Electroluminescent devices

Abstract

Disclosed herein an electroluminescent device for converting an energy of an electric field applied directly to a light energy and capable of producing surface luminescent for a large area different from conventional incandescent lamps, fluorescent lamps or light emitting diodes.

Description

BACKGROUND OF THE INVENTION

The present invention relates to organic electroluminescent devices. More in particular, the present invention relates to electroluminescent devices for converting an energy of an electric field applied directly to a light energy and capable of producing surface luminescence for a large area different from conventional incandescent lamps, fluorescent lamps or light emitting diodes.

Electroluminescent devices are grouped into the following two categories depending on the difference of the luminescent excitation system:

(1) an AC driving electroluminescent device in which luminescent material is excited by the local transfer of electrons or holes in a luminescent layer and emits light only by an AC electric field, and (2) a DC driving electroluminescent device in which luminescent material is excited by the injection of electrons and holes from an electrode and this re-combination in a luminescent layer and actuated only by a DC electric field.

The AC driving electroluminescent device generally uses, as a luminescent material, an inorganic compound comprising ZnS and Mn, Cu, etc. added thereto, but it involves drawbacks of requiring high AC electric field of higher than 200 V for the driving, much production cost, and insufficient luminance and durability.

On the other hand, the DC driving electroluminescent device uses, as a luminescent layer, a thin film comprising an organic compound, and it has high power conversion efficiency and high luminance.

For instance, Japanese Patent Application Laid-Open (KOKAI) No. 59-194393 (U.S. Pat. No. 4,539,507) discloses an electroluminescent device comprising an anode, a hole transporting zone, an organic luminescent zone and a cathode, in which the total film-thickness for the anode, the hole transporting zone and the organic luminescent zone is less than 1 .mu.m, and at least one of the anode and the cathode allows to permeate at least 80% of radiation rays at a wavelength of not less than 400 nm and has at least 9.times.10.sup.-5 W/W of power conversion efficiency. As the fluorescent whitening agent of the electron transporting compound forming the organic luminescent zone, there are used, 2,5-bis(5,7-di-t-benzyl-2-benzoxazolyl)-1,3,4-thiadiazole; 4,4'-bis(5,7-t-benzyl-3-benzoxazolyl)stilbene; 2,5-bis(5,7-di-t-benzyl-2-benzoxazolyl)thiophene; 2,2'-(p-phenylenedivinylene)-bis-benzothiazole; 4,4'-bis(2-benzoxazolyl)biphenyl; 2,5-bis(5-(.alpha.,.alpha.-dimethylbenzyl)-2-benzoxazolyl)thiophene; 4,4'-bis(5,7-di (2-methyl-2-butyl)-2-benzoxazolyl)stilbene; and 2,5-bis(5,7-di-(2-methyl-2-butyl)-2-benzoxazolyl)-3,4-diphenylthiophene.

U.S. Pat. No. 4,720,432 also discloses an electroluminescent device comprising in sequence, an anode, an organic hole injecting and transporting zone, an organic electron injecting and transporting zone, and a cathode, characterized in that the organic hole injecting and transporting zone is comprised of a layer in contact with the anode containing a hole injection porphyrnic compound and a layer containing a hole transporting aromatic tertiary amine interposed between the hole injecting layer and the electro injecting and transporting zone.

Further an electroluminescent device comprising an anode, a hole transporting organic material layer, a luminescent layer, an electron transporting organic material layer and a cathode and emitting yellow light is reported in Jpn. Journal of Applied Physics, Vol. 27, pages 713-715, and there are exemplified N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine as the hole transporting organic material, 3,4,9,10-perylene tetracarbonic acid bisbenzimidazole as the electron transporting organic material and phthaloperinone as the luminescent material.

However, it can not be said that sufficient study has been made on the DC driving electroluminescent device using organic compounds as the luminescent material, with respect to the material and device-forming technique, and there are many problems with respect to the improvement of luminance, the control of wavelength of the emission light, the durability and the increased working life.

