Compound for use in organic EL device and organic EL device

Abstract

An object of the invention is to provide an organic EL device-forming compound and an organic EL device which produce light emission of satisfactory luminance, especially at long wavelength and are durable in that improved light emitting performance lasts for a long time. The object is attained by a compound having a basic skeleton represented by formula (I) and an organic EL device comprising the same.(CF 33) In formula (I), R1 to R8 each are hydrogen or a substituted or unsubstituted aryl or alkenyl group, with the proviso that at least six of R1 to R8 are substituted or unsubstituted aryl or alkenyl groups.

Description

TECHNICAL FIELD This invention relates to an organic electro luminescent (EL) device, and more particularly, to a compound for use in a device of the type wherein an electric field is applied across a thin film of an organic compound to emit light.

BACKGROUND TECHNIQUE

Organic electroluminescent (EL) devices include a thin film containing a luminescent organic compound interleaved between an electron injecting electrode and a hole injecting electrode. Electrons and holes are injected into the thin film where they are recombined to create excitons. Light is emitted by utilizing luminescence (phosphorescence or fluorescence) upon deactivation of excitons.

The organic EL devices are characterized by plane light emission at a high luminance of about 100 to 10,000 cd/m 2 with a voltage of about 10 volts and light emission in a spectrum from blue to red color by a simple choice of the type of fluorescent material.

Doping is one technique for producing light emission of any desired color from EL devices. It was reported in Jpn. J. Appl. Phys., 10, 527 (1971) to change emission color from blue to green by doping anthracene crystals with a minor level of tetracene. With respect to organic thin film EL devices having a multilayer structure, it was reported in JP-A 63-264692 to incorporate in a host reported in JP-A 63-264692 to incorporate in a host material having a light emitting function a minor amount of a fluorescent dye capable of emitting light different from that of the host material in response to light emission from the host material as a dopant to form a light emitting layer, thereby changing the color of light emission from green to orange or red.

With respect to long wavelength light emission of yellow to red, known light emitting materials or dopant materials include laser dyes capable of red oscillation (EP 0281381), compounds capable of exciplex emission (JP-A 2-255788), perylene compounds (JP-A 3-791), coumarin compounds (JP-A 3-792), dicyanomethylene compounds (JP-A 3-162481), thioxanthene compounds (JP-A 3-177486), mixtures of a conjugated polymer and an electron transporting compound (JP-A 6-73374), squalirium compounds (JP-A 6-93257), oxadiazole compounds (JP-A 6-136359), oxynate derivatives (JP-A 6-145146), and pyrene compounds (JP-A 6-240246).

Other light emitting materials disclosed heretofore include condensed polycyclic aromatic compounds (JP-A 5-32966 and 5-214334). Also dopant materials proposed heretofore include various condensed polycyclic aromatic compounds (JP-A 5-258859).

These light emitting systems, however, do not provide high luminance or stable light emitting performance, especially at long wavelength. A further improvement in luminance or durability is thus desired.

DISCLOSURE OF THE INVENTION

An object of the invention is to provide a compound for use in an organic EL device and an organic EL device which produce light emission of satisfactory luminance, especially at long wavelength and are durable in that improved light emitting performance lasts for a long time.

This and other objects of the invention are attained by the following construction.

(1) A compound for organic electroluminescent devices, having a basic skeleton represented by the following formula (I):

(CF 3)

wherein R 1 to R 8 each are hydrogen or a substituted or unsubstituted aryl or alkenyl group, with the proviso that at least six of R 1 to R 8 are substituted or unsubstituted aryl or alkenyl groups.

(2) An organic electroluminescent device comprising a hole injecting electrode, an electron injecting electrode, and an organic layer disposed between the electrodes and including at least a light emitting layer, wherein

said light emitting layer contains the compound of (1).

(3) The organic electroluminescent device of (2), wherein the compound contained in said light emitting layer has a basic skeleton represented by the following formula (II):

(CF 4)

wherein each R group in sets of R 11 to R 15 , R 21 to R 25 , R 31 to R 35 , and R 41 to R 45 is hydrogen or a substituted or unsubstituted alkyl, aryl, amino, heterocyclic or phenoxy group, the R groups in at least two sets have substituted or unsubstituted aryl, heterocyclic or aryloxy groups as substituents; R 5 , R 6 , R 7 and R 8 each are hydrogen or an aryl group, with the proviso that at least two of R 5 to R 8 are aryl groups; at least two R groups in each of the sets of R 11 to R 15 , R 21 to R 25 , R 31 to R 35 , and R 41 to R 45 may form a fused ring.

(4) The organic electroluminescent device of (2) or (3) wherein said light emitting layer further contains an electron injecting and transporting compound and/or a hole injecting and transporting compound.

(5) The organic electroluminescent device of any one of (2) to (4) wherein said light emitting layer contains at least two compounds.

(6) The organic electroluminescent device of any one of (2) to (5) wherein said light emitting layer contains at least two dopants, the content of the dopants combined being up to 30% by weight based on a host material.

(7) The organic electroluminescent device of any one of (2) to (6) wherein the overall content of the compound of (1) in said light emitting layer is up to 30% by weight based on a host material.

(8) The organic electroluminescent device of (6) or (7) wherein said light emitting layer contains at least two compounds having different carrier trapping capabilities.

(9) The organic electroluminescent device of (7) or (8) wherein said light emitting layer contains at least a compound having a hole trapping capability and a compound having an electron trapping capability.

(10) The organic electroluminescent device of any one of (1) to (9) wherein at least two light emitting layers are included, and said light emitting layers contain dopants having different carrier trapping capabilities.

(11) The organic electroluminescent device of any one of (1) to (10) wherein at least two light emitting layers are included, at least one layer of said light emitting layers contains a dopant having a hole trapping capability, and at least one other layer of said light emitting layers contains a dopant having an electron trapping capability.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic cross-sectional view showing the basic construction of an organic EL device according to the invention.

FIG. 2 is a diagram showing a mass analysis spectrum of compound IV-256 according to the invention.

FIG. 3 is a diagram showing a 1 H-NMR spectrum of compound IV-256 according to the invention.

FIG. 4 is a diagram showing an infrared absorption spectrum of compound IV-256 according to the invention.

FIG. 5 is a diagram showing a mass analysis spectrum of compound IV-257 according to the invention.

FIG. 6 is a diagram showing a 1 H-NMR spectrum of compound IV-257 according to the invention.

FIG. 7 is a diagram showing an infrared absorption spectrum of compound IV-257 according to the invention.

FIG. 8 is a diagram showing a mass analysis spectrum of compound IV-213 according to the invention.

FIG. 9 is a diagram showing a 1 H-NMR spectrum of compound IV-213 according to the invention.

FIG. 10 is a diagram showing an infrared absorption spectrum of compound IV-213 according to the invention.

BEST MODE FOR CARRYING OUT THE INVENTION

The compounds of the present invention have a basic skeleton represented by the following formula (I).

(CF 5)

By incorporating a compound of formula (I) in a light emitting layer, there is obtained an organic EL device capable of light emission having a maximum wavelength in the long wavelength range. Particularly when the compound of formula (I) is used in the light emitting layer as a dopant for a host material having a light emitting function in itself or as a dopant in a mix layer with a light emitting function formed from a mixture of an electron injecting and transporting compound and a hole injecting and transporting compound, light emission of blue to red, especially long wavelength light emission is possible at a sufficient luminance and the light emitting performance lasts long.

In formula (I), R 1 to R 8 each are hydrogen or a substituted or unsubstituted aryl or alkenyl group. At least six of R 1 to R 8 are aryl or alkenyl groups.

The aryl groups represented by R 1 to R 8 may be monocyclic or polycyclic, inclusive of fused rings and a collection of rings. Those aryl groups having 6 to 30 carbon atoms in total are preferred and they may have substituents.

The aryl groups represented by R 1 to R 4 are preferably phenyl, o-, m- or p-tolyl, pyrenyl, perylenyl, coronenyl, 1- or 2-naphthyl, anthryl, o-, m- or p-biphenylyl, terphenyl and phenanthryl groups.

The alkenyl groups represented by R 1 to R 4 are preferably those having a phenyl group as at least one substituent, such as 1- and 2-phenylethenyl, 1,2- and 2,2-diphenylethenyl, and 1,2,2-triphenylethenyl, although unsubstituted alkenyl groups are acceptable.

Where R 1 to R 4 have substituents thereon, it is preferable that at least two of these substituents are selected from among aryl, amino, heterocyclic, alkenyl and aryloxy groups. The aryl, amino, heterocyclic and alkenyl groups are as defined above for R 1 to R 4 .

