Organic compound and organic electroluminescence device using the same

Abstract

The present invention discloses an organic compound and an organic electroluminescence device using the organic compound as a host material, a fluorescent guest material, an electron transporting or a hole blocking material in the light emitting layer of the organic electroluminescence device. The organic compound may be for lowering a driving voltage, power consumption or increasing a current efficiency or half-life of the organic electroluminescence device. ##STR00001## The same definition as described in the present invention.

Claims

1. An organic compound represented by the following formula (A): ##STR00206## wherein X is a divalent bridge selected from the group consisting of O, S, SO, SO.sub.2, Se, NR.sub.3 and SiR.sub.4R.sub.5; m represents an integer of 0, 1, 2, 3, 4, 5, 6, 7 or 8; A represents a substituted or unsubstituted fused ring hydrocarbons unit with three rings if X is NR.sub.3; A represents a substituted or unsubstituted fused ring hydrocarbons unit with two to three rings if X is O, S, SO, SO.sub.2, Se or SiR.sub.4R.sub.5; R.sub.1 to R.sub.5 are independently selected from the group consisting of a hydrogen atom, a halogen, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 30 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 30 ring carbon atoms; and G.sub.1 and G.sub.2 independently represent a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted fluorene group, a substituted or unsubstituted benzofluorene group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted pyrenyl group , a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted benzimidazole group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted biscarbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted diphenylphosphine oxide group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted diazinyl group, a substituted or unsubstituted pyridinyl group, a substituted or unsubstituted phenanthroline group, a substituted or unsubstituted dihydroacridine group, a substituted or unsubstituted phenothiazine group, a substituted or unsubstituted phenoxazine group, a substituted or unsubstituted dihydrophenazine group, a substituted or unsubstituted diphenylamine group, a substituted or unsubstituted triphenylamine group, a substituted or unsubstituted phenyldibenzofuranylamine group, or a substituted or unsubstituted phenyldibenzothiophenylamine group.

2. The organic compound according to claim 1, wherein G.sub.1 and G.sub.2 independently represent one of the following substituents: ##STR00207## ##STR00208## ##STR00209## ##STR00210## ##STR00211## ##STR00212## ##STR00213## ##STR00214## ##STR00215## ##STR00216## ##STR00217## ##STR00218## ##STR00219##

3. An organic compound is one of the following compounds: ##STR00220## ##STR00221## ##STR00222## ##STR00223## ##STR00224## ##STR00225## ##STR00226## ##STR00227## ##STR00228## ##STR00229## ##STR00230## ##STR00231## ##STR00232## ##STR00233## ##STR00234## ##STR00235## ##STR00236## ##STR00237## ##STR00238## ##STR00239## ##STR00240## ##STR00241## ##STR00242## ##STR00243## ##STR00244## ##STR00245## ##STR00246## ##STR00247## ##STR00248## ##STR00249## ##STR00250## ##STR00251## ##STR00252## ##STR00253## ##STR00254## ##STR00255## ##STR00256## ##STR00257## ##STR00258## ##STR00259## ##STR00260## ##STR00261## ##STR00262## ##STR00263## ##STR00264## ##STR00265## ##STR00266## ##STR00267## ##STR00268## ##STR00269## ##STR00270## ##STR00271##

4. An organic electroluminescence device comprising a pair of electrodes having a cathode and an anode, and between the pairs of electrodes comprising at least a light emitting layer and one or more layers of organic thin film layers, wherein the light emitting layer and/or the one or more thin film layers comprise the organic compound according to claim 3.

5. The organic electroluminescence device according to claim 4, wherein the light emitting layer comprising the organic compound of formula (A) as a host material.

6. The organic electroluminescence device according to claim 4, wherein the light emitting layer comprising the organic compound of formula (A) as a fluorescent dopant material.

7. The organic electroluminescence device according to claim 4, wherein the organic thin film layer comprising the organic compound of formula (A) as a hole blocking material.

8. The organic electroluminescence device according to claim 4, wherein the organic thin film layer comprising the organic compound of formula (A) is an electron transporting layer.

9. The organic electroluminescence device according to claim 4, wherein the organic electroluminescence device is a lighting panel.