As a result of the present inventors' earnest studies in order to provide an electroluminescent device having high luminance and excellent durability with long lasting luminescent performance, and providing versatile wavelength of emission light, capable of accurately selecting luminescent hues such as blue, green and red while considering the application to full color display, it has been found that an electroluminescent device comprising as a luminescent layer at least one layer of an organic compound sandwiched between an anode and a cathode, in which the said organic compound layer comprises an organic compound represented by the following formula (I'), can be driven at a low applied voltage, can provide an emission light of high luminance for a long period, and can accurately select the luminescent hues. ##STR1## (where B' represents: (1) a cyclic hydrocarbon such as a substituted or unsubstituted cyclobutene, cyclohexene or cyclohexadiene, a substituted or unsubstituted benzene, p-benzoquinone, cyclopentadienone, diphenyl, etc.;

(2) a condensated polycyclic hydrocarbon such as naphthalene, anthracene, naphthacene, phenanthrene, a substituted or unsubstituted indene, indenone, naphthocyclobutene, a substituted or unsubstituted benzocyclohexene, naphthocyclohexene, etc.; (3) an oxygen heterocycle such as a substituted or unsubstituted furane, benzofuran, isobenzofuran, pyrrone, isonaphthofuran, etc.; (4) a sulfur heterocycle such as thiophene, isobenzothiophene and isonaphthothiophene, etc.; (5) a nitrogen heterocycle such as substituted or unsubstituted pyrrole, imidazole, pyridine, pyridazine, pyrazine, pyrimidine, quinoline, quinazoline, triazine, pyrazole, isoindole, etc.; Ar represents benzene, biphenyl, methoxybenzene or naphthalene; m is an integer of 1 to 6; and n is an integer of 1 to 6.

The present invention has been attained based on this finding.

SUMMARY OF THE INVENTION

In an aspect of the present invention, there is provided an electroluminescent device comprising an anode, a cathode and one at least one organic compound layer sandwiched therebetween, in which the said organic compound layer comprises an organic compound, as the constituent ingredient, represented by the following formula (I): ##STR2## wherein B represents ##STR3## (in which X.sup.1 is H, Cl, CH.sub.3, OCH.sub.3, C.sub.2 H.sub.5 or CN, and l is 1,2 or 3) ##STR4## (in which X.sup.2 is H or OCH.sub.3, and X.sup.3 is H, CH.sub.3, ##STR5## (in which X.sup.4 is H or ##STR6## (in which D is O, S, or N, X.sup.5 is H or COOH,

X.sup.6 is H, CH.sub.3, C.sub.2 H.sub.5 or ##STR7## and .kappa. is 0 or 1) ##STR8## (in which X.sup.7 is H or O) ##STR9## (in which X.sup.8 is O or C(CN).sub.2) ##STR10## (in which X.sup.9 is H or CH.sub.3) ##STR11## (in which X.sup.10 is O or C(CN).sub.2) ##STR12## (in which D is O, S or N, Y.sup.1 is H, and i is 0 or 1) ##STR13## (in which E is O or S) ##STR14## (in which E is O or S) ##STR15## (in which G is S or NH) ##STR16## (in which Z represents: (1) substituted or unsubstituted (C.sub.4 -C.sub.6) cycloalkenes containing at least one double bond in the ring, (2) (C.sub.4 -C.sub.6) cycloalkenes having an aromatic ring and containing one double bond in the ring, (3) 5- or 9-membered heterocycles containing a double bond and at least one oxygen in the ring, (4) 5-membered heterocycles having an aromatic ring, and containing one oxygen and at least one double bond in the ring, (5) 6- or 7-membered heterocycles having C.sub.4 or C.sub.6 cycloalkene with at least one double bond, and containing two oxygen atoms in the ring, (6) C.sub.5, C.sub.6 or C.sub.11 heterocycles containing 1 or 2 sulfur atoms in the ring, (7) 5- or 6-membered heterocycles containing 2 to 4 nitrogen atoms and at least one double bond in the ring, (8) 5-, 6- or 8-membered heterocycles having an aromatic ring, and containing at least one double bond and 1 or 2 nitrogen atoms in the ring, (9) 5- or 6-membered heterocycles containing 1 or 2 nitrogen atoms and, optionally, oxygen atom in the ring; Ar represents ##STR17## m represents an integer of 1 to 6; and n represents an integer of 1 to 6.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 to FIG. 3 are schematic cross sectional views of an electroluminescent device according to the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The organic compound consisting a luminescent layer in the electroluminescent device according to the present invention is a compound represented by the formula (I): ##STR18## wherein B represents ##STR19## (in which X.sup.1 is H, Cl, CH.sub.3, OCH.sub.3, C.sub.2 H.sub.5 or CN, and l is 1, 2 or 3) ##STR20## (in which X.sup.2 is H or OCH.sub.3, and X.sup.3 is H, CH.sub.3, ##STR21## (in which X.sup.4 is H or ##STR22## (in which D is O, S, or N, X.sup.5 is H or COOH,

