Heteroaromatic compound and organic electroluminescence device using the same

Abstract

A heteroaromatic compound which can be used as the fluorescent guest material in the light emitting layer of the organic electroluminescence device is disclosed. The organic electroluminescence device employing the heteroaromatic compound of the present invention shows lower power consumption, higher efficiency, and longer half-life time than the existed organic electroluminescence devices.

Claims

1. A heteroaromatic compound of formula (1) below: ##STR00094## wherein Ar.sub.1 and Ar.sub.2 are independently an aryl group or a heteroaryl group having 4 to 6 ring carbon atoms; Ar.sub.3 is a cycloalkyl group, a cycloalkenyl group, or an aryl group having 5 to 6 ring carbon atoms; R.sub.1 and R.sub.2 are independently a hydrogen atom, a unsubstituted alkyl group having 1 to 36 carbon atoms, a unsubstituted aryl group having 6 to 36 carbon atoms, or a unsubstituted aralkyl group having 6 to 36 carbon atoms; W represents a divalent bridge selected from the group consisting of O, S, CR.sub.3R.sub.4, NR.sub.5, and SiR.sub.6R.sub.7, and R.sub.3 to R.sub.7 are independently a hydrogen atom or a unsubstituted alkyl group having 1 to 20 carbon atoms; X is absent or a divalent bridge selected from the group consisting of O, S, CR.sub.8R.sub.9, NR.sub.10, and SiR.sub.11R.sub.12; A is absent or represents formula (2) below: ##STR00095## wherein Y represents a divalent bridge selected from the group consisting of O, S, CR.sub.13R.sub.14, NR.sub.15, and SiR.sub.16R.sub.17; and R.sub.8 to R.sub.17 are independently a hydrogen atom, a unsubstituted alkyl group having 1 to 36 carbon atoms, a unsubstituted aryl group having 6 to 36 carbon atoms, a unsubstituted aralkyl group having 6 to 36 carbon atoms, or a unsubstituted heteroaryl group having 3 to 36 carbon atoms.

2. The heteroaromatic compound according to claim 1, wherein Ar.sub.1 and Ar.sub.2 are independently ##STR00096##

3. The heteroaromatic compound according to claim 1, wherein Ar.sub.3 is ##STR00097##

4. A heteroaromatic compound selected from the group consisting of following compounds: ##STR00098## ##STR00099## ##STR00100## ##STR00101## ##STR00102## ##STR00103## ##STR00104## ##STR00105## ##STR00106## ##STR00107## ##STR00108## ##STR00109## ##STR00110## ##STR00111## ##STR00112## ##STR00113## ##STR00114## ##STR00115## ##STR00116## ##STR00117## ##STR00118## ##STR00119## ##STR00120## ##STR00121## ##STR00122## ##STR00123## ##STR00124## ##STR00125## ##STR00126## ##STR00127## ##STR00128## ##STR00129## ##STR00130## ##STR00131## ##STR00132## ##STR00133## ##STR00134## ##STR00135## ##STR00136## ##STR00137## ##STR00138## ##STR00139## ##STR00140## ##STR00141## ##STR00142## ##STR00143## ##STR00144## ##STR00145## ##STR00146## ##STR00147## ##STR00148## ##STR00149## ##STR00150## ##STR00151## ##STR00152##

5. An organic electroluminescence device, comprising a pair of electrodes composed of a cathode and an anode, and a light emitting layer between the pair of electrodes, wherein the light emitting layer comprises the heteroaromatic compound according to claim 4.

6. The organic electroluminescence device according to claim 5, wherein the heteroaromatic compound of formula (1) is a fluorescent dopant material.

7. The organic electroluminescence device according to claim 5, wherein the light emitting layer emits blue fluorescence.

8. The organic electroluminescence device according to claim 5, wherein the organic electroluminescence device is a lighting panel.

