WO2021034017A1 - Nouveau composé et dispositif électroluminescent organique l'utilisant - Google Patents
Nouveau composé et dispositif électroluminescent organique l'utilisant Download PDFInfo
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- WO2021034017A1 WO2021034017A1 PCT/KR2020/010789 KR2020010789W WO2021034017A1 WO 2021034017 A1 WO2021034017 A1 WO 2021034017A1 KR 2020010789 W KR2020010789 W KR 2020010789W WO 2021034017 A1 WO2021034017 A1 WO 2021034017A1
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- DHXHNTQWDWPCJM-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c2nc([o]c3c4cccc3)c4nc2-[n](c2ccccc2c2c3)c2cc2c3[n]3-c(cccc4)c4-c(cccc4)c4-c4c3c2ccc4)c2)c2c2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c2nc([o]c3c4cccc3)c4nc2-[n](c2ccccc2c2c3)c2cc2c3[n]3-c(cccc4)c4-c(cccc4)c4-c4c3c2ccc4)c2)c2c2c1cccc2 DHXHNTQWDWPCJM-UHFFFAOYSA-N 0.000 description 1
- RXVWRVUXJHRUBU-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c2nc3ccccc3nc2-[n]2c(cc(c3cccc-4c3[n]3-c(cccc5)c5-c5c-4cccc5)c3c3)c3c3ccccc23)c2)c2c2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c2nc3ccccc3nc2-[n]2c(cc(c3cccc-4c3[n]3-c(cccc5)c5-c5c-4cccc5)c3c3)c3c3ccccc23)c2)c2c2c1cccc2 RXVWRVUXJHRUBU-UHFFFAOYSA-N 0.000 description 1
- PYEYBVHEEMZKIP-UHFFFAOYSA-N c(cc1)ccc1-[n]1c2cc(-c3c(c(cccc4)c4[s]4)c4nc(-[n]4c5cc(c6ccccc66)c7[n]6-c(cccc6)c6-c6ccccc6-c7c5c5ccccc45)n3)ccc2c2ccccc12 Chemical compound c(cc1)ccc1-[n]1c2cc(-c3c(c(cccc4)c4[s]4)c4nc(-[n]4c5cc(c6ccccc66)c7[n]6-c(cccc6)c6-c6ccccc6-c7c5c5ccccc45)n3)ccc2c2ccccc12 PYEYBVHEEMZKIP-UHFFFAOYSA-N 0.000 description 1
- NECGOIARMWEUPP-UHFFFAOYSA-N c(cc1)ccc1-[n]1c2cc(-c3c4[s]c(cccc5)c5c4nc(-[n]4c5cc(c6c7cccc6)c6[n]7-c(cccc7)c7-c(cccc7)c7-c6c5c5ccccc45)n3)ccc2c2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c2cc(-c3c4[s]c(cccc5)c5c4nc(-[n]4c5cc(c6c7cccc6)c6[n]7-c(cccc7)c7-c(cccc7)c7-c6c5c5ccccc45)n3)ccc2c2c1cccc2 NECGOIARMWEUPP-UHFFFAOYSA-N 0.000 description 1
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- WHIQEBNNHBVFIG-UHFFFAOYSA-N c(cc1)ccc1-[n]1c2cccc(-c3c(-[n]4c5cc(c6ccccc66)c7[n]6-c(cccc6)c6-c6ccccc6-c7c5c5ccccc45)nc(cccc4)c4n3)c2c2ccccc12 Chemical compound c(cc1)ccc1-[n]1c2cccc(-c3c(-[n]4c5cc(c6ccccc66)c7[n]6-c(cccc6)c6-c6ccccc6-c7c5c5ccccc45)nc(cccc4)c4n3)c2c2ccccc12 WHIQEBNNHBVFIG-UHFFFAOYSA-N 0.000 description 1
- NJPVXLLKXLESLD-UHFFFAOYSA-N c(cc1)ccc1-[n]1c2cccc(-c3c(-[n]4c5cc(c6ccccc66)c7[n]6-c6ccccc6-c6ccccc6-c7c5c5ccccc45)nc(ccc4c5cccc4)c5n3)c2c2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c2cccc(-c3c(-[n]4c5cc(c6ccccc66)c7[n]6-c6ccccc6-c6ccccc6-c7c5c5ccccc45)nc(ccc4c5cccc4)c5n3)c2c2c1cccc2 NJPVXLLKXLESLD-UHFFFAOYSA-N 0.000 description 1
- WHJZYXCKYWKYPG-UHFFFAOYSA-N c(cc1)ccc1-[n]1c2cccc(-c3c(c4ccccc4[o]4)c4nc(-[n](c(cccc4)c4c4c5)c4cc4c5[n]5-c6ccccc6-c(cccc6)c6-c6c5c4ccc6)n3)c2c2ccccc12 Chemical compound c(cc1)ccc1-[n]1c2cccc(-c3c(c4ccccc4[o]4)c4nc(-[n](c(cccc4)c4c4c5)c4cc4c5[n]5-c6ccccc6-c(cccc6)c6-c6c5c4ccc6)n3)c2c2ccccc12 WHJZYXCKYWKYPG-UHFFFAOYSA-N 0.000 description 1
- LIYZHKFHCYLGIR-UHFFFAOYSA-N c(cc1)ccc1-[n]1c2cccc(-c3nc(-[n](c4ccccc44)c(cc5c6c7cccc6)c4c-4c5[n]7-c(cccc5)c5-c5c-4cccc5)nc4c3c3ccccc3[o]4)c2c2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c2cccc(-c3nc(-[n](c4ccccc44)c(cc5c6c7cccc6)c4c-4c5[n]7-c(cccc5)c5-c5c-4cccc5)nc4c3c3ccccc3[o]4)c2c2c1cccc2 LIYZHKFHCYLGIR-UHFFFAOYSA-N 0.000 description 1