X.sup.6 is H, CH.sub.3, C.sub.2 H.sub.5 or ##STR23## and .kappa. is 0 or 1) ##STR24## (in which X.sup.7 is H or O) ##STR25## (in which X.sup.8 is O or C(CN).sub.2) ##STR26## (in which X.sup.9 is H or CH.sub.3) ##STR27## (in which X.sup.10 is O or C(CN).sub.2) ##STR28## (in which D is O, S or N, Y is H, and i is 0 or 1) ##STR29## (in which E is O or S) ##STR30## (in which E is O or S) ##STR31## (in which G is S or NH) ##STR32## (in which Z represents: (1) substituted or unsubstituted (C.sub.4 -C.sub.6) cycloalkenes containing at least one double bond in the ring, (2) (C.sub.4 -C.sub.6) cycloalkenes having an aromatic ring and containing one double bond in the ring, (3) 5- or 9-membered heterocycles containing a double bond and at least one oxygen in the ring, (4) b 5-membered heterocycles having an aromatic ring, and containing one oxygen and at least one double bond in the ring, (5) 6- or 7-membered heterocycles having C.sub.4 or C.sub.6 cycloalkene with at least one double, bond and containing two oxygen atoms in the ring, (6) C.sub.5, C.sub.6 or C.sub.11 heterocycles containing 1 or 2 sulfur atoms in the ring, (7) 5- or 6-membered heterocycles containing 2 to 4 nitrogen atoms and at least one double bond in the ring, (8) 5-, 6- or 8-membered heterocycles having an aromatic ring, and containing at least one double bond and 1 or 2 nitrogen atoms in the ring, (9) 5- or 6-membered heterocycles containing 1 or 2 nitrogen atoms and, optionally, oxygen atom in the ring; Ar represents ##STR33## m represents an integer of 1 to 6; and n represents an integer of 1 to 6.

As the specific compounds represented by the general formula (I), there can be exemplified compounds Nos. 1-174.

For the substituent B in the formula (I):

