COMPOUND AND ORGANIC ELECTRONIC DEVICE USING THE SAME

Abstract

Provided are a novel compound and an organic electronic device using the same. The novel compound is represented by the following Formula (I):

##STR00001## wherein X.sup.1 and X.sup.2 are each independently C(R.sup.a), and the two (R.sup.a)s are the same or different; X.sup.3 and X.sup.4 are each independently C(R.sup.b), and the two (R.sup.b)s are the same or different; the two (R.sup.a)s are joined together to form an aryl ring and the two (R.sup.b)s are joined together to form an oxygen-containing heteroaryl ring, a sulfur-containing heteroaryl ring, or a polycyclic aromatic ring; wherein Y.sup.1 and Y.sup.2 are the same or different; Y.sup.1 and Y.sup.2 are each represented by NR′R″; R′ and R″ are the same or different; at least one of R′ and R″ is an aryl group.

Claims

1. A compound represented by the following Formula (I): ##STR00358## wherein X.sup.1 and X.sup.2 are each independently C(R.sup.a) and the two (R.sup.a)s are the same or different; X.sup.3 and X.sup.4 are each independently C(R.sup.b) and the two (R.sup.b)s are the same or different; the two (R.sup.a)s are joined together to form an aryl ring and the two (R.sup.b)s are joined together to form an oxygen-containing heteroaryl ring, a sulfur-containing heteroaryl ring, or a polycyclic aromatic ring; wherein Y.sup.1 and Y.sup.2 are the same or different; Y.sup.1 and Y.sup.2 are each represented by NR′R″; R′ and R″ are the same or different; at least one of R′ and R″ is an aryl group; wherein Z.sup.1 to Z.sup.3 are each independently selected from the group consisting of: a deuterium atom, a halogen group, a cyano group, a nitro group, an alkyl group having 1 to 40 carbon atoms, an alkenyl group having 2 to 40 carbon atoms, an alkynyl group having 2 to 40 carbon atoms, a cycloalkyl group having 3 to 60 carbon atoms, a heterocycloalkyl group having 3 to 60 carbon atoms, an aryl group having 6 to 60 carbon atoms, a heteroaryl group having 3 to 60 carbon atoms, an alkoxy group having 1 to 40 carbon atoms, an aryloxy group having 6 to 60 carbon atoms, an alkylsilyl group having 1 to 40 carbon atoms, an arylsilyl group having 6 to 60 carbon atoms, an alkylboron group having 1 to 40 carbon atoms, an arylboron group having 6 to 60 carbon atoms, a phosphine group having 1 to 40 carbon atoms, and a phosphine oxide group having 1 to 40 carbon atoms; wherein 1 is an integral from 1 to 4; m is an integral from 0 to 4; n1 is an integral from 0 to 3; n2 is an integral from 0 to 4; n3 is an integral from 0 to 4; the total of n1 and 1 is not more than 4; the total of n2 and m is not more than 4.

2. The compound as claimed in claim 1, wherein the oxygen-containing heteroaryl ring contains at least one furan group.

3. The compound as claimed in claim 2, wherein the compound is represented by the following Formulae (I-I) to (1-VI): ##STR00359## ##STR00360## wherein A.sup.1 and A.sup.2 are each independently C(R.sup.c), the two (R.sup.c)s are the same or different, and the two (R.sup.c)s are joined together to form an aromatic structure contained in the oxygen-containing heteroaryl ring.

4. The compound as claimed in claim 3, wherein the aromatic structure contained in the oxygen-containing heteroaryl ring is a substituted or unsubstituted 6 to 20-membered carbon cyclic structure.

5. The compound as claimed in claim 1, wherein the sulfur-containing heteroaryl ring contains at least one thiofuran group.

6. The compound as claimed in claim 5, wherein the compound is represented by the following Formulae (II-I) to (II-VI): ##STR00361## ##STR00362## wherein A.sup.3 and A.sup.4 are each independently C(R.sup.d), the two (R.sup.d)s are the same or different, and the two (R.sup.d)s are joined together to form an aromatic structure contained in the sulfur-containing heteroaryl ring.

7. The compound as claimed in claim 6, wherein the aromatic structure contained in the sulfur-containing heteroaryl ring is a substituted or unsubstituted 6 to 20-membered carbon cyclic structure.

8. The compound as claimed in claim 1, wherein the polycyclic aromatic ring is selected from the group consisting of: a benzene ring, a dimethylfluorene, a naphthalene ring, an anthracene ring, a phenanthrene ring, a tetracene ring, a chrysene ring, a triphenylene ring, a pyrene ring, a perylene ring, a pentacene ring, a benzopyrene ring, a corannulene ring, a benzoperylene ring, a coronene ring, an ovalene ring, a benzofluorine ring, an indene ring, a fluoranthene ring, and a benzofluoranthene ring.

9. The compound as claimed in claim 8, wherein the compound is represented by the following Formulae (II-I) to (III-XVIII): ##STR00363## ##STR00364## ##STR00365## ##STR00366## ##STR00367##

10. The compound as claimed in claim 1, wherein the aryl ring formed by the two (R.sup.a)s is selected from the group consisting of: a substituted or unsubstituted benzene ring, a substituted or unsubstituted dimethyifluorene, a substituted or unsubstituted naphthalene ring, a substituted or unsubstituted anthracene ring, a substituted or unsubstituted phenanthrene ring, a substituted or unsubstituted tetracene ring, a substituted or unsubstituted chrysene ring, a substituted or unsubstituted triphenylene ring, a substituted or unsubstituted pyrene ring, a substituted or unsubstituted perylene ring, a substituted or unsubstituted pentacene ring, a substituted or unsubstituted benzopyrene ring, a substituted or unsubstituted corannulene ring, a substituted or unsubstituted benzoperylene ring, a substituted or unsubstituted coronene ring, a substituted or unsubstituted ovalene ring, a substituted or unsubstituted benzofluorine ring, a substituted or unsubstituted indene ring, a substituted or unsubstituted fluoranthene ring, and a substituted or unsubstituted benzofluoranthene ring.

11. The compound as claimed in claim 1, wherein the aryl ring formed by the two (R.sup.a)s is a substituted or unsubstituted 6 to 60-membered aryl ring.

12. The compound as claimed in claim 1, wherein R′ contained in Y.sup.1 and Y.sup.2 is the aryl group and R″ contained in Y.sup.1 and Y.sup.2 is selected from the group consisting of: an alkyl group having 1 to 40 carbon atoms, an alkenyl group having 2 to 40 carbon atoms, an alkynyl group having 2 to 40 carbon atoms, a cycloalkyl group having 3 to 60 carbon atoms, and an aryl group having 6 to 60 carbon atoms.