10. The organic electroluminescence device according to claim 4, wherein the organic electroluminescence device is a backlight panel.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The FIGURE is a schematic view showing an organic EL device according to an embodiment of the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

(2) What probed into the invention is the organic compound and organic EL device using the organic compound. Detailed descriptions of the production, structure and elements will be provided as follows such that the invention can be fully understood. Obviously, the application of the invention is not confined to specific details familiar to those skilled in the art. On the other hand, the common elements and procedures that are known to everyone are not described in details to avoid unnecessary limits of the invention. Some preferred embodiments of the present invention will now be described in greater detail as follows. However, it should be recognized that the present invention can be practiced in a wide range of other embodiments besides those explicitly described, that is, this invention can also be applied extensively to other embodiments, and the scope of the present invention is expressly not limited except as specified in the accompanying claims.

(3) In one embodiment of the present invention, an organic compound which can be used as the host and dopant material of the light emitting layer in the organic EL device is disclosed. The organic compound may be represented by the following formula (A):

(4) ##STR00003##

(5) Wherein X may be a divalent bridge selected from the group consisting of O, S, SO, SO.sub.2, Se, NR.sub.3, and SiR.sub.4R.sub.5. The symbol m may represent an integer of 0, 1, 2, 3, 4, 5, 6, 7 or 8. A may represent a substituted or unsubstituted fused ring hydrocarbons unit with three rings, if X is, for example, but not limited to NR.sub.3. A may represent a substituted or unsubstituted fused ring hydrocarbons unit with two to three rings, if X is, for example, but not limited to O, S, SO, SO.sub.2, Se, NR.sub.3 or SiR.sub.4R. G.sub.1 and G.sub.2 are independently selected from the group consisting of a hydrogen, a methyl group, a halogen (e.g., fluoride), a phenylphosphine oxide group, a substituted or unsubstituted aryl group having 6 to 30 (e.g., 10, 12, 14, 16, 18, 20, 24, 26 or 30) ring carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 30 (e.g., 12, 15, 16, 17, 18, 21, 22, 23, 24 or 30) ring carbon atoms, a substituted or unsubstituted arylamine group having 6 to 30 (e.g., 12, 17, 18, 20, 24, 27 or 28) ring carbon atoms, and a substituted or unsubstituted heteroarylamine group having 3 to 30 (e.g., 21 or 27) ring carbon atoms. R.sub.1 to R.sub.5 may be independently selected from the group consisting of a hydrogen atom, a methyl group, a halogen (e.g., fluoride), a substituted or unsubstituted alkyl group having 1 to 30 (e.g., 8 or 10) carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 30 (e.g., 8, 12 or 24,) ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 (e.g., 6 or 12) ring carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 30 (e.g., 5 or 10) ring carbon atom. The heteroaryl group may comprise, for example, a heteroaromatic PAHs unit having two, three, four, five or six rings. The heteroaromatic PAHs may contain an oxygen atom, a sulfur atom or one, two or three N atoms.

(6) In some embodiments, the organic compound can be represented by one of the following formula (1) to formula (18):

(7) ##STR00004## ##STR00005## ##STR00006## ##STR00007## ##STR00008##

(8) In some embodiments, the alkyl group, aralkyl group, aryl group, or heteroaryl group may be substituted by a halogen, an alkyl group, an aryl group, or a heteroaryl group.

(9) In some embodiments, G.sub.1 and G.sub.2 independently represent a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstitutedfluorene group, a substituted or unsubstitutedbenzofluorene group, a substituted or unsubstitutednaphthyl group, a substituted or unsubstitutedanthracenyl group, a substituted or unsubstitutedphenanthrenyl group, a substituted or unsubstitutedpyrenyl group, a substituted or unsubstitutedchrysenyl group, a substituted or unsubstitutedtriphenylenyl group, a substituted or unsubstituted benzimidazole group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted biscarbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted diphenylphosphine oxide group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted diazinyl group, a substituted or unsubstituted pyridinyl group, a substituted or unsubstituted phenanthroline group, a substituted or unsubstituted dihydroacridine group, a substituted or unsubstituted phenothiazine group, a substituted or unsubstituted phenoxazine group, a substituted or unsubstituted dihydrophenazine group, a substituted or unsubstituted diphenylamine group, a substituted or unsubstituted triphenylamine group, a substituted or unsubstituted phenyldibenzofuranylamine group, or a substituted or unsubstituted phenyldibenzothiophenylamine group.