the compound belonging to Group 1 includes Nos. 8-11 and 14-20. the compound belonging to Group 2 includes Nos. 13 and 25-37, the compound belonging to Group 3 includes Nos. 38-43, the compound belonging to Group 4 includes Nos. 44-46, the compound belonging to Group 5 includes Nos. 47-53, the compound belonging to Group 6 includes Nos. 54-62, the compound belonging to Group 7 includes Nos. 65-67, the compound belonging to Group 8 includes Nos. 68 and 69, the compound belonging to Group 9 includes Nos. 12-21, the compound belonging to Group 10 includes Nos. 22, 70-75, 96-99 and 111-118, the compound belonging to Group 11 includes Nos. 85, 86, 91 and 92, the compound belonging to Group 12 includes Nos. 87-90, the compound belonging to Group 13 includes Nos. 23, 24 and 126-136, the compound belonging to Group 14 includes Nos. 137-141, the compound belonging to Group 15 includes Nos. 143-145, the compound belonging to Group 16 includes Nos. 150-156 and 158, the compound belonging to Group 17 includes Nos. 122-123, the compound belonging to Group 18 includes Nos. 119-120, the compound belonging to Group 19 includes Nos. 147-148, the compound belonging to Group 20 includes Nos. 165-166, the compound belonging to Group 21 includes Nos. 161-162, the compound belonging to Group 22 includes Nos. 167-170, the compound belonging to Group 23 includes Nos. 76, 80, 100 and 125, the compound belonging to Group 24 includes Nos. 82-101, the compound belonging to Group 25 includes Nos. 83 and 102, the compound belonging to Group 26 includes Nos. 104 and 142, the compound belonging to Group 27 includes Nos. 106 and 108-110, the compound belonging to Group 28 includes Nos. 171-172, the compounds belonging to Group 29 are respectively as below: Group 29-1 : Compound Nos. 1-7 Group 29-2 : Compound Nos. 63 and 64 Group 29-3 : Compound Nos. 77 and 78 Group 29-4 : Compound Nos. 79, 81, 84 and 93 Group 29-5 : Compound Nos. 94 and 95 Group 29-6 : Compound Nos. 103, 105 and 107 Group 29-7 : Compound Nos. 121, 124, 146 and 149 Group 29-8 : Compound Nos. 157, 160, 163 and 164 Group 29-9 : Compound Nos. 159, 173 and 174

In the substituent B of the formula (I), compounds belonging to Groups 1 to 9, 13 to 19, 21, 23, 24, 29-1 and 29-2, more preferably Groups 1 to 9, 23, 24, 29-1 and 29-2, most preferably Groups 1 and 6, are preferred.

__________________________________________________________________________Compound No. Structural formula__________________________________________________________________________ ##STR34##2 ##STR35##3 ##STR36##4 ##STR37##5 ##STR38##6 ##STR39##7 ##STR40##8 ##STR41##9 ##STR42##10 ##STR43##11 ##STR44##12 ##STR45##13 ##STR46##14 ##STR47##15 ##STR48##16 ##STR49##17 ##STR50##18 ##STR51##19 ##STR52##20 ##STR53##21 ##STR54##22 ##STR55##23 ##STR56##24 ##STR57##25 ##STR58##26 ##STR59##27 ##STR60##28 ##STR61##29 ##STR62##30 ##STR63##31 ##STR64##32 ##STR65##33 ##STR66##34 ##STR67##35 ##STR68##36 ##STR69##37 ##STR70##38 ##STR71##39 ##STR72##40 ##STR73##41 ##STR74##42 ##STR75##43 ##STR76##44 ##STR77##45 ##STR78##46 ##STR79##__________________________________________________________________________47 ##STR80##48 ##STR81##49 ##STR82##50 ##STR83##51 ##STR84##52 ##STR85##53 ##STR86##54 ##STR87##55 ##STR88##56 ##STR89##57 ##STR90##58 ##STR91##59 ##STR92##60 ##STR93##61 ##STR94##62 ##STR95##63 ##STR96##64 ##STR97##65 ##STR98##66 ##STR99##67 ##STR100##68 ##STR101##69 ##STR102##70 ##STR103##71 ##STR104##72 ##STR105##73 ##STR106##74 ##STR107##75 ##STR108##76 ##STR109##77 ##STR110##78 ##STR111##79 ##STR112##80 ##STR113##81 ##STR114##82 ##STR115##83 ##STR116##84 ##STR117##85 ##STR118##86 ##STR119##87 ##STR120##88 ##STR121##89 ##STR122##90 ##STR123##91 ##STR124##92 ##STR125##93 ##STR126##94 ##STR127##95 ##STR128##96 ##STR129##97 ##STR130##98 ##STR131##99 ##STR132##100 ##STR133##101 ##STR134##102 ##STR135##103 ##STR136##104 ##STR137##105 ##STR138##106 ##STR139##107 ##STR140##108 ##STR141##109 ##STR142##110 ##STR143##__________________________________________________________________________111 ##STR144##112 ##STR145##113 ##STR146##114 ##STR147##115 ##STR148##116 ##STR149##117 ##STR150##118 ##STR151##119 ##STR152##120 ##STR153##121 ##STR154##122 ##STR155##123 ##STR156##124 ##STR157##125 ##STR158##126 ##STR159##127 ##STR160##128 ##STR161##129 ##STR162##130 ##STR163##131 ##STR164##132 ##STR165##133 ##STR166##134 ##STR167##135 ##STR168##136 ##STR169##137 ##STR170##138 ##STR171##139 ##STR172##140 ##STR173##141 ##STR174##142 ##STR175##143 ##STR176##144 ##STR177##145 ##STR178##146 ##STR179##147 ##STR180##148 ##STR181##149 ##STR182##150 ##STR183##151 ##STR184##152 ##STR185##153 ##STR186##154 ##STR187##155 ##STR188##156 ##STR189##157 ##STR190##158 ##STR191##159 ##STR192##160 ##STR193##161 ##STR194##162 ##STR195##163 ##STR196##164 ##STR197##165 ##STR198##166 ##STR199##167 ##STR200##168 ##STR201##169 ##STR202##170 ##STR203##171 ##STR204##172 ##STR205##173 ##STR206##174 ##STR207##__________________________________________________________________________

