WO2015134017A1 - Phosphorescent oled devices - Google Patents
Phosphorescent oled devices Download PDFInfo
- Publication number
- WO2015134017A1 WO2015134017A1 PCT/US2014/020899 US2014020899W WO2015134017A1 WO 2015134017 A1 WO2015134017 A1 WO 2015134017A1 US 2014020899 W US2014020899 W US 2014020899W WO 2015134017 A1 WO2015134017 A1 WO 2015134017A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- group
- hole blocking
- layer
- independently selected
- Prior art date
Links
- 239000000463 material Substances 0.000 claims abstract description 139
- 230000000903 blocking effect Effects 0.000 claims abstract description 59
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims abstract description 49
- 229930192474 thiophene Natural products 0.000 claims abstract description 34
- 239000002019 doping agent Substances 0.000 claims abstract description 28
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 13
- 150000003624 transition metals Chemical class 0.000 claims abstract description 13
- 230000021615 conjugation Effects 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 77
- 125000001072 heteroaryl group Chemical group 0.000 claims description 34
- 125000003118 aryl group Chemical group 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 125000001424 substituent group Chemical group 0.000 claims description 27
- 125000003342 alkenyl group Chemical group 0.000 claims description 23
- 239000001257 hydrogen Substances 0.000 claims description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 125000000304 alkynyl group Chemical group 0.000 claims description 22
- 238000006467 substitution reaction Methods 0.000 claims description 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 18
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 15
- 125000000623 heterocyclic group Chemical group 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 9
- 125000001725 pyrenyl group Chemical group 0.000 claims description 9
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000002837 carbocyclic group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims description 2
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- SDTHIDMOBRXVOQ-UHFFFAOYSA-N 5-[bis(2-chloroethyl)amino]-6-methyl-1h-pyrimidine-2,4-dione Chemical compound CC=1NC(=O)NC(=O)C=1N(CCCl)CCCl SDTHIDMOBRXVOQ-UHFFFAOYSA-N 0.000 claims 1
- 239000010410 layer Substances 0.000 description 147
- -1 thiphene compound Chemical class 0.000 description 34
- 125000005580 triphenylene group Chemical group 0.000 description 34
- SLGBZMMZGDRARJ-UHFFFAOYSA-N Triphenylene Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 SLGBZMMZGDRARJ-UHFFFAOYSA-N 0.000 description 27
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000000725 suspension Substances 0.000 description 18
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 16
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 15
- 101000687716 Drosophila melanogaster SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 homolog Proteins 0.000 description 14
- 101001003146 Mus musculus Interleukin-11 receptor subunit alpha-1 Proteins 0.000 description 14
- 101000687741 Mus musculus SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 Proteins 0.000 description 14
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- 150000003384 small molecules Chemical class 0.000 description 12
- 239000007924 injection Substances 0.000 description 11
- 238000002347 injection Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 230000004888 barrier function Effects 0.000 description 10
- 125000005843 halogen group Chemical group 0.000 description 10
- 238000004770 highest occupied molecular orbital Methods 0.000 description 10
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000004305 biphenyl Substances 0.000 description 9
- 230000005525 hole transport Effects 0.000 description 9
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 235000010290 biphenyl Nutrition 0.000 description 8
- 229940125782 compound 2 Drugs 0.000 description 8
- 230000005281 excited state Effects 0.000 description 8
- 239000003446 ligand Substances 0.000 description 8
- 239000000758 substrate Substances 0.000 description 8
- 150000003577 thiophenes Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000000151 deposition Methods 0.000 description 7
- 239000012044 organic layer Substances 0.000 description 7
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 6
- 0 *C1(C2(*)CC1)c1ccccc1-c1*2cccc1 Chemical compound *C1(C2(*)CC1)c1ccccc1-c1*2cccc1 0.000 description 6
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 6
- 229940125797 compound 12 Drugs 0.000 description 6
- 229910052740 iodine Inorganic materials 0.000 description 6
- 230000007246 mechanism Effects 0.000 description 6
- 239000011368 organic material Substances 0.000 description 6
- 125000002524 organometallic group Chemical group 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000005160 1H NMR spectroscopy Methods 0.000 description 5
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229940125904 compound 1 Drugs 0.000 description 5
- 229940126214 compound 3 Drugs 0.000 description 5
- 125000005842 heteroatom Chemical group 0.000 description 5
- 150000002902 organometallic compounds Chemical class 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 230000007704 transition Effects 0.000 description 5
- AWGBKZRMLNVLAF-UHFFFAOYSA-N 3,5-dibromo-n,2-dihydroxybenzamide Chemical compound ONC(=O)C1=CC(Br)=CC(Br)=C1O AWGBKZRMLNVLAF-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229940125898 compound 5 Drugs 0.000 description 4
- 239000000412 dendrimer Substances 0.000 description 4
- 229920000736 dendritic polymer Polymers 0.000 description 4
- 230000005693 optoelectronics Effects 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000011369 resultant mixture Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 3
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 3
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 3
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 3
- WKLCOLQNFQFUTM-UHFFFAOYSA-N 2-(3-bromo-5-chlorophenyl)-4,6-diphenylpyrimidine Chemical compound BrC=1C=C(C=C(C1)Cl)C1=NC(=CC(=N1)C1=CC=CC=C1)C1=CC=CC=C1 WKLCOLQNFQFUTM-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 3
- 229940126543 compound 14 Drugs 0.000 description 3
- 229940125758 compound 15 Drugs 0.000 description 3
- 229940126142 compound 16 Drugs 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 150000002240 furans Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 229910052747 lanthanoid Inorganic materials 0.000 description 3
- 150000002602 lanthanoids Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000011885 synergistic combination Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 3
- IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 2
- BANFGGCAQWUIAJ-UHFFFAOYSA-N (4-pyridin-2-ylphenyl)boronic acid Chemical compound C1=CC(B(O)O)=CC=C1C1=CC=CC=N1 BANFGGCAQWUIAJ-UHFFFAOYSA-N 0.000 description 2
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 2
- AXESFOAWYPCUND-UHFFFAOYSA-N C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C1=CC(=CC(=C1)C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C34)C3=NC=CC=C3 Chemical compound C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C1=CC(=CC(=C1)C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C34)C3=NC=CC=C3 AXESFOAWYPCUND-UHFFFAOYSA-N 0.000 description 2
- WSLAQWOVEZDNFA-UHFFFAOYSA-N C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C1=CC(=CC(=C1)C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C34)Cl Chemical compound C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C1=CC(=CC(=C1)C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C34)Cl WSLAQWOVEZDNFA-UHFFFAOYSA-N 0.000 description 2
- DDXHVRLAEWAIOV-UHFFFAOYSA-N C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C=1C=C(C=C(C1)Cl)C1=CC=C(C=C1)C1=NC=CC=C1 Chemical compound C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C=1C=C(C=C(C1)Cl)C1=CC=C(C=C1)C1=NC=CC=C1 DDXHVRLAEWAIOV-UHFFFAOYSA-N 0.000 description 2
- OPFJDXRVMFKJJO-ZHHKINOHSA-N N-{[3-(2-benzamido-4-methyl-1,3-thiazol-5-yl)-pyrazol-5-yl]carbonyl}-G-dR-G-dD-dD-dD-NH2 Chemical compound S1C(C=2NN=C(C=2)C(=O)NCC(=O)N[C@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(N)=O)=C(C)N=C1NC(=O)C1=CC=CC=C1 OPFJDXRVMFKJJO-ZHHKINOHSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 125000002078 anthracen-1-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([*])=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 2
- 125000000748 anthracen-2-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([H])=C([*])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 2
- 125000005605 benzo group Chemical group 0.000 description 2
- 125000006268 biphenyl-3-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])C(*)=C([H])C([H])=C1[H] 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229940125773 compound 10 Drugs 0.000 description 2
- 229940125810 compound 20 Drugs 0.000 description 2
- 229940126086 compound 21 Drugs 0.000 description 2
- 229940125846 compound 25 Drugs 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 2
- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 238000005286 illumination Methods 0.000 description 2
- 150000002504 iridium compounds Chemical class 0.000 description 2
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000000059 patterning Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000001296 phosphorescence spectrum Methods 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 125000001742 pyren-1-yl group Chemical group [H]C1=C([H])C2=C([H])C([H])=C3C(*)=C([H])C([H])=C4C([H])=C([H])C(=C1[H])C2=C34 0.000 description 2
- MWEKPLLMFXIZOC-UHFFFAOYSA-N pyren-1-ylboronic acid Chemical compound C1=C2C(B(O)O)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 MWEKPLLMFXIZOC-UHFFFAOYSA-N 0.000 description 2
- 125000001732 pyren-2-yl group Chemical group [H]C1=C([H])C2=C([H])C([H])=C3C([H])=C(*)C([H])=C4C([H])=C([H])C(=C1[H])C2=C34 0.000 description 2
- 125000001486 pyren-4-yl group Chemical group [H]C1=C(C2=C34)C([H])=C([H])C([H])=C2C([*])=C([H])C3=C([H])C([H])=C([H])C4=C1[H] 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000010129 solution processing Methods 0.000 description 2
- 238000002207 thermal evaporation Methods 0.000 description 2
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 description 1
- STBLNCCBQMHSRC-BATDWUPUSA-N (2s)-n-[(3s,4s)-5-acetyl-7-cyano-4-methyl-1-[(2-methylnaphthalen-1-yl)methyl]-2-oxo-3,4-dihydro-1,5-benzodiazepin-3-yl]-2-(methylamino)propanamide Chemical compound O=C1[C@@H](NC(=O)[C@H](C)NC)[C@H](C)N(C(C)=O)C2=CC(C#N)=CC=C2N1CC1=C(C)C=CC2=CC=CC=C12 STBLNCCBQMHSRC-BATDWUPUSA-N 0.000 description 1
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
- UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 description 1
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical class C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 1
- IXHWGNYCZPISET-UHFFFAOYSA-N 2-[4-(dicyanomethylidene)-2,3,5,6-tetrafluorocyclohexa-2,5-dien-1-ylidene]propanedinitrile Chemical compound FC1=C(F)C(=C(C#N)C#N)C(F)=C(F)C1=C(C#N)C#N IXHWGNYCZPISET-UHFFFAOYSA-N 0.000 description 1
- NPRYCHLHHVWLQZ-TURQNECASA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynylpurin-8-one Chemical compound NC1=NC=C2N(C(N(C2=N1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C NPRYCHLHHVWLQZ-TURQNECASA-N 0.000 description 1
- IMRWILPUOVGIMU-UHFFFAOYSA-N 2-bromopyridine Chemical compound BrC1=CC=CC=N1 IMRWILPUOVGIMU-UHFFFAOYSA-N 0.000 description 1
- MZSAMHOCTRNOIZ-UHFFFAOYSA-N 3-[4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-yl]oxy-N-phenylaniline Chemical compound NCC1=CC(=NC(=C1)C(F)(F)F)OC=1C=C(NC2=CC=CC=C2)C=CC=1 MZSAMHOCTRNOIZ-UHFFFAOYSA-N 0.000 description 1
- DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical group C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- XRMOZHDQFVCMGY-UHFFFAOYSA-N C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C1=CC(=CC(=C1)C1=NC=CC=C1)Cl Chemical compound C1(=CC=CC=C1)C1=NC(=NC(=C1)C1=CC=CC=C1)C1=CC(=CC(=C1)C1=NC=CC=C1)Cl XRMOZHDQFVCMGY-UHFFFAOYSA-N 0.000 description 1
- BPQUWLPLYQOTGO-UHFFFAOYSA-N C1C=CC=CC1c1nc(-c2cc(-c3c(cccc4)c4cc4c3cccc4)cc(-c(cc3)ccc3-c3ccccn3)c2)nc(-c2ccccc2)c1 Chemical compound C1C=CC=CC1c1nc(-c2cc(-c3c(cccc4)c4cc4c3cccc4)cc(-c(cc3)ccc3-c3ccccn3)c2)nc(-c2ccccc2)c1 BPQUWLPLYQOTGO-UHFFFAOYSA-N 0.000 description 1
- WVLWWHRIAVPBSB-UHFFFAOYSA-N CC(CC12)=CC=C1c1ccccc1-c1c2cccc1 Chemical compound CC(CC12)=CC=C1c1ccccc1-c1c2cccc1 WVLWWHRIAVPBSB-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229940126657 Compound 17 Drugs 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- LJOOWESTVASNOG-UFJKPHDISA-N [(1s,3r,4ar,7s,8s,8as)-3-hydroxy-8-[2-[(4r)-4-hydroxy-6-oxooxan-2-yl]ethyl]-7-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl] (2s)-2-methylbutanoate Chemical compound C([C@H]1[C@@H](C)C=C[C@H]2C[C@@H](O)C[C@@H]([C@H]12)OC(=O)[C@@H](C)CC)CC1C[C@@H](O)CC(=O)O1 LJOOWESTVASNOG-UFJKPHDISA-N 0.000 description 1
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- VHHDLIWHHXBLBK-UHFFFAOYSA-N anthracen-9-ylboronic acid Chemical compound C1=CC=C2C(B(O)O)=C(C=CC=C3)C3=CC2=C1 VHHDLIWHHXBLBK-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- UFVXQDWNSAGPHN-UHFFFAOYSA-K bis[(2-methylquinolin-8-yl)oxy]-(4-phenylphenoxy)alumane Chemical compound [Al+3].C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC([O-])=CC=C1C1=CC=CC=C1 UFVXQDWNSAGPHN-UHFFFAOYSA-K 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 229940127204 compound 29 Drugs 0.000 description 1
- 229940125878 compound 36 Drugs 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 150000001907 coumarones Chemical class 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- YNHIGQDRGKUECZ-UHFFFAOYSA-N dichloropalladium;triphenylphosphanium Chemical compound Cl[Pd]Cl.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000001540 jet deposition Methods 0.000 description 1
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000013086 organic photovoltaic Methods 0.000 description 1
- 150000002908 osmium compounds Chemical class 0.000 description 1
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 230000005610 quantum mechanics Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 150000003643 triphenylenes Chemical class 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- UGOMMVLRQDMAQQ-UHFFFAOYSA-N xphos Chemical group CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 UGOMMVLRQDMAQQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/10—Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/10—Triplet emission
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/30—Highest occupied molecular orbital [HOMO], lowest unoccupied molecular orbital [LUMO] or Fermi energy values
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/14—Carrier transporting layers
- H10K50/15—Hole transporting layers
Definitions
- Embodiments disclosed herein relate to organic light emitting diode devices (OLEDs).