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- DULVVJPEVPEIAA-UHFFFAOYSA-N c(cc1)ccc1-[n]1c2cccc(-c3nc(-c4cc(cccc5)c5cc4)nc(-[n](c4ccccc4c4c5)c4cc4c5[n]5-c(cccc6)c6-c(cccc6)c6-c6c5c4cc(-c4cccc(-[n]5c(ccc(-c7nc(-[n](c(cccc8)c8c8c9)c8cc8c9[n]9-c%10ccccc%10-c(cccc%10)c%10-c%10c9c8ccc%10)nc(-c8cc(cccc9)c9cc8)n7)c7)c7c7c5cccc7)c4)c6)n3)c2c2ccccc12 Chemical compound c(cc1)ccc1-[n]1c2cccc(-c3nc(-c4cc(cccc5)c5cc4)nc(-[n](c4ccccc4c4c5)c4cc4c5[n]5-c(cccc6)c6-c(cccc6)c6-c6c5c4cc(-c4cccc(-[n]5c(ccc(-c7nc(-[n](c(cccc8)c8c8c9)c8cc8c9[n]9-c%10ccccc%10-c(cccc%10)c%10-c%10c9c8ccc%10)nc(-c8cc(cccc9)c9cc8)n7)c7)c7c7c5cccc7)c4)c6)n3)c2c2ccccc12 DULVVJPEVPEIAA-UHFFFAOYSA-N 0.000 description 1
- BAULMFRFLHSBIP-UHFFFAOYSA-N c(cc1)ccc1-c(c1c2cccc1)ccc2-c1c(c(cccc2)c2[o]2)c2nc(-[n](c2ccccc2c2c3)c2cc2c3[n]3-c4ccccc4-c4ccccc4-c4c3c2ccc4)n1 Chemical compound c(cc1)ccc1-c(c1c2cccc1)ccc2-c1c(c(cccc2)c2[o]2)c2nc(-[n](c2ccccc2c2c3)c2cc2c3[n]3-c4ccccc4-c4ccccc4-c4c3c2ccc4)n1 BAULMFRFLHSBIP-UHFFFAOYSA-N 0.000 description 1
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- JIWOIBGEIRRULL-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c1c(c2ccccc2[s]2)c2nc(-[n]2c3cc(c4ccccc44)c5[n]4-c(cccc4)c4-c4ccccc4-c5c3c3ccccc23)n1 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c1c(c2ccccc2[s]2)c2nc(-[n]2c3cc(c4ccccc44)c5[n]4-c(cccc4)c4-c4ccccc4-c5c3c3ccccc23)n1 JIWOIBGEIRRULL-UHFFFAOYSA-N 0.000 description 1
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- ORZLEWGFJUXRLI-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c1nc(-[n](c2ccccc22)c(cc3c4c5cccc4)c2c-2c3[n]5-c(cccc3)c3-c3c-2cccc3)nc2ccc(cccc3)c3c12 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c1nc(-[n](c2ccccc22)c(cc3c4c5cccc4)c2c-2c3[n]5-c(cccc3)c3-c3c-2cccc3)nc2ccc(cccc3)c3c12 ORZLEWGFJUXRLI-UHFFFAOYSA-N 0.000 description 1
- UBFIVTIHCVERSC-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c1nc(-[n](c2ccccc2c2c3)c2cc2c3[n]3-c(cccc4)c4-c(ccc(-c4ccc(c(c([n]5-c6nc(-c7ccc(c8ccccc8[n]8-c9ccccc9)c8c7)nc(-c(cc7)ccc7-c7ccccc7)n6)c6)cc7c6c6cccc-8c6[n]7-c6ccccc6-c6c-8cccc6)c5c4)c4)c4-c4c3c2ccc4)nc(-c(cc2c3ccccc33)ccc2[n]3-c2ccccc2)n1 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c1nc(-[n](c2ccccc2c2c3)c2cc2c3[n]3-c(cccc4)c4-c(ccc(-c4ccc(c(c([n]5-c6nc(-c7ccc(c8ccccc8[n]8-c9ccccc9)c8c7)nc(-c(cc7)ccc7-c7ccccc7)n6)c6)cc7c6c6cccc-8c6[n]7-c6ccccc6-c6c-8cccc6)c5c4)c4)c4-c4c3c2ccc4)nc(-c(cc2c3ccccc33)ccc2[n]3-c2ccccc2)n1 UBFIVTIHCVERSC-UHFFFAOYSA-N 0.000 description 1
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- AZKXFSYVLIPGJS-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c1nc(-c2cc(-[n]3c4cc(c5c6cccc5)c5[n]6-c(cccc6)c6-c(cccc6)c6-c5c4c4ccccc34)cc3ccccc23)nc(-c(cc2)ccc2-c2ccccc2)n1 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c1nc(-c2cc(-[n]3c4cc(c5c6cccc5)c5[n]6-c(cccc6)c6-c(cccc6)c6-c5c4c4ccccc34)cc3ccccc23)nc(-c(cc2)ccc2-c2ccccc2)n1 AZKXFSYVLIPGJS-UHFFFAOYSA-N 0.000 description 1