(10) In some embodiments, G.sub.1 and G.sub.2 independently represent one of the following substituents:

(11) ##STR00009## ##STR00010## ##STR00011## ##STR00012## ##STR00013## ##STR00014## ##STR00015## ##STR00016## ##STR00017## ##STR00018## ##STR00019## ##STR00020##

(12) The organic compound may be one of the following compounds

(13) ##STR00021## ##STR00022## ##STR00023## ##STR00024## ##STR00025## ##STR00026## ##STR00027## ##STR00028## ##STR00029## ##STR00030## ##STR00031## ##STR00032## ##STR00033## ##STR00034## ##STR00035## ##STR00036## ##STR00037## ##STR00038## ##STR00039## ##STR00040## ##STR00041## ##STR00042## ##STR00043## ##STR00044## ##STR00045## ##STR00046## ##STR00047## ##STR00048## ##STR00049## ##STR00050## ##STR00051## ##STR00052##

(14) ##STR00053## ##STR00054## ##STR00055## ##STR00056## ##STR00057## ##STR00058## ##STR00059## ##STR00060## ##STR00061## ##STR00062## ##STR00063## ##STR00064## ##STR00065## ##STR00066## ##STR00067## ##STR00068## ##STR00069## ##STR00070## ##STR00071## ##STR00072## ##STR00073## ##STR00074## ##STR00075## ##STR00076## ##STR00077## ##STR00078## ##STR00079## ##STR00080## ##STR00081## ##STR00082## ##STR00083## ##STR00084## ##STR00085## ##STR00086## ##STR00087## ##STR00088## ##STR00089## ##STR00090## ##STR00091## ##STR00092## ##STR00093##

(15) In another embodiment of the present invention, an organic electroluminescence device is disclosed. The organic electroluminescence device comprises a pair of electrodes composed of a cathode and an anode, and a light emitting layer between the pair of electrodes. The light emitting layer comprises the organic compound represented by formula (A).

(16) In some embodiments, the organic compound of the light emitting layer may be a host material. The host material is capable of, for example, lowering a driving voltage, increasing a current efficiency or extending a half-life of the organic electroluminescence device.

(17) In some embodiments, the organic compound of the light emitting layer may be a fluorescent dopant material. The dopant material is capable of, for example, lowering a driving voltage, increasing a current efficiency or extending a half-life of the organic electroluminescence device.

(18) In some embodiments, the organic compound of the light emitting layer may be an electron transfer material.

(19) In some embodiments, the organic compound of the light emitting layer may be a hole blocking material.

(20) In a further embodiment of the present invention, the organic electroluminescence device is a lighting panel. In other embodiment of the present invention, the organic electroluminescence device is a backlight panel.

(21) Detailed preparation of the organic compounds of the present invention will be clarified by exemplary embodiments below, but the present invention is not limited thereto. EXAMPLES 1 to 31 show the preparation of the organic compounds of the present invention, and EXAMPLE 32 and EXAMPLE 33 show the fabrication and test reports of the organic EL devices.

Example 1

Synthesis of 1-bromo-2-iodo-4-methoxybenzene

(22) ##STR00094##

(23) A mixture of 40 g (171 mmol) of 1-iodo-3-methoxybenzene, 32 g (179 mmol) of N-bromosuccinimide, and 600 ml of DMF was degassed and placed under nitrogen, and then heated at 80° C. for 12 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. Subsequently, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 45 g of 1-bromo-2-iodo-4-methoxybenzene as yellow oil (84.1%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 7.43 (dd, 1H), 7.35 (dd, 1H), 6.73 (dd, 1H), 3.74 (s, 3H).

Synthesis of 2-bromo-5-methoxy-1,1′-biphenyl

(24) ##STR00095##

(25) A mixture of 40 g (127.8 mmol) of 1-bromo-2-iodo-4-methoxybenzene, 15.6 g (127.8 mmol) of phenylboronic acid, 2.95 g (2.56 mmol) of Pd(Ph.sub.3).sub.4, 155 ml of 2M Na.sub.2CO.sub.3, 100 ml of EtOH and 300 ml of toluene was degassed and placed under nitrogen, and then heated to reflux for 12 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. Subsequently, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 30 g of 2-bromo-5-methoxy-1,1′-biphenyl as colorless liquid (89.2%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 7.55 (d, 1H), 7.46-7.38 (m, 5H), 6.89 (d, 1H), 6.79 (dd, 1H), 3.81 (s, 3H).

Synthesis of (5-methoxy-[1,1′-biphenyl]-2-yl)boronic Acid

(26) ##STR00096##

(27) The compound 2-bromo-5-methoxy-1,1′-biphenyl (30 g, 114 mmol) was mixed with 600 ml of dry THF. To the mixture, 54.7 ml of N-butyllithium (137 mmol) was added at −60° C. and the mixture was stirred for 1 hrs. After the reaction finished, 17.8 g (171 mmol) of trimethyl borate was added and the mixture was stirred overnight. 228 ml (228 mmole) of 1M HCl was added and the mixture was stirred for 1 hrs. The mixture was extracted with ethyl acetate/H.sub.2O, and the organic layer was removed under reduced pressure. The crude product was washed by hexane, yielding 19.5 g of (5-methoxy-[1,1′-biphenyl]-2-yl)boronic acid as white solid (75%).

