Electroluminescence

Recent studies have been made on electroluminescence (EL) of organic compounds where light emission occurs upon application of a voltage. Since Tang reported multilayered organic EL devices in 1987, related research and development has rapidly progressed. Today, there are some which are put in practical use. Organic EL devices have characteristic features such as spontaneous emission,
low-voltage driving force, no dependence on view angles, high-speed response properties, and high brightness. They are expected to be useful as flat panel display materials.
The multilayered organic EL devices consist of a hole transport layer, electron transport layer and emitter layer and depending on the combination, either the hole transport layer or electron transport layer may serve dually as the emitter layer. Emission wavelengths are controlled by doping trace amounts of fluorescent dyes in the emitter layer. Furthermore, the polymer-type EL devices such as light-emitting polymers and polymers dispersed with low-molecular weight fluorescent compounds are being studied because of ease of processing.

A1340 A1340 B2694 B2694 D0711 D0711
B2695 B2695 D0905 D0905 B2111 B2111
B2088 B2088 B1549 B1549 B2654 B2654
B2077 B2077 B2078 B2078 B3645 B3645
B1554 B1554 B2713 B2713 B1336 B1336
B1066 B1066 B2079 B2079 B3146 B3146
B2269 B2269 B1564 B1564 B2676 B2676
B2305 B2305 B1677 B1677 B1678 B1678
B3663 B3663 B3634 B3634 B3682 B3682
B1767 B1767 B2696 B2696 P1005 P1005
P1006 P1006 C0386 C0386 C1961 C1961
D3842 D3842 D3932 D3932 D3302 D3302
D3933 D3933 D3934 D3934 D3303 D3303
D4028 D4028 D1910 D1910 D3952 D3952
D2144 D2144 D2849 D2849 D2687 D2687
D3227 D3227 D2347 D2347 D2757 D2757
D3739 D3739 D1689 D1689 D2448 D2448
D3236 D3236 D1429 D1429 N0659 N0659
N0610 N0610 P0078 P0078 P1629 P1629
P0972 P0972 P0984 P0984 P0079 P0079
P0331 P0331 P1766 P1766 P0656 P0656
P1104 P1104 B3561 B3561 Q0001 Q0001
Q0057 Q0057 Q0083 Q0083 Q0018 Q0018
S0220 S0220 T0020 T0020 T2716 T2716
T2206 T2206 T2269 T2269 T1812 T1812
T0168 T0168 T1358 T1358 T0561 T0561
T2233 T2233 T1934 T1934 T2700 T2700
T1735 T1735 T2685 T2685 T1527 T1527
T2238 T2238 V0021 V0021
A1340 4-Amino-p-terphenyl
B2694 Bathocuproine (purified by sublimation)
D0711 Bathocuproine
B2695 Bathophenanthroline (purified by sublimation)
D0905 Bathophenanthroline
B2111 3-(2-Benzimidazolyl)-7-(diethylamino)coumarin
B2088 3-(2-Benzothiazolyl)-7-(diethylamino)coumarin
B1549 9,9-Bis(4-aminophenyl)fluorene
B2654 9,9-Bis(4-aminophenyl)fluorene (purified by sublimation)
B2077 Bis[2-(2-benzothiazolyl)phenolato]zinc(II)
B2078 Bis[2-(2-benzoxazolyl)phenolato]zinc(II)
B3645 9,9-Bis(4-bromophenyl)fluorene
B1554 2,5-Bis(5-tert-butyl-2-benzoxazolyl)thiophene
B2713 4,4'-Bis(9H-carbazol-9-yl)biphenyl
B1336 N,N'-Bis(4-chlorophenyl)-N,N'-diphenyl-1,4-phenylenediamine
B1066 2,5-Bis(4-diethylaminophenyl)-1,3,4-oxadiazole
B2079 1,1-Bis[4-[N,N-di(p-tolyl)amino]phenyl]cyclohexane
B3146 1,1-Bis[4-[N,N-di(p-tolyl)amino]phenyl]cyclohexane (purified by sublimation)
B2269 4,4'-Bis[di(3,5-xylyl)amino]-4''-phenyltriphenylamine
B1564 4,4'-Bis(5-methyl-2-benzoxazolyl)stilbene
B2676 4,4'-Bis(5-methyl-2-benzoxazolyl)stilbene (purified by sublimation)
B2305 4,4'-Bis[N-(1-naphthyl)-N-phenylamino]-4''-phenyltriphenylamine
B1677 Bis(8-quinolinolato)copper(II)
B1678 Bis(8-quinolinolato)zinc(II) Hydrate
B3663 2-Bromo-5-phenylthiophene
B3634 1-(4-Bromophenyl)-1,2,2-triphenylethylene
B3682 2-Bromoselenophene
B1767 2-(4-tert-Butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole
B2696 2-(4-tert-Butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole (purified by sublimation)
P1005 Copper(II) Phthalocyanine (alpha-form)
P1006 Copper(II) Phthalocyanine (beta-form)
C0386 Coronene
C1961 Coronene (purified by sublimation)
D3842 4,7-Dibromo-2,1,3-benzothiadiazole
D3932 2,7-Dibromocarbazole
D3302 4,4'-Dibromo-4''-cyclohexyltriphenylamine
D3933 2,7-Dibromo-9,9-dihexylfluorene
D3934 2,7-Dibromo-9,9-di-n-octylfluorene
D3303 4,4'-Dibromo-4''-phenyltriphenylamine
D4028 2,5-Dibromoselenophene
D1910 4,4'-Dibromotriphenylamine
D3952 3,6-Di-tert-butylcarbazole
D2144 1,2-Dichlorotetramethyldisilane
D2849 4-(Dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4H-pyran
D2687 N,N'-Dimethylquinacridone
D3227 N,N'-Dimethylquinacridone (purified by sublimation)
D2347 4,4'-Dimethyltriphenylamine
D2757 2,5-Di(1-naphthyl)-1,3,4-oxadiazole
D3739 3-(Diphenylamino)dibenzo[g,p]chrysene
D1689 9,10-Diphenylanthracene
D2448 N,N'-Diphenyl-N,N'-di(m-tolyl)benzidine
D3236 N,N'-Diphenyl-N,N'-di(m-tolyl)benzidine (purified by sublimation)
D1429 2,5-Diphenyl-1,3,4-oxadiazole
N0659 Nile Red
N0610 4-Nitro-p-terphenyl
P0078 Perylene
P1629 Perylene (purified by sublimation)
P0972 3,4,9,10-Perylenetetracarboxylic Dianhydride
P0984 3,4,9,10-Perylenetetracarboxylic Diimide
P0079 Phenanthrene
P0331 Phenanthrene Zone Refined (number of passes:30)
P1766 (1,10-Phenanthroline)tris[4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedionato]europium(III)
P0656 Poly(N-vinylcarbazole)
P1104 Pyrene
B3561 2-(2-Pyridyl)benzo[b]thiophene
Q0001 p-Quaterphenyl
Q0057 Quinacridone
Q0083 Quinacridone (purified by sublimation)
Q0018 p-Quinquephenyl
S0220 p-Sexiphenyl
T0020 p-Terphenyl
T2716 1,3,6,8-Tetrabromopyrene
T2206 Tetradecafluoro-alpha-sexithiophene (purified by sublimation)
T2269 N,N,N',N'-Tetrakis(p-tolyl)benzidine
T1812 N,N,N',N'-Tetraphenylbenzidine
T0168 1,1,4,4-Tetraphenyl-1,3-butadiene
T1358 meso-Tetraphenylchlorin
T0561 5,6,11,12-Tetraphenylnaphthacene
T2233 5,6,11,12-Tetraphenylnaphthacene (purified by sublimation)
T1934 1,3,5-Tri(9H-carbazol-9-yl)benzene (purified by sublimation)
T2700 2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine
T1735 Tris(1,3-diphenyl-1,3-propanedionato)(1,10-phenanthroline)europium(III)
T2685 Tris[1-phenylisoquinoline-C2,N]iridium(III) (purified by sublimation)
T1527 Tris(8-quinolinolato)aluminum
T2238 Tris(8-quinolinolato)aluminum (purified by sublimation)
V0021 9-Vinylcarbazole