The aryloxy groups to substitute on R 1 to R 4 are preferably those of aryl groups having 6 to 18 carbon atoms in total, for example, o-, m- and p-phenoxy.

The amino groups to substitute on R 1 to R 4 may be selected from among alkylamino, arylamino, aralkylamino and analogous groups. They preferably have aliphatic groups having 1 to 6 carbon atoms in total and/or aromatic carbocyclic groups having 1 to 4 rings. Illustrative examples include dimethylamino, diethylamino, dibutylamino, diphenylamino, ditolylamino, bisdiphenylylamino, and bisnaphthylamino groups.

The heterocyclic groups to substitute on R 1 to R 4 include 5- or 6-membered ring aromatic heterocyclic groups containing O, N or S as a hetero atom, and fused polycyclic aromatic heterocyclic groups having 2 to 20 carbon atoms.

Examples of the aromatic heterocyclic groups and fused polycyclic aromatic heterocyclic groups to substitute on R 1 to R 4 include thienyl, furyl, pyrolyl, pyridyl, quinolyl, and quinoxalyl groups.

At least two of these substituents may form a fused ring. Also, these substituents may be further substituted ones, in which preferred substituents are as described above.

When R 1 to R 4 have substituents, it is preferred that at least two of the substituents have the above-described substituents. The position of substitution is not particularly limited and may be a meta, para or ortho position. R 1 and R 4 , and R 2 and R 3 in the respective pairs are preferably identical although they may be different.

Further preferably, the compounds for organic electroluminescent devices according to the invention are those having a basic skeleton represented by the following formula (II):

(CF 6)

In formula (II), R 11 to R 15 , R 21 to R 25 R 31 to R 35 and R 41 to R 45 are hydrogen, aryl, amino, heterocyclic, aryloxy or alkenyl groups. It is preferred that the R groups in at least one set have aryl, amino, heterocyclic or aryloxy groups as substituents. At least two R groups may form a fused ring. R 5 , R 6 , R 7 , and R 8 are hydrogen, aryl or alkenyl groups, with the proviso that at least two of R 5 to R 8 are aryl or alkenyl groups.

Preferred examples of the aryl, amino, heterocyclic and aryloxy groups are the same as exemplified above for R 1 to R 4 . It is preferred that R 11 to R 15 and R 41 to R 45 , and R 21 to R 25 and R 31 to R 35 in the respective set pairs are identical although they may be different.

The amino groups to substitute on R 11 to R 15 , R 21 to R 25 , R 31 to R 35 , and R 41 to R 45 may be alkylamino, arylamino, aralkylamino and analogous groups. They preferably have aliphatic groups with 1 to 6 carbon atoms in total and/or aromatic carbocyclic groups of 1 to 4 rings. Illustrative examples are dimethylamino, diethylamino, dibutylamino, diphenylamino, ditolylamino, and bisbiphenylylamino groups.

Examples of the fused ring formed include indene, naphthalene, anthracene, phenanthrene, quinoline, isoquinoline, quinoxaline, phenazine, acridine, indole, carbazole, phenoxazine, phenothiazine, benzothiazole, benzothiophene, benzofuran, acridone, benzimidazole, coumarin, and flavone.

Especially preferred illustrative examples of the compound of the invention are shown below in Tables 1 to 37. The substituents R 1 to R 8 are represented by R 10 to R 80 , respectively.

TABLE 1
	Substituent
Compound No.	R 10	R 20	R 30	R 40
I-239
I-240
I-241
I-245
I-246
I-247
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	I-239			—H	—H
	I-240			—H	—H
	I-241			—H	—H
	I-245
	I-246
	I-247

TABLE 2
	Substituent
Compound No.	R 10	R 20	R 30
I-257
I-258
I-259
I-263
I-264
I-265
	Substituent
Compound No.	R 40	R 50	R 60	R 70	R 80
I-257				—H	—H
I-258				—H	—H
I-259				—H	—H
I-263
I-264
I-265

TABLE 3
	Substituent
Compound No.	R 10	R 20	R 30
I-251
I-252
I-253
I-269
I-270
I-271
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	I-251				—CH 3	—CH 3
	I-252				—CH 3	—CH 3
	I-253				—CH 3	—CH 3
	I-269				—CH 3	—CH 3
	I-270				—CH 3	—CH 3
	I-271				—CH 3	—CH 3

TABLE 4
Compound No.	R 10	R 20	R 30
I-272
I-273
I-274
I-275
I-276
I-277
	Compound No.	R 40	R 50	R 60	R 70	R 80
	I-272				H	H
	I-273				H	H
	I-274				H	H
	I-275				H	H
	I-276				H	H
	I-277				H	H

TABLE 5
Compound No.	R 10	R 20	R 30
I-278
I-279
I-280
I-281
I-282
	Compound No.	R 40	R 50	R 60	R 70	R 80
	I-278				H	H
	I-279				H	H
	I-280				H	H
	I-281				H	H
	I-282				H	H

TABLE 6
Compound No.	R 10	R 20	R 30
I-283
I-284
I-285
I-286
I-287
I-288
	Compound No.	R 40	R 50	R 60	R 70	R 80
	I-283
	I-284
	I-285
	I-286
	I-287
	I-288

TABLE 7
Compound No.	R 10	R 20	R 30
I-289
I-290
I-291
I-292
I-293
	Compound No.	R 40	R 50	R 60	R 70	R 80
	I-289
	I-290
	I-291
	I-292
	I-293

	TABLE 8
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-31
IV-32
IV-33
IV-34
IV-35
IV-36
	Substituent
Compound No.	R 50	R 60	R 70	R 80
IV-31
IV-32
IV-33
IV-34
IV-35
IV-36

	TABLE 9
	Substituent
Compound No.	R 10	R 20	R 30	R 40	R 50
IV-39
IV-40
IV-41
IV-42
IV-43
IV-44
IV-45
IV-46
IV-47
IV-48
	Substituent
Compound No.	R 60	R 70	R 80
IV-39
IV-40
IV-41
IV-42
IV-43
IV-44
IV-45
IV-46
IV-47
IV-48

	TABLE 10
	Substituent
Compound No.	R 10	R 20	R 30	R 40	R 50
IV-49
IV-50
IV-51
IV-52
IV-53
IV-54
IV-55
IV-56
IV-57
IV-58
IV-59
IV-60
IV-61
IV-62
	Substituent
Compound No.	R 60	R 70	R 80
IV-49
IV-50
IV-51
IV-52
IV-53
IV-54
IV-55
IV-56
IV-57
IV-58
IV-59
IV-60
IV-61
IV-62

	TABLE 11
	Substituent
Compound No.	R 10	R 20	R 30
IV-63
IV-64
IV-65
IV-66
IV-67
IV-68
IV-69
IV-70
IV-71
IV-72
IV-73
IV-74
	Substituent
Compound No.	R 40	R 50	R 60	R 70	R 80
IV-63
IV-64
IV-65
IV-66
IV-67
IV-68
IV-69
IV-70
IV-71
IV-72
IV-73
IV-74

	TABLE 12
	Substituent
Compound No.	R 10	R 20	R 30
IV-75
IV-76
IV-77
IV-78
IV-79
IV-80
IV-81
IV-82
IV-83
IV-84
IV-85
IV-86
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	IV-75				H	H
	IV-76				H	H
	IV-77				H	H
	IV-78				H	H
	IV-79				H	H
	IV-80				H	H
	IV-81				H	H
	IV-82				H	H
	IV-83				H	H
	IV-84				H	H
	IV-85				H	H
	IV-86				H	H

	TABLE 13
	Substituent
Compound No.	R 10	R 20	R 30	R 40	R 50
IV-87
IV-88
IV-89
IV-90
IV-91
IV-92
IV-93
IV-94
IV-95
IV-96
IV-97
IV-98
IV-99
	Substituent
	Compound No.	R 60	R 70	R 80
	IV-87		H	H
	IV-88		H	H
	IV-89		H	H
	IV-90		H	H
	IV-91		H	H
	IV-92		H	H
	IV-93		H	H
	IV-94		H	H
	IV-95		H	H
	IV-96		H	H
	IV-97		H	H
	IV-98		H	H
	IV-99		H	H

	TABLE 14
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-212
IV-213
IV-214
IV-215
IV-216
IV-217
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-212
	IV-213
	IV-214
	IV-215
	IV-216
	IV-217

	TABLE 15
	Substituent
Compound No.	R 10	R 20	R 30
IV-218
IV-219
IV-220
IV-221
IV-222
IV-223
IV-224
IV-225
IV-226
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	IV-218
	IV-219
	IV-220
	IV-221
	IV-222
	IV-223
	IV-224
	IV-225
	IV-226