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- AVATUZVQWIKTJI-UHFFFAOYSA-N c(cc1)ccc1-c(cccc1)c1-c1nc(-[n](c(cccc2)c2c2c3)c2cc2c3[n]3-c(cccc4)c4-c(ccc(-c(cc4)cc(-c5ccccc5)c4-c4nc([s]c5c6cccc5)c6nc4-[n](c(cccc4)c4c4c5)c4cc4c5[n]5-c(cccc6)c6-c(cccc6)c6-c6c5c4ccc6)c4)c4-c4c3c2ccc4)nc2c1[s]c1c2cccc1 Chemical compound c(cc1)ccc1-c(cccc1)c1-c1nc(-[n](c(cccc2)c2c2c3)c2cc2c3[n]3-c(cccc4)c4-c(ccc(-c(cc4)cc(-c5ccccc5)c4-c4nc([s]c5c6cccc5)c6nc4-[n](c(cccc4)c4c4c5)c4cc4c5[n]5-c(cccc6)c6-c(cccc6)c6-c6c5c4ccc6)c4)c4-c4c3c2ccc4)nc2c1[s]c1c2cccc1 AVATUZVQWIKTJI-UHFFFAOYSA-N 0.000 description 1
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- XNUVVHVFAAQPQY-UHFFFAOYSA-L manganese(2+) quinolin-8-olate Chemical compound N1=CC=CC2=CC=CC(=C12)[O-].[Mn+2].N1=CC=CC2=CC=CC(=C12)[O-] XNUVVHVFAAQPQY-UHFFFAOYSA-L 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GVOISEJVFFIGQE-YCZSINBZSA-N n-[(1r,2s,5r)-5-[methyl(propan-2-yl)amino]-2-[(3s)-2-oxo-3-[[6-(trifluoromethyl)quinazolin-4-yl]amino]pyrrolidin-1-yl]cyclohexyl]acetamide Chemical compound CC(=O)N[C@@H]1C[C@H](N(C)C(C)C)CC[C@@H]1N1C(=O)[C@@H](NC=2C3=CC(=CC=C3N=CN=2)C(F)(F)F)CC1 GVOISEJVFFIGQE-YCZSINBZSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 239000007773 negative electrode material Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 150000002964 pentacenes Chemical class 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 150000002987 phenanthrenes Chemical class 0.000 description 1
- 150000005041 phenanthrolines Chemical class 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- XPPWLXNXHSNMKC-UHFFFAOYSA-N phenylboron Chemical group [B]C1=CC=CC=C1 XPPWLXNXHSNMKC-UHFFFAOYSA-N 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002098 polyfluorene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 239000007774 positive electrode material Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 150000003220 pyrenes Chemical class 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- JYRWUSXRTGACLY-UHFFFAOYSA-N tert-butyl 4-[[3-(4-methylsulfonylphenyl)-[1,2]oxazolo[4,5-d]pyrimidin-7-yl]oxy]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1OC1=NC=NC2=C1ON=C2C1=CC=C(S(C)(=O)=O)C=C1 JYRWUSXRTGACLY-UHFFFAOYSA-N 0.000 description 1
- JLBRGNFGBDNNSF-UHFFFAOYSA-N tert-butyl(dimethyl)borane Chemical group CB(C)C(C)(C)C JLBRGNFGBDNNSF-UHFFFAOYSA-N 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 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 1
- KWQNQSDKCINQQP-UHFFFAOYSA-K tri(quinolin-8-yloxy)gallane Chemical compound C1=CN=C2C(O[Ga](OC=3C4=NC=CC=C4C=CC=3)OC=3C4=NC=CC=C4C=CC=3)=CC=CC2=C1 KWQNQSDKCINQQP-UHFFFAOYSA-K 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical group CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 1
- WXRGABKACDFXMG-UHFFFAOYSA-N trimethylborane Chemical group CB(C)C WXRGABKACDFXMG-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- MXSVLWZRHLXFKH-UHFFFAOYSA-N triphenylborane Chemical group C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 MXSVLWZRHLXFKH-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- JQSHBVHOMNKWFT-DTORHVGOSA-N varenicline Chemical compound C12=CC3=NC=CN=C3C=C2[C@H]2C[C@@H]1CNC2 JQSHBVHOMNKWFT-DTORHVGOSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
- HTPBWAPZAJWXKY-UHFFFAOYSA-L zinc;quinolin-8-olate Chemical compound [Zn+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 HTPBWAPZAJWXKY-UHFFFAOYSA-L 0.000 description 1
Images
Classifications
-
- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/16—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