- OLEDs organic light emitting diode devices
- embodiments disclosed herein relate to a combination of device materials to provide OLED devices having enhanced luminous efficacy, low voltage, and increased device lifetime.
- an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode.
- the anode injects holes and the cathode injects electrons into the organic layer(s).
- the injected holes and electrons each migrate toward the oppositely charged electrode.
- an "exciton” which is a localized electron-hole pair having an excited energy state, is formed.
- Light is emitted when the exciton relaxes via a photoemissive mechanism.
- the exciton may be localized on an excimer or an exciplex. Non-radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.
- FIG. 1 is a schematic drawing showing an outline constitution of one example of the OLED according to one embodiment of the present disclosure. The drawing is not drawn to scale.
- FIG. 2 shows an inverted OLED according to another embodiment of the present disclosure.
- FIG. 3 shows an exemplary multilayered OLED device in accordance with embodiments disclosed herein.
- OLED organic light-emitting diode
- the host material comprises a benzo-fused thiophene and the phosphorescent dopant comprises a heteroleptic transition metal complex having extended conjugation, a hole blocking layer disposed on the emissive layer, the hole blocking layer comprising a hole blocking material, an electron transport layer disposed on the hole blocking layer, wherein the OLED device has a luminous efficacy of at least about 40 Im W at 1 ,000 cd/m2 (nits).
- Opto-etectronic devices that make use of organic materials are becoming increasingly desirable for a number of reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials. For example, the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
- OLEDs organic light emitting devices
- the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
- OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly utilized technology in applications such as flat panel displays, illumination, and backlighting. Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.
- phosphorescent emissive molecules are full color display.
- Industry standards for such a display call for pixels adapted to emit particular colors, referred to as "saturated" colors.
- these standards call for saturated red, green, and blue pixels. Color may be measured using CIE coordinates, which are well known to the art.
- Fluorescence emissive molecules that emitted light from their singlet states
- Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.
- Phosphorescence may be referred to as a "forbidden" transition because the transition requires a change in spin states, and quantum mechanics indicates that such a transition is not favored.
- phosphorescence generally occurs in a time frame exceeding at least 10 nanoseconds, and typically greater than 100 nanoseconds. If the natural radiative lifetime of phosphorescence is too long, triplets may decay by a non-radiative mechanism, such that no light is emitted.
- Organic phosphorescence is also often observed in molecules containing heteroatoms with unshared pairs of electrons at very low temperatures. 2,2'-bipyridine is such a molecule.
- Non-radiative decay mechanisms are typically temperature dependent, such that an organic material that exhibits phosphorescence at liquid nitrogen temperatures typically does not exhibit phosphorescence at room temperature. But, as demonstrated by Baldo, this problem may be addressed by selecting phosphorescent compounds that do phosphoresce at room temperature.
- Representative emissive layers include doped or un-doped
- phosphorescent organometallic materials such as disclosed in U.S. Pat. Nos. 6,303,238 and 6,310,360; U.S. Patent Application Publication Nos. 2002-0034656; 2002-0182441 ; 2003- 0072964; and WO-02/074015.
- the excitons in an OLED are believed to be created in a ratio of about 3:1 , i.e., approximately 75% triplets and 25% singlets. See, Adachi et al., "Nearly 100% Internal Phosphorescent Efficiency In An Organic Light Emitting Device," J. Appl. Phys., 90, 5048 (2001 ), which is incorporated by reference in its entirety.
- singlet excitons may readily transfer their energy to triplet excited states via "intersystem crossing," whereas triplet excitons may not readily transfer their energy to singlet excited states.
- 100% internal quantum efficiency is theoretically possible with phosphorescent OLEDs.
- Phosphorescence may be preceded by a transition from a triplet excited state to an intermediate non-triplet state from which the emissive decay occurs.
- organic molecules coordinated to lanthanide elements often phosphoresce from excited states localized on the lanthanide metal.
- such materials do not phosphoresce directly from a triplet excited state but instead emit from an atomic excited state centered on the lanthanide metal ion.
- the europium diketonate complexes illustrate one group of these types of species.
- Phosphorescence from triplets can be enhanced over fluorescence by confining, such as through bonding, the organic molecule in close proximity to an atom of high atomic number. This phenomenon, called the heavy atom effect, is created by a mechanism known as spin-orbit coupling. Such a phosphorescent transition may be observed from an excited metal-to-ligand charge transfer (MLCT) state of an organometallic molecule such as tris(2- phenylpyndine)iridium(lll).
- MLCT excited metal-to-ligand charge transfer
- triplet energy refers to an energy corresponding to the highest energy feature discernable in the phosphorescence spectrum of a given material.
- the highest energy feature is not necessarily the peak having the greatest intensity in the phosphorescence spectrum, and could, for example, be a local maximum of a clear shoulder on the high energy side of such a peak.
- FIG. 1 shows an organic light emitting device 100.
- Device 100 may include a substrate 1 10. an anode 1 15, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170.
- Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164.
- Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in US 7,279,704 at cols. 6-10, which are incorporated by reference.
- each of these layers are available.
- a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety.
- An example of a p-doped hole transport layer is m- MTDATA doped with F 4 -TCNQ at a molar ratio of 50:1 , as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety.
- Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al.. which is incorporated by reference in its entirety.
- An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1 :1 , as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety.
- the theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No.
- FIG. 2 shows an inverted OLED 200.
- the device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230.
- Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an "inverted" OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200.
- FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.
- barrier layer One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc.
- the barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge.
- the barrier layer may comprise a single layer, or multiple layers.
- the barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer.
- the barrier layer may incorporate an inorganic or an organic compound or both.
- the barrier layer comprises a mixture of a polymeric material and a non-polymeric material as described in U.S. Pat, No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and
- the aforesaid polymeric and non-polymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time.
- the weight ratio of polymeric to non-polymeric material may be in the range of 95:5 to 5:95.
- the polymeric material and the non-polymeric material may be created from the same precursor material.
- the mixture of a polymeric material and a non-polymeric material consists essentially of polymeric silicon and inorganic silicon.
- Embodiments disclosed herein provide phosphorescent organic light emiting devices (PHOLED) having high power efficiency and operational stability. Superior power efficacy and long device lifetime were achieved via a synergistic combination of materials within the devices.
- a combination of appropriate host material, phosphorescent dopant and electron transport material are disclosed herein to provide devices with improved lifetimes as measured by LT97 (time for luminance to decrease to 97% of its intial level) of about 51 hours at 10,000 cd/m 2 (nits).
- Devices disclosed herein may also achieve power efficacies of about 61 Im/W. These device characteristics are obtained at low voltage making the combination of materials unexpectedly superior to state of the art devices.
- organic light-emitting diode (OLED) devices comprising an emissive layer comprising a host material and a phosphorescent dopant, wherein the host material comprises a benzo-fused thiophene and the phosphorescent dopant comprises a heteroleptic transition metal complex having extended conjugation and an electron transport layer disposed on the hole blocking layer, wherein the OLED device has a luminous efficacy of at least about 40 Im/W at 1 ,000 cd/m 2 (nits).
- such devices may further comprise a hole blocking layer disposed between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that may be the same or different from the host material in the emissive layer.
- the hole blocking material comprises the same benzo-fused thiphene compound as the host material.
- heteroleptic means a complex having at least two different ligands.
- extended conjugation refers to an extended array of pi bonds capable of distribution of electron density over many atoms.
- luminous efficacy refers to a measure of how well a light source produces visible light and is generally computed as the ratio of luminous flux to power.
- halo halogen, alkyl, cycloalkyi, alkenyl, alkynyl, aralkyi, heterocyclic group, aryl, aromatic group, and heteroaryl are known to the art, but are defined here for ease of reference.
- halo or halogen as used herein includes fluorine, chlorine, bromine and iodine.
- alkyl as used herein contemplates both straight and branched chain alkyl radicals.
- exemplary alkyl groups may contain from one to fifteen carbon atoms and includes methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, and the like. Additionally, the alkyl group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic-amino, N02, and OR, wherein each R is independently selected from H, alkyl, alkenyl, alkynyl, aralkyi, aryl and heteroaryl.
- cycloalkyi as used herein contemplates cyclic alkyl radicals.
- exemplary cycloalkyi groups include those containing 3 to 7 carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, and the like. Additionally, the cycloalkyi group may be optionally substituted with one or more substituents selected from halo, CN , C02R. C(0)R, NR2, cyclic- amino, N02. and OR.
- alkenyl as used herein contemplates both straight and branched chain alkene radicals.
- exemplary alkenyl groups include those containing two to fifteen carbon atoms. Additionally, the alkenyl group may be optionally substituted with one or more substituents selected from halo. CN , C02R, C(0)R, NR2, cyclic-amino, N02. and OR.
- alkynyl as used herein contemplates both straight and branched chain alkyne radicals.
- exemplary alkyl groups include those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted with one or more substituents selected from halo, CN, C02R , C(0)R, N R2. cyclic-amino, N02, and OR.
- aralkyi contemplates an alkyl group that has as a substituent an aromatic group. Additionally, the aralkyi group may be optionally substituted on the aryl with one or more substituents selected from halo. CN , C02R, C(0)R, NR2, cyclic- amino, N02. and OR.
- heterocyclic group contemplates non-aromatic cyclic radicals.
- exemplary heterocyclic groups include those containing 3 or 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperdmo, pyrrolidino, and the like, and cyclic ethers, such as tetrahydrofuran, tetrahydropyran , and the like.
- the heterocyclic group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic-amino, N02, and OR.
- aryl or "aromatic group” as used herein contemplates single-ring groups and polycyclic ring systems.
- the polycyclic rings may have two or more rings in which two carbons are common by two adjoining rings (the rings are "fused") wherein at least one of the rings is aromatic, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles and/or heteroaryls.
- the aryl group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic-amino, N02, and OR.
- heteroaryl as used herein contemplates single-ring hetero-aromatic groups that may include from one to three heteroatoms, for example, pyrrole, furan, thiophene, imidazole, oxazole, thiazole, triazole, pyrazole, pyridine, pyrazine and pyrimidine, and the like.
- heteroaryl also includes polycyclic hetero-aromatic systems having two or more rings in which two atoms are common to two adjoining rings (the rings are "fused") wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles and/or heteroaryls. Additionally, the heteroaryl group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic- amino, N02, and OR.
- organic includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices.
- Small molecule refers to any organic material that is not a polymer, and "small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances For example, using a long chain alkyl group as a substituent does not remove a molecule from the "small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety.
- the core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter.
- a dendrimer may be a "small molecule.” and it is believed that all dendnmers currently used in the field of OLEDs are small molecules.
- top means furthest away from the substrate, while “bottom” means closest to the substrate.
- first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is "in contact with” the second layer.
- a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.
- solution processible means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.
- a first "Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is "greater than” or "higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative).
- IP ionization potentials
- EA electron affinity
- the LUMO energy level of a material is higher than the HOMO energy level of the same material.
- a "higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a "lower” HOMO or LUMO energy level.
- a first work function is "greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a "higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.
- device 300 in accordance with embodiments disclosed herein. From the bottom up, device 300 includes anode 310, a hole injection layer 320, a hole transport layer 330, an emissive layer 340, a hole blocking layer 350, an electron transport layer 360, an eletron injection layer 370, and a cathode 380.
- the synergistic combination of materials comprise emissive layer 340, a combination of host material benzo-fused thiophene and phosphorescent dopantand electron transport layer 360.
- hole blocking layer (HBL) 350 comprising a hole blocking material may be incorporated between emissive layer 340 and electron transport layer 360 to confine excitons within emissive.
- the HBL material should have HOMO and LUMO energy levels suitable to block hole transport from the emissive layer (EML) to the electron transport layer (ETL) and to pass electrons from the ETL to the EML.
- the HBL material may be selected from known HBL materials, for example. BAlq which is is a well-known electron transporting blocking layer material.
- the material in hole blocking layer 350 may comprise the same benzo-fused thiophene compound that is used as a host material in emissive layer 340.
- the layered structures illustrated in Figures 1 , 2 and 3 are provided by way of non- limiting example, and it is understood that embodiments disclosed herein may be used in connection with a wide variety of other structures.
- the specific materials and structures described are exemplary in nature, and other materials and structures may be used.
- Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used.
- the layers may have various sublayers.
- the names given to the various layers herein are not intended to be strictly limiting.
- hole transport layers 130 and 330 transport holes and inject holes into emissive layers 140 and 340, and may be described as hole transport layers or hole injection layers.
- any of the layers of the various embodiments may be deposited by any suitable method.
- methods may include thermal evaporation, ink-jet deposition, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102, which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431 ,968, which is incorporated by reference in its entirety.
- OVPD organic vapor phase deposition
- OJP organic vapor jet printing
- Other suitable deposition methods include spin coating and other solution based processes.