13. The compound as claimed in claim 1, wherein Y.sup.1 and Y.sup.2 in Formula (I) are each independently selected from the group consisting of: ##STR00368## ##STR00369## ##STR00370## ##STR00371## ##STR00372## ##STR00373## ##STR00374## wherein R.sup.1 to R.sup.5 are each independently selected from the group consisting of: a deuterium atom, a halogen group, a cyano group, a nitro group, an alkyl group having 1 to 12 carbon atoms, an alkenyl group having 2 to 12 carbon atoms, an alkynyl group having 2 to 12 carbon atoms, a cycloalkyl group having 3 to 30 carbon atoms, a heterocycloalkyl group having 3 to 30 carbon atoms, an aryl group having 6 to 30 carbon atoms, a heteroaryl group having 3 to 20 carbon atoms, an alkoxy group having 1 to 40 carbon atoms, an aryloxy group having 6 to 30 carbon atoms, an alkylsilyl group having 1 to 40 carbon atoms, an arylsilyl group having 6 to 30 carbon atoms, an alkylboron group having 1 to 40 carbon atoms, an arylboron group having 6 to 30 carbon atoms, a phosphine group having 1 to 30 carbon atoms, and a phosphine oxide group having 1 to 30 carbon atoms; wherein p is an integral from 0 to 5; n is an integral from 0 to 4; q is an integral from 0 to 3.

14. The compound as claimed in claim 1, wherein the compound is selected from the group consisting of: ##STR00375## ##STR00376## ##STR00377## ##STR00378## ##STR00379## ##STR00380## ##STR00381## ##STR00382## ##STR00383## ##STR00384## ##STR00385## ##STR00386## ##STR00387## ##STR00388## ##STR00389## ##STR00390## ##STR00391## ##STR00392## ##STR00393## ##STR00394## ##STR00395## ##STR00396## ##STR00397## ##STR00398## ##STR00399## ##STR00400## ##STR00401## ##STR00402## ##STR00403## ##STR00404## ##STR00405## ##STR00406## ##STR00407## ##STR00408## ##STR00409## ##STR00410## ##STR00411## ##STR00412## ##STR00413## ##STR00414## ##STR00415## ##STR00416## ##STR00417## ##STR00418## ##STR00419## ##STR00420## ##STR00421## ##STR00422## ##STR00423## ##STR00424## ##STR00425## ##STR00426## ##STR00427## ##STR00428## ##STR00429## ##STR00430## ##STR00431## ##STR00432## ##STR00433## ##STR00434## ##STR00435## ##STR00436## ##STR00437## ##STR00438## ##STR00439## ##STR00440## ##STR00441## ##STR00442## ##STR00443## ##STR00444## ##STR00445## ##STR00446## ##STR00447## ##STR00448## ##STR00449## ##STR00450## ##STR00451## ##STR00452## ##STR00453## ##STR00454## ##STR00455## ##STR00456## ##STR00457## ##STR00458## ##STR00459## ##STR00460## ##STR00461## ##STR00462## ##STR00463## ##STR00464## ##STR00465## ##STR00466## ##STR00467## ##STR00468## ##STR00469## ##STR00470## ##STR00471## ##STR00472## ##STR00473## ##STR00474## ##STR00475## ##STR00476## ##STR00477## ##STR00478## ##STR00479## ##STR00480## ##STR00481## ##STR00482## ##STR00483## ##STR00484## ##STR00485## ##STR00486## ##STR00487## ##STR00488## ##STR00489## ##STR00490## ##STR00491## ##STR00492## ##STR00493## ##STR00494## ##STR00495## ##STR00496## ##STR00497## ##STR00498## ##STR00499## ##STR00500## ##STR00501## ##STR00502## ##STR00503## ##STR00504## ##STR00505## ##STR00506## ##STR00507## ##STR00508## ##STR00509## ##STR00510## ##STR00511## ##STR00512## ##STR00513## ##STR00514## ##STR00515## ##STR00516## ##STR00517## ##STR00518## ##STR00519## ##STR00520## ##STR00521## ##STR00522## ##STR00523## ##STR00524## ##STR00525## ##STR00526## ##STR00527## ##STR00528## ##STR00529## ##STR00530## ##STR00531## ##STR00532## ##STR00533## ##STR00534## ##STR00535## ##STR00536## ##STR00537## ##STR00538## ##STR00539## ##STR00540## ##STR00541## ##STR00542## ##STR00543## ##STR00544## ##STR00545## ##STR00546## ##STR00547## ##STR00548## ##STR00549## ##STR00550## ##STR00551## ##STR00552## ##STR00553## ##STR00554## ##STR00555## ##STR00556## ##STR00557## ##STR00558## ##STR00559## ##STR00560## ##STR00561## ##STR00562## ##STR00563## ##STR00564## ##STR00565## ##STR00566## ##STR00567## ##STR00568## ##STR00569## ##STR00570## ##STR00571## ##STR00572## ##STR00573## ##STR00574## ##STR00575## ##STR00576## ##STR00577## ##STR00578## ##STR00579## ##STR00580## ##STR00581## ##STR00582## ##STR00583## ##STR00584## ##STR00585## ##STR00586## ##STR00587## ##STR00588## ##STR00589## ##STR00590## ##STR00591## ##STR00592## ##STR00593## ##STR00594## ##STR00595## ##STR00596## ##STR00597## ##STR00598## ##STR00599## ##STR00600## ##STR00601## ##STR00602## ##STR00603## ##STR00604## ##STR00605## ##STR00606## ##STR00607## ##STR00608## ##STR00609## ##STR00610## ##STR00611## ##STR00612## ##STR00613## ##STR00614## ##STR00615## ##STR00616## ##STR00617## ##STR00618## ##STR00619## ##STR00620## ##STR00621## ##STR00622## ##STR00623## ##STR00624## ##STR00625## ##STR00626## ##STR00627## ##STR00628## ##STR00629## ##STR00630## ##STR00631## ##STR00632## ##STR00633## ##STR00634## ##STR00635## ##STR00636## ##STR00637## ##STR00638## ##STR00639## ##STR00640## ##STR00641## ##STR00642## ##STR00643## ##STR00644## ##STR00645## ##STR00646## ##STR00647## ##STR00648## ##STR00649## ##STR00650## ##STR00651## ##STR00652## ##STR00653## ##STR00654## ##STR00655## ##STR00656## ##STR00657## ##STR00658## ##STR00659## ##STR00660## ##STR00661## ##STR00662## ##STR00663## ##STR00664## ##STR00665## ##STR00666## ##STR00667## ##STR00668## ##STR00669## ##STR00670## ##STR00671## ##STR00672## ##STR00673## ##STR00674## ##STR00675## ##STR00676## ##STR00677## ##STR00678## ##STR00679## ##STR00680## ##STR00681## ##STR00682## ##STR00683## ##STR00684## ##STR00685## ##STR00686## ##STR00687## ##STR00688## ##STR00689## ##STR00690## ##STR00691## ##STR00692## ##STR00693## ##STR00694## ##STR00695## ##STR00696## ##STR00697## ##STR00698## ##STR00699## ##STR00700## ##STR00701## ##STR00702## ##STR00703## ##STR00704## ##STR00705## ##STR00706## ##STR00707## ##STR00708## ##STR00709## ##STR00710## ##STR00711## ##STR00712## ##STR00713## ##STR00714##

15. The compound as claimed in claim 1, wherein Z.sup.3 in Formula (I) is selected from the group consisting of: a deuterium atom, a halogen group, a cyano group, a nitro group, an alkyl group having 1 to 12 carbon atoms, an alkenyl group having 2 to 12 carbon atoms, and an alkynyl group having 2 to 12 carbon atoms.