Synthesis of 9-(5-methoxy-[1,1′-biphenyl]-2-yl)benzo[b]naphtha-[1,2-d]thiophene

(28) ##STR00097##

(29) A mixture of 20 g (87.7 mmol) of (5-methoxy-[1,1′-biphenyl]-2-yl)-boronic acid, 30.2 g (96.5 mmol) of 9-bromobenzo[b]naphtho[1,2-d]thiophene, 2.03 g (1.75 mmol) of Pd(Ph.sub.3).sub.4, 87.7 ml of 2M Na.sub.2CO.sub.3, 200 ml of EtOH and 400 ml of toluene was degassed and placed under nitrogen, and then heated to reflux for 12 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. Subsequently, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 25.2 g of 9-(5-methoxy-[1,1′-biphenyl]-2-yl)benzo[b]naphtha-[1,2-d]-thiophene as white solid (69%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.47 (d, 1H), 8.12-8.06 (m, 3H), 8.01 (d, 1H), 7.77-7.72 (m, 4H), 7.51-7.45 (m, 5H), 7.40-7.36 (m, 2H), 7.02 (d, 1H), 3.81 (s, 3H).

Synthesis of 11-methoxynaphtho[2,1-b]triphenyleno[2,3-d]thiophene

(30) ##STR00098##

(31) The compound 9-(5-methoxy-[1,1′-biphenyl]-2-yl)benzo[b]naphtha-[1,2-d]thiophene (20 g, 48 mmol) was mixed with 700 ml of CH.sub.2Cl.sub.2. To the mixture, 77.9 g of FeCl.sub.3 (480 mmol) was added and the mixture was stirred for 1 hrs. After the reaction finished, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 7.6 g of 11-methoxynaphtho[2,1-b]triphenyleno-[2,3-d]thiophene as white solid (39%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.91-8.89 (m, 2H), 8.81 (d, 1H), 8.49 (d, 1H), 8.14 (m, 2H), 7.99 (d, H), 7.88-7.82 (m, 3H), 7.62 (s, 1H), 7.57-7.52 (m, 3H), 7.36 (d, 1H), 3.82 (s, 3H).

Synthesis of naphtho[2,1-b]triphenyleno[2,3-d]thiophen-11-ol

(32) ##STR00099##

(33) The compound 11-methoxynaphtho[2,1-b]triphenyleno[2,3-d]-thiophene (10 g, 27.4 mmol) was mixed with 400 ml of CH.sub.2Cl.sub.2. To the mixture, 7.24 g of BBr.sub.3 (28.9 mmol) was added and the mixture was stirred overnight. After the reaction finished, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 8.4 g of naphtho[2,1-b]triphenyleno[2,3-d]thiophen-11-ol as white solid (87%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.89-8.87 (m, 2H), 8.78 (d, 1H), 8.45 (d, 1H), 8.09 (m, 2H), 7.94 (d, H), 7.89-7.84 (m, 3H), 7.58 (s, 1H), 7.55-7.49 (m, 3H), 7.31 (d, 1H), 5.41 (s, 1H).

Synthesis of naphtho[2,1-b]triphenyleno[2,3-d]thiophen-11-yl trifluoromethanesulfonate

(34) ##STR00100##

(35) The compound naphtho[2,1-b]triphenyleno[2,3-d]thiophen-11-ol (10 g, 25 mmol) was mixed with 450 ml of CH.sub.2Cl.sub.2. To the mixture, 2.98 g of pyridine (37.5 mmol) was added and the mixture was stirred for 1 hrs. To the mixture, 12 g of (CF.sub.3SO.sub.2).sub.2O (42.5 mmol) was added and the mixture was stirred for 1 hrs. After the reaction finished, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 6.9 g of naphtho[2,1-b]triphenyleno[2,3-d]-thiophen-11-yl trifluoromethanesulfonate as yellow solid (52%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.99-8.95 (m, 3H), 8.47 (d, 1H), 8.14-8.11 (m, 3H), 7.97 (d, H), 7.91-7.84 (m, 3H), 7.58 (s, 1H), 7.55-7.50 (m, 3H).