- Solution based processes may be carried out under nitrogen or other inert atmosphere.
- methods may include thermal evaporation.
- patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and OVJD. Other methods may also be used.
- the materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and typically containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having up 20 carbons or more may be used, and thus a range from about 3 to about 20 carbons may be typical.
- Materials with asymmetric structures may have better solution processibility than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize.
- Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.
- Devices fabricated in accordance with embodiments disclosed herein may be incorporated into a wide variety of consumer products, including flat panel displays, computer monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads up displays, fully transparent displays, flexible displays, laser printers, telephones, cell phones, personal digital assistants (PDAs), laptop computers, digital cameras, camcorders viewfmders, micro-displays, 3-D displays, vehicles, a large area wall, theater or stadium screen, or a sign.
- PDAs personal digital assistants
- Various control mechanisms may be used to control devices fabricated in accordance with the present embodiments, including passive matrix and active matrix.
- the materials and structures described herein may have applications in devices other than OLEDs.
- other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures disclosed herein.
- organic devices such as organic transistors, may also employ the materials and structures disclosed herein.
- host material of emissive layer 340 comprise the benzo-fused thiophene comprises a compound of Formula I, Formula II or Formula III:
- R 1 , R 2 and R 3 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen.
- compounds of Formula I, II and III may comprise at least one aryl group that is a triphenylene group: triphenylene
- Triphenylene is a polyaromatic hydrocarbon with high triplet energy, yet high pi- conjugation and a relatively small energy difference between the first singlet and first triplet levels, Thus, triphenylene has relatively accessible HOMO and LUMO levels compared to other aromatic compounds with similar triplet energy such as biphenyl. Triphenylene can readily accommodate red, green and even blue phosphorescent dopants to give high efficiency without energy quenching. Benzo-fused thiophenes may be used as hole transporting organic conductors. In addition, the triplet energies of benzothiophenes of Formula I Hare relatively high. A combination of benzo-fused thiophenes and triphenylene as hosts in PHOLED may be particularly beneficial.
- Benzo-fused thiophenes are typically more hole transporting than electron transporting, and triphenylene is more electron transporting than hole transporting. Therefore, combining these two moieties in one molecule may offer improved charge balance which may improve device performance in terms of lifetime, efficiency and low voltage.
- Different chemical linking motifs of the two moieties can be used to tune the properties of the resulting compound to match a particular phosphorescent emitter, device architecture, and / or fabrication process. For example, m-phenylene linkage may provide higher triplet energy and higher solubility relative to p-phenylene.
- Compounds of Formula I , I I and I I I may be substituted with groups that are not necessarily triphenylenes.
- any group that is used as a substituent of Formula I may be selected with a triplet energy high enough to maintain the benefit of having triphenylene benzo-fused thiophenes.
- the compounds described herein may have a sufficiently high triplet energy to be suitable for use in a device having phosphorescent blue emissive materials.
- substituents of the compounds described herein are generally unfused such that the substituents are not fused to the triphenylene, benzo-fused furan or benzo-fused thiophene moieties of the compound. However, the substituents may optionally be inter-fused (i.e. fused to each other).
- benzo-fused furans are also typically hole transporting materials having relatively high triplet energy.
- benzo-fused furans include benzofuran and dibenzofuran. Therefore, a material containing both triphenylene and benzofuran may be advantageously used as host or hole blocking material in PHOLED. A compound containing both of these two groups may offer improved electron stabilization which may improve device stability and efficiency with low voltage.
- the properties of the triphenylene containing benzofuran compounds may be tuned as necessary by using different chemical linkages to link the triphenylene and the benzofuran.
- triphenylene-containing benzo-fused thiophenes useful in the devices disclosed herein include compounds having the structure of the following formulae (H- I), (H-l l) and (H-lll)
- R 1 ,R 2 and R 3 are independently selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl, heteroaryl and hydrogen. Each of R 1 ,R 2 and R 3 may represent multiple substituents. At least one of R 1 ,R 2 and R 3 in Formula (H-l) and at least one of R 1 and R 2 in Formulas (H-!l) and (H-lll) includes a triphenylene group.
- triphenylene group may be linked directly to the structure of formulae (H-l), (H-ll) or (H-lll), but there may also be a "spacer” in between the triphenylene group and the structure of formulae (H-l), (H-ll) or (H-lll).
- Examples of triphenylene-containing benzo-fused thiophenes or benzo-fused furans include compounds having the structure of the following formulae (H-IV), (H-V), and (H-VI);
- Each of R 1 R 2 and R 3 may represent mono, di, tri, or tetra substitutions, n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10.
- An and Ar 2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof. At least one of R 1 ,R 2 and R 3 in Formula (H-IV) and at least one of R 1 and R 2 in Formulas (H-V) and (HVI) includes a triphenylene group.
- Ri to R 7 represents, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl and heteroaryl, or no substitution.
- Examples of compounds having the structure of the formula (H-ll) include:
- R 5 represent, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyi, aryl and heteroaryl, or no substitution.
- Each of Ri to R 5 may represent mono, di, tri, or tetra substitutions.
- n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10.
- a ⁇ and Ar 2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
- Compound 15'G Compound 15' where R 4 , R 5 , R 6 , R 7 , R 10 , R and R 12 represent, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyi, aryl and heteroaryl, or no substitution(H).
- X is S or O.
- X is S
- R 4 , R 5 , R 6 , R ? , Re, R9, R10, R11 and R 12 are independently selected from the group consisting of C n H 2n+1 , OC n H 2 n + i, OAn ,
- R-, to R n may represent mono, di, tri, or tetra substitutions, n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10.
- An and Ar 2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
- the present disclosure comprises an OLED which comprises a benzo-fused thiophene host material, wherein the triplet energy of the host material is from about 2.0 eV to about 2.8 eV.
- the benzo-fused thiophene comprises a compound of Formula la:
- each R 1 and R 2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyi, aryl, aralkyl, heteroaryl, and hydrogen;
- L is bond or an optionally substituted pheny R 4 are independently selected from the group
- Examples of compounds of Formula III or Ilia include the following: Examples of re of Formula(H-lll) include: .
- R-i to R? represents, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl and heteroaryl, or no substitution (i.e., hydrogen).
- the benzofused thiophene host is Compound 2' (hereinafter
- the host material and hole blocking material are the same, i.e., both are triphenylene containing benzo-fused thiophenes. That is, in embodiments, the host material of the emissive layer and the hole blocking material of the hole blocking layer may be the same. In some such embodiments, the host material and the hole blocking material
- emissive layer 340 has a thickness from about 100 to about 600 angstroms or about 200 angstroms to about 400 angstroms, or about 250 to about 350 angstroms, or about 280 to about 320 angstroms.
- hole blocking layer 150 which may comprise the same host material as the emissive layer, has a thickness from about 10 to about 100 angstroms, or about 25 to about 75 angstroms, or about 35 to about 65 angstroms, or about 45 to about 55 angstroms.
- Some examples of the phosphorescent emitter material doped into emissive layer 340 are heteroleptic phosphorescent organometallic compounds represented by the formula L 2 MX. LL'MX, LL'I_"M, or LMXX'. wherein L, U, L", X, and X' are inequivalent, bidentate ligands and M is a metal that forms octahedral complexes, wherein L, L', and L" are monoanionic inequivalent bidentate ligands coordinated to M through an sp 2 hybridized carbon and a heteroatom.
- the phosphorescent organometallic compound may be a compound selected from the group consisting of phosphorescent organometallic platinum compounds, organometallic iridium compounds and organometallic osmium compounds.
- the organometallic platinum compounds, iridium compounds and osmium compounds can each include an aromatic ligand,
- the phosphorescent dopant present in emissive layer 340 comprises a heteroleptic transition metal com of Formula -l 11 :
- B and C are each independently a 5 or 6-membered carbocyclic or heterocyclic rings; wherein A-B is a bonded pair of carbocyclic or heterocyclic rings coordinated to a metal M via a nitrogen atom in ring A and an sp 2 hybridized atom in ring B; wherein A-C is a bonded pair of carbocyclic or heterocyclic rings; wherein each R a , R b , and R c are independently mono, di, tri, or tetra substitutions and each R a , R b , and R c are independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl, and heteroaryl, any of which may be optionally substituted; wherein X 1 t X 2 , X 3 , X 4 , X s , X 6 , X 7 , X 8 , and X 9 are independently selected
- phosphorescent emissive compounds comprise Ir (III) heteroleptic complexes having extended conjugation on the heterocyclic ring which coordinates to the metal through nitrogen.
- the compounds provided have the formula selected from the group consisting of:
- Heteroleptic iridium compounds are provided, which may be used in organic light emitting devices as the emissive dopant of such devices.
- the heteroleptic compounds may be selected from the group consisting of:
- the heteroleptic transition metal complex is a Compound 12
- the phosphorescent dopant is present in emissive layer 140 in a range from about .5 to about 30 percent by weight of the layer or about 1 to about 20 percent by weight of the layer or about 5 percent to about 15 percent by weight of the layer.
- electron transport layer 360 comprises a compound of Formula V:
- X represents a single chemical bond or phenylene group
- Y represents anthraceny! group or pyrenyl group.
- a phenylene group for X include 1 ,2-phenylene. 1 ,3- phenylen and 1 ,4-phenylene.
- anthracenyl group of Y include anthracen-9-yl, anthracen-1-yl and anthracen-2-yl.
- pyrenyl group of Y include pyren-1 -yl, pyren- 2-yl and pyren-4-yl.
- Exemplary compounds of structure V include structures ETL-1 , ETL-2, and ETL-3 below:
- the electron transport layer has a thickness from about 10 to about 600 angstroms or about 350 angstroms to about 550 angstroms, or about 400 to about 500 angstroms.
- the materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device.
- emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present
- the materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.
- devices configured with the combination of materials disclosed herein may have a voltage below about 4.5 volts at 1 ,000 cd/m 2 and a luminance of at least 18,500 cd/m at 40 rnA/cm 2 .
- organic light-emitting diode (OLED) device comprising an emissive layer comprising a host material and a phosphorescent dopant.
- the host material comprises a benzo-fused thiophene and the phosphorescent dopant comprises a heteroleptic transition metal complex having extended conjugation, and an electron transport layer disposed on the hole blocking layer, wherein the OLED device has a luminous efficacy of at least about 40 Im/W and voltage below about 4.5 volts at 1 ,000 cd/m 2 (nits), and a luminance of at least 18,500 cd/m 2 at 40 mA/cm 2 .
- the benzo-fused thiophene comprises a compound of Formula Ilia:
- each R 1 and R 2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen;
- L is bond or an optionally substituted phenyl group; and
- R 3 and R 4 are independently selected from the group
- the heteroleptic transition metal complex is a compound of Formula L 2 MX, LL'MX, LL'L"M, or LMXX', wherein L, L', L", X, and X' are inequivalent, bidentate ligands and M is a transition metal that forms octahedral complexes, wherein L, L', and L" are monoanionic inequivalent bidentate ligands coordinated to M through an sp 2 hybridized carbon and a heteroatom such as, for example.
- X represents a single chemical bond or phenylene group
- Y represents anthracenyl group or pyrenyl group
- Exemplary compounds of structure V include structures ETL-1 , ETL-2, and ETL-3 below:
- such devices may also exhibit a time for luminance to decrease to 97% of its initial level of about 50 hours at 10,000 cd/m 2 .
- organic light-emitting diode (OLED) devices comprising an emissive layer comprising a host material and a phosphorescent dopant, wherein the host material comprises a benzo-fused thiophene compound of Formula H-llla:
- each R 1 and R 2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen;
- L is bond or an optionally substituted pheny R 4 are independently selected from the group
- the phosphorescent dopant comprises
- X represents a single chemical bond or phenylene group
- Y represents anthracenyl group or pyrenyl group
- Exemplary compounds of structure V include structures ETL-1 , ETL-2, and ETL-3 below:
- such devices may further comprise a hole blocking layer between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that_may be the same or different from the host material in the emissive layer.
- the hole blocking material may be a benzo fused thiophene compound.
- the hole blocking material may be the same benzo fused thiophene compound as the host material in the emissive layer.
- This Example shows the preparation and performace of devices prepared from the synergistic combination of materials disclosed herein.
- Experimental Devices #1 , #2 and #3 all bearing the structure shown in FIG. 3 were fabricated according to the present disclosure as follows: LG101 (LGChem, Seoul, South Korean) was used in all devices to form a 10 nm thick hole injection layer, NPD was used in all devices to form a 30 nm thick hole transport layer.
- phosphorescent emitter compound G1 (previously disclosed as Compound 12 in WO2010/028151 including synthesis) was doped at 12 % doping level into Compound H as a host material (previously disclosed as Compound 2' in WO 2009/021 126 including synthesis) to form a 30 nm thick emissive layer layer.
- An undoped layer of compound H was used in all devices to form a 5 nm thick hole blocking layer.
- a 40 nm thick electron transport layer was deposited over the hole blocking layer using one of ETL-1 , ETL-2 and ETL-3 respectively in Devices #1 , #2, #3.
- Li F was used in all devices to form 1 nm thick electron injection layer.
- a 100 nm thick layer of Aluminum formed the cathode in all devices and an 80 nm thick layer of ITO formed the anode in all devices.
- hole blocking/host compound H , dopant compound G1 and hole transport compound NPD are shown in Table 2 below.
- Hole injection material LG101 was obtained from LG Chem, Seoul, South Korea. Table 2
- the device was transferred directly from vacuum into an inert environment glove-box, where it was encapsulated using a UV-curable epoxy, and a glass lid with a moisture getter.