- the present invention relates to a novel compound and an organic light emitting device using the same.
- the organic light emission phenomenon refers to a phenomenon in which electrical energy is converted into light energy using an organic material.
- An organic light-emitting device using the organic light-emitting phenomenon has a wide viewing angle, excellent contrast, and fast response time, and has excellent luminance, driving voltage, and response speed characteristics, and thus many studies are being conducted.
- the organic light emitting device generally has a structure including an anode and a cathode, and an organic material layer between the anode and the cathode.
- the organic material layer is often made of a multi-layered structure composed of different materials in order to increase the efficiency and stability of the organic light emitting device.For example, it may be formed of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer, and the like.
- a voltage is applied between the two electrodes
- holes are injected from the anode and electrons from the cathode are injected into the organic material layer, and excitons are formed when the injected holes and electrons meet. It glows when it falls back to the ground.
- Patent Document 0001 Korean Patent Publication No. 10-2013-073537
- the present invention relates to a novel compound and an organic light emitting device comprising the same.
- the present invention provides a compound represented by the following formula 1:
- R is linked at position 1 or 2 to form a single bond
- L is a single bond, or a substituted or unsubstituted C 6-60 arylene
- Het is a substituted or unsubstituted C 5-60 heteroaryl containing any one or more hetero atoms selected from the group consisting of N, O and S,
- R 1 , R 2 , R 3 , R 4 and R 5 are each independently hydrogen, deuterium, or substituted or unsubstituted C 1-60 alkyl,
- n1, n3, n4 and n5 are each independently an integer of 0 to 4,
- n2 is an integer from 0 to 2.
- the present invention is a first electrode; A second electrode provided to face the first electrode; And one or more organic material layers provided between the first electrode and the second electrode, wherein at least one of the organic material layers comprises the compound of the present invention.
- the compound represented by Chemical Formula 1 may be used as a material for an organic material layer of an organic light-emitting device, and may improve efficiency, low driving voltage, and/or lifetime characteristics in the organic light-emitting device.
- the compound represented by Formula 1 described above may be used as a host material for the emission layer.
- FIG. 1 shows an example of an organic light-emitting device comprising a substrate 1, an anode 2, a hole transport layer 3, a light-emitting layer 4, an electron injection and transport layer 5, and a cathode 6.
- FIG. 2 shows a substrate 1, an anode 2, a hole injection layer 7, a hole transport layer 3, an electron suppression layer 8, a light emitting layer 4, a hole suppression layer 9, an electron injection and transport layer ( 5) and a cathode 6 is shown as an example of an organic light-emitting device.