Purification just before use is recommended.

Anthracenes


Anthraquinones


Carbazoles


Fluorenes


Fluorenones


Porphyrins


Phthalocyanines


Pyrenes


Reagents for Conducting Polymer Research


Dichlorosilanes (for Polysilanes)

Literature

1) C. W. Tang, S. A. VanSlyke, Appl. Phys. Lett., 1987, 51, 913 [DOI].
2) C. Adachi, T. Tsutsui, S. Saito, Appl. Phys. Lett., 1990, 56, 799 [DOI].
3) J. H. Burroughes, D. D. C. Bradley, A. R. Brown, R. N. Marks, K. Mackay, R. H. Friend, P. L. Burns, A. B. Holmes, Nature, 1990, 347, 539 [DOI].
4) R. H. Friend, R. W. Gymer, A. B. Holmes, J. H. Burroughes, R. N. Marks, C. Taliani, D. D. C. Bradley, D. A. Dos Santos, J. L. Bredas, M. Logdlund, W. R. Salaneck, Nature, 1999, 397, 121 [DOI].
5) S. Seki, S. Miyashita, Oyo Butsuri, 2001, 70, 70.
6) J. Kido, Oyo Butsuri, 2001, 70, 333.
7) K. Hachise, N. Takada, N. Tanigaki, Oyo Butsuri, 2001, 70, 455.


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