	TABLE 16
	Substituent
Compound No.	R 10	R 20
IV-227
IV-228
IV-229
IV-230
IV-231
IV-232
IV-233
IV-234
IV-235
	Substituent
Compound No.	R 30	R 40
IV-227
IV-228
IV-229
IV-230
IV-231
IV-232
IV-233
IV-234
IV-235
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-227
	IV-228
	IV-229
	IV-230
	IV-231
	IV-232
	IV-233
	IV-234
	IV-235

	TABLE 17
	Substituent
Compound No.	R 10	R 20
IV-236
IV-237
IV-238
IV-239
	Substituent
Compound No.	R 30	R 40
IV-236
IV-237
IV-238
IV-239
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-236
	IV-237
	IV-238
	IV-239

	TABLE 18
	Substituent
Compound No.	R 10	R 20	R 30
IV-240
IV-241
IV-242
IV-243
IV-244
IV-245
IV-246
IV-247
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	IV-240
	IV-241
	IV-242
	IV-243
	IV-244
	IV-245
	IV-246
	IV-247

	TABLE 19
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-248
IV-249
IV-250
IV-251
IV-252
IV-253
IV-254
IV-255
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-248
	IV-249
	IV-250
	IV-251
	IV-252
	IV-253
	IV-254
	IV-255

	TABLE 20
	Substituent
Compound No.	R 10	R 20	R 30
IV-256
IV-257
IV-258
IV-259
IV-260
IV-261
IV-262
IV-263
IV-264
IV-265
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	IV-256				H	H
	IV-257				H	H
	IV-258				H	H
	IV-259				H	H
	IV-260				H	H
	IV-261				H	H
	IV-262				H	H
	IV-263				H	H
	IV-264				H	H
	IV-265				H	H

	TABLE 21
	Substituent
Compound No.	R 10	R 20	R 30
IV-266
IV-267
IV-268
IV-269
IV-270
IV-271
IV-272
IV-273
IV-274
IV-275
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	IV-266				H	H
	IV-267				H	H
	IV-268				H	H
	IV-269				H	H
	IV-270				H	H
	IV-271				H	H
	IV-272				H	H
	IV-273				H	H
	IV-274				H	H
	IV-275				H	H

	TABLE 22
	Substituent
Compound No.	R 10	R 20
IV-276
IV-277
IV-278
IV-279
IV-280
IV-281
IV-282
IV-283
IV-284
	Substituent
Compound No.	R 30	R 40
IV-276
IV-277
IV-278
IV-279
IV-280
IV-281
IV-282
IV-283
IV-284
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-276			H	H
	IV-277			H	H
	IV-278			H	H
	IV-279			H	H
	IV-280			H	H
	IV-281			H	H
	IV-282			H	H
	IV-283			H	H
	IV-284			H	H

	TABLE 23
	Substituent
Compound No.	R 10	R 20
IV-285
IV-286
IV-287
IV-288
	Substituent
Compound No.	R 30	R 40
IV-285
IV-286
IV-287
IV-288
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-285			H	H
	IV-286			H	H
	IV-287			H	H
	IV-288			H	H

	TABLE 24
	Substituent
Compound No.	R 10	R 20	R 30
IV-289
IV-290
IV-291
IV-292
IV-293
IV-294
IV-295
IV-296
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	IV-289				H	H
	IV-290				H	H
	IV-291				H	H
	IV-292				H	H
	IV-293				H	H
	IV-294				H	H
	IV-295				H	H
	IV-296				H	H

	TABLE 25
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-297
IV-298
IV-299
IV-300
IV-301
IV-302
IV-303
IV-304
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-297			H	H
	IV-298			H	H
	IV-299			H	H
	IV-300			H	H
	IV-301			H	H
	IV-302			H	H
	IV-303			H	H
	IV-304			H	H

	TABLE 26
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-305
IV-306
IV-307
IV-308
IV-309
IV-310
IV-311
IV-312
IV-313
IV-314
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-305			H	H
	IV-306			H	H
	IV-307			H	H
	IV-308			H	H
	IV-309			H	H
	IV-310			H	H
	IV-311			H	H
	IV-312			H	H
	IV-313			H	H
	IV-314			H	H

	TABLE 27
	Substituent
Compound No.	R 10	R 20	R 30
IV-315
IV-316
IV-317
IV-318
IV-319
IV-320
IV-321
IV-322
IV-323
IV-324
	Substituent
	Compound No.	R 40	R 50	R 60	R 70	R 80
	IV-315				H	H
	IV-316				H	H
	IV-317				H	H
	IV-318				H	H
	IV-319				H	H
	IV-320				H	H
	IV-321				H	H
	IV-322				H	H
	IV-323				H	H
	IV-324				H	H

	TABLE 28
	Substituent
Compound No.	R 10	R 20
IV-325
IV-326
IV-327
	Substituent
Compound No.	R 30	R 40
IV-325
IV-326
IV-327
	Substituent
Compound No.	R 50	R 60	R 70	R 80
IV-325			H	H
IV-326			H	H
IV-327			H	H

	TABLE 29
	Substituent
Compound No.	R 10	R 20
IV-328
IV-329
IV-330
IV-331
	Substituent
Compound No.	R 30	R 40
IV-328
IV-329
IV-330
IV-331
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-328			H	H
	IV-329			H	H
	IV-330			H	H
	IV-331			H	H

	TABLE 30
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-332
IV-333
IV-334
IV-335
IV-336
IV-337
IV-338
IV-339
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-332			H	H
	IV-333			H	H
	IV-334			H	H
	IV-335			H	H
	IV-336			H	H
	IV-337			H	H
	IV-338			H	H
	IV-339			H	H

	TABLE 31
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-340
IV-341
IV-342
IV-343
IV-344
IV-345
IV-346
IV-347
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-340			H	H
	IV-341			H	H
	IV-342			H	H
	IV-343			H	H
	IV-344			H	H
	IV-345			H	H
	IV-346			H	H
	IV-347			H	H

	TABLE 32
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-348
IV-349
IV-350
IV-351
IV-352
IV-353
IV-354
IV-355
IV-356
IV-357
	Substituent
Compound No.	R 50	R 60	R 70	R 80
IV-348
IV-349
IV-350
IV-351
IV-352
IV-353
IV-354
IV-355
IV-356
IV-357

	TABLE 33
	Substituent
Compound No.	R 10	R 20	R 30
IV-358
IV-359
IV-360
IV-361
IV-362
IV-363
IV-364
IV-365
IV-366
IV-367
	Substituent
Compound No.	R 40	R 50	R 60
IV-358
IV-359
IV-360
IV-361
IV-362
IV-363
IV-364
IV-365
IV-366
IV-367
	Substituent
	Compound No.	R 70	R 80
	IV-358
	IV-359
	IV-360
	IV-361
	IV-362
	IV-363
	IV-364
	IV-365
	IV-366
	IV-367

	TABLE 34
	Substituent
Compound No.	R 10	R 20	R 30	R 40
IV-368
IV-369
IV-370
IV-371
IV-372
IV-373
IV-374
IV-375
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-368
	IV-369
	IV-370
	IV-371
	IV-372
	IV-373
	IV-374
	IV-375

	TABLE 35
	Substituent
Compound No.	R 10	R 20	R 30	R 40	R 50
IV-376
IV-377
IV-378
IV-379
IV-380
IV-381
IV-382
IV-383
	Substituent
	Compound No.	R 60	R 70	R 80
	IV-376
	IV-377
	IV-378
	IV-379
	IV-380
	IV-381
	IV-382
	IV-383

	TABLE 36
	Substituent
Compound No.	R 10	R 20
IV-384
IV-385
IV-386
	Substituent
Compound No.	R 30	R 40
IV-384
IV-385
IV-386
	Substituent
Compound No.	R 50	R 60	R 70	R 80
IV-384
IV-385
IV-386

	TABLE 37
	Substituent
Compound No.	R 10	R 20
IV-387
IV-388
IV-389
IV-390
	Substituent
Compound No.	R 30	R 40
IV-387
IV-388
IV-389
IV-390
	Substituent
	Compound No.	R 50	R 60	R 70	R 80
	IV-387
	IV-388
	IV-389
	IV-390

The compound of the invention is obtained by effecting synthesis using diphenylnaphthoquinone, for example. Typical synthetic schemes are shown below.