- substituted or unsubstituted refers to deuterium (D); Halogen group; Nitrile group; Nitro group; Hydroxy group; Carbonyl group; Ester group; Imide group; Amino group; Phosphine oxide group; Alkoxy group; Aryloxy group; Alkyl thioxy group; Arylthioxy group; Alkyl sulfoxy group; Arylsulfoxy group; Silyl group; Boron group; Alkyl group; Cycloalkyl group; Alkenyl group; Aryl group; Aralkyl group; Aralkenyl group; Alkylaryl group; Alkylamine group; Aralkylamine group; Heteroarylamine group; Arylamine group; Arylphosphine group; Or it means a substituted or unsubstituted substituted or unsubstituted with one or more substituents selected from the group consisting of a heterocyclic group containing one or more of N, O and S atoms,
- a substituent to which two or more substituents are connected may be a biphenyl group. That is, the biphenyl group may be an aryl group or may be interpreted as a substituent to which two phenyl groups are connected.
- the number of carbon atoms of the carbonyl group is not particularly limited, but it is preferably 1 to 40 carbon atoms. Specifically, it may be a compound having the following structure, but is not limited thereto.
- the ester group may be substituted with an oxygen of the ester group with a straight chain, branched or cyclic alkyl group having 1 to 25 carbon atoms or an aryl group having 6 to 25 carbon atoms.
- it may be a compound of the following structural formula, but is not limited thereto.
- the number of carbon atoms of the imide group is not particularly limited, but it is preferably 1 to 25 carbon atoms. Specifically, it may be a compound having the following structure, but is not limited thereto.
- the silyl group is specifically trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, triphenylsilyl group, diphenylsilyl group, phenylsilyl group, etc. However, it is not limited thereto.
- the boron group specifically includes a trimethyl boron group, a triethyl boron group, a t-butyldimethyl boron group, a triphenyl boron group, and a phenyl boron group, but is not limited thereto.
- examples of the halogen group include fluorine, chlorine, bromine or iodine.
- the alkyl group may be a linear or branched chain, and the number of carbon atoms is not particularly limited, but is preferably 1 to 40. According to an exemplary embodiment, the alkyl group has 1 to 20 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 10 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 6 carbon atoms.
- alkyl group examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n -Pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl , n-heptyl, 1-methylhexyl, cyclopentylmethyl, cycloheptylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhex
- the alkenyl group may be a linear or branched chain, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. According to an exemplary embodiment, the alkenyl group has 2 to 20 carbon atoms. According to another exemplary embodiment, the alkenyl group has 2 to 10 carbon atoms. According to another exemplary embodiment, the alkenyl group has 2 to 6 carbon atoms.
- Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1- Butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2-( Naphthyl-1-yl)vinyl-1-yl, 2,2-bis(diphenyl-1-yl)vinyl-1-yl, stilbenyl group, styrenyl group, and the like, but are not limited thereto.
- the cycloalkyl group is not particularly limited, but is preferably 3 to 60 carbon atoms, and according to an exemplary embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 20 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 6 carbon atoms.
- the aryl group is not particularly limited, but is preferably 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to an exemplary embodiment, the aryl group has 6 to 30 carbon atoms. According to an exemplary embodiment, the aryl group has 6 to 20 carbon atoms.
- the aryl group may be a phenyl group, a biphenyl group, or a terphenyl group, but the monocyclic aryl group is not limited thereto.
- the polycyclic aryl group may be a naphthyl group, an anthracenyl group, a phenanthryl group, a pyrenyl group, a perylenyl group, a chrysenyl group, a fluorenyl group, and the like, but is not limited thereto.
- the fluorenyl group may be substituted, and two substituents may be bonded to each other to form a spiro structure.
- Etc When the fluorenyl group is substituted, Etc.
- Etc it is not limited thereto.
- the heterocyclic group is a heterocyclic group including at least one of O, N, Si and S as a heterogeneous element, and the number of carbons is not particularly limited, but it is preferably 2 to 60 carbon atoms.
- the heterocyclic group include thiophene group, furan group, pyrrole group, imidazole group, thiazole group, oxazole group, oxadiazole group, triazole group, pyridyl group, bipyridyl group, pyrimidyl group, triazine group, acridyl group , Pyridazine group, pyrazinyl group, quinolinyl group, quinazoline group, quinoxalinyl group, phthalazinyl group, pyrido pyrimidinyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group, isoquinoline group, indole group , Car
- the aryl group among the aralkyl group, aralkenyl group, alkylaryl group, and arylamine group is the same as the example of the aryl group described above.
- the alkyl group among the aralkyl group, the alkylaryl group and the alkylamine group is the same as the example of the aforementioned alkyl group.
- the description of the aforementioned heterocyclic group may be applied.
- the alkenyl group of the aralkenyl group is the same as the example of the alkenyl group described above.
- the description of the aryl group described above may be applied except that the arylene is a divalent group.
- the description of the aforementioned heterocyclic group may be applied except that the heteroarylene is a divalent group.