9. The organic electroluminescence device according to claim 5, wherein the organic electroluminescence device is a backlight panel.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The FIGURES 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 heteroaromatic compound and organic EL device using the heteroaromatic 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, a heteroaromatic compound which can be used as the fluorescent dopant material of the light emitting layer in the organic EL device is disclosed. The heteroaromatic compound is represented by the following formula (1):

(4) ##STR00003##
wherein Ar.sub.1 and Ar.sub.2 are independently an aryl group or a heteroaryl group having 4 to 6 ring carbon atoms; Ar.sub.3 is a cycloalkyl group, a cycloalkenyl group, or an aryl group having 5 to 6 ring carbon atoms; R.sub.1 and R.sub.2 are independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 36 carbon atoms, a substituted or unsubstituted aryl group having 6 to 36 carbon atoms, or a substituted or unsubstituted aralkyl group having 6 to 36 carbon atoms; W represents a divalent bridge selected from the group consisting of O, S, CR.sub.3R.sub.4, NR.sub.5, and SiR.sub.6R.sub.7, and R.sub.3 to R.sub.7 are independently a hydrogen atom or a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms; X is absent or a divalent bridge selected from the group consisting of O, S, CR.sub.8R.sub.9, NR.sub.10, and SiR.sub.11R.sub.12; A is absent or represents formula (2) below:

(5) ##STR00004##
wherein Y represents a divalent bridge selected from the group consisting of O, S, CR.sub.13R.sub.14, NR.sub.15, and SiR.sub.16R.sub.17; and R.sub.8 to R.sub.17 are independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 36 carbon atoms, a substituted or unsubstituted aryl group having 6 to 36 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 36 carbon atoms, or a substituted or unsubstituted heteroaryl group having 3 to 36 carbon atoms.

(6) In some embodiments, Ar.sub.1 and Ar.sub.2 are independently

(7) ##STR00005##

(8) In some embodiments, Ar.sub.3 is

(9) ##STR00006##

(10) Preferably, the heteroaromatic compound is one of the following compounds:

(11) ##STR00007## ##STR00008## ##STR00009## ##STR00010## ##STR00011## ##STR00012## ##STR00013## ##STR00014## ##STR00015## ##STR00016## ##STR00017## ##STR00018## ##STR00019## ##STR00020## ##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## ##STR00053## ##STR00054## ##STR00055## ##STR00056## ##STR00057## ##STR00058## ##STR00059## ##STR00060## ##STR00061##

(12) 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 heteroaromatic compound of formula (1).

(13) In some embodiments, the light emitting layer comprising the heteroaromatic compound of formula (1) is a fluorescent dopant material. In particular, the light emitting layer emits blue fluorescence.

(14) 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.

(15) Detailed preparation of the heteroaromatic compounds of the present invention will be clarified by exemplary embodiments below, but the present invention is not limited thereto. EXAMPLES 1 to 7 show the preparation of the heteroaromatic compounds of the present invention, and EXAMPLE 8 shows the fabrication and test reports of the organic EL devices.

Example 1

Synthesis of Intermediate A

(16) ##STR00062##

(17) A mixture of 13 g (40 mmol) of 4,6-dibromobenzofuran, 11.3 g (40 mmol) of bis(4-tert-butylphenyl)amine, 0.9 g (0.8 mmol) of Pd.sub.2(dba).sub.3, 1.2 g (0.6 mmol) of tri-tert-butylphosphine, 5.0 g (52 mmol) of sodium tert-butoxide, and 150 ml of toluene was placed under nitrogen, and then heated and stirred at 70° C. for 24 hrs. After the reaction finished, the mixture was allowed to cool to room temperature. The solution was extracted with 100 ml of ethyl acetate and 300 ml of water. The organic layer was dried with anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica to give product (16 g, 30.4 mmol, 76%).

Synthesis of Intermediate B

(18) ##STR00063##

(19) A mixture of 16 g (30.4 mmol) of Intermediate A and 100 ml of THF was placed under nitrogen and stirred at −78° C. After n-BuLi (2.5 M in hexane, 13.6 mL) was added dropwise, the temperature was raised to 0° C. and the mixture was stirred for 30 minutes. Afterwards, the temperature was lowered to −75° C. and 3.8 g (37 mmol) of trimethylborate was slowly added dropwise. Subsequently, the temperature was slowly raised to room temperature, and then the mixture was stirred for 3 hours. After the mixture had acidity by adding 3 N HCl, it was extracted with ethyl acetate and water. The organic layer was dried with anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was recrystallized from toluene to give product (11.2 g, 22.8 mmol, 75%).