16. An organic electronic device, comprising a first electrode, a second electrode, and an organic layer disposed between the first electrode and the second electrode, wherein the organic layer comprises the compound as claimed in claim 1.

17. The organic electronic device as claimed in claim 16, wherein the organic electronic device is an organic light emitting device.

18. The organic electronic device as claimed in claim 17, wherein the organic light emitting device comprises: a hole injection layer formed on the first electrode; a hole transport layer formed on the hole injection layer, wherein the organic layer is the hole transport layer; an emission layer formed on the hole transport layer; an electron transport layer formed on the emission layer; and an electron injection layer formed between the electron transport layer and the second electrode.

19. The organic electronic device as claimed in claim 17, wherein the organic light emitting device comprises: a hole injection layer fornied on the first electrode; a hole transport layer formed on the hole injection layer; an electron blocking layer formed on the hole injection layer, wherein the organic layer is the electron blocking layer; an emission layer formed on the electron blocking layer; an electron transport layer fo ied on the emission layer; and an electron injection layer formed between the electron transport layer and the second electrode.

20. The organic electronic device as claimed in claim 17, wherein the compound is selected from the group consisting of: ##STR00715## ##STR00716## ##STR00717## ##STR00718## ##STR00719## ##STR00720## ##STR00721## ##STR00722## ##STR00723## ##STR00724## ##STR00725## ##STR00726## ##STR00727## ##STR00728## ##STR00729## ##STR00730## ##STR00731## ##STR00732## ##STR00733## ##STR00734## ##STR00735## ##STR00736## ##STR00737## ##STR00738## ##STR00739## ##STR00740## ##STR00741## ##STR00742## ##STR00743## ##STR00744## ##STR00745## ##STR00746## ##STR00747## ##STR00748## ##STR00749## ##STR00750## ##STR00751## ##STR00752## ##STR00753## ##STR00754## ##STR00755## ##STR00756## ##STR00757## ##STR00758## ##STR00759## ##STR00760## ##STR00761## ##STR00762## ##STR00763## ##STR00764## ##STR00765## ##STR00766## ##STR00767## ##STR00768## ##STR00769## ##STR00770## ##STR00771## ##STR00772## ##STR00773## ##STR00774## ##STR00775## ##STR00776## ##STR00777## ##STR00778## ##STR00779## ##STR00780## ##STR00781## ##STR00782## ##STR00783## ##STR00784## ##STR00785## ##STR00786## ##STR00787## ##STR00788## ##STR00789## ##STR00790## ##STR00791## ##STR00792## ##STR00793## ##STR00794## ##STR00795## ##STR00796## ##STR00797## ##STR00798## ##STR00799## ##STR00800## ##STR00801## ##STR00802## ##STR00803## ##STR00804## ##STR00805## ##STR00806## ##STR00807## ##STR00808## ##STR00809## ##STR00810## ##STR00811## ##STR00812## ##STR00813## ##STR00814## ##STR00815## ##STR00816## ##STR00817## ##STR00818## ##STR00819## ##STR00820## ##STR00821## ##STR00822## ##STR00823## ##STR00824## ##STR00825## ##STR00826## ##STR00827## ##STR00828## ##STR00829## ##STR00830## ##STR00831## ##STR00832## ##STR00833## ##STR00834## ##STR00835## ##STR00836## ##STR00837## ##STR00838## ##STR00839## ##STR00840## ##STR00841## ##STR00842## ##STR00843## ##STR00844## ##STR00845## ##STR00846## ##STR00847## ##STR00848## ##STR00849## ##STR00850## ##STR00851## ##STR00852## ##STR00853## ##STR00854## ##STR00855## ##STR00856## ##STR00857## ##STR00858## ##STR00859## ##STR00860## ##STR00861## ##STR00862## ##STR00863## ##STR00864## ##STR00865## ##STR00866## ##STR00867## ##STR00868## ##STR00869## ##STR00870## ##STR00871## ##STR00872## ##STR00873## ##STR00874## ##STR00875## ##STR00876## ##STR00877## ##STR00878## ##STR00879## ##STR00880## ##STR00881## ##STR00882## ##STR00883## ##STR00884## ##STR00885## ##STR00886## ##STR00887## ##STR00888## ##STR00889## ##STR00890## ##STR00891## ##STR00892## ##STR00893## ##STR00894## ##STR00895## ##STR00896## ##STR00897## ##STR00898## ##STR00899## ##STR00900## ##STR00901## ##STR00902## ##STR00903##

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0067] FIG. 1 illustrates a schematic cross-sectional view of an OLED;

[0068] FIGS. 2 to 18 respectively are .sup.1H nuclear magnetic resonance (NMR) spectra of Compounds 1 to 17.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0069] Hereinafter, one skilled in the arts can easily realize the advantages and effects of a novel compound and an organic light emitting device using the same in accordance with the present invention from the following examples. It should be understood that the descriptions proposed herein are just preferable examples only for the purpose of illustrations, not intended to limit the scope of the invention. Various modifications and variations could be made in order to practice or apply the present invention without departing from the spirit and scope of the invention.

[0070] Synthesis of Intermediate A1

[0071] Intermediate A1 used for preparing a novel compound was synthesized by the following steps. The synthesis pathway of the Intermediate A1 was summarized in Scheme A1.

##STR00208##

[0072] Step 1: synthesis of Intermediate A1-1

[0073] A mixture of 3-bromodibenzo[a,d]cyclohepten-5-one (86 g, 1.0 eq), N-bromosuccinimide (NBS) (106 g, 2 eq), benzyl peroxide (0.7 g, 0.01 eq) in carbon tetrachloride (CCl.sub.4) (430 ml) was heated to 85° C. The reaction was monitored by high performance liquid chromatography (HPLC). After completion of a reaction, the precipitate was separated by filtration and washed with CH.sub.3OH and then purified by recrystalization. The purified product was concentrated to dryness, whereby a white solid product was obtained in an amount of 123 g and a yield of 92.3%.

[0074] The solid product was identified as Intermediate A1-1 by a field desorption mass spectroscopy (FD-MS) analysis. FD-MS analysis: C.sub.15H.sub.9Br.sub.3O: theoretical value of 444.94 and observed value of 444.94.

[0075] Step 2: synthesis of Intermediate A1-2

[0076] The obtained Intermediate A1-1 (116.0 g, 1.0 eq) was dissolved in 960 ml of furan/THF (v/v=2/1), the reaction was cooled to 0° C. and then treated with potassium tert-butoxide (KO-t-Bu) (87.8 g, 3.0 eq). The reaction was allowed to stir at 0° C. for 1 hour, and then stirred at room temperature for another 12 hours. Quenched by DI water, the organic layer was recovered by solvent extraction operation and dried over sodium sulfate. The solvent was removed from the organic layer by distillation under reduced pressure, and the resulting residue was purified by silica gel column chromatography. The purified product was concentrated to dryness, whereby a light yellow solid product was obtained in an amount of 46.8 g and a yield of 51.1%.