The layer constituting the luminescence (light emission) of the electroluminescent device according to the present invention comprises at least one of the ingredients represented by the formula (I) and, if necessary, may also contain at least one known luminescent material for the stabilization of film crystallization. The layer constituting the luminescence of the electroluminescent device according to the present invention means a luminescent layer, or light-emitting electron transporting layer and hole transporting layer.

The thickness of the layer constituting the luminescence of the present invention is not more than 2 .mu.m, preferably, from 0.05 to 0.5 .mu.m.

For improving the charge injection efficiency from the electrode, a conventional charge injecting and transporting layer can be independently disposed between an anode and a cathode. As the charge injecting and transporting layer, there cen be exemplified a hole transporting layer for properly transporting holes to the cathode when the holes are injected and an electron transporting layer for properly transporting electrons to the anode.

As the electroluminescent device according to the present invention, for example, the electroluminescent device having at least one conventional hole transporting layer, at least one conventional electron transporting layer, or at least one conventional hole transporting layer and at least one conventional electron transporting layer other than the luminescent layer of the present invention may be exemplified.

As the electron transporting substance constituting the conventional electron transporting layer in the present invention, those compounds as disclosed in U.S. Pat. Nos. 4720432 and 4539507 can be used. As preferred conventional electron transporting substance, there can be mentioned aluminum trisoxine, perylene tetracarboxylic acid derivatives.

The thickness of the electron transporting layer of the present invention is not more than 2000 .ANG..

As the hole transporting substance constituting the conventional hole transporting layer in the present invention, those compounds as disclosed in U.S. Pat. Nos. 4539507 and 4,720,432 can be used. As preferred conventional hole transporting compounds, there can be mentioned those having a hole mobility coefficient of at least 10.sup.-5 cm.sup.2 /V-sec between electrodes applied with an electric field of 10.sup.4 -10.sup.6 V/cm, for example, aromatic amine compound: N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl 4,4'-diamine.

The thickness of the hole transporting layer in the present invention is not more than 2000 .ANG..

The anode, in the present invention comprises metal of great work function, alloys or compounds thereof, electroconductive polymers of great work function, etc. As specific examples, there can be mentioned nickel, gold, platinum and palladium and alloys thereof, tin oxide (SnO.sub.2), indium-tin oxide (ITO), copper iodide, poly(3-methylthiophene), polypyrrole, etc.

The thickness of the anode of the present invention is from 100 to 5000 .ANG., preferably, 200 to 2000 .ANG..