Synthesis of 5,6-Dibromo-1,2-dihydroacenaphthylene

(20) ##STR00064##

(21) A mixture of 100 g (650 mmol) of Acenaphthene and 150 ml of DMF was placed under nitrogen and stirred at 0° C. After 250 g (1430 mmol) of N-bromosuccinimide in 500 ml of DMF was added dropwise, the temperature was raised to room temperature and the mixture was stirred for 18 hours. The precipitated product was filtered off with suction and washed with EtOH. The residue was recrystallized from EtOH to give product (46.5 g, 149.5 mmol, 23%).

Synthesis of Intermediate C

(22) ##STR00065##

(23) A mixture of 3.1 g (10 mmol) of 5,6-Dibromo-1,2-dihydro-acenaphthylene, 4.9 g (10 mmol) of Intermediate B, 0.58 g (0.5 mmol) of Pd(PPh.sub.3).sub.4, 7 ml of 2M K.sub.2CO.sub.3, 40 ml of EtOH, and 40 ml of toluene was degassed and placed under nitrogen, and then heated at 90° C. overnight. After the reaction finished, the mixture was allowed to cool to room temperature. The organic phase was separated and washed with ethyl acetate and water. After being dried over magnesium sulfate, the solvent was removed in vacuo. The residue was purified by column chromatography on silica to give product (4.4 g, 6.5 mmol, 65%).

Synthesis of EX1

(24) ##STR00066##

(25) A mixture of 4.4 g (6.5 mmol) of Intermediate C and 70 ml of THF was placed under nitrogen and stirred at −78° C. After 3.4 mL of n-BuLi (2.5 M in hexane) was added dropwise, the mixture was stirred for 1 hour. Afterwards, 1.17 g (6.5 mmol) of 9H-fluoren-9-one dissolved in 15 ml of THF was slowly added dropwise, the temperature was slowly raised to room temperature, and the mixture was stirred for 12 hours. The reaction was finished by adding 70 ml of saturated NaHCO.sub.3 aqueous solution, and the mixture was extracted with DCM and water to receive the organic layer. The organic layer was dried over magnesium sulfate, and the solvent was removed in vacuo. The residue was dissolved in 30 ml acetic acid, and then a small amount of 3 N HCl was added thereto. After being stirred at 100° C. for 12 hours, the solution was cooled down to room temperature and then filtered. The filtrate was purified by column chromatography on silica to give product (2.6 g, 3.4 mmol, 52%). MS(m/z, EI.sup.+): 760.3.

Example 2

Synthesis of EX6

(26) ##STR00067##

(27) The same synthesis procedure as in Synthesis of EX1 was used, except that 0.77 g (4.0 mmol) of Cyclopentadithiophene Ketone was used instead of 9H-fluoren-9-one to obtain 1.2 g (40%) of EX6. MS(m/z, EI.sup.+): 772.2.

Example 3

Synthesis of methyl 2-((9,9-dimethyl-9H-fluoren-2-yl)amino)-benzoate

(28) ##STR00068##

(29) A mixture of 10 g (36.6 mmol) of 2-bromo-9,9-dimethyl-9H-fluorene, 6.64 g (43.9 mmol) of methyl 2-aminobenzoate, 0.3 g (1.46 mmol) of Pd(OAc).sub.2, 17.9 g (54.9 mmol) of cesium carbonate, and 120 ml of o-xylene 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 10 g of methyl 2-((9,9-dimethyl-9H-fluoren-2-yl)amino)benzoate as yellow oil (79.6%), .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.97 (s, 1H), 8.11 (d, 1H), 7.87 (d, 1H), 7.75-7.64 (m, 3H), 7.41-7.29 (m, 3H), 7.08 (m, 1H), 6.92 (d, 1H), 6.77 (d, 1H), 3.79 (s, 3H), 1.57 (s, 3H), 1.54 (s, 3H).