[0077] The solid product was identified as Intermediate Al-2 by FD-MS analysis. FD-MS analysis C.sub.19H.sub.11BrO.sub.2: theoretical value of 351.19 and observed value of 351.19.

[0078] Step 3: synthesis of Intermediate A1-3

[0079] A suspension of Intermediate A1-2 (53.5 g, 1.0 eq) and 5% Pd/C (8.1 g, 0.025 eq) in 535 ml of ethyl acetate (EA) was stirred for 3 hours to 6 hours under a hydrogen atmosphere (H.sub.2) provided by a balloon of hydrogen. The resulting mixture was filtered through a pad of celite and washed with EA, and the filtrate was concentrated under reduced pressure to obtain 100 g (100%) of yellow solid product.

[0080] The solid product was identified as Intermediate A1-3 by FD-MS analysis. FD-MS analysis C.sub.19H.sub.13BrO.sub.2: theoretical value of 353.21 and observed value of 353.21. The intermediate A1-3 can be directly used in the following step without further purification.

[0081] Step 4: synthesis of Intermediate A1-4

[0082] Intermediate A1-3 (53 g, 1.0 eq) and p-toluenesulfonic acid (PTSA) (57 g, 2.0 eq) in 530 ml of toluene was heated to reflux for 12 hours. The reaction mixture was cooled to room temperature and then quenched with a saturated aqueous solution of NaHCO.sub.3 and extracted with CH.sub.2Cl.sub.2. The organic layer was washed with water, brine and dried with anhydrous Na.sub.2SO.sub.4 subsequently. Then the resulting solution was concentrated under reduced pressure and purified by column chromatography on silica gel with CH.sub.2Cl.sub.2/hexane (1:1 v/v) as an eluent, whereby a light yellow solid product was obtained in an amount of 46.0 g and a yield of 91.5%.

[0083] The solid product was identified as Intermediate A1 by FD-MS analysis. FD-MS analysis C.sub.19H.sub.11BrO: theoretical value of 335.19 and observed value of 335.19.

[0084] Synthesis of Intermediate A2

[0085] Intermediate A2 used for preparing a novel compound was synthesized in a similar manner as Intermediate A1 through steps 1 to 4, except that the starting material 3-bromodibenzo[a,d]cyclohepten-5-one was replaced by 2-bromodibenzo[a,d]cyclohepten-5-one (CAS No. 198707-82-3). The synthesis pathway of Intermediate A2 was summarized in Scheme A2. All intermediates were analyzed according to the methods as described above, and the results were listed in Table 1.

##STR00209##

[0086] Synthesis of Intermediate A3

[0087] Intermediate A3 used for preparing a novel compound was synthesized in a similar manner as Intermediate A1 through steps 1 to 4, except that the starting material 3-bromodibenzo[a,d]cyclohepten-5-one was replaced by 3,7-dibromodibenzo[a,d]cyclohepten-5-one (CAS No. 226946-20-9). The synthesis pathway of Intermediate A3 was summarized in Scheme A3. All intermediates were analyzed as described above, and the results were listed in Table 1.

##STR00210##

TABLE-US-00001 TABLE 1 chemical structures, yields, formulae, and mass (M.sup.+) analyzed by FD-MS of intermediates. Intermediate A1-1 A1-2 Chemical Structure [00211] [00212] Yield 92.3% 51.1% Formula C.sub.15H.sub.9Br.sub.3O C.sub.19H.sub.11BrO.sub.2 Mass(M.sup.+) 444.94 351.19 A2-1 A2-2 Chemical Structure [00213] [00214] Yield 91.5% 58.2% Formula C.sub.15H.sub.9Br.sub.3O C.sub.19H.sub.11BrO.sub.2 Mass(M.sup.+) 444.94 351.19 A3-1 A3-2 Chemical Structure [00215] [00216] Yield 93.7% 55.8% Formula C.sub.15H.sub.8Br.sub.4O C.sub.19H.sub.10Br.sub.2O.sub.2 Mass(M.sup.+) 523.84 430.09 A1 -3 A1 Chemical Structure [00217] [00218] Yield NA 91.5% Formula C.sub.19H.sub.13BrO.sub.2 C.sub.19H.sub.11BrO Mass(M.sup.+) 353.21 335.19 A2-3 A2 Chemical Structure [00219] [00220] Yield NA 93.5% Formula C.sub.19H.sub.13BrO.sub.2 C.sub.19H.sub.11BrO Mass(M.sup.+) 353.21 335.19 A3-3 A3 Chemical Structure [00221] [00222] Yield NA 93.0% Formula C.sub.19H.sub.12Br.sub.2O.sub.2 C.sub.19H.sub.10Br.sub.2O Mass(M.sup.+) 432.11 414.09

[0088] Modifications of Intermediates A1 to A3

[0089] In addition to the Intermediates A1 to A3, one person skilled in the art can adopt other starting materials and successfully synthesize other desired intermediates through a reaction mechanism similar to Schemes A1 to A3. Applicable modifications of Intermediates A1 to A3 may be, for example, but not limited to, Intermediates A4 to A15 as follows.

##STR00223## ##STR00224##

[0090] Synthesis of Intermediates B1 to B8

[0091] Intermediates B1 to B8 were synthesized by reacting 1-bromo-2-iodobenzene and aryl boronic acid (Reactant A). A general synthesis pathway for Intermediate B was summarized in Scheme B1. In the following Scheme B 1, “Reactant A” may be any one of Reactants A 1 to A8 as listed in Table 2 and the R.sup.HR in Reactant A is a heteroaryl ring containing furan group or thiofuran group. “Intermediate B” may be any one of Intermediates B1 to B8 as listed in Table 2.

##STR00225##

[0092] According to the Scheme B1, each of Intermediates B1 to B8 was synthesized by the steps as follows.

[0093] Water and toluene were poured into a round-bottomed flask, fitted with a condenser and argon flow, and bubbled through with argon. Potassium carbonate (1.5 eq), 1-bromo-2-iodobenzene (1.0 eq), Reactant A (1.05 eq), tri(m-tolyl)phosphine (P(m-toyl).sub.3) (0.04 eq) and Pd(OAc).sub.2 (0.01 eq) were added to the mixture, which was heated at 65° C. for 5 hours in an oil bath. The reaction mixture was allowed to be cooled to room temperature, toluene was evaporated, and water and EA were added. The layers were separated and the aqueous layer was extracted with EA twice. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and evaporated in vacuo to obtain a yellow oil. The yellow oil was further purified using column chromatography on silica gel (eluent: 30% EA in heptane) to give Intermediate B. All intermediates were analyzed according to the methods as described above, and the results were listed in Table 2.