- the emission profiles were assumed to be Lambertian, so EQE was calculated from
- Comparative Example Device CE For performance comparison, Comparative Example Device CE , also bearing the structure shown in FIG. 3, was also constructed . Comparative Example Device CE was fabricated in the same manner as Experimental devices #1 , #2 and #3 except that Alq3 was used to form the electron transport layer rather than ETL- 1 , ETL-2 or ETL-3.
- Table 2 shows a summary of the fou r devices' construction in terms of the materials used for the electron transporting layer and the emitter layer.
- Table 3 shows the performance comparison of Experimental Devices #1 , #2 and #3 and Comparative Example device CE .
- the power efficacies of devices in accordance with embodiments disclosed herein using ETL-1 , ETL-2 or ETL-3 as electron transport material in combination with H:G1 (12%) were 49, 55, and 61 ImA V at 1 ,000 nits respectively compared to 37 ImA/V for comparative device using previously known Alq 3 as ETL material .
- Devcies #1 and #3 achieved the higher efficiency while maintaining comparable operational lifetime.
- Device #2 demonstrated improved operational lifetime in addition to higher efficiency.
- the LT97 (time for luminance to decrease to 97% of its initial level) at 10,000 nits was estimated to be 51 hrs for Device #2 compared to 38 hours for Device CE using known ETL material Alq.
- This example shows the preparation of exemplary electron transport materials.
- ETL-1 , ETL-2 or ETL-3 synthesized above may be further refined by sublimation under vacuum before its use for the provision of the layered structure, in accordance with embodiments disclosed herein.
- OLEDS incorporating the teachings of the present disclosure exhbit unexpected and substantial improved working lifetime characteristics and improved luminous efficiency
- an organic light emitting device comprising an anode, a cathode and a plurality of organic layers sandwiched between them, the plurality of organic layers comprising: an emitter layer comprising a host material and a phosphorescent emitter material wherein the host material comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan and wherein the phosphorescent emitter material comprises a phosphorescent organometallic compound that emits phosphorescent radiation from a triplet molecular excited state when a voltage is applied across the device;
- the electron transport layer disposed between the emitter layer and the cathode, the electron transport layer comprising an electron transport material represented by the following general formula V:
- X represents a single chemical bond or phenylene group
- Y represents anthraceny! group or pyrenyl group
- phosphorescent organometallic compound is selected from the group consisting of phosphorescent organometallic platinum compounds, organometallic iridium compounds and organometallic osmium compounds
- the phenylene group may be selected from 1 .2-phenylene. 1 ,3-phenylen and 1 ,4-phenylene. 10 1 15) According to the disclosed is an organic light emitting device, the
- phosphorescent organometallic compound may comprise an aromatic ligand.
- the anthracenyl group is selected from anthracen-9-yl, anthracen-1 -yl and anthracen-2-yl.
- the pyrenyl group is selected from pyren-1 -yl, pyren-2-yl and pyren-4-yl.
- the electron transport material is selected from the group consisting of:
- the electron transport material is selected from the group consisting of
- R 1 R 2 and R 3 may represent mono, di, tri, or tetra substitutions, n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10.
- An and Ar 2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
- At least one of R 1 ,R 2 and R 3 in Formula (H-IV) and at least one of R 1 and R 2 in Formulas (H-V) and (HVI) includes a triphenylene group.
- R 1 ,R 2 and R 3 are independently selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl, heteroaryl and hydrogen. Each of R 1 ,R 2 and R 3 may represent multiple substituents. At least one of R 1 ,R 2 and R 3 in Formula (H-l) and at least one of R 1 and R 2 in Formulas (H-ll) and (H-lll) includes a triphenylene group.
- the device further comprise a hole blocking layer disposed between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that may be the same or different from the host material in the emissive layer.
- the device further comprise a hole blocking layer disposed between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that is the same as the host material in the emissive layer.
Abstract
An organic light-emitting diode (OLED) device includes an emissive layer having a host material and a phosphorescent dopant, the host material including a benzo-fused thiophene and the phosphorescent dopant including a heteroleptic transition metal complex having extended conjugation, a hole blocking layer disposed on the emissive layer, the hole blocking layer including a hole blocking material, an electron transport layer disposed on the hole blocking layer, the OLED device having a luminous efficacy of at least about 40 lm/W at 1,000 cd/m2 (nits).
Description
PHOSPHORESCENT OLED DEVICES
BACKGROUND
[0001] Embodiments disclosed herein relate to organic light emitting diode devices (OLEDs). In particular, embodiments disclosed herein relate to a combination of device materials to provide OLED devices having enhanced luminous efficacy, low voltage, and increased device lifetime.
[0002] Generally, an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode. When a current is applied, the anode injects holes and the cathode injects electrons into the organic layer(s). The injected holes and electrons each migrate toward the oppositely charged electrode. When an electron and hole localize on the same molecule, an "exciton," which is a localized electron-hole pair having an excited energy state, is formed. Light is emitted when the exciton relaxes via a photoemissive mechanism. In some cases, the exciton may be localized on an excimer or an exciplex. Non-radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.
BRIEF DESCRIPTION OF THE FIGURES [0003] FIG. 1 is a schematic drawing showing an outline constitution of one example of the OLED according to one embodiment of the present disclosure. The drawing is not drawn to scale.
[0004] FIG. 2 shows an inverted OLED according to another embodiment of the present disclosure.
[0005] FIG. 3 shows an exemplary multilayered OLED device in accordance with embodiments disclosed herein.
SUMMARY
[0006] In some aspects, embodiments disclosed herein relate to organic light-emitting diode (OLED) devices comprising an emissive layer comprising a host material and a
phosphorescent dopant, wherein the host material comprises a benzo-fused thiophene and the phosphorescent dopant comprises a heteroleptic transition metal complex having extended conjugation, a hole blocking layer disposed on the emissive layer, the hole blocking layer comprising a hole blocking material, an electron transport layer disposed on the hole blocking layer, wherein the OLED device has a luminous efficacy of at least about 40 Im W at 1 ,000 cd/m2 (nits).
DETAILED DESCRIPTION
[0007] Opto-etectronic devices that make use of organic materials are becoming increasingly desirable for a number of reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials. For example, the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
[0008] OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly utilized technology in applications such as flat panel displays, illumination, and backlighting. Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.
[0009] One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as "saturated" colors. In particular, these standards call for saturated red, green, and blue pixels. Color may be measured using CIE coordinates, which are well known to the art.
[0010] Early OLEDs used emissive molecules that emitted light from their singlet states ("fluorescence") as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.
[0011] More recently, OLEDs having emissive materials that emit light from triplet states ("phosphorescence") have been demonstrated. Baldo et al. , "Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices," Nature, vol. 395, 151-154, 1998;
("Baldo-I") and Baldo et al. , "Very high-efficiency green organic light-emitting devices based on electrophosphorescence," Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) ("Baldo-H"), which are incorporated by reference in their entireties.
[0012] Phosphorescence may be referred to as a "forbidden" transition because the transition requires a change in spin states, and quantum mechanics indicates that such a transition is not favored. As a result, phosphorescence generally occurs in a time frame exceeding at least 10 nanoseconds, and typically greater than 100 nanoseconds. If the natural radiative lifetime of phosphorescence is too long, triplets may decay by a non-radiative mechanism, such that no light is emitted. Organic phosphorescence is also often observed in molecules containing heteroatoms with unshared pairs of electrons at very low temperatures. 2,2'-bipyridine is such
a molecule. Non-radiative decay mechanisms are typically temperature dependent, such that an organic material that exhibits phosphorescence at liquid nitrogen temperatures typically does not exhibit phosphorescence at room temperature. But, as demonstrated by Baldo, this problem may be addressed by selecting phosphorescent compounds that do phosphoresce at room temperature. Representative emissive layers include doped or un-doped
phosphorescent organometallic materials such as disclosed in U.S. Pat. Nos. 6,303,238 and 6,310,360; U.S. Patent Application Publication Nos. 2002-0034656; 2002-0182441 ; 2003- 0072964; and WO-02/074015.
[0013] Generally, the excitons in an OLED are believed to be created in a ratio of about 3:1 , i.e., approximately 75% triplets and 25% singlets. See, Adachi et al., "Nearly 100% Internal Phosphorescent Efficiency In An Organic Light Emitting Device," J. Appl. Phys., 90, 5048 (2001 ), which is incorporated by reference in its entirety. In many cases, singlet excitons may readily transfer their energy to triplet excited states via "intersystem crossing," whereas triplet excitons may not readily transfer their energy to singlet excited states. As a result, 100% internal quantum efficiency is theoretically possible with phosphorescent OLEDs. In a fluorescent device, the energy of triplet excitons is generally lost to radiationless decay processes that heat-up the device, resulting in much lower internal quantum efficiencies. OLEDs utilizing phosphorescent materials that emit from triplet excited states are disclosed, for example, in U.S. Pat. No. 6,303,238, which is incorporated by reference in its entirety,
[0014] Phosphorescence may be preceded by a transition from a triplet excited state to an intermediate non-triplet state from which the emissive decay occurs. For example, organic molecules coordinated to lanthanide elements often phosphoresce from excited states localized on the lanthanide metal. However, such materials do not phosphoresce directly from a triplet excited state but instead emit from an atomic excited state centered on the lanthanide metal ion. The europium diketonate complexes illustrate one group of these types of species.
[0015] Phosphorescence from triplets can be enhanced over fluorescence by confining, such as through bonding, the organic molecule in close proximity to an atom of high atomic number. This phenomenon, called the heavy atom effect, is created by a mechanism known as spin-orbit coupling. Such a phosphorescent transition may be observed from an excited metal-to-ligand charge transfer (MLCT) state of an organometallic molecule such as tris(2- phenylpyndine)iridium(lll).
[0016] As used herein, the term "triplet energy" refers to an energy corresponding to the highest energy feature discernable in the phosphorescence spectrum of a given material. The highest energy feature is not necessarily the peak having the greatest intensity in the phosphorescence spectrum, and could, for example, be a local maximum of a clear shoulder on the high energy side of such a peak.
[0017] FIG. 1 shows an organic light emitting device 100. The figures are not necessarily drawn to scale. Device 100 may include a substrate 1 10. an anode 1 15, a hole injection layer
120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170. Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164. Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in US 7,279,704 at cols. 6-10, which are incorporated by reference.
[0018] More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a p-doped hole transport layer is m- MTDATA doped with F4-TCNQ at a molar ratio of 50:1 , as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al.. which is incorporated by reference in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1 :1 , as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.
[0019] FIG. 2 shows an inverted OLED 200. The device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230. Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an "inverted" OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200. FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.
[0020] Devices fabricated in accordance with embodiments disclosed herein may
further optionally comprise a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc. The barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge. The
barrier layer may comprise a single layer, or multiple layers. The barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate an inorganic or an organic compound or both. In some embodiments, the barrier layer comprises a mixture of a polymeric material and a non-polymeric material as described in U.S. Pat, No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and
PCT/US2009/042829, which are herein incorporated by reference in their entireties. To be considered a "mixture", the aforesaid polymeric and non-polymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time. The weight ratio of polymeric to non-polymeric material may be in the range of 95:5 to 5:95. The polymeric material and the non-polymeric material may be created from the same precursor material. In one example, the mixture of a polymeric material and a non-polymeric material consists essentially of polymeric silicon and inorganic silicon.
[0021] Embodiments disclosed herein provide phosphorescent organic light emiting devices (PHOLED) having high power efficiency and operational stability. Superior power efficacy and long device lifetime were achieved via a synergistic combination of materials within the devices. In particular, a combination of appropriate host material, phosphorescent dopant and electron transport material are disclosed herein to provide devices with improved lifetimes as measured by LT97 (time for luminance to decrease to 97% of its intial level) of about 51 hours at 10,000 cd/m2 (nits). Devices disclosed herein may also achieve power efficacies of about 61 Im/W. These device characteristics are obtained at low voltage making the combination of materials unexpectedly superior to state of the art devices. These and other advantages will be apparent to those skilled in the art.
In embodiments, there are provided organic light-emitting diode (OLED) devices comprising an emissive layer comprising a host material and a phosphorescent dopant, wherein the host material comprises a benzo-fused thiophene and the phosphorescent dopant comprises a heteroleptic transition metal complex having extended conjugation and an electron transport layer disposed on the hole blocking layer, wherein the OLED device has a luminous efficacy of at least about 40 Im/W at 1 ,000 cd/m2 (nits). In embodiments, such devices may further comprise a hole blocking layer disposed between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that may be the same or different from the host material in the emissive layer. In some such embodiments the hole blocking material comprises the same benzo-fused thiphene compound as the host material.
[0022] Although the terms used herein are generally intended to have their ordinary meaning as understood by those skilled in the art. the following definitions are nonetheless provided :
[0023] As used herein, "heteroleptic" means a complex having at least two different ligands.
[0024] As used herein, "extended conjugation" refers to an extended array of pi bonds capable of distribution of electron density over many atoms.
[0025] As used herein, "luminous efficacy" refers to a measure of how well a light source produces visible light and is generally computed as the ratio of luminous flux to power.
[0026] The terms halo, halogen, alkyl, cycloalkyi, alkenyl, alkynyl, aralkyi, heterocyclic group, aryl, aromatic group, and heteroaryl are known to the art, but are defined here for ease of reference.
[0027] The term "halo" or "halogen" as used herein includes fluorine, chlorine, bromine and iodine.
[0028] The term "alkyl" as used herein contemplates both straight and branched chain alkyl radicals. Exemplary alkyl groups may contain from one to fifteen carbon atoms and includes methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, and the like. Additionally, the alkyl group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic-amino, N02, and OR, wherein each R is independently selected from H, alkyl, alkenyl, alkynyl, aralkyi, aryl and heteroaryl.