Synthesis of 2-(2-((9,9-dimethyl-9H-fluoren-2-yl)amino)phenyl)-propan-2-ol

(30) ##STR00069##

(31) The compound methyl 2-((9,9-dimethyl-9H-fluoren-2-yl)amino)-benzoate (10 g, 29.1 mmol) was mixed with 100 ml of THF. To the mixture, 58 ml of 3 M methylmagnesium bromide was added slowly at room temperature and then stirred at room temperature for 3 hrs. After the reaction finished, ammonium chloride solution was added to the reaction mixture, which was then extracted with ethyl acetate/water to receive the organic layer. The solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 9 g of 2-(2-((9,9-dimethyl-9H-fluoren-2-yl)amino)phenyl)-propan-2-ol as yellow oil (90%), .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.91 (s, 1H), 7.81 (d, 1H), 7.59 (d, 1H), 7.54 (d, 1H), 7.35-7.39 (m, 3H), 7.29 (m, 1H), 6.92 (m, 1H), 6.76-6.74 (d, 2H), 6.58 (d, 1H), 3.88 (s, 1H), 1.53 (s, 3H), 1.51 (s, 3H), 1.35 (s, 6H).

Synthesis of 7,7,13,13-tetramethyl-7,13-dihydro-5H-indeno-[1,2-b]-acridine

(32) ##STR00070##

(33) The compound 2-(2-((9,9-dimethyl-9H-fluoren-2-yl)amino)-phenyl)-propan-2-ol (27 g, 78.6 mmol) was mixed with 400 ml of CH.sub.2Cl.sub.2. To the mixture, 51 ml of methane sulfonic acid and 37 ml of phosphoric acid was added slowly at room temperature and then stirred at room temperature for 12 hrs. After the reaction finished, ice-cold water was added to the reaction mixture, and then 20% sodium hydroxide solution was added thereto. The reaction mixture was extracted with ethyl acetate/water to receive the organic layer. The solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 15 g of 7,7,13,13-tetramethyl-7,13-dihydro-5H-indeno-[1,2-b]-acridine as yellow solid (58.8%). .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.95 (s, 1H), 7.79 (s, 1H), 7.72 (d, 1H), 7.43 (d, 1H), 7.36 (d, 1H), 7.25 (m, 1H), 7.16 (dd, 1H), 7.04 (m, 1H), 6.87 (s, 1H), 6.81-6.78 (m, 2H) 1.55 (s, 6H), 1.38 (s, 6H).

Synthesis of Intermediate D

(34) ##STR00071##

(35) The same synthesis procedure as in Synthesis of Intermediate A was used, except that 4,6-dibromobenzothiophene (6.8 g, 20 mmol) was used instead of 4,6-dibromobenzofuran and 7,7,13,13-tetramethyl-7,13-dihydro-5H-indeno-[1,2-b]acridine (6.5 g, 20 mmol) was used instead of bis(4-tert-butylphenyl)amine to obtain 8.3 g (71%) of Intermediate D.

Synthesis of Intermediate E

(36) ##STR00072##

(37) The same synthesis procedure as in Synthesis of Intermediate B was used, except that Intermediate D (8.3 g, 14.2 mmol) was used instead of Intermediate A to obtain 5.7 g (73%) of Intermediate E.

Synthesis of Intermediate F

(38) ##STR00073##

(39) The same synthesis procedure as in Synthesis of Intermediate C was used, except that Intermediate E (5.7 g, 10.3 mmol) was used instead of Intermediate B to obtain 4.6 g (61%) of Intermediate F.

Synthesis of EX9

(40) ##STR00074##

(41) The same synthesis procedure as in Synthesis of EX1 was used, except that Intermediate F (3.6 g, 4.8 mmol) was used instead of Intermediate C to obtain 2.0 g (51%) of EX9. MS(m/z, EI.sup.+): 820.4.

Example 4

Synthesis of EX10

(42) ##STR00075##

(43) The same synthesis procedure as in Synthesis of EX6 was used, except that Intermediate F (3.6 g, 4.8 mmol) was used instead of Intermediate C to obtain 2.5 g (48%) of EX10. MS(m/z, EI.sup.+): 832.3.