[0094] Synthesis of Intermediates B9 to B12

[0095] Intermediates B9 to B12 were synthesized by reacting 1-bromo-2-iodobenzene and aryl boronic acid (Reactant A). A general synthesis pathway for Intermediates B9 to B12 was summarized in Scheme B2. In the following Scheme B2, “Reactant A” may be any one of Reactants A9 to A12 as listed in Table 2 and the R.sup.PA in Reactant A is a polycyclic aromatic group. “Intermediate B” may be any one of Intermediates B9 to B12 as listed in Table 2.

##STR00226##

[0096] According to the Scheme B2, each of Intermediates B9 to B12 was synthesized by the steps as follows.

[0097] 1-bromo-2-iodobenzene (1.0 eq), Reactant A (1.2 eq), potassium carbonate (3.0 eq), 200 ml of toluene, trim-tolyl)phosphine (P(m-toyl).sub.3) (0.06 eq) and Pd(OAc).sub.2 (0.015 eq) were mixed and stirred at 80° C. for 12 hours. The reaction mixture was then cooled to room temperature, and an organic layer was extracted with saturated aqueous solution of sodium chloride and EA and dried over magnesium sulfate, and then treated with activated characoal, followed by filtering with silica gel. After a solid prepared by concentrating the filtrate under reduced pressure was suspended in hexane, the suspension was filtered again and washed with hexane to obtain Intermediate B. All intermediates were analyzed according to the methods as described above, and the results were listed in Table 2.

TABLE-US-00002 TABLE 2 Reactant A used for preparing Intermediates B1 to B12, and the chemical structures, yields, formulae, and mass analyzed by FD-MS of Intermediates B1 to B12. Intermediate B Reactant A Yield Formula/ Chemical Structure Chemical Structure (%) Mass (M.sup.+) [00227] [00228] 80 C.sub.18H.sub.11BrO/ (323.18) [00229] [00230] 63 C.sub.18H.sub.11BrO/ (323.18) [00231] [00232] 85 C.sub.18H.sub.11BrO/ (323.18) [00233] [00234] 87 C.sub.18H.sub.11BrO/ (323.18) [00235] [00236] 90 C.sub.18H.sub.11BrS/ (339.25) [00237] [00238] 63 C.sub.18H.sub.11BrS/ (339.25) [00239] [00240] 88 C.sub.18H.sub.11BrS/ (339.25) [00241] [00242] 84 C.sub.18H.sub.11BrS/ (339.25) [00243] [00244] 93 C.sub.16H.sub.11Br/ (283.16) [00245] [00246] 84 C.sub.22H.sub.13Br/ (357.24) [00247] [00248] 62 C.sub.20H.sub.13Br/ (333.22) [00249] [00250] 80 C.sub.22H.sub.13Br/ (357.24)

[0098] Synthesis of Intermediates B13

[0099] In addition to Schemes B1 and B2, another synthesis pathway for Intermediate B was summarized in Scheme B3.

##STR00251##

[0100] Step 1: Synthesis of o-(phenylethynyl)benzaldehyde

[0101] Referring to Chemistry—A European Journal, 2007, 13(19), 5632, 2-bromobenzaldehyde (1 eq, CAS No. 6630-33-7), CuI (0.025 eq), Pd(PPh.sub.3).sub.2Cl.sub.2 (0.05 eq), Et.sub.3N (0.6 ml), and the ethynylbenzene (1.2 eq, CAS No. 536-74-3) were added under argon to a stirred solution of quinoline (1 mmol) in anhydrous DMF (1.0M to 2-bromobenzaldehyde). The mixture was stirred at room temperature and monitored by thin layer chromatography (TLC). After evaporation under vacuum, the crude mixture was purified by column chromatography on silica gel to give o-(phenylethynyl)benzaldehyde.

[0102] Step 2: Synthesis of Intermediate B13 (2-bromo-3-phenylnapthalene)

[0103] Referring to Journal of the American Chemical Society, 2003, 125(36), 10921, a mixture of o-(phenylethynyl)benzaldehyde (0.5 mmol, CAS No. 59046-72-9) and Cu(OTf).sub.2(5 mol %) in 1,2-dichloroethane (2 ml) were added with (bromoethynyl)benzene (0.6 mmol, CAS No. 932-87-6) and CF.sub.2HCO.sub.2H (0.5 mmol) successively at room temperature under N.sub.2 atmosphere. The resulting mixture was stirred at 100° C. for 15 min and then cooled to room temperature. A saturated aqueous solution of NaHCO.sub.3 was added, and the mixture was extracted with ether three times. The combined extracts were washed with brine, dried over MgSO.sub.4, and evaporated to leave the crude product, which was purified by silica gel column chromatography using hexane as eluent to give 2-bromo-3-phenylnaphthalene (0.43 mmol) in 86% yield.

[0104] Modifications of Intermediates B1 to B13

[0105] In addition to the Intermediates B1 to B12, one person skilled in the art can adopt any dihalobenzenes other than 1-bromo-2-iodobenzene and any aryl boronic acids other than Reactants A1 to A12 to successfully synthesize other desired Intermediates B through a reaction mechanism similar to Scheme B1 or Scheme B2. Similarly, one person skilled in the art can also synthesize other desired Intermediates B through a reaction mechanism similar to Scheme B3.

[0106] Synthesis of Intermediates C

[0107] The foresaid Intermediates B1 to B13 were further adopted to synthesize Intermediate C. A general synthesis pathway for Intermediate C was summarized in Scheme C. In the following Scheme C, “Intermediate A” may be any one of foresaid Inteiinediates A1 to A3, “Inteintediate B” may be any one of foresaid Intermediates B1 to B13, and “Intermediate C” may be any one of Intermediates C1 to C29 as listed in Table 3. Intermediates C1 to C29 were each synthesized by the following steps.

##STR00252##

[0108] Step 1: Synthesis of Alcohol Intermediate

[0109] 1.3 g (52 mmol) of magnesium was put into a 200 ml three-neck flask and stirred for 0.5 hours while reducing pressure with a rotary pump. Then 5.0 ml of diethyl ether and one drop of dibromoethane were added under a nitrogen gas stream. A solution in which Intermediate B (50 mmol) was dissolved in 15 ml of diethyl ether was dropped into this mixture at a pace that maintained reflux flow. After completion of dropping, the reaction mixture was heated at 40° C. for 3 hours so as to become a Grignard reagent. The foresaid Intermediate A (45 mmol) was put into a 200 ml three-neck flask, and after nitrogen substitution in the flask was carried out, 40 ml of diethyl ether was added into the flask. The synthesized Grignard reagent was dropped into this solution, and after completion of dropping, the solution was refluxed at 50° C. for 3 hours, and then stirred at room temperature for 24 hours. When the reaction was completed, the reaction solution was washed with water, and a water layer was extracted with ethyl acetate. The extracted solution and an organic layer were combined and washed with saturated saline, and then dried with MgSO.sub.4. After drying, this mixture was subjected to suction filtration, and a filtrate was concentrated to give a light yellow, powdery solid of “alcohol intermediate”.