The light emitting layer containing the compound of the invention has functions of injecting holes and electrons, transporting them, and recombining holes and electrons to create excitons. The use of relatively electronically neutral compounds in the light emitting layer in addition to the compound of the invention enables easy and well-balanced injection and transportation of electrons and holes.

In the light emitting layer of the organic EL device of the invention, it is preferred to use the inventive compound in combination with a host material capable of light emission by itself, that is, to use the compound as a dopant. In this embodiment, the content of the inventive compound in the light emitting layer is preferably 0.01 to 10% by weight, especially 0.1 to 5% by weight. By using the compound in combination with the host material, the light emission wavelength of the host material can be altered, enabling light emission shifted to a longer wavelength and improving the luminous efficiency and stability of the device.

Preferred host materials are quinolinolato complexes, more preferably aluminum complexes having 8-quinolinol or a derivative thereof as a ligand. Examples of the aluminum complex are disclosed in JP-A 63-264692, 3-255190, 5-70733, 5-258859, and 6-215874.

Examples of the former include tris(8-quinolinolato)-aluminum, bis(8-quinolinolato)magnesium, bis(benzo[f]-8-quinolinolato)zinc, bis(2-methyl-8-quinolinolato)aluminum oxide, tris(8-quinolinolato)indium, tris(5-methyl-8-quinolinolato)aluminum, 8-quinolinolatolithium, tris(5-chloro-8-quinolinolato)gallium, bis(5-chloro-8-quinolinolato)calcium, 5,7-dichloro-8-quinolinolatoaluminum, tris(5,7-dibromo-8-hydroxyquinolinolato)aluminum, and poly[zinc(II)-bis(8-hydroxy-5-quinolinyl)methane].

Also useful are aluminum complexes having another ligand in addition to 8-quinolinol or a derivative thereof. Examples include bis(2-methyl-8-quinolinolato)(phenolato)-aluminum(III), bis(2-methyl-8-quinolinolato)(ortho-cresolato)aluminum(III), bis(2-methyl-8-quinolinolato)-(meta-cresolato)aluminum(III), bis(2-methyl-8-quinolinolato)(para-cresolato)aluminum(III), bis(2-methyl-8-quinolinolato)(ortho-phenylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(meta-phenylphenolato)-aluminum(III), bis(2-methyl-8-quinolinolato)(para-phenylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(2,3-dimethylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(2,6-dimethylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(3,4-dimethylphenolato)-aluminum(III), bis(2-methyl-8-quinolinolato)(3,5-dimethylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(3,5-di-tert-butylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(2,6-diphenyl-phenolato)aluminum(III), bis(2-methyl-8-quinolinolato)-(2,4,6-triphenylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(2,3,6-trimethylphenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(2,3,5,6-tetramethyl-phenolato)aluminum(III), bis(2-methyl-8-quinolinolato)(1-naphtholato)aluminum(III), bis(2-methyl-8-quinolinolato)(2-naphtholato)aluminum(III), bis(2,4-dimethyl-8-quinolinolato)(ortho-phenylphenolato)aluminum(III), bis(2,4-dimethyl-8-quinolinolato)(para-phenylphenolato)-aluminum(III), bis(2,4-dimethyl-8-quinolinolato)(meta-phenylphenolato)aluminum(III), bis(2,4-dimethyl-8-quinolinolato)(3,5-dimethylphenolato)aluminum(III), bis(2,4-dimethyl-8-quinolinolato)(3,5-di-tert-butylphenolato)aluminum(III), bis(2-methyl-4-ethyl-8-quinolinolato)(para-cresolato)aluminum(III), bis(2-methyl-4-methoxy-8-quinolinolato)(para-phenylphenolato)-aluminum(III), bis(2-methyl-5-cyano-8-quinolinolato)(ortho-cresolato)aluminum(III), and bis(2-methyl-6-trifluoromethyl-8-quinolinolato) (2-naphtholato)-aluminum(III).

Also acceptable are bis(2-methyl-8-quinolinolato)-aluminum(III)-μ-oxo-bis(2-methyl-8-quinolinolato)aluminum (III), bis(2,4-dimethyl-8-quinolinolato)aluminum(III)-μ-oxo-bis(2,4-dimethyl-8-quinolinolato)aluminum (III), bis(4-ethyl-2-methyl-8-quinolinolato)aluminum(III)-μ-oxo-bis(4-ethyl-2-methyl-8-quinolinolato)aluminum (III), bis(2-methyl-4-methoxyquinolinolato)aluminum(III)-μ-oxo-bis(2-methyl-4-methoxyquinolinolato)aluminum (III), bis(5-cyano-2-methyl-8-quinolinolato)aluminum(III)-μ-oxo-bis(5-cyano-2-methyl-8-quinolinolato)aluminum (III), and bis(2-methyl-5-trifluoromethyl-8-quinolinolato)aluminum(III)-μ-oxo-bis(2-methyl-5-trifluoromethyl-8-quinolinolato)aluminum (III).

Other useful host materials are the phenylanthracene derivatives described in Japanese Patent Application No. 6-110569 and the tetraarylethene derivatives described in Japanese Patent Application No. 6-114456. Also, triphenylamine derivatives as typified by TPD are preferred host materials.

The light emitting layer may contain another luminescent material. Such a luminescent material may be at least one compound selected from compounds as disclosed in JP-A 63-264692, for example, quinacridone and styryl dyes. Also included are quinoline derivatives, for example, metal complex dyes having 8-quinolinol or a derivative thereof as a ligand such as tris(8-quinolinolato)aluminum, tetraphenylbutadiene, anthracene, perylene, coronene, and 12-phthaloperinone derivatives. Further included are the phenylanthracene derivatives of Japanese Patent Application No. 6-110569 and the tetraarylethene derivatives of Japanese Patent Application No. 6-114456.

The light emitting layer may also serve as an electron injecting and transporting layer. In this embodiment, the use of tris(8-quinolinolato)aluminum or the like is preferred. These fluorescent materials may be evaporated.

If desired, the light emitting layer is a layer of a mixture of at least one hole injecting and transporting compound and at least one electron injecting and transporting compound in which the inventive compound is contained as a dopant. In such a mix layer, the content of the inventive compound is preferably 0.01 to 20% by weight, especially 0.1 to 15% by weight.

In the mix layer, carrier hopping conduction paths are created, allowing carriers to move through a polarly predominant material while injection of carriers of opposite polarity is rather inhibited. The organic compound is less susceptible to damage, resulting in the advantage of an extended device life. By incorporating the above-described dopant in such a mix layer, the light emission wavelength the mix layer itself possesses can be altered, enabling light emission shifted to a longer wavelength and improving the luminous intensity and stability of the device. In particular, the inventive compound, which is stable to both electron and hole injection, can contribute to a drastic increase of the light emission life even at a doping level of about 2% by weight.

When the carrier trapping capability of a dopant is biased toward the electron or hole side, at least two dopants having different carrier trapping capabilities may be used to improve recombination and hence, to increase the probability of recombination. By using dopants having different carrier trapping capabilities, the probability of recombination of holes and electrons in the light emitting layer is improved so that the light emission efficiency and luminous intensity are improved. The especially preferred combination is a combination of a dopant having a high electron trapping capability to the host material with a dopant having a high hole trapping capability to the host material.

The hole injecting and transporting compound and electron injecting and transporting compound used in the mix layer may be selected from compounds for the hole injecting and transporting layer and compounds for the electron injecting and transporting layer to be described later, respectively. Specifically, the compounds for the hole injecting and transporting layer are preferably amine derivatives having strong fluorescence, for example, triphenyldiamine (TPD) derivatives, styrylamine derivatives and amine derivatives having an aromatic fused ring known as the hole injecting and transporting material.

The compounds for the electron injecting and transporting layer are preferably quinoline derivatives and metal complexes having 8-quinolinol or a derivative thereof as a ligand, especially tris(8-quinolinolato)aluminum (Alq3). The phenylanthracene derivatives and tetraarylethene derivatives described above are also preferably used.

The compounds for the hole injecting and transporting layer are preferably amine derivatives having strong fluorescence, for example, triphenyldiamine derivatives, styrylamine derivatives and amine derivatives having an aromatic fused ring known as the hole injecting and transporting material.

With respect to the mix ratio, which is determined in consideration of the respective carrier mobility and carrier concentration, it is preferred that the weight ratio of the hole injecting and transporting compound to the electron injecting and transporting compound range from about 1/99 to 99/1, more preferably from about 10/90 to 90/10, especially from about 20/80 to 80/20.

The thickness of the mix layer preferably ranges from the thickness corresponding to a single molecule layer to less than the thickness of an organic compound layer, for example, preferably from 1 to 85 nm, more preferably 5 to 60 nm, most preferably 5 to 50 nm.