Example 5

Synthesis of methyl 2-(dibenzo[b,d]thiophen-3-ylamino)benzoate

(44) ##STR00076##

(45) A mixture of 5 g (19 mmol) of 3-bromodibenzo[b,d]thiophene, 3.45 g (22.8 mmol) of methyl 2-aminobenzoate, 0.17 g (0.76 mmol) of Pd(OAc).sub.2, 9.28 g (28.5 mmol) of cesium carbonate, and 60 ml of o-xylene 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 4.8 g of methyl 2-(dibenzo[b,d]thiophen-3-ylamino)benzoate as yellow oil (75.8%), .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.99 (s, 1H), 8.14 (d, 1H), 7.89 (d, 1H), 7.79-7.68 (m, 3H), 7.45-7.33 (m, 3H), 7.12 (m, 1H), 6.97 (d, 1H), 6.81 (d, 1H), 3.79 (s, 3H).

Synthesis of 2-(2-(dibenzo[b,d]thiophen-3-ylamino)phenyl)propan-2-ol

(46) ##STR00077##

(47) The compound methyl 2-(dibenzo[b,d]thiophen-3-ylamino)-benzoate (4.8 g, 14.4 mmol) was mixed with 50 ml of THF. To the mixture, 28 ml of 3 M methylmagnesium bromide was added slowly at room temperature and then stirred at room temperature for 3 hrs. After the reaction finished, ammonium chloride solution was added to the reaction mixture, which was then extracted with ethyl acetate/water to receive the organic layer. The solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 4.5 g of 2-(2-(dibenzo[b,d]thiophen-3-ylamino)phenyl)propan-2-ol as yellow oil (93.7%), .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.94 (s, 1H), 7.83 (d, 1H), 7.62 (d, 1H), 7.55 (d, 1H), 7.41-7.36 (m, 3H), 7.29 (m, 1H), 6.94 (m, 1H), 6.78-6.75 (d, 2H), 6.59 (d, 1H), 3.91 (s, 1H), 1.35 (s, 6H).

Synthesis of 12,12-dimethyl-7,12-dihydrobenzo[4,5]thieno[3,2-b]-acridine

(48) ##STR00078##

(49) The compound 2-(2-(dibenzo[b,d]thiophen-3-ylamino)phenyl)-propan-2-ol (10 g, 30 mmol) was mixed with 150 ml of CH.sub.2Cl.sub.2. To the mixture, 19 ml of methane sulfonic acid and 14 ml of phosphoric acid were added slowly at room temperature and then stirred at room temperature for 12 hrs. After the reaction finished, ice-cold water was added to the reaction mixture, and 20% sodium hydroxide solution was added thereto. The reaction mixture was extracted with ethyl acetate/water to receive the organic layer. The solvent was removed under reduced pressure, and the crude product was purified by column chromatography, yielding 5.3 g of 12,12-dimethyl-7,12-dihydrobenzo[4,5]thieno[3,2-b]acridine as yellow solid (56%), .sup.1H NMR (CDCl.sub.3, 400 MHz): chemical shift (ppm) 8.97 (s, 1H), 7.81 (s, 1H), 7.73 (d, 1H), 7.45 (d, 1H), 7.38 (d, 1H), 7.28 (m, 1H), 7.18 (dd, 1H), 7.07 (m, 1H), 6.89 (s, 1H), 6.83-6.79 (m, 2H), 1.38 (s, 6H).

Synthesis of Intermediate G

(50) ##STR00079##

(51) The same synthesis procedure as in Synthesis of Intermediate A was used, except that 1,8-dibromo-9,9-dimethyl-9H-fluorene (7.0 g, 20 mmol) was used instead of 4,6-dibromobenzofuran and 12,12-dimethyl-7,12-dihydro-benzo[4,5]thieno[3,2-b]acridine (6.3 g, 20 mmol) was used instead of bis(4-tert-butylphenyl)amine to obtain 7.6 g (65%) of Intermediate G.

Synthesis of Intermediate H

(52) ##STR00080##

(53) The same synthesis procedure as in Synthesis of Intermediate B was used, except that Intermediate G (7.6 g, 13 mmol) was used instead of Intermediate A to obtain 4.9 g (69%) of Intermediate H.