[0029] The term "cycloalkyi" as used herein contemplates cyclic alkyl radicals. Exemplary cycloalkyi groups include those containing 3 to 7 carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, and the like. Additionally, the cycloalkyi group may be optionally substituted with one or more substituents selected from halo, CN , C02R. C(0)R, NR2, cyclic- amino, N02. and OR.
[0030] The term "alkenyl" as used herein contemplates both straight and branched chain alkene radicals. Exemplary alkenyl groups include those containing two to fifteen carbon atoms. Additionally, the alkenyl group may be optionally substituted with one or more substituents selected from halo. CN , C02R, C(0)R, NR2, cyclic-amino, N02. and OR.
[0031] The term "alkynyl" as used herein contemplates both straight and branched chain alkyne radicals. Exemplary alkyl groups include those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted with one or more substituents selected from halo, CN, C02R , C(0)R, N R2. cyclic-amino, N02, and OR.
[0032] The terms "aralkyi" as used herein contemplates an alkyl group that has as a substituent an aromatic group. Additionally, the aralkyi group may be optionally substituted on the aryl with one or more substituents selected from halo. CN , C02R, C(0)R, NR2, cyclic- amino, N02. and OR.
[0033] The term "heterocyclic group" as used herein contemplates non-aromatic cyclic radicals. Exemplary heterocyclic groups include those containing 3 or 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperdmo, pyrrolidino, and the like, and cyclic ethers, such as tetrahydrofuran, tetrahydropyran , and the
like. Additionally, the heterocyclic group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic-amino, N02, and OR.
[0034] The term "aryl" or "aromatic group" as used herein contemplates single-ring groups and polycyclic ring systems. The polycyclic rings may have two or more rings in which two carbons are common by two adjoining rings (the rings are "fused") wherein at least one of the rings is aromatic, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles and/or heteroaryls. Additionally, the aryl group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic-amino, N02, and OR.
[0035] The term "heteroaryl" as used herein contemplates single-ring hetero-aromatic groups that may include from one to three heteroatoms, for example, pyrrole, furan, thiophene, imidazole, oxazole, thiazole, triazole, pyrazole, pyridine, pyrazine and pyrimidine, and the like. The term heteroaryl also includes polycyclic hetero-aromatic systems having two or more rings in which two atoms are common to two adjoining rings (the rings are "fused") wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles and/or heteroaryls. Additionally, the heteroaryl group may be optionally substituted with one or more substituents selected from halo, CN, C02R, C(0)R, NR2, cyclic- amino, N02, and OR.
[0036] As used herein, the term "organic" includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices. "Small molecule" refers to any organic material that is not a polymer, and "small molecules" may actually be quite large. Small molecules may include repeat units in some circumstances For example, using a long chain alkyl group as a substituent does not remove a molecule from the "small molecule" class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a "small molecule." and it is believed that all dendnmers currently used in the field of OLEDs are small molecules.
[0037] [As used herein, "top" means furthest away from the substrate, while "bottom" means closest to the substrate. Where a first layer is described as "disposed over" a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is "in contact with" the second layer. For example, a cathode may be described as "disposed over" an anode, even though there are various organic layers in between.
[0038] As used herein, "solution processible" means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.
[0039] As used herein, and as would be generally understood by one skilled in the art. a first "Highest Occupied Molecular Orbital" (HOMO) or "Lowest Unoccupied Molecular Orbital"
(LUMO) energy level is "greater than" or "higher than" a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A "higher" HOMO or LUMO energy level appears closer to the top of such a diagram than a "lower" HOMO or LUMO energy level.
[0040] As used herein, and as would be generally understood by one skilled in the art, a first work function is "greater than" or "higher than" a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a "higher" work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a "higher" work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.
[0041] More details on OLEDs, and the definitions described above, can be found in US Pat. No. 7,279.704, which is incorporated herein by reference in its entirety.
[0042] 399Referring now to Figure 3, there is shown a device 300 in accordance with embodiments disclosed herein. From the bottom up, device 300 includes anode 310, a hole injection layer 320, a hole transport layer 330, an emissive layer 340, a hole blocking layer 350, an electron transport layer 360, an eletron injection layer 370, and a cathode 380.
[0043] In accordance with embodiments disclosed herein, the synergistic combination of materials comprise emissive layer 340, a combination of host material benzo-fused thiophene and phosphorescent dopantand electron transport layer 360. In embodiments, hole blocking layer (HBL) 350 comprising a hole blocking material may be incorporated between emissive layer 340 and electron transport layer 360 to confine excitons within emissive. To perform this role, the HBL material should have HOMO and LUMO energy levels suitable to block hole transport from the emissive layer (EML) to the electron transport layer (ETL) and to pass electrons from the ETL to the EML. In embodiments, the HBL material may be selected from known HBL materials, for example. BAlq which is is a well-known electron transporting blocking layer material. In embodiments, the material in hole blocking layer 350 may comprise the same benzo-fused thiophene compound that is used as a host material in emissive layer 340.
[0044] The layered structures illustrated in Figures 1 , 2 and 3 are provided by way of non- limiting example, and it is understood that embodiments disclosed herein may be used in connection with a wide variety of other structures. The specific materials and structures described are exemplary in nature, and other materials and structures may be used.
Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers. The names given to the various layers herein are not intended to be strictly limiting. For example, in devices 100 and 300, hole transport layers 130 and 330 transport holes and inject holes into emissive layers 140 and 340, and may be described as hole transport layers or hole injection layers.
[0045] Unless otherwise specified, any of the layers of the various embodiments may be deposited by any suitable method. For organic layers, methods may include thermal evaporation, ink-jet deposition, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102, which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431 ,968, which is incorporated by reference in its entirety. Other suitable deposition methods include spin coating and other solution based processes. Solution based processes may be carried out under nitrogen or other inert atmosphere. For the other layers, methods may include thermal evaporation. In embodiments, patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and OVJD. Other methods may also be used. The materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and typically containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having up 20 carbons or more may be used, and thus a range from about 3 to about 20 carbons may be typical.
Materials with asymmetric structures may have better solution processibility than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.
[0046] Devices fabricated in accordance with embodiments disclosed herein may be incorporated into a wide variety of consumer products, including flat panel displays, computer monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads up displays, fully transparent displays, flexible displays, laser printers, telephones, cell phones, personal digital assistants (PDAs), laptop computers, digital cameras, camcorders viewfmders, micro-displays, 3-D displays, vehicles, a large area wall, theater or stadium
screen, or a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present embodiments, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18 degrees C to 30 degrees C, and those close to "room temperature" (i.e., about 20 to 25 degrees C), but could be used outside this temperature range, for example, from -40 degree C to +80 degree C.
[0047] The materials and structures described herein may have applications in devices other than OLEDs. For example, other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures disclosed herein. More generally, organic devices, such as organic transistors, may also employ the materials and structures disclosed herein.
[0048] Returning now to Figure 3, in embodiments, host material of emissive layer 340 comprise the benzo-fused thiophene comprises a compound of Formula I, Formula II or Formula III:
wherein R1, R2 and R3 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen.
[0049] In embodiments, compounds of Formula I, II and III may comprise at least one aryl group that is a triphenylene group:
triphenylene
[0050] Triphenylene is a polyaromatic hydrocarbon with high triplet energy, yet high pi- conjugation and a relatively small energy difference between the first singlet and first triplet levels, Thus, triphenylene has relatively accessible HOMO and LUMO levels compared to other aromatic compounds with similar triplet energy such as biphenyl. Triphenylene can readily accommodate red, green and even blue phosphorescent dopants to give high efficiency without energy quenching. Benzo-fused thiophenes may be used as hole transporting organic conductors. In addition, the triplet energies of benzothiophenes of Formula I Hare relatively high. A combination of benzo-fused thiophenes and triphenylene as hosts in PHOLED may be particularly beneficial. Benzo-fused thiophenes are typically more hole transporting than electron transporting, and triphenylene is more electron transporting than hole transporting. Therefore, combining these two moieties in one molecule may offer
improved charge balance which may improve device performance in terms of lifetime, efficiency and low voltage. Different chemical linking motifs of the two moieties can be used to tune the properties of the resulting compound to match a particular phosphorescent emitter, device architecture, and / or fabrication process. For example, m-phenylene linkage may provide higher triplet energy and higher solubility relative to p-phenylene.
[0051] Compounds of Formula I , I I and I I I may be substituted with groups that are not necessarily triphenylenes. In embodiments, any group that is used as a substituent of Formula I may be selected with a triplet energy high enough to maintain the benefit of having triphenylene benzo-fused thiophenes. Examples of such groups that may be used as substituents of Formula I , I I and II I may include a substituent selected from the group consisting of CnH2n+1 , OCnH2n+1 , OAn , N(A^ )(Ar2), CH=CH-CnH2n+1 , C=CHCnH2n+1 , An , Ar,-Ar2l CnH2n-Ari , or no substitution, wherein n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10, and wherein Ar, and Ar2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof. The compounds described herein may have a sufficiently high triplet energy to be suitable for use in a device having phosphorescent blue emissive materials.
[0052] The substituents of the compounds described herein are generally unfused such that the substituents are not fused to the triphenylene, benzo-fused furan or benzo-fused thiophene moieties of the compound. However, the substituents may optionally be inter-fused (i.e. fused to each other).
[0053] Similar to the characterization of benzo-fused thiophenes, benzo-fused furans are also typically hole transporting materials having relatively high triplet energy. Examples of benzo-fused furans include benzofuran and dibenzofuran. Therefore, a material containing both triphenylene and benzofuran may be advantageously used as host or hole blocking material in PHOLED. A compound containing both of these two groups may offer improved electron stabilization which may improve device stability and efficiency with low voltage. The properties of the triphenylene containing benzofuran compounds may be tuned as necessary by using different chemical linkages to link the triphenylene and the benzofuran.
[0054] Examples of triphenylene-containing benzo-fused thiophenes useful in the devices disclosed herein include compounds having the structure of the following formulae (H- I), (H-l l) and (H-lll)
(H-l) (H-ll) (H-lll)
[0055] Where R1 ,R2 and R3 are independently selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl, heteroaryl and hydrogen. Each of R1 ,R2 and R3 may represent multiple substituents. At least one of R1 ,R2 and R3 in Formula (H-l) and at least one of R1 and R2 in Formulas (H-!l) and (H-lll) includes a triphenylene group. The triphenylene group may be linked directly to the structure of formulae (H-l), (H-ll) or (H-lll), but there may also be a "spacer" in between the triphenylene group and the structure of formulae (H-l), (H-ll) or (H-lll). [0056] Examples of triphenylene-containing benzo-fused thiophenes or benzo-fused furans include compounds having the structure of the following formulae (H-IV), (H-V), and (H-VI);
(H-IV) (H-V) (H-VI)
where X is S or O and wherein R1 R2 and R3 are unfused substituents that are independently selected from CnH2n+1 , OCnH2n+h OAr,, N(CnH2n+i)2, N(Ar,)(Ar2), CH=CH- CnH2n«i , C=CHCnH2n+1 , Ar^ Ar Ar2, CnH2n-Ar1, or no substitution. Each of R1 R2 and R3 may represent mono, di, tri, or tetra substitutions, n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10. An and Ar2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof. At least one of R1 ,R2 and R3 in Formula (H-IV) and at least one of R1 and R2 in Formulas (H-V) and (HVI) includes a triphenylene group.
[00573
[0058] Ex de;
Ri to R7 represents, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl and heteroaryl, or no substitution.
[0059] Ex
wherein R3, R4, R5, R6, and R7, at each occurrence, are selected independently from the group consisting of CnH2n+1, OCnH2n+1 > OAr, , N(CnH2r)+1)2, N(Ari)(Ar2), CH=CH— CnH2n+1,
C≡CHCnH2n+1, Ar1 f A^— Ar2, CnH2n— Ar,, and no substitution, wherein n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10, and wherein Ar-ι and Ar2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
[0060] Examples of compounds having the structure of the formula (H-ll) include:
Compound 12'G Compound 12'
Compound 16!G Compound 16'
Compound 1 ?*G
where to R5 represent, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyi, aryl and heteroaryl, or no substitution.
[0061] of the formula (H-V) include:
Compound 16
Compound 18
where X is S or O. In some embodiments, X is S. R1 to R5 are independently selected from the group consisting of CnH2n+1 , OCnH2n+i, OAr, , N(CnH2n+1 )2,
, C=CHCnH2n+1 , ΑΓτ , Ar!-Ar2, CnH2n-Ar1 , or no substitution. Each of Ri to R5 may represent mono, di, tri, or tetra substitutions., n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10. A^ and Ar2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
[0062] e: .
Compound 5'G Compound 5
Compound 10'
Compound 15'G Compound 15' where R4, R5, R6, R7, R10, R and R12 represent, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyi, aryl and heteroaryl, or no substitution(H).
ounds having the formula (H-VI) include
Compound 1 G Compound 1
Compound 2G Compound 2
Compound 6G Compound 6
Compound 10G Compound 10
Compound 21 G Compound 21
Compound 25 G Compound 25
Compound 29G Compound 29
Compound 32G Compound 32
where X is S or O. In some embodiments, X is S, wherein R4, R5, R6, R?, Re, R9, R10, R11 and R12 are independently selected from the group consisting of CnH2n+1, OCnH2n+i, OAn ,
N(CnH2n+1)2, N(Ar1)(Ar2), CH=CH-CnH2n+1, C=CHCnH2n+1, Ar,, ΑΓ,-ΑΓΖ, CnH2n-Ari , or no substitution. Each of R-, to Rn may represent mono, di, tri, or tetra substitutions, n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10. An and Ar2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.