Preferably the mix layer is formed by a co-deposition process of evaporating the compounds from distinct sources. If both the compounds have equal or very close vapor pressure or evaporation temperature, they may be pre-mixed in a common evaporation boat, from which they are evaporated together. The mix layer is preferably a uniform mixture of both the compounds although the compounds can be present in island form. The light emitting layer is generally formed to a predetermined thickness by evaporating an organic fluorescent material or coating a dispersion thereof in a resin binder.

One exemplary construction of the organic EL light emitting device fabricated using the inventive compound has on a substrate, a hole injecting electrode, a hole injecting and transporting layer, a light emitting and electron injecting and transporting layer, and an electron injecting electrode in the described order. If desired, an auxiliary electrode and a sealing layer are provided on the electron injecting electrode.

The organic EL device of the invention is not limited to the above exemplary construction and may have various other constructions. In another exemplary construction, the light emitting layer is provided singly and an electron injecting and transporting layer is interposed between the light emitting layer and the electron injecting electrode. Also, the light emitting layer may be mixed with the hole injecting and transporting layer, if desired.

The thicknesses of the light emitting layer, hole injecting and transporting layer, and electron injecting and transporting layer are not critical and vary with a particular formation technique. Usually a single layer is about 5 to 500 nm thick, especially about 10 to 300 nm thick.

The thicknesses of the hole injecting and transporting layer and electron injecting and transporting layer are equal to or range from 1/10 to 10 times the thickness of the light emitting layer although they depend on the design of a recombination/light emitting region. When the electron or hole injecting and transporting layer is divided into an injecting layer and a transporting layer, preferably the injecting layer is at least 1 nm thick and the transporting layer is at least 1 nm thick. The upper limit of thickness is generally about 500 nm for the injecting layer and about 500 nm for the transporting layer. The same applies when two injecting and transporting layers are provided.

The hole injecting and transporting layer has functions of facilitating injection of holes from the hole injecting electrode, transporting them stably, and obstructing electrons. The electron injecting and transporting layer has functions of facilitating injection of electrons from the electron injecting electrode, transporting them stably, and obstructing holes. These layers are effective for increasing the number of holes and electrons injected into the light emitting layer and confining holes and electrons therein for optimizing the recombination region to improve light emission efficiency.

In the hole injecting and transporting layer, there may be used various organic compounds as described, for example, in JP-A 63-295695, 2-191694, 3-792, 5-234681, 5-239455, 5-299174, 7-126225, 7-126226, and 8-100172, and EP 0650955A1. Exemplary are tetraarylbenzidine compounds (triaryldiamines or triphenyldiamines: TPD), aromatic tertiary amines, hydrazone derivatives, carbazole derivatives, triazole derivatives, imidazole derivatives, oxadiazole derivatives having an amino group, and polythiophenes. Two or more of these compounds may be used, and on such combined use, they may be formed as separate layers or mixed.

Where the hole injecting and transporting layer is formed separately as a hole injecting layer and a hole transporting layer, two or more compounds are selected in a proper combination from the compounds commonly used in hole injecting and transporting layers. In this regard, it is preferred to laminate layers in such an order that a layer of a compound having a lower ionization potential may be disposed adjacent the hole injecting electrode (ITO). It is also preferred to use a compound having good thin film forming ability at the hole injecting electrode surface. The order of lamination also applies where a plurality of hole injecting and transporting layers are provided. Such an order of lamination is effective for lowering the drive voltage and preventing current leakage and the development and growth of dark spots. Since evaporation is utilized in the manufacture of devices, films as thin as about 1 to 10 nm can be formed uniform and pinhole-free, which restrains any change in color tone of light emission and a drop of efficiency by re-absorption even if a compound having a low ionization potential and absorption in the visible range is used in the hole injecting layer. Like the light emitting layer, the hole injecting and transporting layer may be formed by evaporating the above-mentioned compounds.

In the electron injecting and transporting layer which is optionally provided, there may be used quinoline derivatives including organic metal complexes having 8-quinolinol or a derivative thereof as a ligand such as tris(8-quinolinolato)aluminum (Alq3), oxadiazole derivatives, perylene derivatives, pyridine derivatives, pyrimidine derivatives, quinoxaline derivatives, diphenylquinone derivatives, and nitro-substituted fluorene derivatives. The electron injecting and transporting layer can also serve as the light emitting layer. In this case, use of tris(8-quinolinolato)aluminum etc. is preferred. Like the light emitting layer, the electron injecting and transporting layer may be formed by evaporation or the like.

Where the electron injecting and transporting layer is formed separately as an electron injecting layer and an electron transporting layer, two or more compounds are selected in a proper combination from the compounds commonly used in electron injecting and transporting layers. In this regard, it is preferred to stack layers in such an order that a layer of a compound having a greater electron affinity may be disposed adjacent the electron injecting electrode. The order of stacking also applies where a plurality of electron injecting and transporting layers are provided.

In forming the hole injecting and transporting layer, the light emitting layer, and the electron injecting and transporting layer, vacuum evaporation is preferably used because homogeneous thin films are available. By utilizing vacuum evaporation, there is obtained a homogeneous thin film which is amorphous or has a crystal grain size of less than 0.1 μm. If the grain size is more than 0.1 μm, uneven light emission would take place and the drive voltage of the device must be increased with a substantial drop of charge injection efficiency.

The conditions for vacuum evaporation are not critical although a vacuum of 10 −4 Pa or lower and a deposition rate of about 0.01 to 1 nm/sec are preferred. It is preferred to successively form layers in vacuum because the successive formation in vacuum can avoid adsorption of impurities on the interface between the layers, thus ensuring better performance. Also, the drive voltage of a device can be reduced and the development and growth of dark spots be restrained.

In the embodiment wherein the respective layers are formed by vacuum evaporation, where it is desired for a single layer to contain two or more compounds, preferably boats having the compounds received therein are individually temperature controlled to achieve co-deposition.

The electron injecting electrode is preferably made of metals, alloys or intermetallic compounds having a work function of up to 4 eV. With a work function of more than 4 eV, the electron injecting efficiency lowers and consequently, the light emission efficiency lowers. Examples of the metal having a work function of up to 4 eV of which the electron injecting electrode film is constructed include alkali metals such as Li, Na and K, alkaline earth metals such as Mg, Ca, Sr and Ba, rare earth metals such as La and Ce, and Al, In, Ag, Sn, Zn, and Zr. Examples of the film-forming alloy having a work function of up to 4 eV include Ag—Mg (Ag: 0.1 to 50 at %), Al—Li (Li: 0.01 to 12 at %), In—Mg (Mg: 50 to 80 at %), and Al—Ca (Ca: 0.01 to 20 at %). These materials may be present alone or in combination of two or more. Where two or more materials are combined, their mixing ratio is arbitrary. It is also acceptable that an oxide or halide of an alkali metal, alkaline earth metal or rare earth metal is thinly deposited and a supporting electrode (auxiliary electrode or wiring electrode) of aluminum etc. is used.

The electron injecting electrode may be formed by evaporation or sputtering.

The electron injecting electrode may have at least a sufficient thickness to effect electron injection, for example, a thickness of at least 0.5 nm, preferably at least 1 nm. Although the upper limit is not critical, the electrode thickness is typically about 1 to about 500 nm.

The hole injecting electrode is preferably formed of such a material to such a thickness that the electrode may have a transmittance of at least 80% of emitted light. Illustratively, oxide transparent conductive thin films are preferred. For example, materials based on tin-doped indium oxide (ITO), zinc-doped indium oxide (IZO), indium oxide (In 2 O 3 ), tin oxide (SnO 2 ) or zinc oxide (ZnO) are preferable. These oxides may deviate somewhat from their stoichiometry. An appropriate proportion of SnO 2 mixed with In 2 O 3 is about 1 to 20%, more preferably about 5 to 12% by weight. An appropriate proportion of ZnO 2 mixed with In 2 O 3 is about 12 to 32% by weight.

The hole injecting electrode should preferably have a light transmittance of at least 80%, especially at least 90% in the light emission band, typically from 350 to 800 nm, and especially at each light emission. Since the emitted light is generally taken out through the hole injecting electrode, with a lower transmittance, the light emitted by the light emitting layer would be attenuated through the electrode, failing to provide a luminance necessary as a light emitting device. It is noted that only the side from which the emitted light exits has a transmittance of at least 80%.

