE, CE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1956, 78 (12) :2678-2682
[4]   FLUORESCENCE PROPERTIES OF COUMARIN LASER-DYES IN AQUEOUS POLYMER MEDIA - CHROMOPHORE ISOLATION IN POLY(METHACRYLIC ACID) HYPERCOILS [J].
JONES, G ;
RAHMAN, MA .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (49) :13028-13037
[5]   Optical materials for organic light-emitting devices [J].
Kalinowski, J. .
OPTICAL MATERIALS, 2008, 30 (05) :792-799
[6]  
Kalinowski J., 2005, Organic Light-Emitting Diodes: Principles, Characteristics, and Processes
[7]   Hydrogen bonding properties and intermediate structure of N-(2-carboxyphenyl)salicylidenimine [J].
Ligtenbarg, AGJ ;
Hage, R ;
Meetsma, A ;
Feringa, BL .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1999, (04) :807-812
[8]   Effective color tuning in organic light-emitting diodes based on aluminum tris(5-aryl-8-hydroxyquinoline) complexes [J].
Montes, VA ;
Li, G ;
Pohl, R ;
Shinar, J ;
Anzenbacher, P .
ADVANCED MATERIALS, 2004, 16 (22) :2001-+
[9]   METAL-COMPLEXES OF AROMATIC SCHIFF-BASE COMPOUNDS .1. FLUORESCENCE PROPERTIES OF ALUMINUM AND GALLIUM COMPLEXES OF AROMATIC SCHIFF-BASES AND THEIR USE IN FLUORIMETRY [J].
MORISIGE, K .
ANALYTICA CHIMICA ACTA, 1974, 72 (02) :295-305
[10]   FLUORESCENCE PROPERTIES OF METAL-COMPLEXES OF AROMATIC SCHIFF-BASE AND THEIR USE IN FLUORIMETRY [J].
MORISIGE, K .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1978, 40 (05) :843-851