[0064] In embodiments, the present disclosure comprises an OLED which comprises a benzo-fused thiophene host material, wherein the triplet energy of the host material is from about 2.0 eV to about 2.8 eV.
[0065] In embodiments, the benzo-fused thiophene comprises a compound of Formula la:
wherein each R1 and R2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyi, aryl, aralkyl, heteroaryl, and hydrogen; L is bond or an optionally substituted pheny R4 are independently selected from the group
[0066] Examples of compounds of Formula III or Ilia include the following: Examples of re of Formula(H-lll) include: .
Compound 1'G Compound 1 '
Compound 2'G Compound 2'
Compound 5'
Compound 15'G Compound 1 5'
.where R-i to R? represents, independently, mono, di, tri or tetra substitutions selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl and heteroaryl, or no substitution (i.e., hydrogen).
[0067] In embodiments, the benzofused thiophene host is Compound 2' (hereinafter
Compound "H"):
In embodiments, the host material and hole blocking material are the same, i.e., both are triphenylene containing benzo-fused thiophenes. That is, in embodiments, the host material of the emissive layer and the hole blocking material of the hole blocking layer may be the same. In some such embodiments, the host material and the hole blocking material
comprisecompound H The preparation of compounds of Formula I , I I and II I , including Compound H (previously disclosed as Compound 2'), are disclosed in U.S. Pat. Application Publication No. 201 1/084599 (WO 2009/021 126) which is incorporated herein by reference in its entirety.
[0068] In emobdiments. emissive layer 340 has a thickness from about 100 to about 600 angstroms or about 200 angstroms to about 400 angstroms, or about 250 to about 350 angstroms, or about 280 to about 320 angstroms. In embodiments, hole blocking layer 150, which may comprise the same host material as the emissive layer, has a thickness from about 10 to about 100 angstroms, or about 25 to about 75 angstroms, or about 35 to about 65 angstroms, or about 45 to about 55 angstroms.
[0069] Some examples of the phosphorescent emitter material doped into emissive layer 340 are heteroleptic phosphorescent organometallic compounds represented by the formula L2MX. LL'MX, LL'I_"M, or LMXX'. wherein L, U, L", X, and X' are inequivalent,
bidentate ligands and M is a metal that forms octahedral complexes, wherein L, L', and L" are monoanionic inequivalent bidentate ligands coordinated to M through an sp2 hybridized carbon and a heteroatom.
[0070] The phosphorescent organometallic compound may be a compound selected from the group consisting of phosphorescent organometallic platinum compounds, organometallic iridium compounds and organometallic osmium compounds. The organometallic platinum compounds, iridium compounds and osmium compounds can each include an aromatic ligand,
[0071] In embodiments, the phosphorescent dopant present in emissive layer 340 comprises a heteroleptic transition metal com of Formula -l 11 :
wherein B and C are each independently a 5 or 6-membered carbocyclic or heterocyclic rings; wherein A-B is a bonded pair of carbocyclic or heterocyclic rings coordinated to a metal M via a nitrogen atom in ring A and an sp2 hybridized atom in ring B; wherein A-C is a bonded pair of carbocyclic or heterocyclic rings; wherein each Ra, Rb, and Rc are independently mono, di, tri, or tetra substitutions and each Ra, Rb, and Rc are independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl, and heteroaryl, any of which may be optionally substituted; wherein X1 t X2, X3, X4, Xs, X6, X7, X8, and X9 are independently selected from carbon and nitrogen; wherein R1 and R2 are independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl, and heteroaryl, any of which may be optionally substituted; and wherein at least one of Ri , R2, and the Ra substituents adjacent to C is not hydrogen; wherein M is a coordinated metal having an atomic number greater than 40, m is the oxidation state of the metal, and n is an integer of at least 1 ,
In embodiments, phosphorescent emissive compounds are provided that comprise Ir (III) heteroleptic complexes having extended conjugation on the heterocyclic ring which coordinates to the metal through nitrogen. The compounds provided have the formula selected from the group consisting of:
Heteroleptic iridium compounds are provided, which may be used in organic light emitting devices as the emissive dopant of such devices. The heteroleptic compounds may be selected from the group consisting of:
Compound 12 Compound 13 Compound 14
[0072] In embodiments, the heteroleptic transition metal complex is a Compound 12
(hereinafter Compound G1 ):
[0073] Methods of preparing such phosphorescent dopants, including compound 12 are disclosed in U.S. Patent Application Publication No. 2011/227049, which is incorporated herein by reference in its entirety. In embodiments, the phosphorescent dopant is present in emissive layer 140 in a range from about .5 to about 30 percent by weight of the layer or about 1 to about 20 percent by weight of the layer or about 5 percent to about 15 percent by weight of the layer.
[0074] In embodiments, electron transport layer 360 comprises a compound of Formula V:
where X represents a single chemical bond or phenylene group, and Y represents anthraceny! group or pyrenyl group. Examples of a phenylene group for X include 1 ,2-phenylene. 1 ,3- phenylen and 1 ,4-phenylene. Examples of anthracenyl group of Y include anthracen-9-yl, anthracen-1-yl and anthracen-2-yl. Examples of pyrenyl group of Y include pyren-1 -yl, pyren- 2-yl and pyren-4-yl.
ETL-1 ETL-2 ETL-3
[0076] Further examples of compound 5 are provided below which are described in U.S. Application Publication No. 2012/0214993, which is incorporated herein by reference in its entirety:
[0077] In embodiments, the electron transport layer has a thickness from about 10 to about 600 angstroms or about 350 angstroms to about 550 angstroms, or about 400 to about 500 angstroms.
[0078] The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device. For example, emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present The materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed
herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.
[0079] In addition to and/or in combination with the materials disclosed herein, many hole injection materials, hole transporting materials, host materials, dopant materials, exiton/hole blocking layer materials, electron transporting and electron injecting materials may be used in an OLED. Non- limiting examples of the materials that may be used in an OLED in combination with materials disclosed herein are listed in Table 1 below. Table 1 lists non- limiting classes of materials, non- limiting examples of compounds for each class, and references that disclose the materials.
compounds , i { >■<' } > ( > < ? 1832 (2000)
[0080] In embodiments, devices configured with the combination of materials disclosed herein may have a voltage below about 4.5 volts at 1 ,000 cd/m2 and a luminance of at least 18,500 cd/m at 40 rnA/cm2. Thus, in embodiments, there are provided organic light-emitting diode
(OLED) device comprising an emissive layer comprising a host material and a phosphorescent dopant.wherein the host material comprises a benzo-fused thiophene and the phosphorescent dopant comprises a heteroleptic transition metal complex having extended conjugation, and an electron transport layer disposed on the hole blocking layer, wherein the OLED device has a luminous efficacy of at least about 40 Im/W and voltage below about 4.5 volts at 1 ,000 cd/m2 (nits), and a luminance of at least 18,500 cd/m2 at 40 mA/cm2.
[0081] In some such embodiments, the benzo-fused thiophene comprises a compound of Formula Ilia:
wherein each R1 and R2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen; L is bond or an optionally substituted phenyl group; and R3 and R4 are independently selected from the group
consisting of hydrogen and xample, Compound H below:
Compound H
[0082] In some such embodiments, the heteroleptic transition metal complex is a compound of Formula L2MX, LL'MX, LL'L"M, or LMXX', wherein L, L', L", X, and X' are inequivalent, bidentate ligands and M is a transition metal that forms octahedral complexes, wherein L, L', and L" are monoanionic inequivalent bidentate ligands coordinated to M through an sp2 hybridized carbon and a heteroatom such as, for example. Compound G1 below:
and the electron transport layer co rmula V:
where X represents a single chemical bond or phenylene group, and Y represents anthracenyl group or pyrenyl group.
[0083] Exemplary compounds of structure V include structures ETL-1 , ETL-2, and ETL-3 below:
ETL-1 ETL-2 ETL-3 [0084] In embodiments, such devices may also exhibit a time for luminance to decrease to 97% of its initial level of about 50 hours at 10,000 cd/m2.
[0085] In embodiments, there are provided organic light-emitting diode (OLED) devices comprising an emissive layer comprising a host material and a phosphorescent dopant, wherein the host material comprises a benzo-fused thiophene compound of Formula H-llla:
wherein each R1 and R2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen; L is bond or an optionally substituted pheny R4 are independently selected from the group
consisting of hydrogen and , and the phosphorescent dopant comprises
Compound G1 :
; and an electron transport layer disposed over the emissive layer, wherein the electron transport layer comprises a compound of Formula V:
where X represents a single chemical bond or phenylene group, and Y represents anthracenyl group or pyrenyl group.
ETL-1 ETL-2 ETL-3
[0087] In embodiments, such devices may further comprise a hole blocking layer between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that_may be the same or different from the host material in the emissive layer. In embodiments, the hole blocking material may be a benzo fused thiophene compound. In embodiments, the hole blocking material may be the same benzo fused thiophene compound as the host material in the emissive layer.
EXAMPLES
EXAMPLE 1
[0088] This Example shows the preparation and performace of devices prepared from the synergistic combination of materials disclosed herein.
DEVICE FABRICATION AND MEASUREMENT
[0089] Experimental Devices #1 , #2 and #3 all bearing the structure shown in FIG. 3 were fabricated according to the present disclosure as follows: LG101 (LGChem, Seoul, South Korean) was used in all devices to form a 10 nm thick hole injection layer, NPD was used in all devices to form a 30 nm thick hole transport layer. In all devices, phosphorescent emitter compound G1 (previously disclosed as Compound 12 in WO2010/028151 including synthesis) was doped at 12 % doping level into Compound H as a host material (previously disclosed as Compound 2' in WO 2009/021 126 including synthesis) to form a 30 nm thick emissive layer layer. An undoped layer of compound H was used in all devices to form a 5 nm thick hole blocking layer. A 40 nm thick electron transport layer was deposited over the hole blocking layer using one of ETL-1 , ETL-2 and ETL-3 respectively in Devices #1 , #2, #3. Li F was used in all devices to form 1 nm thick electron injection layer. A 100 nm thick layer of Aluminum formed the cathode in all devices and an 80 nm thick layer of ITO formed the anode in all devices. The chemical strucures of experimental electron transport compounds ETL-1 , ETL-2 and ETL-3. comparative electron transport compound Alq3. hole blocking/host compound H , dopant compound G1 and hole transport compound NPD are shown in Table 2 below. Hole injection material LG101 was obtained from LG Chem, Seoul, South Korea.
Table 2
The device was transferred directly from vacuum into an inert environment glove-box, where it was encapsulated using a UV-curable epoxy, and a glass lid with a moisture getter. The emission profiles were assumed to be Lambertian, so EQE was calculated from
measurements, made with a SpectraScan PR705, of the emission intensity normal to the substrate. The current and voltage measurements were obtained using a Keithley 236 source measure unit.
[0091 ] For performance comparison, Comparative Example Device CE , also bearing the structure shown in FIG. 3, was also constructed . Comparative Example Device CE was fabricated in the same manner as Experimental devices #1 , #2 and #3 except that Alq3 was used to form the electron transport layer rather than ETL- 1 , ETL-2 or ETL-3.
[0092] Table 2 shows a summary of the fou r devices' construction in terms of the materials used for the electron transporting layer and the emitter layer. Table 3 shows the performance comparison of Experimental Devices #1 , #2 and #3 and Comparative Example device CE .
TABLE 2
Electron Transport
Device # Material Emitter Dopant Em itter Host
heteroleptic triphenylene containing organometallic benzo-fused thiophene
1 ETL 1 compound G 1 compound H heteroleptic triphenylene containing organometallic benzo-fused thiophene
2 ETL 2 compou nd G 1 compound H
heteroleptic triphenylene containing organometallic benzo-fused thiophene
3 ETL 3 compound G1 compound H heteroleptic triphenylene containing organometallic benzo-fused thiophene
CE Aiq3 compound G1 compound H
Table 3
[0093] As seen in Table 3, the power efficacies of devices in accordance with embodiments disclosed herein using ETL-1 , ETL-2 or ETL-3 as electron transport material in combination with H:G1 (12%) were 49, 55, and 61 ImA V at 1 ,000 nits respectively compared to 37 ImA/V for comparative device using previously known Alq3 as ETL material . Devcies #1 and #3 achieved the higher efficiency while maintaining comparable operational lifetime. Device #2 demonstrated improved operational lifetime in addition to higher efficiency. The LT97 (time for luminance to decrease to 97% of its initial level) at 10,000 nits was estimated to be 51 hrs for Device #2 compared to 38 hours for Device CE using known ETL material Alq.
EXAMPLE 2
[0094] This example shows the preparation of exemplary electron transport materials.
[0095] Synthesis of ETL-1
[0096] In a stream of argon, 7.0 g of 2-(3-bromo-5-chlorophenyl)-4,6- diphenylpyrimidine, 4.5 g of 1 -pyreneboronic acid, 1 17 mg of bis(triphenylphosphine)palladium dichloride, and 17 mL of aqueous 4N-NaOH solution were suspended in 75 mL of THF, and the resultant suspension was heated under reflux for one hour. Then, the suspension was cooled to room temperature, and water and methanol were added to the suspension. The deposited solid was collected by filtration and rinsed with water and with methanol to give 1 .24 g of 4,6-diphenyl -2-[3-chloro-5-(1-pyrenyl)phenyl]pyrimidine as a pale yellow powder
(yield:99%).