The hole injecting electrode has at least a sufficient thickness to effect hole injection, preferably a thickness of 50 to 500 nm, especially 50 to 300 nm. Although the upper limit of the electrode thickness is not critical, a too thick electrode would have the risk of separation. Too thin an electrode would have problems with respect to film strength during fabrication, hole transporting ability, and resistance value.

In depositing the hole injecting electrode, a sputtering process is preferred. The sputtering process may be a high-frequency sputtering process using an RF power supply although a dc sputtering process is preferably used when the ease of control of physical properties of the hole injecting electrode being deposited and the flatness of the deposited film are taken into account.

A protective film may be formed if necessary. The protective film may be formed using an inorganic material such as SiOx or an organic material such as Teflon. The protective film may be either transparent or opaque and have a thickness of about 50 to 1,200 nm. Apart from the reactive sputtering process mentioned above, the protective film may also be formed by an ordinary sputtering or evaporation process.

Further, a sealing layer is provided on the device in order to prevent the organic layers and electrodes from oxidation. In order to prevent the ingress of moisture, the sealing layer is formed by attaching a sealing plate such as a glass plate to the substrate with an adhesive resin layer such as a commercially available low moisture absorption photo-curable adhesive, epoxy base adhesive, silicone base adhesive, or crosslinking ethylene-vinyl acetate copolymer adhesive sheet. Metal plates and plastic plates may also be used instead of the glass plate.

Transparent or translucent materials such as glass, quartz and resins are used as the substrate when the emitted light exits from the substrate side. The substrate may be provided with a color filter film, a fluorescent material-containing color conversion film or a dielectric reflecting film for controlling the color of light emission. In the case of the inversely stacked layer structure, the substrate may be either transparent or opaque. For the opaque substrate, ceramic and other materials may be used.

The color filter film used herein may be a color filter as used in liquid crystal displays and the like. The properties of a color filter may be adjusted in accordance with the light emission of the organic EL device so as to optimize the extraction efficiency and color purity.

It is also preferred to use a color filter capable of cutting external light of short wavelength which is otherwise absorbed by the EL device materials and fluorescence conversion layer, because the light resistance and display contrast of the device are improved.

An optical thin film such as a dielectric multilayer film may be used instead of the color filter.

The fluorescence conversion filter film is to convert the color of light emission by absorbing electroluminescence and allowing the fluorescent material in the film to emit light. It is formed from three components: a binder, a fluorescent material, and a light absorbing material.

The fluorescent material used may basically have a high fluorescent quantum yield and desirably exhibits strong absorption in the electroluminescent wavelength region. In practice, laser dyes are appropriate. Use may be made of rhodamine compounds, perylene compounds, cyanine compounds, phthalocyanine compounds (including sub-phthalocyanines), naphthalimide compounds, fused ring hydrocarbon compounds, fused heterocyclic compounds, styryl compounds, and coumarin compounds.

The binder is selected from materials which do not cause extinction of fluorescence, preferably those materials which can be finely patterned by photolithography or printing technique. Also, those materials which are not damaged during deposition of ITO are preferable.

The light absorbing material is used when the light absorption of the fluorescent material is short and may be omitted if unnecessary. The light absorbing material may also be selected from materials which do not cause extinction of fluorescence of the fluorescent material.

Referring to FIG. 1 , there is illustrated one exemplary construction of the organic EL device fabricated according to the invention. The organic EL device is shown in FIG. 1 as having on a substrate 1 , a hole injecting electrode 2 , a hole injecting and transporting layer 3 , a light emitting layer 4 , an electron injecting and transporting layer 5 , and an electron injecting electrode 6 in the described order. The organic EL device of the invention is not limited to the illustrated construction and various other constructions are possible.

The organic EL device of the invention is generally of the dc or pulse drive type while it can be of the ac drive type. The applied voltage is generally about 2 to 30 volts.

EXAMPLE

Examples of the present invention are given below together with Comparative Examples for further illustrating the invention.

Synthetic Example 1

Synthesis of 2,3,5,6,11,12-hexaphenylnaphthacene (Illustrative Compound IV-256)

By effecting Dieles-Alder reaction of 1,4-benzoquinone with 2,3-dimethylbutadiene, 6,7-diphenyl-1,4-naphthoquinone was synthesized.

Next, boron tribromide was added over one hour to a mixed solution of 5.2 g (16.7 mmol) of the 6,7-diphenyl-1,4-naphthoquinone and 5.4 g (20 mmol) of 1,3-diphenyl-isobenzofuran in methylene chloride, yielding 7.5 g of 2,3,6,11-tetraphenyl-5,12-naphthoquinone (yellow acicular crystal: 80%).

Next, from the above-prepared 2,3,6,11-tetraphenyl-5,12-naphthoquinone and bromobenzene, 1.6 g of a diol product was obtained (white powder: 86%), from which 1.2 g of an end product of the following structure was obtained (red solid: 78%). Sublimation of 1 g of the red solid for purification left 0.8 g of a red solid. The results of analysis of the resulting red solid are shown below.

Mass analysis: m/e 685 ((M+1) + ) (the spectrum shown in FIG. 2 ); 1 H-NMR spectrum: shown in FIG. 3 ; Infrared absorption spectrum: shown in FIG. 4 .

Synthetic Example 2

Synthesis of 6,11-bis(biphenylyl)-2,3,5,12-tetraphenylnaphthacene (Illustrative Compound IV-257)

By effecting Dieles-Alder reaction of dibenzoylethylene with 2,3-diphenylbutadiene, 4,5-diphenyl-1,2-dibenzoylbenzene tetrahydro-compound was synthesized.

The tetrahydro-compound was subject to cyclization in acetic anhydride in the presence of phosphoric acid catalyst, yielding 4,7-dihydro-1,3,5,6-tetraphenyl-isobenzofuran.

Next, the dihydro-compound of furan and tetrachloro-p-benzoquinone (chloranyl) in toluene were heated under reflux to effect dehydrogenation, yielding 1,3,5,6-tetraphenylisobenzofuran.

Next, as in Synthetic Example 1, from the 1,3,5,6-tetraphenylisobenzofuran and 1,4-naphthoquinone, 6,8,9,11-tetraphenyl-5,12-naphthacenequinone was synthesized.

Further, from the 6,8,9,11-tetraphenyl-5,12-naphthacenequinone and p-bromobiphenyl, there was yielded 1.7 g of a diol product (white powder: 73%), from which 1.1 g of an end product of the following structure was obtained (red solid: 71%). Sublimation of 1 g of the red solid for purification left 0.9 g of a red solid. The results of analysis of the resulting red solid are shown below.

Mass analysis: m/e 837 ((M+1) + ) (the spectrum shown in FIG. 5 ); 1 H-NMR spectrum: shown in FIG. 6 ; Infrared absorption spectrum: shown in FIG. 7 .

Synthetic Example 3

Synthesis of 5,12-bis(biphenylyl)-2,3,6,8,9,11-hexaphenylnaphthacene (Illustrative Compound IV-213)

By following the same reaction procedure as in Synthetic Example 1, but using 5,6-diphenyl-1,4-naphthoquinone and 1,3,5,6-tetraphenylisobenzofuran, 2,3,6,8,9,11-hexaphenyl-5,12-naphthacenequinone was synthesized.

Next, from the 2,3,6,8,9,11-hexaphenyl-5,12-naphthacenequinone and p-bromobiphenyl, there was yielded 1.8 g of a diol product (white powder: 83%), from which 1.1 g of an end product of the following structure was obtained (red solid: 65%). Sublimation of 1 g of the red solid for purification left 0.8 g of a red solid. The results of analysis of the resulting red solid are shown below.

Mass analysis: m/e 989 ((M+1) + ) (the spectrum shown in FIG. 8 ); 1 H-NMR spectrum: shown in FIG. 9 ; Infrared absorption spectrum: shown in FIG. 10 .

Example 1

On a glass substrate, a transparent ITO electrode thin film was deposited to a thickness of 100 nm by RF sputtering and patterned. The glass substrate having the transparent ITO electrode was subjected to ultrasonic washing with neutral detergent, acetone, and ethanol, pulled up from boiling ethanol, and dried. The transparent electrode surface was further cleaned with UV/ozone. Thereafter, the substrate was secured by a holder in a vacuum evaporation chamber, which was evacuated to a vacuum of 1×10 −4 Pa or lower.

With the vacuum kept, N,N′-diphenyl-N,N′-bis[N-(4-methylphenyl)-N-phenyl-(4-aminophenyl)]-1,1′-biphenyl-4,4′-diamine was evaporated at a deposition rate of 0.2 nm/sec. to a thickness of 50 nm, forming a hole injecting layer.