- the hydrocarbon ring is not a monovalent group, and the description of the aryl group or the cycloalkyl group described above may be applied except that the hydrocarbon ring is formed by bonding of two substituents.
- the heterocycle is not a monovalent group, and the description of the above-described heterocyclic group may be applied, except that two substituents are bonded to each other.
- the present invention provides a compound represented by Chemical Formula 1.
- the compound represented by Formula 1 has an indolocarbazole core structure, forms a seven-membered ring in which two benzene rings are further condensed around one nitrogen atom of the core structure, and is added to the other nitrogen atom. Characterized in that it contains a heteroaryl group.
- the condensed ring structure has high stability against electrons and holes, and when applied as a host compound, energy transfer to the dopant is easy. Accordingly, when employed as an emission layer compound in an organic light emitting device, characteristics of a low driving voltage, high efficiency, and long life can all be improved.
- the compound represented by Formula 1 is specifically as follows:
- R is connected at the 1st or 2nd position to form a single bond, thereby forming a 7-membered ring around the N atom,
- L is a single bond or a substituted or unsubstituted C 6-60 arylene
- Het is a substituted or unsubstituted C 5-60 heteroaryl containing any one or more hetero atoms selected from the group consisting of N, O and S,
- R 1 , R 2 , R 3 , R 4 and R 5 are each independently hydrogen, deuterium, or substituted or unsubstituted C 1-60 alkyl,
- n1, n3, n4 and n5 are each independently an integer of 0 to 4,
- n2 is an integer from 0 to 2.
- R is connected at the 1st or 2nd position to form a seven-membered ring, in which case the compound represented by Formula 1 is represented by the following Formula 1-1 or 1-2:
- n'2 is 0 or 1
- n'3 is an integer from 0 to 3
- L is a single bond, phenylene, or naphthylene.
- Het is any one selected from the group consisting of:
- Each R′ is independently a substituted or unsubstituted C 6-60 aryl, or a C 5-60 heteroaryl comprising at least one hetero atom selected from the group consisting of substituted or unsubstituted N, O and S. .
- R' is each independently, phenyl, biphenylyl, naphthyl, terphenylyl, phenylnaphthyl, naphthylphenyl, phenanthrenyl, triphenylenyl, dimethylfluorenyl, dibenzofuranyl, Dibenzothiophenyl, carbazol-9-yl or 9-phenyl-9H-carbazolyl.
- R 1 , R 2 , R 3 , R 4 and R 5 are each independently hydrogen or deuterium, more preferably all of them are hydrogen.
- the compound represented by Formula 1 may be any one selected from the group consisting of:
- each of X is independently halogen, preferably bromo or chloro, and the definition of other substituents is as described above.
- the compound represented by Formula 1 may be prepared through a reaction of introducing an additional hetero substituent to the core structures of Core 1-1 and Core 1-2, and a specific example may be prepared through Reaction Scheme 1-3.
- the reactor for the reaction may be appropriately changed, and the method for preparing the compound represented by Formula 1 may be more specific in Preparation Examples to be described later.
- the present invention provides an organic light-emitting device including the compound represented by Formula 1 above.
- the present invention provides a first electrode; A second electrode provided to face the first electrode; And one or more organic material layers provided between the first electrode and the second electrode, wherein at least one of the organic material layers includes a compound represented by Formula 1 .
- the organic material layer of the organic light emitting device of the present invention may have a single-layer structure, but may have a multilayer structure in which two or more organic material layers are stacked.
- the organic light emitting device of the present invention may have a structure including a hole injection layer, a hole transport layer, an electron suppression layer, a light emitting layer, a hole suppression layer, an electron transport layer, an electron injection layer, and the like as an organic material layer.
- the structure of the organic light emitting device is not limited thereto and may include a smaller number of organic layers.
- the organic material layer may include a hole injection layer, a hole transport layer, or a layer that simultaneously injects and transports holes, and the hole injection layer, a hole transport layer, or a layer that simultaneously injects and transports holes is represented by Formula 1 above. Including the indicated compound.
- the organic material layer may include an emission layer, and the emission layer includes the compound represented by Chemical Formula 1.
- the compound represented by Formula 1 is used as a host compound of the emission layer.
- the organic material layer of the organic light emitting device of the present invention may have a single-layer structure, but may have a multilayer structure in which two or more organic material layers are stacked.
- the organic light emitting device of the present invention further includes a hole injection layer and a hole transport layer between the first electrode and the emission layer, and an electron transport layer and an electron injection layer between the emission layer and the second electrode in addition to the emission layer as an organic material layer. It can have a structure to However, the structure of the organic light-emitting device is not limited thereto, and may include a smaller number or a larger number of organic layers.