[0110] The alcohol intermediate could be directly used in step 2 without further purification. Each alcohol intermediates synthesized by reacting different Intermediate A with Inteimediate B was identified by FD-MS. The chemical structure of each alcohol intermediate was listed in Table 3.

[0111] Step 2: Synthesis of Intermediate C

[0112] 93 mmol of alcohol inteii iediate obtained from step 1, 900 ml of acetic acid, and 0.5 ml of HCl were added, and the mixture was stirred at 110° C. for 6 hours. The solvent was then removed by a rotary evaporator, and the remaining substance was purified with column chromatography to obtain Intermediate C.

[0113] Intermediates C1 to C29 obtained from different alcohol intermediates were identified by FD-MS. The chemical structures of Intermediates C1 to C29 were listed in Table 3.

TABLE-US-00003 TABLE 3 Intermediates A and B used for preparing Intermediates C1 to C29, chemical structures of alcohol intermediates, and chemical structures, yields, formulae, and mass analyzed by FD-MS of Intermediates C1 to C29. Inter- Inter- Intermediate C mediate mediate Alcohol intermediate Yield Formula/ A B Chemical Structure Chemical Structure (%) Mass (M.sup.+) A1 B1 [00253] [00254] 65 C.sub.37H.sub.21BrO/ (561.47) A3 B1 [00255] [00256] 66 C.sub.37H.sub.20Br.sub.2O/ (640.36) A1 B2 [00257] [00258] 78 C.sub.37H.sub.21BrO/ (561.47) A3 B2 [00259] [00260] 88 C.sub.37H.sub.20Br.sub.2O/ (640.36) A1 B3 [00261] [00262] 84 C.sub.37H.sub.21BrO/ (561.47) A3 B3 [00263] [00264] 81 C.sub.37H.sub.20Br.sub.2O/ (640.36) A1 B4 [00265] [00266] 86 C.sub.37H.sub.21BrO/ (561.47) A3 B4 [00267] [00268] 86 C.sub.37H.sub.20Br.sub.2O/ (640.36) A2 B3 [00269] [00270] 73 C.sub.37H.sub.21BrO/ (561.47) A1 B7 [00271] [00272] 82 C.sub.37H.sub.21BrS/ (577.53) A2 B7 [00273] [00274] 84 C.sub.37H.sub.21BrS/ (577.53) A3 B7 [00275] [00276] 84 C.sub.37H.sub.20Br.sub.2S/ (656.43) A1 B6 [00277] [00278] 71 C.sub.37H.sub.21BrS/ (577.53) A3 B6 [00279] [00280] 72 C.sub.37H.sub.20Br.sub.2S/ (656.43) A1 B5 [00281] [00282] 68 C.sub.37H.sub.21BrS/ (577.53) A3 B5 [00283] [00284] 58 C.sub.37H.sub.20Br.sub.2S/ (656.43) A1 B8 [00285] [00286] 67 C.sub.37H.sub.21BrS/ (577.53) A3 B8 [00287] [00288] 71 C.sub.37H.sub.20Br.sub.2S/ (656.43) A1 B9 [00289] [00290] 83 C.sub.35H.sub.21Br/ (521.45) A2 B9 [00291] [00292] 79 C.sub.35H.sub.21Br/ (521.45) A3 B9 [00293] [00294] 76 C.sub.35H.sub.20Br.sub.2/ (600.34) A1 B13 [00295] [00296] 63 C.sub.35H.sub.21Br/ (521.45) A3 B13 [00297] [00298] 68 C.sub.35H.sub.20Br.sub.2/ (600.34) A1 B11 [00299] [00300] 71 C.sub.39H.sub.23Br/ (571.5) A3 B11 [00301] [00302] 77 C.sub.39H.sub.22Br.sub.2/ (650.4) A1 B12 [00303] [00304] 58 C.sub.41H.sub.23Br/ (595.53) A3 B12 [00305] [00306] 73 C.sub.41H.sub.22Br.sub.2/ (674.42) A1 B10 [00307] [00308] 63 C.sub.41H.sub.23Br/ (595.53) A3 B10 [00309] [00310] 84 C.sub.41H.sub.23Br.sub.2/ (674.42)

[0114] Modifications of Intermediates C1 to C29

[0115] In addition to the Intetinediates C1 to C29, one person skilled in the art can adopt any intermediate A other than Intermediates A1 to A3 and any Intermediate B other than Intermediates B1 to B13 to successfully synthesize other desired Intermediates C through a reaction mechanism similar to Scheme C.

[0116] Synthesis of Novel Compounds

[0117] Each of Intermediates C1 to C29 could be reacted with various reactants to synthesize various claimed novel compounds. The general synthesis pathway of the claimed novel compound was summarized in Scheme I. In the following Scheme I, “Reactant B” may be any one of Reactants B1 to B5 as listed in Table 4, and “Intermediate C” may be any one of foresaid Intermediates C1 to C29. The compounds were each synthesized by the following steps.

##STR00311##

TABLE-US-00004 TABLE 4 chemical structure and CAS No. of Reactants B1 to B5. Reactant No. Reactant B1 Reactant B2 Reactant B3 Chemical Structure [00312] [00313] [00314] CAS No. 122-39-4 102113-98-4 NA Reactant B4 Reactant B5 Chemical Structure [00315] [00316] CAS No. NA NA

[0118] Reactants B1 to B5 were used to prepare the novel compounds. Among them, Reactants B1 to B2 were purchased from Aldrich or Alfa, and CAS numbers were listed in Table 4. In addition, Reactants B3 to B5 were synthesized by the Scheme I-I below.

[0119] Synthesis of Reactants B3 to B5

[0120] Reactants B3 to B5 were synthesized by the Scheme I-I. The Reactants B3 to B5 can be prepared according to the above Scheme I-I. The starting materials Ar.sub.1-NH.sub.2 (arylamine) and Br—Ar.sub.2 (arylbromide) to prepare the Reactants B3 to B5 are listed in the following Table 5.

##STR00317##

[0121] A mixture of arylbromide (1.0 eq), arylamine (1.05 eq), Pd(OAc).sub.2 (0.01 eq), 1,1′-Bis(diphenylphosphino)ferrocene (DPPF) (0.04 eq), sodium tert-butoxide (1.5 eq), and toluene was taken in a pressure tube and heated at 80° C. for 12h under N.sub.2 atmosphere. After completion of the reaction, the volatiles were removed under vacuum, and the resulting solution extracted with 60 mL dichloromethane for 3 times. The combined organic extract was washed with brine solution, dried over Na.sub.2SO.sub.4, and concentrated to leave a yellow solid. Further, the crude product was purified by column chromatography on silica gel by using hexane/dichloromethane mixture (2:1 v/v) as an eluent. The analysis data of the obtained products, i.e. Reactants B3 to B5, are listed in the following Table 5.