Then, N,N,N′,N′-tetrakis(m-biphenyl)-1,1′-biphenyl-4,4′-diamine (TPD) was evaporated at a deposition rate of 0.2 nm/sec to a thickness of 20 nm, forming a hole transporting layer.

With the vacuum kept, the compound of the following structure according to the invention (Illustrative Compound IV-256) and tris(8-quinolinolato)aluminum (Alq3) were evaporated in a weight ratio of 2:100 and at an overall deposition rate of 0.2 nm/sec to a thickness of 70 nm, forming an electron injecting and transporting/light emitting layer.

Next, with the vacuum kept, Mg—Ag (weight ratio 10:1) was evaporated at a deposition rate of 0.2 nm/sec to a thickness of 200 nm, forming an electron injecting electrode. Aluminum was evaporated to a thickness of 100 nm to form a protective electrode, completing an organic EL device.

A dc voltage was applied across the organic EL device, which was found to produce light emission at a current density of 10 MA/cm 2 and a drive voltage of 8.88 volts to a luminance of 675 cd/M 2 . The light emission had a maximum wavelength λmax of 574 nm and chromaticity coordinates (x, y) of (0.53, 0.46).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 145 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 MA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 3,000 hours.

Example 2

An organic EL device was fabricated as in Example 1 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Example 1 was changed to the compound of the following structure (Illustrative Compound IV-257).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 9.0 volts to a luminance of 720 cd/m 2 . The light emission had a maximum wavelength λmax of 580 nm and chromaticity coordinates (x, y) of (0.54, 0.46).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 155 cd/m 2 1 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 3,000 hours.

Example 3

An organic EL device was fabricated as in Example 1 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Example 1 was changed to the compound of the following structure (Illustrative Compound IV-213).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 9.3 volts to a luminance of 500 cd/m 2 . The light emission had a maximum wavelength λmax of 590 nm and chromaticity coordinates (x, y) of (0.58, 0.42).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 135 cd/m 2 1 a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.68, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 3,000 hours.

Example 4

An organic EL device was fabricated as in Example 1 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Example 1 was changed to the compound of the following structure (Illustrative Compound IV-78).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 8.6 volts to a luminance of 750 cd/m 2 . The light emission had a maximum wavelength λmax of 578 nm and chromaticity coordinates (x, y) of (0.54, 0.46).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 152 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 4,000 hours.

Example 5

An organic EL device was fabricated as in Example 1 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Example 1 was changed to the compound of the following structure (Illustrative Compound IV-259).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 8.5 volts to a luminance of 700 cd/m 2 . The light emission had a maximum wavelength λmax of 585 nm and chromaticity coordinates (x, y) of (0.56, 0.44).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 155 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 3,000 hours.

Example 6

Organic EL devices were fabricated as in Example 1 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer was changed to the compounds of classes I to IV other than the Illustrative Compounds used in the foregoing Examples, obtaining substantially the same results.

Example 7

An organic EL device was fabricated as in Example 1 except that when the hole injecting and transporting layer was formed by evaporation in Example 1, the compound used along with TPD was changed to the compound of the following structure (Illustrative Compound IV-256), TPD and the compound were evaporated in a weight ratio of 2:100, and Alq3 was evaporated as a single layer.

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 5.72 volts to a luminance of 810 cd/m 2 . The light emission had a maximum wavelength λmax of 572 nm and chromaticity coordinates (x, y) of (0.48, 0.50).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 141 cd/m 2 , a maximum wavelength λmax of 615 nm, and chromaticity coordinates (x, y) of (0.61, 0.37).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 1,800 hours.

Example 8

An organic EL device was fabricated as in Example 7 except that the compound used along with TPD in evaporating the hole injecting and transporting layer in Example 7 was changed to the compound of the following structure (Illustrative Compound IV-257).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 5.94 volts to a luminance of 866 cd/m 2 . The light emission had a maximum wavelength λmax of 578 nm and chromaticity coordinates (x, y) of (0.51, 0.47).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 145 cd/m 2 , a maximum wavelength λmax of 616 nm, and chromaticity coordinates (x, y) of (0.62, 0.37).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 2,000 hours.

Example 9

Organic EL devices were fabricated as in Example 7 except that the compound used along with TPD in evaporating the hole injecting and transporting layer in Example 7 was changed to the compounds shown in Tables 1 to 32 other than the Illustrative Compounds used in the foregoing Examples 1 to 8, obtaining substantially the same results.

Example 10

After the hole injecting layer was formed as in Example 1, two inventive compounds of the following structure having different carrier trapping capabilities (I-1) and (IV-213) and N,N,N′,N′-tetrakis(m-biphenyl)-1,1′-biphenyl-4,4′-diamine (TPD) were evaporated in a weight ratio of 2:2:100 at a deposition rate of 0.2 nm/sec to a thickness of 40 nm, forming a light emitting layer.

With the vacuum kept, tris(8-quinolinolato)aluminum (Alq3) was evaporated at a deposition rate of 0.2 nm/sec to a thickness of 30 nm, forming an electron injecting and transporting layer.

Subsequently as in Example 1, an electron injecting electrode of Mg—Ag (weight ratio 10:1) and a protective electrode of aluminum were formed, completing an organic EL device.

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 6.3 volts to a luminance of 1,000 cd/m 2 . The light emission had a maximum wavelength λmax of 585 nm and chromaticity coordinates (x, y) of (0.57, 0.40).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 153 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extremely extended life as demonstrated by a luminance half-life period of more than 4,000 hours.

Example 11

An organic EL device was fabricated as in Example 7 except that the compound used along with TPD in evaporating the hole injecting and transporting layer in Example 7 was changed to the compound of the following structure (Illustrative Compound IV-78).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 5.7 volts to a luminance of 950 cd/m 2 . The light emission had a maximum wavelength λmax of 570 nm and chromaticity coordinates (x, y) of (0.51, 0.46).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 153 cd/m 2 , a maximum wavelength λmax of 615 nm, and chromaticity coordinates (x, y) of (0.61, 0.37).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 3,000 hours.

Example 12

An organic EL device was fabricated as in Example 7 except that the compound used along with TPD in evaporating the hole injecting and transporting layer in Example 7 was changed to the compound of the following structure (Illustrative Compound IV-259).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 5.75 volts to a luminance of 900 cd/m 2 . The light emission had a maximum wavelength λmax of 577 nm and chromaticity coordinates (x, y) of (0.45, 0.52).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 160 cd/m 2 , a maximum wavelength λmax of 615 nm, and chromaticity coordinates (x, y) of (0.61, 0.37).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited an extended life as demonstrated by a luminance half-life period of more than 2,500 hours.

Comparative Example 1

An organic EL device was fabricated as in Example 1 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Example 1 was changed to rubrene of the following structure.

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 9.0 volts to a luminance of 700 cd/m 2 . The light emission had a maximum wavelength λmax of 558 nm and chromaticity coordinates (x, y) of (0.48, 0.51).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 90 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.65, 0.35).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 1,500 hours.

Comparative Example 2

On a glass substrate, a transparent ITO electrode thin film was deposited to a thickness of 100 nm by RF sputtering and patterned. The glass substrate having the transparent ITO electrode was subjected to ultrasonic washing with neutral detergent, acetone, and ethanol, pulled up from boiling ethanol, and dried. The transparent electrode surface was further cleaned with UV/ozone. Thereafter, the substrate was secured by a holder in a vacuum evaporation chamber, which was evacuated to a vacuum of 1×10 −4 Pa or lower.

With the vacuum kept, N,N′-diphenyl-N,N′-bis[N-(4-methylphenyl)-N-phenyl-(4-aminophenyl)]-1,1′-biphenyl-4,4′-diamine was evaporated at a deposition rate of 0.2 nm/sec. to a thickness of 50 nm, forming a hole injecting layer.

Then, N,N,N′,N′-tetrakis(m-biphenyl)-1,1′-biphenyl-4,4′-diamine (TPD) was evaporated at a deposition rate of 0.2 nm/sec to a thickness of 20 nm, forming a hole transporting layer.

With the vacuum kept, the compound of the following structure (Compound I-1) and tris(8-quinolinolato)aluminum (Alq3) were evaporated in a weight ratio of 2:100 and at an overall deposition rate of 0.2 nm/sec to a thickness of 70 nm, forming an electron injecting and transporting/light emitting layer.

Next, with the vacuum kept, Mg—Ag (weight ratio 10:1) was evaporated at a deposition rate of 0.2 nm/sec to a thickness of 200 nm, forming an electron injecting electrode. Aluminum was evaporated to a thickness of 100 nm to form a protective electrode, completing an organic EL device.