- the first electrode is an anode and the second electrode is a cathode, and an anode, one or more organic material layers, and a cathode are sequentially stacked on a substrate (normal type). It can be a device.
- the first electrode is a cathode and the second electrode is an anode, and a cathode, one or more organic material layers, and an anode are sequentially stacked on a substrate. It may be a light emitting device.
- FIGS. 1 and 2 the structure of an organic light-emitting device according to an embodiment of the present invention is illustrated in FIGS. 1 and 2.
- the compound represented by Formula 1 may be included in the emission layer.
- the compound represented by Formula 1 may be included in the emission layer.
- the organic light-emitting device according to the present invention may be manufactured by materials and methods known in the art, except that at least one of the organic material layers includes the compound represented by Chemical Formula 1.
- the organic material layers may be formed of the same material or different materials.
- the organic light emitting device may be manufactured by sequentially stacking a first electrode, an organic material layer, and a second electrode on a substrate.
- a PVD (physical vapor deposition) method such as sputtering or e-beam evaporation
- the anode is formed by depositing a metal or a conductive metal oxide or an alloy thereof on the substrate.
- an organic material layer including a hole injection layer, a hole transport layer, an electron suppression layer, an emission layer, a hole suppression layer and an electron transport layer is formed thereon, and then a material that can be used as a cathode may be deposited thereon.
- an organic light-emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.
- the compound represented by Formula 1 may be formed as an organic material layer by a solution coating method as well as a vacuum deposition method when manufacturing an organic light emitting device.
- the solution coating method refers to spin coating, dip coating, doctor blading, inkjet printing, screen printing, spray method, roll coating, and the like, but is not limited thereto.
- an organic light-emitting device may be manufactured by sequentially depositing an organic material layer and an anode material from a cathode material on a substrate (WO 2003/012890).
- the manufacturing method is not limited thereto.
- the first electrode is an anode
- the second electrode is a cathode
- the first electrode is a cathode
- the second electrode is an anode
- the cathode material a material having a large work function is preferable so that holes can be smoothly injected into the organic material layer.
- the cathode material include metals such as vanadium, chromium, copper, zinc, and gold, or alloys thereof; Metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); Combinations of metals and oxides such as ZnO:Al or SnO 2 :Sb; Poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), conductive polymers such as polypyrrole and polyaniline, and the like, but are not limited thereto.
- the cathode material is a material having a small work function to facilitate electron injection into the organic material layer.
- the negative electrode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, and lead, or alloys thereof; There are multi-layered materials such as LiF/Al or LiO 2 /Al, but are not limited thereto.
- the hole injection layer is a layer that injects holes from an electrode, and has the ability to transport holes as a hole injection material, so that it has a hole injection effect at the anode, an excellent hole injection effect for a light emitting layer or a light emitting material.
- a compound that prevents the movement of excitons to the electron injection layer or the electron injection material and has excellent ability to form a thin film is preferable.
- the HOMO (highest occupied molecular orbital) of the hole injection material is between the work function of the positive electrode material and the HOMO of the surrounding organic material layer.
- hole injection materials include metal porphyrin, oligothiophene, arylamine-based organic substances, hexanitrile hexaazatriphenylene-based organic substances, quinacridone-based organic substances, and perylene-based organic substances.
- the hole transport layer is a layer that receives holes from the hole injection layer and transports holes to the emission layer
- the hole transport material is a material capable of transporting holes from the anode or the hole injection layer to the emission layer, and has high mobility for holes.
- the material is suitable.
- the hole transport material the compound represented by Formula 1 may be used, or an arylamine-based organic material, a conductive polymer, and a block copolymer having a conjugated portion and a non-conjugated portion may be used, but the present invention is not limited thereto. .
- the electron inhibiting layer (or electron blocking layer, electron blocking layer) is formed on the hole transport layer, and is preferably provided in contact with the light emitting layer to control hole mobility and prevent excessive movement of electrons, thereby preventing the hole-electron It refers to a layer that serves to improve the efficiency of an organic light emitting device by increasing the probability of coupling.
- the electron inhibiting layer includes an electron blocking material, and an arylamine-based organic material may be used as an example of the electron blocking material, but is not limited thereto.
- the light-emitting material of the light-emitting layer a material capable of emitting light in the visible region by transporting and combining holes and electrons from the hole transport layer and the electron transport layer, respectively, and a material having good quantum efficiency for fluorescence or phosphorescence is preferable.