For the cathode in the present invention, metals of small work function may be used. For example, silver, tin, lead, magnesium, manganese and aluminum or alloys thereof may be used. The thickness of the cathode of the present invention is not less than 500 .ANG..

It is preferable that at least one of substances used for the anode and the cathode has a sufficient transparency in the region of a luminous wavelength (light emitting wavelength) of the device. Specifically, it is preferable that the substance has a light transmittance of not lower than 80%.

The electroluminescent device according to the present invention is manufactured by successively laminating the respective layers described above on a transparent substrate such as glass in accordance with a customary method. For instance, the luminescent layer (organic compound layer) in the present invention is prepared by forming the foregoing compounds into thin films by means of vacuum vapor deposition, solution coating, etc.

For the improvement of the stability, particularly, for the protection against moisture in air of the device, there may be mentioned a method of laminating a protecting layer, or a method of placing the entire device into a cell and sealing silicon oil, etc. therein.

In a case where the compound used has hole transporting property, electron transporting property and luminescent property by itself, or compounds having respective property are used in admixture, a constitution as shown in FIG. 1 (1: luminescent layer, 2: cathode, 3: anode and 4: substrate) can be taken.

FIG. 2 (1: luminescent layer, 2: cathode, 3: anode, 4: substrate, 5: electron transporting compound layer and 6: hole transporting compound layer) shows a constitution in which a luminescent layer 1 is formed by the combination of a hole transporting compound layer 6 and an electron transporting compound layer 5. Preferred properties of organic compounds are combined in this constitution, intended for the development of a device of excellent luminescence property in which holes or electrons can be transported smoothly from the electrode by the combination of layers of excellent hole transporting compound and/or electron transporting compound. Either one of the compound layers emits light depending on the combination of the compound layers.

FIG. 3 (1: luminescent layer, 1': luminescent compound layer, 2: cathode, 3: anode, 4: substrate, 5: electron transporting compound layer and 6: hole transporting compound layer) shows a structure in which a luminescent layer 1 is formed by the combination of a hole transporting compound layer 6, a luminescent compound layer 1' and an electron transporting compound layer 5, which is based on an improvement for the concept of the function separation described above. By the function separation the selection for the compounds facilitates while taking notice of the hole transporting, electron transporting and luminescent properties, and as a result a wide range of compounds can be used and the versatility of the wavelength of luminescence is increased. Any of the organic compounds according to the present invention is excellent in luminescent property and can be constituted, as occasion demand, as shown in FIGS. 1, 2 and 3.

Further, the compound represented by the formula (I) according to the present invention is excellent in the hole transporting property or the electron transporting property depending on B, Ar in the formula (I). Accordingly, two or more kinds of compounds according to the present invention may be used in the constitution as shown in FIGS. 2 and 3.

The electroluminescent device according to the present invention emits light under the application of an electric bias to the luminescent layer, but even slight pinholes, if any, will cause short circuit making the device to function no more. Accordingly, it is desired to use a compound of excellent film-forming property for constituting the luminescent layer and, if necessary, the luminescent layer may be formed in combination with a compound of good film-forming property, for example, a polymer binder. As the polymer binder usable herein, there can be exemplified polystyrene, polyvinyl toluene, poly-N-vinyl carbazole, polymethyl methacrylate, polymethyl acrylate, polyester, polycarbonate and polyimide.

In the electroluminescent device according to the present invention, since the compound represented by the formula (I) is used as the material for constituting the luminescent layer, light-emission at high luminance can be obtained for a long period even with a low driving voltage. The electroluminescent devices according to the present invention emits light of various tones by using the compounds according to the present invention.

Further, since in the present invention the devices can easily be prepared by means of vacuum vapor deposition, etc. there is provided a merit that inexpensive devices of large area can be produced efficiently.

EXAMPLES

The present invention will be more precisely explained while referring to Examples as follows.

However, the present invention is not restricted to examples under mentioned. From the foregoing description, one skilled in the art can easily asserting the essential characteristics of the present invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.