A dc voltage was applied across the organic EL device. Initially, the device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 9.0 volts to a luminance of 800 cd/m 2 . The light emission had a maximum wavelength λmax of 572 nm and chromaticity coordinates (x, y) of (0.53, 0.46).

While the device was operated to continue light emission with a constant current of 10 mA/cm 2 conducted, measurement was made by means of a luminance meter equipped with a red filter for LCD, finding emission of red light at a luminance of 153 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34). The red filter used herein was to cut wavelengths of shorter than 590 nm and had a transmittance of 30% at a wavelength of 600 nm.

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 2,500 hours.

Comparative Example 3

An organic EL device was fabricated as in Comparative Example 2 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Comparative Example 2 was changed to the compound of the following structure (I-85).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 9.4 volts to a luminance of 870 cd/m 2 . The light emission had a maximum wavelength λmax of 570 nm and chromaticity coordinates (x, y) of (0.52, 0.47).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 147 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 2,500 hours.

Comparative Example 4

An organic EL device was fabricated as in Comparative Example 2 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Comparative Example 2 was changed to the compound of the following structure (II-40).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 8.2 volts to a luminance of 790 cd/m 2 . The light emission had a maximum wavelength λmax of 583 nm and chromaticity coordinates (x, y) of (0.54, 0.45).

Measurement was similarly made using the same red filter as in Comparative Example 2, finding emission of red light at a luminance of 156 cd/m 2 , a maximum wavelength λmax of 621 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 1,500 hours.

Comparative Example 5

An organic EL device was fabricated as in Comparative Example 2 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Example 2 was changed to the compound of the following structure (III-38).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 8.3 volts to a luminance of 580 cd/m 2 . The light emission had a maximum wavelength λmax of 591 nm and chromaticity coordinates (x, y) of (0.53, 0.45).

Measurement was similarly made using the same red filter as in Comparative Example 2, finding emission of red light at a luminance of 125 cd/m 2 , a maximum wavelength λmax of 622 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 1,500 hours.

Comparative Example 6

An organic EL device was fabricated as in Comparative Example 2 except that the compound used along with Alq3 in the electron injecting and transporting/light emitting layer in Comparative Example 2 was changed to the compound of the following structure (IV-114).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 8.7 volts to a luminance of 810 cd/m 2 . The light emission had a maximum wavelength λmax of 567 nm and chromaticity coordinates (x, y) of (0.52, 0.47).

Measurement was similarly made using the same red filter as in Comparative Example 2, finding emission of red light at a luminance of 141 cd/m 2 , a maximum wavelength λmax of 620 nm, and chromaticity coordinates (x, y) of (0.66, 0.34).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 1,000 hours.

Comparative Example 7

An organic EL device was fabricated as in Example 7 except that the compound used along with TPD in forming the hole injecting and transporting layer by evaporation in Example 7 was changed to rubrene of the following structure.

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 5.46 volts to a luminance of 788 cd/r 2 . The light emission had a maximum wavelength λmax of 553 nm and chromaticity coordinates (x, y) of (0.43, 0.54).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 80 cd/m 2 , a maximum wavelength λmax of 612 nm, and chromaticity coordinates (x, y) of (0.59, 0.39).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 900 hours.

Comparative Example 8

An organic EL device was fabricated as in Example 1 except that when the hole injecting and transporting layer was formed by evaporation in Comparative Example 7, TPD and the compound of the following structure (I-1) were evaporated in a weight ratio of 2:100, and Alq3 was evaporated as a single layer.

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 5.77 volts to a luminance of 974 cd/m 2 . The light emission had a maximum wavelength λmax of 563 nm and chromaticity coordinates (x, y) of (0.44, 0.53).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 140 cd/m 2 , a maximum wavelength λmax of 615 nm, and chromaticity coordinates (x, y) of (0.61, 0.37).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 1,700 hours.

Comparative Example 9

An organic EL device was fabricated as in Comparative Example 8 except that the compound used along with TPD in forming the hole injecting and transporting layer by evaporation in Comparative Example 8 was changed to the compound of the following structure (IV-114).

A dc voltage was applied across the organic EL device. The device was found to produce light emission at a current density of 10 mA/cm 2 and a drive voltage of 5.73 volts to a luminance of 1,005 cd/m 2 . The light emission had a maximum wavelength λmax of 560 nm and chromaticity coordinates (x, y) of (0.45, 0.52).

Measurement was similarly made using the same red filter as in Example 1, finding emission of red light at a luminance of 138 cd/m 2 1 a maximum wavelength λmax of 615 nm, and chromaticity coordinates (x, y) of (0.61, 0.37).

The device was continuously operated for light emission with a constant current of 50 mA/cm 2 conducted. It exhibited a luminance half-life period of less than 1,700 hours.

BENEFITS OF THE INVENTION

There have been described compounds for organic EL devices and organic EL devices which produce light emission of satisfactory luminance, especially at long wavelength and are durable in that improved light emitting performance lasts for a long time.

Claims

1. A compound for organic electroluminescent devices, having a basic skeleton represented by the following formula (I): wherein R1 to R8 each are hydrogen or a substituted or unsubstituted aryl or alkenyl group, with the proviso that at least six of R1 to R8 are substituted or unsubstituted aryl or alkenyl groups.

2. An organic electroluminescent device comprising a hole injecting electrode, an electron injecting electrode, and an organic layer disposed between the electrodes and including at least a light emitting layer, whereinsaid light emitting layer contains the compound of claim 1.

3. The organic electroluminescent device of claim 2, wherein the compound contained in said light emitting layer has a basic skeleton represented by the following formula (II): wherein each R group in sets of R11 to R15, R21 to R25, R31 to R35, and R41 to R45 is hydrogen or a substituted or unsubstituted alkyl, aryl, amino, heterocyclic or phenoxy group, the R groups in at least two sets have substituted or unsubstituted aryl, heterocyclic or aryloxy groups as substituents; R5, R6, R7, and R8 each are hydrogen or an aryl group, with the proviso that at least two of R5 to R8 are aryl groups; at least two R groups in each of the sets of R11 to R15, R21 to R25, R31 to R35, and R41 to R45 may form a fused ring.

4. The organic electroluminescent device of claim 2 wherein said light emitting layer further contains an electron injecting and transporting compound and/or a hole injecting and transporting compound.

5. The organic electroluminescent device of claim 2 wherein said light emitting layer contains at least two compounds.

6. The organic electroluminescent device of claim 2 wherein said light emitting layer contains at least two dopants, the content of the dopants combined being up to 30% by weight based on a host material.

7. The organic electroluminescent device of claim 2, wherein the overall content of said compound in said light emitting layer is up to 30% by weight based on a host material.

8. The organic electroluminescent device of claim 6 wherein said light emitting layer contains at least two compounds having different carrier trapping capabilities.

9. The organic electroluminescent device of claim 7 wherein said light emitting layer contains at least a compound having a hole trapping capability and a compound having an electron trapping capability.

10. The organic electroluminescent device of claim 2, wherein the device contains at least two light emitting layers, each of said light emitting layers containing a dopant having different carrier trapping capabilities from the dopants of the other layers.

11. The organic electroluminescent device of claim 2, wherein the device contains at least two light emitting layers, one of which contains a dopant having a hole trapping capability, and a second of said at least one other layers contains a dopant having an electron trapping capability.

12. The organic electroluminescent device of claim 7, wherein said light emitting layer contains at least two compounds having different carrier trapping capabilities.

13. The organic electroluminescent device of claim 2, wherein the device contains at least two light emitting layers, each of said light emitting layers containing at least two dopant compounds, the content of the dopants combined being up to 30% by weight based on a host material, the dopants of each layer having different carrier trapping capabilities from the dopants of the other layers.

14. The organic electroluminescent device of claim 2, wherein the device contains at least two light emitting layers, each of said light emitting layers containing at least two dopant compounds, the content of the dopants combined being up to 30% by weight based on a host material, and wherein the dopants of one layer have a hole trapping capability and the dopants of a second layer have an electron trapping capability.

15. The organic electroluminescent device of claim 2, wherein the device contains at least two light emitting layers, each of said light emitting layers containing a dopant compound having a hole trapping capability and a dopant compound having an electron trapping capability and each layer having different carrier trapping capabilities from the dopants of the other layers.

16. The organic electroluminescent device of claim 2, wherein the device contains at least two light emitting layers, one of which contains a dopant having a hole trapping capability and a dopant compound having an electron trapping capability, and a second of said at least one other layers contains a dopant having an electron trapping capability and a hole trapping capability.