Synthesis of 4,4,5,5-tetramethyl-2-(naphtho[2,1-b]triphenyleno[2,3-d]-thiophen-11-yl)-1,3,2-dioxaborolane

(36) ##STR00101##

(37) A mixture of 5 g (9.4 mmol) of naphtho[2,1-b]triphenyleno[2,3-d]-thiophen-11-yl trifluoromethanesulfonate, 2.87 g (11.3 mmol) of bis(pinacolato)diboron, 0.43 g (0.36 mmol) of Pd(Ph.sub.3).sub.4, 1.84 g (18.8 mmol) of potassium acetate, and 60 ml of 1,4-dioxane was degassed and placed under nitrogen, and then heated to reflux for 12 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. Subsequently, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 3.26 g of 4,4,5,5-tetramethyl-2-(naphtho[2,1-b]triphenyleno[2,3-d]-thiophen-11-yl)-1,3,2-dioxaborolane as white solid (68%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.94-8.88 (m, 3H), 8.47 (d, 1H), 8.15-8.12 (m, 3H), 7.99 (d, 1H), 7.88-7.82 (m, 4H), 7.57-7.53 (m, 3H), 1.27 (s, 12H).

Synthesis of 11-([1,1′:3′,1″-terphenyl]-3-yl)naphtho[2,1-b]-triphenyleno[2,3-d]thiophene (Compound 78)

(38) ##STR00102##

(39) A mixture of 5 g (9.8 mmol) of 4,4,5,5-tetramethyl-2-(naphtho[2,1-b]-triphenyleno[2,3-d]thiophen-11-yl)-1,3,2-dioxaborolane, 3.33 g (10.8 mmol) of 3-bromo-1,1′:3′,1″-terphenyl, 0.23 g (0.2 mmol) of Pd(Ph.sub.3).sub.4, 9.8 ml of 2M Na.sub.2CO.sub.3, 30 ml of EtOH and 60 ml of toluene was degassed and placed under nitrogen, and then heated to reflux for 12 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. Subsequently, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 3.9 g of 11-([1,1′:3′,1″-terphenyl]-3-yl)naphtho[2,1-b]-triphenyleno[2,3-d]thiophene as yellow solid (65%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.99-8.93 (m, 3H), 8.46 (d, 1H), 8.33 (s, 1H), 8.29-8.23 (m, 4H), 8.14-8.09 (m, 3H), 7.97 (d, H), 7.85-7.81 (m, 2H), 7.56-7.46 (m, 7H), 7.47-7.42 (m, 3H).

Example 2-13

(40) We have used the same synthesis methods to get a series of intermediates and the following compounds are synthesized analogously.

(41) TABLE-US-00001 Ex. IntermediateIII IntermediateIV  2 03 04  3 05 06  4 07 08  5 09 0  6  7  8  9 10 0 11 12 13 Ex. Product Yield  2 58%  3 64%  4 69%  5 0 62%  6 68%  7 61%  8 63%  9 59% 10 63% 11 66% 12 55% 13 57%

Example 14

Synthesis of 5-bromo-10-iodonaphtho[2,1-b]benzofuran

(42) ##STR00139##

(43) A mixture of 10 g (33.7 mmol) of 5-bromonaphtho[2,1-b]benzofuran, 60 ml of acetic acid, 6 ml of water, 6 ml of concentrated sulfuric acid, 8.55 g (33.7 mmol) of iodine, 7.67 g (33.7 mmol) of periodic acid and 60 ml of chloroform was heated at 50° C. overnight with good stirring. After cooling to room temperature, the product mixture was poured into water and extracted with dichloromethane (3×100 mL). The combined dark purple organic layer was decolorized with sodium sulfite, washed with water, dried with anhydrous Na.sub.2SO.sub.4, filtered, and evaporated to dryness. The crude product was purified by column chromatography, yielding 6.8 g of 5-bromo-10-iodonaphtho[2,1-b]benzofuran as yellow solid (47.8%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.57 (d, 1H), 8.48 (s, 1H), 8.13 (d, 1H), 7.82 (s, 1H), 7.54-7.58 (m, 3H), 7.43 (d, 1H).