EXAMPLE 1

A device was manufactured by forming an anode sized 3 mm.times.3 mm, 500 .ANG. in thickness comprising indium tin oxide (ITO) on a glass substrate, and forming, thereover, a hole transporting layer of 500 .ANG. in thickness comprising a benzidine derivative represented by the following formula (a), a luminescent layer of 1000 .ANG. in thickness comprising the compound No. 8 described above and an anode of 1500 .ANG. in thickness comprising silver-magnesium alloy (silver: 7.7 atm %, and purity: 99.9%) respectively by means of vacuum vapor deposition. The vacuum degree was about 1.times.10.sup.-6 Torr and the substrate temperature was at a room temperature upon vapor deposition. A DC power source was connected by way of lead wires to the anode and the cathode of the thus manufactured device and, when 30 V of voltage was applied, a current density of 70 mA/cm.sup.2 flowed to the device and clear blue luminescence was confirmed for a long period. ##STR208##

In this example, the compound (No. 8) according to the present invention functioned as electron transporting and luminescent material.

EXAMPLE 2-5

Devices were manufactured in the same manner as in Example 1 except for using the compounds shown below instead of the compound No. 8 used in Example 1. The results thereof are set forth below.

______________________________________Example No. Compound No. Tone of emitted light______________________________________2 No. 162 blue3 No. 77 blue4 No. 63 yellow5 No. 62 yellow______________________________________

EXAMPLE 6

A device was manufactured in the same manner as in Example 1 except for using the compound No. 9 as the ingredient for forming the luminescent layer and the perylene derivative represented by the following formula (b) as the ingredient for forming the electron transporting layer. The film thickness of the electron transporting layer was 500 .ANG.. When the device was driven in the same manner as in Example 1, a current of 30 mA/cm.sup.2 flowed to the device under a voltage of 20 V, and clear blue luminescence was observed for long period. ##STR209##

In this example, the compound (No. 9) according to the present invention functioned as hole transporting and luminescent material.

EXAMPLES 7-10

Devices were manufactured in the same manner as in Example 6 except for using the compounds shown below instead of the compound No. 9 used in Example 6. The results thereof are set forth below.

______________________________________Example No. Compound No. Tone of emitted light______________________________________7 No. 10 blue8 No. 11 blue9 No. 44 orange10 No. 65 blue______________________________________

EXAMPLE 11

Using the substrate having an anode as in Example 1, a luminescent layer of 1000 .ANG. in thickness comprising the compound No. 9 and a silver-magnesium alloy layer of 1500 .ANG. in thickness as the cathode were respectively formed on the anode under the same conditions as described above by means of vacuum vapor deposition. When the device was driven in the same manner as in Example 1, a current of 20 mA/cm.sup.2 flowed to the device at a voltage of 20 V, and clear blue luminescence was observed for long period.

In this example, the compound (No. 8) according to the present invention functioned as a luminescent layer.

EXAMPLES 12

A device was manufactured in the same manner as in Example 11 except for using the compound No. 119 instead of the compound No. 9 used in Example 11. The result thereof is set forth below.

______________________________________Example No. Compound No. Tone of emitted light______________________________________12 No. 119 blue______________________________________

EXAMPLE 13

A device was manufactured by using the substrate having an anode as in Example 1 and then vapor-depositing under vacuum, on the anode, a hole transporting layer of 600 .ANG. in thickness comprising a triphenylamine derivative represented by the following formula (c), a luminescent layer of 600 .ANG. in thickness comprising the compound No. 120, an electron transporting layer of 600 .ANG. in thickness comprising perylene derivative represented by the formula (b) and a silver-magnesium alloy as the cathode were successively formed under the same conditions as those in Example 1. When the device was driven in the same manner as in Example 1, a current of 20 mA/cm.sup.2 flowed to the device at a voltage of 30 V and blue luminescence was observed for a long period. ##STR210##

EXAMPLES 14-15

Devices were manufactured in the same manner as in Example 13 except for using the compounds shown below instead of the compound No. 120 used in Example 13. The results thereof are set forth below.