TABLE-US-00005 TABLE 5 the arylbromide and the arylamine used to prepare the Reactants B3 to B5 and the yield and the chemical structures, yields, formulae, and mass analyzed by FD-MS of Reactants B3 to B5. Yield Formula/ Arylbromide Arylamine Reactant (%) Mass (M.sup.+) [00318] [00319] [00320] 83 C.sub.27H.sub.23N/ (361.48) [00321] [00322] [00323] 80 C.sub.21H.sub.19NO/ (301.38) [00324] [00325] [00326] 82 C.sub.24H.sub.17NO/ (335.4)

[0122] Intermediate C (1.0 eq) and Reactant B (2.1 eq) were dissolved in toluene (105 ml) and saturated with N.sub.2. Pd(OAc).sub.2 (0.02 g, 0.005 eq), 10% (w/w) P(t-Bu).sub.3 in xylene and NaO-t-Bu (5.24 g, 3.0 eq) were added in the solution in succession and heated at 80° C. for 12 hours. DI water (20 ml) was poured into the resulting suspension and the mixed solution was stirred for 30 min. After that, the mixed solution was filtered with suction to obtain solid. Then, the solid was washed by H.sub.2O and methanol and recrystallized (3 times) with toluene to obtain the white solid of the claimed novel compound.

[0123] The reactants B and intermediates C adopted to synthesize Compounds 1 to 17 were listed in Table 6. Compounds 1 to 17 were identified by H.sup.1-NMR and FD-MS, and the chemical structure, yield, formulae and mass of each of Compounds 1 to 17 were also listed in Table 6. Take Compounds 1 to 17 as examples, the .sup.1H-NMR spectra were shown in FIGS. 2 to 18.

TABLE-US-00006 TABLE 6 reactants and intermediates adopted to prepare Compounds 1 to 17 and their yields, formulae, and FD-MS data. Claimed Compound Reactant Intermediate Formula/ No. No. Chemical Structure Yield Mass (M.sup.+) B3 C19 [00327] 82 C.sub.62H.sub.43N/ (802.01) B2 C5 [00328] 87 C.sub.61H.sub.39NO/ (801.97) B2 C10 [00329] 91 C.sub.61H.sub.39NS/ (818.03) B2 C19 [00330] 89 C.sub.59H.sub.39N/ (761.95) B2 C20 [00331] 92 C.sub.59H.sub.39N/ (761.95) B1 C24 [00332] 78 C.sub.51H.sub.33N/ (659.81) B1 C26 [00333] 75 C.sub.53H.sub.33N/ (683.84) B1 C6 [00334] 81 C.sub.61H.sub.10N.sub.2O/ (816.98) B4 C7 [00335] 93 C.sub.58H.sub.39NO.sub.2/ (781.94) B1 C23 [00336] 68 C.sub.59H.sub.40N.sub.2/ (776.96) B2 C9 [00337] 94 C.sub.61H.sub.39NO/ (801.97) B3 C1 [00338] 68 C.sub.64H.sub.43NO/ (842.03) B1 C3 [00339] 76 C.sub.49H.sub.31NO/ (649.78) B1 C18 [00340] 95 C.sub.61H.sub.40N.sub.2S/ (833.05) B4 C11 [00341] 80 C.sub.58H.sub.39NOS/ (798.01) B5 C10 [00342] 85 C.sub.61H.sub.37NOS/ (832.02) B4 C24 [00343] 82 C.sub.60H.sub.41NO/ (791.97)

[0124] Modifications of Compounds 1 to 17

[0125] In addition to the Compounds 1 to 17, one person skilled in the art can react any Intermediate C with any Reactant B through a reaction mechanism similar to Scheme I to synthesize other desired claimed novel compounds.

[0126] Preparation of OLED devices

[0127] A glass substrate coated with ITO layer in a thickness of 1500 Å was placed in distilled water containing a detergent dissolved therein, and was ultrasonically washed. The detergent was a product manufactured by Fischer Co., and the distilled water was distilled water filtered twice through a filter (Millipore Co.). After the ITO layer had been washed for 30 minutes, it was ultrasonically washed twice with distilled water for 10 minutes. After the completion of washing, the glass substrate was ultrasonically washed with isopropyl alcohol, acetone and methanol solvents and then dried, after which it was transported to a plasma cleaner. Then the substrate was cleaned with oxygen plasma for 5 minutes, and then transferred to a vacuum evaporator.

[0128] After that, various organic materials and metal materials were sequentially deposited on the ITO substrate to obtain the OLED device of Examples 1 to 43. The vacuum degree during the deposition was maintained at 1×10.sup.−6 to 3×10.sup.−7 torr. Herein, the ITO substrate was deposited with a first hole injection layer (HIL-1), a second hole injection layer (HIL-2), a first hole transporting layer (HTL-1), a second hole transporting layer (HTL-2), a blue/green/red emission layer (BEL/GEL/REL), an electron transporting layer (ETL), an electron injection layer (EIL), and a cathode (Cthd).

[0129] Herein, HAT was a material for forming HIL-1 and HID; HI-2 was a material for forming HIL-2; HT-1, HT-1′, and the novel compounds of the present invention were a material for forming HTL-1; HT-2, HT-2′, and the novel compounds of the present invention were materials for forming HTL-2; conventional ET was materials for forming ETL; Liq was a material for forming ETD and EIL. RH/GH/BH were host material for forming REL/GEL/BEL, and RD/GD/BD were dopant for forming REL/GEL/BEL. The detailed chemical structures of foresaid commercial materials were listed in Table 7, and the novel compounds of the present invention were listed in Table 6.

TABLE-US-00007 TABLE 7 chemical structures of commercial materials for OLED devices. HAT [00344] HI-2 [00345] HT-1 [00346] HT-2 [00347] ET [00348] Liq [00349] RH [00350] GH [00351] BH [00352] RD [00353] GD [00354] BD [00355] HT-1′ [00356] HT-2′ [00357]

[0130] Preparation of Red OLED Devices

[0131] To prepare the red OLED device, multiple organic layers were respectively deposited on the ITO substrate according to the sequence as listed in Table 8, and the materials and the thicknesses of the organic layers in red OLED devices were also listed in Table 8.

TABLE-US-00008 TABLE 8 coating sequence, materials and thickness of the organic layers in red OLED device. Coating Sequence Layer Material Thickness 1 HIL-1 HAT 100 Å 2 HIL-2 HI-2 doped with 5.0 wt % of HAT 2100 Å  3 HTL-1 Commercial HT-1/HT-1′/Novel 100 Å compound 4 HTL-2 Commercial HT-2/HT-2′/Novel 100 Å compound 5 REL RH doped with 3.5 wt of RD 300 Å 6 ETL ET doped with 35.0 wt of Liq 350 Å 7 EIL Liq  15 Å 8 Cthd Al 1500 Å 

[0132] Preparation of Green OLED Devices

[0133] To prepare the green OLED device, multiple organic layers were respectively deposited on the ITO substrate according to the sequence as listed in Table 9, and the materials and the thicknesses of the organic layers in green OLED devices were also listed in Table 9.