Synthesis of 10-([1,1′-biphenyl]-2-yl)-5-bromonaphtho[2,1-b]-benzofuran

(44) ##STR00140##

(45) A mixture of 10 g (23.6 mmol) of 5-bromo-10-iodonaphtho[2,1-b]-benzofuran, 4.68 g (23.6 mmol) of [1,1′-biphenyl]-2-ylboronic acid, 0.23 g (0.2 mmol) of Pd(Ph.sub.3).sub.4, 23.6 ml of 2M Na.sub.2CO.sub.3, 80 ml of EtOH and 160 ml of toluene was degassed and placed under nitrogen, and then heated to reflux for 12 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. Subsequently, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 6.9 g of 10-([1,1′-biphenyl]-2-yl)-5-bromonaphtho[2,1-b]benzofuran as white solid (64.9%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.59 (d, 1H), 8.45 (s, 1H), 8.11 (d, 1H), 7.86-7.79 (m, 5H), 7.74-7.72 (s, 2H), 7.54-7.39 (m, 7H).

Synthesis of 5-bromonaphtho[2,1-b]triphenyleno[2,3-d]furan

(46) ##STR00141##

(47) The compound 10-([1,1′-biphenyl]-2-yl)-5-bromonaphtho[2,1-b]-benzofuran (8 g, 17.8 mmol) was mixed with 100 ml of CH.sub.2Cl.sub.2. To the mixture, 28.9 g of FeCl.sub.3 (178 mmol) was added and the mixture was stirred for 1 hrs. After the reaction finished, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 3.2 g of 5-bromonaphtho[2,1-b]triphenyleno[2,3-d]furan as white solid (40.1%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.58 (d, 1H), 8.47 (s, 1H), 8.12 (d, 1H), 7.84-7.79 (m, 3H), 7.75-7.73 (s, 2H), 7.52-7.39 (m, 7H).

Synthesis of 5-([1,1′:3′,1″-terphenyl]-3-yl)naphtho[2,1-b]-triphenyleno[2,3-d]furan (Compound 2)

(48) ##STR00142##

(49) A mixture of 5 g (11.2 mmol) of 5-bromonaphtho[2,1-b]triphenyleno-[2,3-d]furan, 3.37 g (12.3 mmol) of [1,1′:3′,1″-terphenyl]-3-ylboronic acid, 0.26 g (0.22 mmol) of Pd(Ph.sub.3).sub.4, 11.2 ml of 2M Na.sub.2CO.sub.3, 30 ml of EtOH and 60 ml of toluene was degassed and placed under nitrogen, and then heated to reflux for 12 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. Subsequently, the solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 3.5 g of 5-([1,1′:3′,1″-terphenyl]-3-yl)naphtho[2,1-b]triphenyleno-[2,3-d]furan as white solid (52.5%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.94-8.89 (m, 3H), 8.57 (d, 2H), 8.14-8.10 (m, 3H), 7.89-7.84 (m, 4H), 7.72 (s, 2H), 7.65 (s, H), 7.59-7.54 (m, 4H), 7.50-7.44 (m, 8H), 7.39 (m, 1H).

Example 15-31

(50) We have used the same synthesis methods to get a series of intermediates and the following compounds are synthesized analogously.

(51) TABLE-US-00002 Ex. IntermediateI IntermediateII 15 16 17 18 0 19 20 21 22 23 0 24 25 26 27 28 0 29 30 31 Ex. Product Yield 15 61% 16 59% 17 63% 18 0 57% 19 65% 20 58% 21 55% 22 60% 23 52% 24 54% 25 52% 26 50% 27 61% 28 0 57% 29 44% 30 41% 31 41%

General Method of Producing Organic EL Device

(52) ITO-coated glasses with 9-12 ohm/square in resistance and 120˜160 nm in thickness are provided (hereinafter ITO substrate) and cleaned in a number of cleaning steps in an ultrasonic bath (e.g. detergent, deionized water). Before vapor deposition of the organic layers, cleaned ITO substrates are further treated by UV and ozone. All pre-treatment processes for ITO substrate are under clean room (class 100).

(53) These organic layers are applied onto the ITO substrate in order by vapor deposition in a high-vacuum unit (10.sup.−7 Torr), such as: resistively heated quartz boats. The thickness of the respective layer and the vapor deposition rate (0.1-0.3 nm/sec) are precisely monitored or set with the aid of a quartz-crystal monitor. It is also possible, as described above, for individual layers to consist of more than one compound, i.e. in general a host material doped with a dopant material and/or co-deposited with a co-host. This is successfully achieved by co-vaporization from two or more sources, which means the naphthotriphenylenofuran and naphthotriphenylenothiophene derivatives of the present invention are thermally stable.