______________________________________Example No. Compound No. Tone of emitted light______________________________________14 No. 159 blue15 No. 57 blue______________________________________

Claims

1. An electroluminescent device comprising an anode, a cathode and one or a plurality of organic compound layers sandwiched therebetween, in which said organic compound layers comprise an organic compound, as the constituent ingredient, represented by the following formula (I): ##STR211## wherein B represents ##STR212## (in which X.sup.1 is H, Cl, CH.sub.3, OCH.sub.3, C.sub.2 H.sub.5 or CN, and l is 1, 2 or 3), ##STR213## (in which X.sup.2 is H or OCH.sub.3, and X.sup.3 is H, CH.sub.3, ##STR214## (in which X.sup.4 is H or ##STR215## (in which D is O, S, or N, X.sup.5 is H or COOH,

X.sup.6 is H, CH.sub.3, C.sub.2 H.sub.5 or ##STR216## and .kappa. is 0 or 1), ##STR217## (in which X.sup.7 is H or O), ##STR218## (in which X.sup.8 is O or C(CN).sub.2), ##STR219## (in which X.sup.9 is H or CH.sub.3), ##STR220## (in which X.sup.10 is O or C(CN).sub.2), ##STR221## (in which D is O, S or N,

Y.sup.1 is H, and

i is 0 or 1), ##STR222## (in which E is O or S), ##STR223## (in which E is O or S), ##STR224## (in which G is S or NH), ##STR225## (in which Z represents: (1) substituted or unsubstituted (C.sub.4 -C.sub.6) cycloalkenes containing at least one double bond in the ring,

(2) (C.sub.4 -C.sub.6) cycloalkenes having an aromatic ring and containing one double bond in the ring,

(3) 5- or 9-membered heterocycles containing a double bond and at least one oxygen in the ring,

(4) 5-membered heterocycles having an aromatic ring, and containing one oxygen and at least one double bond in the ring,

(5) 6- or 7-membered heterocycles having C.sub.4 or C.sub.6 cycloalkene with at least one double bond, and containing two oxygen atoms in the ring,

(6) C.sub.5, C.sub.6 or C.sub.11 heterocycles containing 1 or 2 sulfur atoms in the ring,

(7) 5- or 6-membered heterocycles containing 2 to 4 nitrogen atoms and at least one double bond in the ring,

(8) 5-, 6- or 8-membered heterocycles having an aromatic ring, and containing at least one double bond and 1 or 2 nitrogen atoms in the ring, or

(9) 5- or 6-membered heterocycles containing 1 or 2 nitrogen atoms and, optionally, oxygen atom in the ring;

Ar represents ##STR226## m represents an integer of 1 to 6; and n represents an integer of 1 to 6.

2. An electroluminescent device according to claim 1, wherein at least one selected from the group consisting of electron transporting layer and hole transporting layer is further disposed between the anode and the cathode.

3. An electroluminescent device according to claim 1, wherein B represents ##STR227## (wherein X.sup.1 and l are the same as defined above), ##STR228## (wherein X.sup.2 and X.sup.3 are the same as defined above), ##STR229## (wherein X.sup.4 is the same as defined above), ##STR230## (wherein X.sup.9 is the same as defined above), ##STR231## (wherein D, Y.sup.1 and i are the same as defined above), ##STR232## (wherein E is the same as defined above), or Z (which represents (1) substituted or unsubstituted (C.sub.4 -C.sub.6) cycloalkenes containing at least one double bond in the ring or (2) (C.sub.4 -C.sub.6) cycloalkenes having an aromatic ring and containing one double bond in the ring).

4. An electroluminescent device according to claim 1, wherein the thickness of the organic compound layer is not more than 2 .mu.m.

5. An electroluminescent device according to claim 1, wherein said organic compound is selected from the group consisting of the compounds represented by the following formula: ##STR233## ##STR234## ##STR235##