[0097] 1H-NMR (400 MHz, CDCI3) δ (ppm): 7.54-7.58 (m, 6H), 7.79 (s, 1 H), 8.07 (t, J = 7.6 Hz, 1 H), 8.09-8.12 (m, 3H), 8.17 (s, 2H), 8.22-8.32 (m, 8H), 8.86 (s, 1 H), 8.89(s, 1 H).
[0098] In a stream of argon, 6.5 g of 4,6-diphenyl -2-[3-chloro-5-(1 - pyrenyl)phenyl]pyrimidine, 2.9 g of 4-(2-pyridyl)phenylboronic acid, 26.9 mg of palladium(ll) acetate, 171 mg of 2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl, and 9.6 mL aqueous 3M-K2C03 solution were suspended in a mixed solvent composed of 54 mL of toluene and 6.0 mL of 1-butanol, and the resultant suspension was heated to 100 dgree Celsius and maintained at that temperature for 3 hours while being stirred. Then, the suspension was cooled to room temperature, and water and methanol were added to the suspension. The deposited solid was collected by filtration and rinsed with water and with methanol to give 7.53 g of 4,6-diphenyl -2-[5-(1 -pyrenyl)-4'-(2-pyndyl)biphenyl-3-yl]pyrimidine (ETL-1 ) as a yellow powder (yield:98%).
[0099] 1H-NMR (400 MHz, CDCI3) 5(ppm): 7.26-7.30 (m, 1 H), 7.55-7.60 (m, 6H), 7.80 (t, J = 7.6 Hz, 1 H), 7.85 (d, J = 7.0 Hz, 1 H), 8.01 (d, J = 8.5 Hz, 2H), 8.06 (t, J = 7.6 Hz, 1 H), 8.09- 8.1 1 (m, 3H), 8.17-8.23 (m, 6H), 8.25 (d, J = 7.6 Hz, 1 H), 8,31-8.38 (m, 6H), 8,76 (d, J = 4,8 Hz, 1 H), 9.02 (s, 1 H), 9.19 (s, 1 H).
[00100] Synthesis of ETL-2
[00101] In a stream of argon, a solution of 2.84 g of 2-bromopyridine and 75 mL of THF was cooled to -78 degree Celsius. 23.3 mL of 1.61 M tert-butyl lithium in pentane was added dropwise into the solution. The resultant mixture was being stirred for 30 minutes at -78 degree Celsius, and then 6.8 g of ZnCI2-N ,N ,N',N'-tetramethylethylenediamine complex was added to the cooled mixture. The resultant mixture was warmed to room temperature while being stirred. Then 6.3 g of 2-(3-bromo-5-chlorophenyl)-4,6-diphenylpyrimidine and 347 mg of tetrakis(triphenylphosphine)palladium was added into the warmed mixture. The resultant mixture was distilled under the reduce pressure to remove pentane, and then was heated under reflux for 3 hours while being stirred, and then was cooled to room temperature.
Saturated aqueous NH4CI solution was added to the mixture, and the resultant mixture was extracted with chloroform. The obtained crude product was purified by silica gel
chromatography to give 5.5 g of 4 6-diphenyl-2-[3-chloro-5-(2-pyridyl)phenyl]pyrimidine as a pale yellow powder (yield:87%).
[00102] 1 H-NMR (400 MHz, CDCI3)6(ppm): 7.34 (dd, J = 7.4, 4.8 Hz, 1 H), 7.57-7.64 (m, 6H), 7.87 (t, J = 7.7 Hz, 1 H), 7.94 (d, J = 8.0 Hz, 1 H), 8.10 (s, 1 H), 8.25 (s, 1 H), 8.31 -8.35 (m, 4H), 8.
[00103] In a stream of argon, 1 .0 g of 4,6-diphenyl-2-[3-chloro-5-(2- pyridyl)phenyl]pyrimidine, 645 mg of 1-pyreneboronic acid, 10.7 mg of palladium(ll) acetate, 68 mg of 2-dicyclohexylphosphino-2\4',6'-triisopropylbiphenyl, and 1 .6 mL of aqueous 3M- potassium phosphate solution were suspended in a mixed solvent composed of 9.5 mL of toluene and 2.4 mL of 1 -butanol, and the resultant suspension was heated to 100 degree Celsius and maintained at that temperature for 19 hours. Then, the suspension was cooled to room temperature, and water and methanol was added to the suspension. The deposited solid was collected by filtration and rinsed with water and with methanol to give 1 .35 g of 4,6- diphenyl -2-[5-(1 -pyrenyl)-3-(2-pyridyl)phenyl]pyrimidine (ETL-2) as a yellow powder
(yield:97%).
[00104] H-NMR (400 MHz, CDCI3) 6(ppm): 7.34 (dd, J = 7.6, 4.8 Hz, 1 H), 7.54-7.60
(m, 6H), 7.88 (t, J = 7.6 Hz, 1 H), 8.03-8.1 1 (m, 4H), 8.1 5-8.23 (m, 4H). 8.25 (d, J = 7.6 Hz. 1 H), 8.32-8 35 (m, 6H), 8.49 (s, 1 H), 8.81 (d, J = 4.8 Hz. 1 H), 9.07 (s,1 H), 9.44 (s, 1 H).
[00106] In a stream of argon, 8.4 g of 2-(3-bromo-5-chlorophenyl)-4,6- diphenylpyrimidine, 4.4 g of 4-(2-pyridyl)phenylboronic acid, 328 mg of
tetrakis(triphenylphosphin)palladium, and 7.5 mL of aqueous 4N-NaOH solution were suspended in 100 mL of THF, and the resultant suspension was heated under reflux for 24 hours. Then, the suspension was cooled to room temperature. Water was added to the suspension, and the resultant suspension was extracted with chloroform. The obtained crude product was purified by silica gel chromatography by using a chloroform as an eluent to give 8.3 g of 4,6-diphenyl-2-[5-chloro-4'-(2-pyridyl)biphenyl-3-yl]pyrimidine as a white powder (yield:83%).
[00107] 1H-NMR (400 MHz, CDCI3) 6(ppm): 7.28-7.32 (m, 1 H), 7.59-7.64 (m, 6H), 7.80- 7.85 (m, 3H), 7.87 (d, J = 8.5 Hz, 2H), 8.1 1 (s, 1 H), 8.18 (d, J = 8.5 Hz, 2H), 8.32-8.35 (m, 4H), 8.
[00108] In a stream of argon, 600 mg of 4,6-diphenyl-2-[5-chloro-4'-(2-pyridyl)biphenyl- 3-yl]pyrimidine, 403 mg of 9-anthraceneboronic acid, 5.4 mg of palladium(l l) acetate, 34.2 mg of 2 dicyclohexylphosphino-2\4',6'-triisopropylbiphenyl, and 1.2 mL of aqueous 3M-potassium phosphate solution were suspended in a mixed solvent composed of 4.8 mL of toluene and 1 .2 mL of 1 -butanol, and the resultant suspension was heated to 100 degree Celsius and maintained at that temperature for 2 hours. Then, the suspension was cooled to room temperature, and water was added to the suspension. The resultant suspension was extracted with chloroform. The obtained oganic layer was distilled under reduce pressure to remove volatile materials to give 584 mg of 4.6-diphenyl-2-[5-(9-anthracenyl)-4'-(2- pyridyl)biphenyl-3-yl]pyrimidine (ETL-3) as a yellow powder (yield:76%).
[00109] 1H-N R (400 MHz. CDCI3) 6(ppm): 7.27 (t, J = 6.2 Hz, 1 H), 7.41 (d, J = 6.5 Hz. 1 H), 7.44 (d, J = 6.6 Hz, 1 H), 7.51 -7.60 (m, 8H), 7.80 (t, J = 7.5 Hz, 1 H), 7.83 (d, J = 7.7 Hz, 1 H). 7 90 (d, J = 8.8 Hz: 2H), 7 94 (s, 1 H). 7.99 (d, J = 8 5 Hz. 2H), 8 1 1 (s, 1 H), 8.14 (d, J =
8.5 Hz, 2H), 8.18 (d, J = 8.5 Hz, 2H), 8.29-8.32 (m, 4H), 8.62 (s, 1 H), 8.76 (d, J = 4.8 Hz, 1 H), 8.85 (s, 1 H), 9.28 (s, 1 H)..
[00110] Any of ETL-1 , ETL-2 or ETL-3 synthesized above may be further refined by sublimation under vacuum before its use for the provision of the layered structure, in accordance with embodiments disclosed herein.
CONCLUSIONS
[00111] OLEDS incorporating the teachings of the present disclosure exhbit unexpected and substantial improved working lifetime characteristics and improved luminous efficiency
[00112] . Disclosed is an organic light emitting device comprising an anode, a cathode and a plurality of organic layers sandwiched between them, the plurality of organic layers comprising: an emitter layer comprising a host material and a phosphorescent emitter material wherein the host material comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan and wherein the phosphorescent emitter material comprises a phosphorescent organometallic compound that emits phosphorescent radiation from a triplet molecular excited state when a voltage is applied across the device;
an electron transport layer disposed between the emitter layer and the cathode, the electron transport layer comprising an electron transport material represented by the following general formula V:
where X represents a single chemical bond or phenylene group, and Y represents anthraceny! group or pyrenyl group
[00113J According to the disclosed is an organic light emitting device, the
phosphorescent organometallic compound is selected from the group consisting of phosphorescent organometallic platinum compounds, organometallic iridium compounds and organometallic osmium compounds
|0()1 14J According to an embodiment of the disclosed organic light emitting device, the phenylene group may be selected from 1 .2-phenylene. 1 ,3-phenylen and 1 ,4-phenylene. 10 1 15) According to the disclosed is an organic light emitting device, the
phosphorescent organometallic compound may comprise an aromatic ligand.
1001 16) According to an embodiment of the disclosed organic light emitting device, the anthracenyl group is selected from anthracen-9-yl, anthracen-1 -yl and anthracen-2-yl.
[00117] According to an embodiment of the disclosed organic light emitting device, the pyrenyl group is selected from pyren-1 -yl, pyren-2-yl and pyren-4-yl.
[00118| According to an embodiment of the disclosed organic light emitting device, the electron transport material is selected from the group consisting of:
[00120] According to another embodiment of the disclosed organic light emitting device, the electron transport material is selected from the group consisting of
and the host material is a compound comprising a triphenylene containing benzo-fused tniophene or benzo-fused furan, wherein any substituent in the compound is an unfused substituent independently selected from the group consisting of CnH2n+i , OCnH2n+i, OAr N(CnH2n+1 )2, N(Ar1)(Ar2), CH=CH-CnH2n+1 l C=CHCnH2n+1 , Ar, , ArrAr2, CnH2n-Ar1 , or no substitution, wherein n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10, and wherein An, and Ar2 are
independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereofOOOOOOOOOOOO
[00121] According to another embodiment of the disclosed organic light emitting device, thE
where X is S or O and wherein R1 R2 and R3 are unfused substituents that are independently selected from CnH2n+1, OCnH2n+h OAr-ι , N(CnH2n+1)2, N^XA^), CH=CH-CnH2n+1 ,
C=CHCnH2n+1 , Ar, , Ar Ar2, CnH2n-Ar1 , or no substitution. Each of R1 R2 and R3 may represent mono, di, tri, or tetra substitutions, n is 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10. An and Ar2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof. At least one of R1 ,R2 and R3 in Formula (H-IV) and at least one of R1 and R2 in Formulas (H-V) and (HVI) includes a triphenylene group.
[00122] According to another embodiment of the disclosed organic light emitting device
(H-l) (H-lll)
Where R1,R2 and R3 are independently selected from alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyl, aryl, heteroaryl and hydrogen. Each of R1,R2 and R3 may represent multiple substituents. At least one of R1,R2 and R3 in Formula (H-l) and at least one of R1 and R2 in Formulas (H-ll) and (H-lll) includes a triphenylene group.
[00123] According to another embodiment of the disclosed organic light emitting device, the device further comprise a hole blocking layer disposed between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that may be the same or different from the host material in the emissive layer.
[00124] According to another embodiment of the disclosed organic light emitting device, the device further comprise a hole blocking layer disposed between the emissive layer and the electron transport layer, the hole blocking layer comprising a hole blocking material that is the same as the host material in the emissive layer.
Claims
1 . An organic light-emitting diode (OLED) device comprising:
an emissive layer comprising a host material and a phosphorescent dopant;
wherein the host material comprises a benzo-fused thiophene and the phosphorescent dopant comprises a heteroleptic transition metal complex having extended conjugation;
a hole blocking layer disposed on the emissive layer, the hole blocking layer comprising a hole blocking material;
an electron transport layer disposed on the hole blocking layer
wherein the OLED device has a luminous efficacy of at least about 40 Im W at 1 ,000 cd/m2 (nits).
2. The device of claim 1 , wherein the benzo-fused thiophene comprises a compound of Formula I I I :
wherein R1 and R2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen.
3, The device of claim 2 , wherein the benzo-fused thiophene comprises a compound of Formula I l ia:
wherein each R1 and R^ are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl , arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen; L is bond or an optionally substituted p R4 are independently selected from the group
4. The device of claim 1 , wherein the heteroleptic transition metal complex comprises compound of Formula D-ll l :
wherein B and C are each independently a 5 or 6-membered carbocyclic or heterocyclic rings; wherein A-B is a bonded pair of carbocyclic or heterocyclic rings coordinated to a metal M via a nitrogen atom in ring A and an sp2 hybridized atom in ring B; wherein A-C is a bonded pair of carbocyclic or heterocyclic rings; wherein each RA, RB, and RC are independently mono, di, tri, or tetra substitutions and each RA, RB, and RC are independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyi, aryl, and heteroaryl, any of which may be optionally substituted; wherein X-i , X2, X3, X4, X5, Xe, X7, e, and X9 are independently selected from carbon and nitrogen; wherein R, and R2 are independently selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkenyl, alkynyl, arylkyi, aryl, and heteroaryl, any of which may be optionally substituted; and wherein at least one of RL R2, and the RA substituents adjacent to C is not hydrogen; wherein M is a coordinated metal having an atomic number greater than 40, m is the oxidation state of the metal, and n is an integer of at least 1 .