TABLE-US-00009 TABLE 9 coating sequence, materials and thickness of the layers in green OLED device. Coating Sequence Layer Material Thickness 1 HIL-1 HAT 100 Å 2 HIL-2 HI-2 doped with 5.0 wt % of HAT 1300 Å  3 HTL-1 Commercial HT-1/HT-1′/Novel 100 Å compound 4 HTL-2 Commercial HT-2/HT-2′/Novel 100 Å compound 5 GEL GH doped with 10.0 wt % of GD 400 Å 6 ETL ET doped with 35.0 wt % of Liq 350 Å 7 EIL Liq  1.5 Å 8 Cthd Al 1500 Å 

[0134] Preparation of Blue OLED Devices

[0135] To prepare the blue OLED device, multiple organic layers were respectively deposited on the ITO substrate according to the sequence as listed in Table 10, and the materials and the thicknesses of the organic layers in green OLED devices were also listed in Table 10.

TABLE-US-00010 TABLE 10 coating sequence, materials and thickness of the layers in blue OLED device. Coating Sequence Layer Material Thickness 1 HIL-1 HAT 100 Å 2 HIL-2 HI-2 doped with 5.0 wt % of HAT 750 Å 3 HTL-1 Commercial HT-1/HT-1′/Novel 100 Å compound 4 HTL-2 Commercial HT-2/HT-2′/Novel 100 Å compound 5 BEL BH doped with 3.5 wt % of BD 250 Å 6 ETL ET doped with 35.0 wt % of Liq 250 Å 7 EIL Liq  15 Å 8 Cthd Al 1500 Å 

[0136] Performance of OLED Device

[0137] To evaluate the performance of OLED devices, red, green, and blue OLED devices were measured by PR650 as photometer and Keithley 2400 as power supply. Color coordinates (x,y) were determined according to the CIE chromaticity scale (Commission Internationale de L'Eclairage, 1931). The results were shown in Table 11. For the blue and red OLED devices, the data were collected at 1000 nits. For the green OLED devices, the data were collected at 3000 nits. The materials of HTL, color and data of CIE, driving voltage, and current efficiency of Examples 1 to 43 and Comparative Examples 1 to 4 were listed in Table 11.

TABLE-US-00011 TABLE 11 materials of HTL-1, materials of HTL-2, characteristics and performance of OLED devices of Examples 1 to 43 (E1 to E43) and Comparative Examples 1 to 4(C1 to C4). Material of Material of HTL-1 HTL-2 Current (novel compound or Efficiency commercial materials) Color, CIE(x, y) Voltage (V) (cd/A) Red OLED devices E1 Compound 2 HT-2 R(0.659, 0.339) 3.64 24.0 E2 Compound 3 HT-2 R(0.660, 0.339) 3.64 26.1 E3 Compound 4 HT-2 R(0.661, 0.338) 3.62 25.2 E4 Compound 5 HT-2 R(0.658, 0.340) 3.68 23.6 E5 Compound 6 HT-2 R(0.659, 0.339) 3.61 26.9 E6 Compound 7 HT-2 R(0.660, 0.338) 3.61 25.5 E7 Compound 8 HT-2 R(0.661, 0.337) 3.62 27.2 E8 Compound 9 HT-2 R(0.659, 0.339) 3.71 30.4 E9 Compound 14 HT-2 R(0.659, 0.340) 3.48 26.8 E10 Compound 17 HT-2 R(0.658, 0.340) 3.52 24.3 E11 HT-1 Compound 10 R(0.657, 0.340) 3.57 19.2 E12 HT-1 Compound 11 R(0.659, 0.339) 3.46 23.1 E13 HT-1 Compound 13 R(0.659, 0.339) 3.56 24.6 E14 HT-1 Compound 15 R(0.660, 0.338) 3.44 26 E15 HT-1 Compound 6 R(0.661, 0.338) 3.58 25.3 Green OLED devices E16 Compound 2 HT-2 G(0.316, 0.637) 3.06 77.0 E17 Compound 3 HT-2 G(0.318, 0.636) 3.09 70.8 E18 Compound 4 HT-2 G(0.316, 0.637) 2.95 77.7 E19 Compound 5 HT-2 G(0.316, 0.638) 3.08 81.0 E20 Compound 6 HT-2 G(0.317, 0.637) 3.03 77.3 E21 Compound 7 HT-2 G(0.316, 0.637) 3.02 74.3 E22 Compound 8 HT-2 G(0.322, 0.634) 3.08 80.7 E23 Compound 9 HT-2 G(0.313, 0.639) 3.09 82.5 E24 Compound 16 HT-2 G(0.319, 0.637) 3.05 79.5 E25 Compound 17 HT-2 G(0.312, 0.639) 3.05 75.4 E26 HT-1 Compound 11 G(0.314, 0.638) 2.91 73.6 E27 HT-1 Compound 13 G(0.317, 0.637) 2.94 75.2 E28 HT-1 Compound 15 G(0.318, 0.636) 3.02 76.8 E29 HT-1 Compound 6 G(0.314, 0.639) 3.03 74.4 C1 HT-1′ HT-2 G(0.318, 0.637) 3.10 70.1 C2 HT-1 HT-2′ G(0.314, 0.639) 3.12 42.7 Blue OLED devices E30 Compound 2 HT-2 B(0.130, 0.146) 4.55 9.83 E31 Compound 3 HT-2 B(0.130, 0.151) 4.71 10.1 E32 Compound 4 HT-2 B(0.129, 0.151) 4.66 10.2 E33 Compound 5 HT-2 B(0.130, 0.149) 4.68 10.2 E34 Compound 6 HT-2 B(0.129, 0.154) 4.54 10.7 E35 Compound 7 HT-2 B(0.128, 0.161) 4.54 11.2 E36 Compound 8 HT-2 B(0.129, 0.149) 4.54 11.4 E37 Compound 14 HT-2 B(0.129, 0.153) 4.63 11.6 E38 Compound 17 HT-2 B(0.129, 0.152) 4.63 11.5 E39 HT-1 Compound 10 B(0.130, 0.154) 4.30 10.9 E40 HT-1 Compound 11 B(0.129, 0.157) 4.47 11.0 E41 HT-1 Compound 13 B(0.130, 0.151) 4.45 11.1 E42 HT-1 Compound 15 B(0.129, 0.150) 4.25 11.5 E43 HT-1 Compound 6 B(0.129, 0.158) 4.30 11.7 C3 HT-1′ HT-2 B(0.129, 0.160) 4.77 9.5 C4 HT-1 HT-2′ B(0.129, 0.159) 4.49 9.1

[0138] Based on the results, in comparison with the commercial electron transport material, adopting Compounds 1 to 17 as the hole transport material can reduce the driving voltage and improve the current efficiency of the red, green, or blue OLEDs. It demonstrates that the novel compound of the present invention is suitable as a hole transport material for any color OLEDs, and allows the OLEDs using the same to have low driving voltage and improved current efficiency.

[0139] Even though numerous characteristics and advantages of the present invention have been set forth in the foregoing description, together with details of the structure and function of the invention, the disclosure is illustrative only. Changes may be made in the details, especially in matters of shape, size, and arrangement of parts within the principles of the invention to the full extent indicated by the broad general meaning of the Willis in which the appended claims are expressed.