Synthesis of 5,6-dibromoacenaphthylene

(54) ##STR00081##

(55) A mixture of 70 g (460 mmol) of Acenaphthylene and 100 ml of DMF was placed under nitrogen and stirred at 0° C. After 180 g (1012 mmol) of N-bromosuccinimide in 300 ml of DMF was added dropwise, the temperature was raised to room temperature and the mixture was stirred for 18 hours. The precipitated product was filtered off with suction and washed with EtOH. The residue was recrystallized from EtOH to give product (47 g, 151.8 mmol, 33%).

Synthesis of Intermediate I

(56) ##STR00082##

(57) The same synthesis procedure as in Synthesis of Intermediate C was used, except that 5,6-dibromoacenaphthylene (2.7 g, 8.9 mmol) was used instead of 5,6-dibromo-1,2-dihydroacenaphthylene and Intermediate H (4.9 g, 8.9 mmol) was used instead of Intermediate B to obtain 4.1 g (63%) of Intermediate I.

Synthesis of EX95

(58) ##STR00083##

(59) The same synthesis procedure as in Synthesis of EX1 was used, except that Intermediate I (4.1 g, 5.6 mmol) was used instead of Intermediate C and 4,5-Diazafluoren-9-one (1.0 g, 5.6 mmol) was used instead of 9H-fluoren-9-one to obtain 1.6 g (35%) of EX95. MS(m/z, EI.sup.+): 818.3.

Example 6

Synthesis of Intermediate J

(60) ##STR00084##

(61) The same synthesis procedure as in Synthesis of Intermediate A was used, except that 6.7 g (20 mmol) of N,9-diphenyl-9H-carbazol-2-amine was used instead of bis(4-tert-butylphenyl)amine to obtain 6.8 g (59%) of Intermediate J.

Synthesis of Intermediate K

(62) ##STR00085##

(63) The same synthesis procedure as in Synthesis of Intermediate B was used, except that 6.8 g (11.8 mmol) of Intermediate J was used instead of Intermediate A to obtain 4.8 g (75%) of Intermediate K.

Synthesis of Intermediate L

(64) ##STR00086##

(65) The same synthesis procedure as in Synthesis of Intermediate C was used, except that 4.8 g (8.8 mmol) of Intermediate K was used instead of Intermediate B to obtain 4.0 g (62%) of Intermediate L.

Synthesis of EX21

(66) ##STR00087##

(67) The same synthesis procedure as in Synthesis of EX1 was used, except that 4.0 g (5.5 mmol) of Intermediate L was used instead of Intermediate C to obtain 1.9 g (43%) of EX21. MS(m/z, EI.sup.+): 813.3.

Example 7

Synthesis of EX23

(68) ##STR00088##

(69) The same synthesis procedure as in Synthesis of EX1 was used, except that 4.0 g (5.5 mmol) of Intermediate L was used instead of Intermediate C and 1.0 g (5.5 mmol) of Cyclopentadithiophene Ketone was used instead of 9H-fluoren-9-one to obtain 2.1 g (47%) of EX23. MS(m/z, EI.sup.+): 825.2.

General Method of Producing Organic EL Device

(70) 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).

(71) 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 5,12-dihydrotetracene derivatives of the present invention are thermally stable.

(72) 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. 10,10-dimethyl-13-(3-(pyren-1-yl)phenyl)-10H-indeno[2,1-b]triphenylene (H1), 10,10-dimethyl-12-(4-(pyren-1-yl)phenyl)-10H-indeno[2,1-b]triphenylene (H2), and 10,10-dimethyl-12-(10-(4-(naphthalene-1-yl)-phenyl) anthracen-9-yl)-1 OH-indeno[2,1-b]triphenylene (H3) are used as emitting hosts in organic EL devices, and N1,N1,N6,N6-tetram-tolylpyrene-1,6-diamine (D1) is used as blue dopant for comparison. HB3 (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 (ET2) is used as electron transporting material to co-deposit with 8-hydroxyquinolato-lithium (LiQ, as shown below) in organic EL devices. The chemical structures of conventional OLED materials and the exemplary heteroaromatic compounds of the present invention for producing control and exemplary organic EL devices in this invention are shown as follows:

(73) ##STR00089## ##STR00090## ##STR00091##

(74) 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-film electron injecting layer is introduced between the cathode and the electron transporting layer. Conventional 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 8