(54) Dipyrazino[2,3-f:2,3-]quinoxaline-2,3,6,7,10,11-hexacarbonitrile(HAT-CN) is used as hole injection layer in this organic EL device. N,N-Bis(naphthalene-1-yl)-N,N-bis(phenyl)-benzidine(NPB) is most widely used as the hole transporting layer. 12-(4,6-diphenyl-1,3,5-triazin-2-yl)-10,10-dimethyl-10,12-dihydrophenanthro[9′,10′:5,6]indeno[2,1-b]carbazole (H1) and 14,14-dimethyl-11-(10-(3-(naphthalen-1-yl)phenyl) anthracen-9-yl)-14H-indeno[1,2-b]triphenylene (H2) are used as emitting hosts for comparison, and bis(2-phenylpyridinato) (2,4-diphenylpyridinato)iridium(III) (D1) and N1,N1,N6,N6-tetra-m-tolylpyrene-1,6-diamine(D2) are used as guest in the emitting layer. HB1 (see the following chemical structure) is used as hole blocking material(HBM), and 2-(naphthalen-1-yl)-9-(4-(1-(4-(10-(naphthalene-2-yl)anthracen-9-yl)-phenyl)-1H-benzo[d]imidazol-2-yl)phenyl)-1,10-phenanthroline(ET1) is used as electron transporting material to co-deposit with 8-hydroxyquinolato-lithium(LiQ) in organic EL devices. The chemical structures of conventional OLED materials and the exemplary organic compounds of the present invention for producing control and exemplary organic EL devices in this invention are shown as follows:

(55) ##STR00194## ##STR00195## ##STR00196## ##STR00197## ##STR00198## ##STR00199## ##STR00200## ##STR00201## ##STR00202## ##STR00203## ##STR00204## ##STR00205##

(56) A typical organic EL device consists of low work function metals, such as Al, Mg, Ca, Li and K, as the cathode by thermal evaporation, and the low work function metals can help electrons injecting the electron transporting layer from cathode. In addition, for reducing the electron injection barrier and improving the organic EL device performance, a thin electron injecting layer is introduced between the cathode and the electron transporting layer. The materials of electron injecting layer are metal halide or metal oxide with low work function, such as: LiF, LiQ, MgO, or Li.sub.2O. On the other hand, after the organic EL device fabrication, EL spectra and CIE coordination are measured by using a PR650 spectra scan spectrometer. Furthermore, the current/voltage, luminescence/voltage, and yield/voltage characteristics are taken with a Keithley 2400 programmable voltage-current source. The above-mentioned apparatuses are operated at room temperature (about 25° C.) and under atmospheric pressure.

Example 32

(57) Using a procedure analogous to the above mentioned general method, organic EL devices emitting green and blue light and having the following device structure as shown in the FIGURE. From the bottom layer 10 to the top layer 80, the following components were produced: ITO/HAT-CN(20 nm)/NPB (110 nm)/Emitting host doped with 15% dopant (30 nm)/HB1/ET1 doped 50% LiQ(35 nm)/LiQ(1 nm)/Al(160 nm). In the device illustrated in the FIGURE, the hole injection layer 20 (HAT-CN) is deposited onto the transparent electrode 10 (ITO), the hole transport layer 30 (NPB) is deposited onto the hole injection layer 20. The emitting layer 40 is deposited onto the hole transport layer 30. The emitting layer 40 may comprise an emitting host material and an emitting guest (dopant) material, as shown in, for example, Table 1. The emitting host material may be doped with about 15% emitting guest material. The emitting layer 40 may have a thickness of about 30 nm.

(58) The hole blocking layer 50 (HB1) is deposited onto the emitting layer 40, the electron transport layer 60 (ET1 doped with 50% LiQ) is deposited onto the hole blocking layer 50, the electron injection layer 70 (LiQ) is deposited onto the electron transport layer 60. The metal electrode 80(Al) is deposited onto the electron injection layer 70. The I-V-B (at 1000 nits) test reports of these organic EL devices are summarized in Table 1 below. The half-life time is defined as the time the initial luminance of 1000 cd/m.sup.2 has dropped to half.