5. The device of claim 4, wherein the heteroleptic transition metal complex is Compound G1 :
6. The device of claim 1 , wherein the host material and hole blocking material are the same.
7. The device of claim 1 , wherein the electron transport layer comprises a compound of Formula V:
5 wherein X represents a single chemical bond or phenylene group, and Y represents
anthracenyl group or pyrenyl group
8. The device of claim 1 , wherein phosphorescent dopant is present in a range from about 5 percent to about 15 percent by weight of the layer.
9. The device of claim 1 , wherein the emissive layer has a thickness from about 200
10 angstroms to about 400 angstroms.
10. The device of claim 1 , wherein the hole blocking layer has a thickness from about 25 to about 75 angstroms.
1 1. The device of claim 1 , wherein the electron transport layer has a thickness from about 350 angstroms to about 550 angstroms.
1 5 12. The device of claim 1 , having a voltage below about 4.5 volts at 1 ,000 cd/m2.
13. The device of claim 1 , having a luminance of at least 18,500 cd/m2 at 40 mA/cm2.
14. An organic light-emitting diode (OLED) device comprising:
an emissive layer comprising a host material and a phosphorescent dopant;
wherein the host material comprises a benzo-fused thiophene and the phosphorescent 0 dopant comprises a heteroleptic transition metal complex having extended conjugation;
a hole blocking layer disposed on the emissive layer, the hole blocking layer comprising a hole blocking material: and
an electron transport layer disposed on the hole blocking layer;
wherein the OLED device has a luminous efficacy of at least about 40 Im/W and voltage 5 below about 4.5 volts at 1 ,000 cd/m2 (nits), and a luminance of at least 18,500 cd/m2 at 40 mA cm2.
15. The device of claim 14, wherein the benzo-fused thiophene comprises a compound of Formula Il ia:
wherein each R1 and R2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen; L is bond or an optionally substituted pheny R4 are independently selected from the group
16. The device of claim 14, wherein the heteroleptic transition metal complex is Compound G1 :
17. The device of claim 14, wherein the electron transport layer comprises a compound of Formula V:
wherein X represents a single chemical bond or phenylene group, and Y represents anthracenyl group or pyrenyl group
18. The device of claim 14, wherein the device has a time for luminance to decrease to 97% of its initial level of about 50 hours at 10,000 cd/m2.
19. An organic light-emitting diode (OLED) device comprising:
an emissive layer comprising a host material and a phosphorescent dopant;
wherein the host material comprises benzo-fused thiophene comprises a compound of
Formula Ilia:
wherein each R1 and R2 are independently selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, arylalkyl, aryl, aralkyl, heteroaryl, and hydrogen; L is bond or an optionally substituted pheny independently selected from the group
consisting of hydrogen and
the phosphorescent dopan :
a hole blocking layer disposed on the emissive layer, the hole blocking layer comprising a hole blocking material; and
an electron transport layer disposed on the hole blocking layer;
wherein the electron transport layer comprises a compound of Formula V:
wherein X represents a single chemical bond or phenylene group, and Y represents anthracenyl group or pyrenyl group
20, The device of claim 19, wherein the host material and hole blocking material are the same.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2014/020899 WO2015134017A1 (en) | 2014-03-05 | 2014-03-05 | Phosphorescent oled devices |
TW104106987A TWI663245B (en) | 2014-03-05 | 2015-03-05 | Phosphorescent oled devices |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2014/020899 WO2015134017A1 (en) | 2014-03-05 | 2014-03-05 | Phosphorescent oled devices |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2015134017A1 true WO2015134017A1 (en) | 2015-09-11 |
Family
ID=50440813
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2014/020899 WO2015134017A1 (en) | 2014-03-05 | 2014-03-05 | Phosphorescent oled devices |
Country Status (2)
Country | Link |
---|---|
TW (1) | TWI663245B (en) |
WO (1) | WO2015134017A1 (en) |
Citations (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4769292A (en) | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
US5703436A (en) | 1994-12-13 | 1997-12-30 | The Trustees Of Princeton University | Transparent contacts for organic devices |
US5707745A (en) | 1994-12-13 | 1998-01-13 | The Trustees Of Princeton University | Multicolor organic light emitting devices |
US5844363A (en) | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
US6013982A (en) | 1996-12-23 | 2000-01-11 | The Trustees Of Princeton University | Multicolor display devices |
US6087196A (en) | 1998-01-30 | 2000-07-11 | The Trustees Of Princeton University | Fabrication of organic semiconductor devices using ink jet printing |
US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
US6294398B1 (en) | 1999-11-23 | 2001-09-25 | The Trustees Of Princeton University | Method for patterning devices |
US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
US6310360B1 (en) | 1999-07-21 | 2001-10-30 | The Trustees Of Princeton University | Intersystem crossing agents for efficient utilization of excitons in organic light emitting devices |
US6337102B1 (en) | 1997-11-17 | 2002-01-08 | The Trustees Of Princeton University | Low pressure vapor phase deposition of organic thin films |
US20020034656A1 (en) | 1998-09-14 | 2002-03-21 | Thompson Mark E. | Organometallic complexes as phosphorescent emitters in organic LEDs |
WO2002074015A2 (en) | 2001-03-14 | 2002-09-19 | The Trustees Of Princeton University | Materials and devices for blue phosphorescence based organic light emitting diodes |
US20020182441A1 (en) | 2000-08-11 | 2002-12-05 | Trustee Of Princeton University | Organometallic compounds and emission-shifting organic electrophosphorescence |
US20030072964A1 (en) | 2001-10-17 | 2003-04-17 | Kwong Raymond C. | Phosphorescent compounds and devices comprising the same |
US20030230980A1 (en) | 2002-06-18 | 2003-12-18 | Forrest Stephen R | Very low voltage, high efficiency phosphorescent oled in a p-i-n structure |
US20040174116A1 (en) | 2001-08-20 | 2004-09-09 | Lu Min-Hao Michael | Transparent electrodes |
US7279704B2 (en) | 2004-05-18 | 2007-10-09 | The University Of Southern California | Complexes with tridentate ligands |
US7431968B1 (en) | 2001-09-04 | 2008-10-07 | The Trustees Of Princeton University | Process and apparatus for organic vapor jet deposition |
WO2009021126A2 (en) | 2007-08-08 | 2009-02-12 | Universal Display Corporation | Benzo-fused thiophene or benzo-fused furan compounds comprising a triphenylene group |
WO2010028151A1 (en) | 2008-09-03 | 2010-03-11 | Universal Display Corporation | Phosphorescent materials |
WO2010111175A1 (en) * | 2009-03-23 | 2010-09-30 | Universal Display Corporation | Heteroleptic iridium complex |
US20110084599A1 (en) | 2007-08-08 | 2011-04-14 | Universal Display Corporation | Single triphenylene chromophores in phosphorescent light emitting diodes |
US7968146B2 (en) | 2006-11-01 | 2011-06-28 | The Trustees Of Princeton University | Hybrid layers for use in coatings on electronic devices or other articles |
EP2468731A1 (en) * | 2009-08-21 | 2012-06-27 | Tosoh Corporation | Cyclic azine derivatives, processes for producing these, and organic electroluminescent element containing these as component |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102095764B1 (en) * | 2012-07-25 | 2020-04-02 | 도레이 카부시키가이샤 | Light emitting element material and light emitting element |
-
2014
- 2014-03-05 WO PCT/US2014/020899 patent/WO2015134017A1/en active Application Filing
-
2015
- 2015-03-05 TW TW104106987A patent/TWI663245B/en active
Patent Citations (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4769292A (en) | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
US5703436A (en) | 1994-12-13 | 1997-12-30 | The Trustees Of Princeton University | Transparent contacts for organic devices |
US5707745A (en) | 1994-12-13 | 1998-01-13 | The Trustees Of Princeton University | Multicolor organic light emitting devices |
US6013982A (en) | 1996-12-23 | 2000-01-11 | The Trustees Of Princeton University | Multicolor display devices |
US5844363A (en) | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
US6337102B1 (en) | 1997-11-17 | 2002-01-08 | The Trustees Of Princeton University | Low pressure vapor phase deposition of organic thin films |
US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
US6087196A (en) | 1998-01-30 | 2000-07-11 | The Trustees Of Princeton University | Fabrication of organic semiconductor devices using ink jet printing |
US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
US20020034656A1 (en) | 1998-09-14 | 2002-03-21 | Thompson Mark E. | Organometallic complexes as phosphorescent emitters in organic LEDs |
US6310360B1 (en) | 1999-07-21 | 2001-10-30 | The Trustees Of Princeton University | Intersystem crossing agents for efficient utilization of excitons in organic light emitting devices |
US6294398B1 (en) | 1999-11-23 | 2001-09-25 | The Trustees Of Princeton University | Method for patterning devices |
US6468819B1 (en) | 1999-11-23 | 2002-10-22 | The Trustees Of Princeton University | Method for patterning organic thin film devices using a die |
US20020182441A1 (en) | 2000-08-11 | 2002-12-05 | Trustee Of Princeton University | Organometallic compounds and emission-shifting organic electrophosphorescence |
WO2002074015A2 (en) | 2001-03-14 | 2002-09-19 | The Trustees Of Princeton University | Materials and devices for blue phosphorescence based organic light emitting diodes |
US20040174116A1 (en) | 2001-08-20 | 2004-09-09 | Lu Min-Hao Michael | Transparent electrodes |
US7431968B1 (en) | 2001-09-04 | 2008-10-07 | The Trustees Of Princeton University | Process and apparatus for organic vapor jet deposition |
US20030072964A1 (en) | 2001-10-17 | 2003-04-17 | Kwong Raymond C. | Phosphorescent compounds and devices comprising the same |
US20030230980A1 (en) | 2002-06-18 | 2003-12-18 | Forrest Stephen R | Very low voltage, high efficiency phosphorescent oled in a p-i-n structure |
US7279704B2 (en) | 2004-05-18 | 2007-10-09 | The University Of Southern California | Complexes with tridentate ligands |
US7968146B2 (en) | 2006-11-01 | 2011-06-28 | The Trustees Of Princeton University | Hybrid layers for use in coatings on electronic devices or other articles |
WO2009021126A2 (en) | 2007-08-08 | 2009-02-12 | Universal Display Corporation | Benzo-fused thiophene or benzo-fused furan compounds comprising a triphenylene group |
US20110084599A1 (en) | 2007-08-08 | 2011-04-14 | Universal Display Corporation | Single triphenylene chromophores in phosphorescent light emitting diodes |
WO2010027583A1 (en) * | 2008-09-03 | 2010-03-11 | Universal Display Corporation | Phosphorescent materials |
WO2010028151A1 (en) | 2008-09-03 | 2010-03-11 | Universal Display Corporation | Phosphorescent materials |
US20110227049A1 (en) | 2008-09-03 | 2011-09-22 | Universal Display Corporation | Phosphorescent materials |
WO2010111175A1 (en) * | 2009-03-23 | 2010-09-30 | Universal Display Corporation | Heteroleptic iridium complex |
EP2468731A1 (en) * | 2009-08-21 | 2012-06-27 | Tosoh Corporation | Cyclic azine derivatives, processes for producing these, and organic electroluminescent element containing these as component |
US20120214993A1 (en) | 2009-08-21 | 2012-08-23 | Sagami Chemical Research Institute, | Cyclic azine derivatives, processes for producing these, and organic electroluminescent element containing these as component |
Non-Patent Citations (3)
Title |
---|
ADACHI ET AL.: "Nearly 100% Internal Phosphorescent Efficiency In An Organic Light Emitting Device", J. APPL. PHYS., vol. 90, 2001, pages 5048 |
BALDO ET AL.: "Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices", NATURE, vol. 395, 1998, pages 151 - 154, XP001002103, DOI: doi:10.1038/25954 |
BALDO ET AL.: "Very high-efficiency green organic light-emitting devices based on electrophosphorescence", APPL. PHYS. LETT., vol. 75, no. 3, 1999, pages 4 - 6, XP012023409, DOI: doi:10.1063/1.124258 |
Also Published As
Publication number | Publication date |
---|---|
TW201602307A (en) | 2016-01-16 |
TWI663245B (en) | 2019-06-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR102118826B1 (en) | Cyclometallated tetradentate pt(ii) complexes comprised of one or two imidazole rings with a twisted aryl group bonded to n-1 | |
JP6574872B2 (en) | Heteroleptic iridium complexes as dopants | |
JP5981603B2 (en) | Heteroleptic iridium complex | |
EP3399005B1 (en) | Phosphorescent materials | |
EP2520571B1 (en) | 2-azatriphenylene materials for organic light emitting diodes | |
EP3064563B1 (en) | Triphenylene hosts in phosphorescent light emitting diodes | |
JP6000966B2 (en) | Phosphorescent substance | |
EP2826775B1 (en) | Organic light emitting diode materials | |
WO2012102967A1 (en) | Aza - dibenzothiophene, aza - dibenzofuran and aza - dibenzoselenophene derivatives for use in oled ' s | |
KR20100061831A (en) | Complexes with tridentate ligands | |
TWI663245B (en) | Phosphorescent oled devices | |
KR20240051905A (en) | Organic electroluminescent materials and devices |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 14715735 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 14715735 Country of ref document: EP Kind code of ref document: A1 |