(75) Using a procedure analogous to the above mentioned general method, organic EL devices emitting blue light and having the following device structure as shown in the FIGURE were produced: ITO/HAT-CN (20 nm)/NPB (110 nm)/Emitting host doped with 5% Emitting dopant (30 nm)/HB3/ET2 doped 50% LiQ(35 nm)/LiQ(1 nm)/Al(160 nm). In the device illustrated in the FIGURE, the hole injection layer 20 is deposited onto the transparent electrode 10, the hole transport layer 30 is deposited onto the hole injection layer 20, the emitting layer 40 is deposited onto the hole transport layer 30, the hole blocking layer 50 is deposited onto the emitting layer 40, the electron transport layer 60 is deposited onto the hole blocking layer 50, the electron injection layer 70 is deposited onto the electron transport layer 60, and the metal electrode 80 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.

(76) TABLE-US-00001 TABLE 1 Emitting Emitting Voltage Efficiency Device Half-life Host dopant (V) (cd/A) Colour time(hour) H1 EX1 2.8 6.3 blue 250 H1 EX6 2.9 6.1 blue 245 H1 EX9 3.0 5.9 blue 231 H1 EX10 2.8 6.5 blue 260 H1 Ex21 3.0 5.8 blue 220 H1 EX23 3.1 5.7 blue 210 H1 EX95 3.1 5.6 blue 195 H1 D1 3.5 5.3 blue 180 H2 EX1 2.8 6.9 blue 300 H2 EX6 2.9 6.7 blue 290 H2 EX9 2.9 6.6 blue 285 H2 EX10 2.8 7.1 blue 310 H2 Ex21 3.0 6.5 blue 280 H2 EX23 3.3 6.3 blue 230 H2 EX95 3.4 6.0 blue 210 H2 D1 3.8 5.5 blue 210 H3 EX1 3.0 7.0 blue 330 H3 EX6 3.0 6.8 blue 310 H3 EX9 3.1 6.5 blue 300 H3 EX10 2.8 7.2 blue 350 H3 Ex21 3.2 6.4 blue 295 H3 EX23 3.2 6.2 blue 291 H3 EX95 3.3 6.1 blue 285 H3 D1 3.5 5.5 blue 280

(77) In the above test report of organic EL devices (see Table 1), we show that the organic material with formula (1) used as emitting dopant material for organic EL devices in the present invention exhibits better performance than the prior art organic EL materials. More specifically, the organic EL devices of the present invention use the organic material with formula (1) as emitting dopant material to collocate with emitting host material, such as H1, H2 and H3, show lower power consumption, higher efficiency, and longer half-life time.

(78) To sum up, the present invention discloses a heteroaromatic compound, which can be used as the fluorescent dopant material of the light emitting layer in organic EL devices. The mentioned heteroaromatic compound is represented by the following formula (1):

(79) ##STR00092##
wherein Ar.sub.1 and Ar.sub.2 are independently an aryl group or a heteroaryl group having 4 to 6 ring carbon atoms; Ar.sub.3 is a cycloalkyl group, a cycloalkenyl group, or an aryl group having 5 to 6 ring carbon atoms; R.sub.1 and R.sub.2 are independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 36 carbon atoms, a substituted or unsubstituted aryl group having 6 to 36 carbon atoms, or a substituted or unsubstituted aralkyl group having 6 to 36 carbon atoms; W represents a divalent bridge selected from the group consisting of O, S, CR.sub.3R.sub.4, NR.sub.5, and SiR.sub.6R.sub.7, and R.sub.3 to R.sub.7 are independently a hydrogen atom or a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms; X is absent or a divalent bridge selected from the group consisting of O, S, CR.sub.8R.sub.9, NR.sub.10, and SiR.sub.11R.sub.12; A is absent or represents formula (2) below:

(80) ##STR00093##
wherein Y represents a divalent bridge selected from the group consisting of O, S, CR.sub.13R.sub.14, NR.sub.15, and SiR.sub.16R.sub.17; and R.sub.8 to R.sub.17 are independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 36 carbon atoms, a substituted or unsubstituted aryl group having 6 to 36 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 36 carbon atoms, or a substituted or unsubstituted heteroaryl group having 3 to 36 carbon atoms.

(81) 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.