(59) TABLE-US-00003 TABLE 1 (The Comp. is short for Compound) Current Emitting Emitting Driving Efficiency Half-life Host Dopant Voltage (Yield; time Material Material (V) cd/A) CIE(y) (hours) H1 D1 5.1 18 0.53 350 Comp. 37 D1 3.9 39 0.54 710 Comp. 55 D1 4.6 27 0.54 440 Comp. 113 D1 4.5 30 0.56 470 Comp. 114 D1 4.8 24 0.54 410 Comp. 115 D1 4.9 22 0.54 390 Comp. 133 D1 4.6 28 0.56 450 Comp. 150 D1 3.6 42 0.55 760 Comp. 152 D1 3.5 44 0.54 770 Comp. 154 D1 3.7 41 0.53 740 Comp. 156 D1 3.8 40 0.56 730 Comp. 222 D1 4.3 34 0.55 600 Comp. 223 D1 4.4 33 0.53 580 H2 D2 4.3 4.6 0.182 250 H2 Comp. 38 4.1 4.8 0.183 280 H2 Comp. 197 3.9 5.0 0.184 330 H2 Comp. 199 3.5 5.7 0.182 400 H2 Comp. 205 3.6 5.4 0.181 380 H2 Comp. 206 3.7 5.2 0.180 350 H2 Comp. 209 4.0 4.9 0.182 300 H2 Comp. 210 4.2 4.7 0.181 270 H2 Comp. 211 4.0 5.0 0.183 310 H2 Comp. 218 3.4 6.0 0.182 450

Example 33

(60) Using a procedure analogous to the above mentioned general method, organic EL devices emitting green and blue light and having the following device structure as shown in the FIGURE. From the bottom layer 10 to the top layer 80, the following components were produced: ITO/HAT-CN(20 nm)/NPB (110 nm)/Emitting host doped with 15% dopant (30 nm)/HB1/ET1 doped 50% LiQ(35 nm)/LiQ(1 nm)/Al(160 nm). In the device illustrated in the FIGURE, the hole injection layer 20 (HAT-CN) is deposited onto the transparent electrode 10 (ITO), the hole transport layer 30(NPB) is deposited onto the hole injection layer 20. The emitting layer 40 is deposited onto the hole transport layer 30. The emitting layer 40 may comprise an emitting host material and an emitting guest (dopant) material, as shown in, for example, Table 1. The emitting host material may be doped with about 15% emitting guest material. The emitting layer 40 may have a thickness of about 30 nm.

(61) The hole blocking layer (HBL) 50 (e.g., HB1) is deposited onto the emitting layer 40, the electron transport layer (ETL) 60 (e.g., ET1 doped with 50% LiQ) is deposited onto the hole blocking layer 50, the electron injection layer 70 (LiQ) is deposited onto the electron transport layer 60. The metal electrode 80(Al) is deposited onto the electron injection layer 70. The I-V-B (at 1000 nits) test reports of these organic EL devices are summarized in Table 1 below. The half-life time is defined as the time the initial luminance of 1000 cd/m.sup.2 has dropped to half.

(62) TABLE-US-00004 TABLE 2 (The Comp. is short for Compound) Current Driving Efficiency Half-life Voltage (Yield; time HBL ETL (V) cd/A) CIE(y) (hours) HB1 ET1 5.1 18 0.53 350 HB1 Comp. 157 3.9 33 0.55 540 HB1 Comp. 161 3.6 37 0.55 600 HB1 Comp. 163 3.7 35 0.54 580 HB1 Comp. 169 3.8 34 0.55 550 HB1 Comp. 171 4.1 30 0.54 510 HB1 Comp. 174 4.8 21 0.55 410 HB1 Comp. 182 4.6 23 0.54 440 HB1 Comp. 186 4.5 25 0.55 450 HB1 Comp. 194 4.4 27 0.53 480 Comp. 56 ET1 4.8 24 0.56 420 Comp. 131 ET1 4.9 21 0.53 400 Comp. 158 ET1 4.5 28 0.53 450 Comp. 162 ET1 4.1 33 0.56 530 Comp. 170 ET1 4.3 31 0.54 480 Comp. 172 ET1 4.6 26 0.56 430

(63) In the above test reports of an organic EL device (see Table 1 and Table 2), the organic compound represented by formula (A) used as an emitting host material, a fluorescent dopant material, an electron transfer or a hole blocking material for the organic EL device in the present invention displays better performance than a prior art organic EL material. More specifically, an organic compound represented by formula (A) for an organic EL device of the present invention is used as an emitting host material, an electron transfer or a hole blocking material to collocate with an emitting guest material, such as D1, and used as an fluorescent emitting dopant material to collocate with an emitting host material, such as H2, thereby lowering a driving voltage, increasing a current efficiency or extending a half-life of the organic EL device.

(64) Obviously, many modifications and variations are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims the present invention can be practiced otherwise than as specifically described herein. Although specific embodiments have been illustrated and described herein, it is obvious to those skilled in the art that many modifications of the present invention may be made without departing from what is intended to be limited solely by the appended claims.