- 8-hydroxy-quinoline aluminum complex Alq 3
- Carbazole-based compounds Dimerized styryl compounds
- BAlq 10-hydroxybenzo quinoline-metal compound
- Benzoxazole, benzthiazole, and benzimidazole-based compounds Poly(p-phenylenevinylene) (PPV)-based polymer
- Spiro compounds Polyfluorene, rubrene, and the like, but are not limited thereto.
- the light emitting layer includes a host material and a dopant material, and a compound represented by Formula 1 herein is used as a host material.
- condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds
- heterocycle-containing compounds include carbazole derivatives, dibenzofuran derivatives, ladder type Furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.
- Dopant materials include aromatic amine derivatives, strylamine compounds, boron complexes, fluoranthene compounds, and metal complexes.
- the aromatic amine derivative is a condensed aromatic ring derivative having a substituted or unsubstituted arylamino group, and includes pyrene, anthracene, chrysene, and periflanthene having an arylamino group
- the styrylamine compound is substituted or unsubstituted
- the aromatic amine derivative is a condensed aromatic ring derivative having a substituted or unsubstituted arylamino group, and includes pyrene, anthracene, chrysene, and periflanthene having an arylamino group
- the styrylamine compound is substituted or unsubstituted
- at least one arylvinyl group is substituted on the arylamine, one or two or more substituents selected from the group consisting
- the metal complex includes an iridium complex, a platinum complex, and the like, but is not limited thereto.
- the light emitting layer may include the following iridium complex compound as a dopant material, but is not limited thereto.
- the hole inhibiting layer (or hole blocking layer, hole blocking layer) is formed on the light emitting layer, and is preferably provided in contact with the light emitting layer, to control electron mobility and prevent excessive movement of holes, thereby increasing the probability of hole-electron bonding. It refers to a layer that serves to improve the efficiency of an organic light-emitting device by increasing it.
- the hole-suppressing layer includes a hole-suppressing material, and examples of such a hole-blocking material include a subazine derivative including triazine; Triazole derivatives; Oxadiazole derivatives; Phenanthroline derivatives; A compound into which an electron withdrawing group such as a phosphine oxide derivative has been introduced may be used, but is not limited thereto.
- the electron injection and transport layer is a layer that simultaneously serves as an electron transport layer and an electron injection layer for injecting electrons from an electrode and transporting received electrons to the emission layer, and is formed on the emission layer or the hole suppression layer.
- an electron injection and transport material a material capable of receiving electrons from the cathode and transferring them to the light emitting layer is suitable, and a material having high mobility for electrons is suitable.
- specific electron injection and transport materials include Al complex of 8-hydroxyquinoline; Complexes containing Alq 3; Organic radical compounds; Hydroxyflavone-metal complex; Triazine derivatives and the like, but are not limited thereto.
- fluorenone anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, fluorenylidene methane, anthrone, and their derivatives, metal complex compounds , Or a nitrogen-containing 5-membered cyclic derivative, but may be used, but is not limited thereto.
- the electron injection and transport layer may be formed as separate layers such as an electron injection layer and an electron transport layer.
- the electron transport layer is formed on the emission layer or the hole suppression layer, and the electron injection and transport material described above may be used as the electron transport material included in the electron transport layer.
- the electron injection layer is formed on the electron transport layer, and electron injection materials included in the electron injection layer include LiF, NaCl, CsF, Li 2 O, BaO, fluorenone, anthraquinodimethane, diphenoquinone, Thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, fluorenylidene methane, anthrone, and the like, their derivatives, metal complex compounds, and nitrogen-containing 5-membered ring derivatives may be used.
- electron injection materials included in the electron injection layer include LiF, NaCl, CsF, Li 2 O, BaO, fluorenone, anthraquinodimethane, diphenoquinone, Thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, fluorenylidene methane, anthrone
- the metal complex compound examples include lithium 8-hydroxyquinolinato, bis(8-hydroxyquinolinato)zinc, bis(8-hydroxyquinolinato)copper, bis(8-hydroxyquinolinato)manganese, Tris(8-hydroxyquinolinato)aluminum, tris(2-methyl-8-hydroxyquinolinato)aluminum, tris(8-hydroxyquinolinato)gallium, bis(10-hydroxybenzo[h] Quinolinato)beryllium, bis(10-hydroxybenzo[h]quinolinato)zinc, bis(2-methyl-8-quinolinato)chlorogallium, bis(2-methyl-8-quinolinato)( o-cresolato)gallium, bis(2-methyl-8-quinolinato)(1-naphtholato)aluminum, bis(2-methyl-8-quinolinato)(2-naphtholato)gallium, etc. It is not limited thereto.
- the organic light emitting device may be a top emission type, a bottom emission type, or a double-sided emission type depending on the material used.
- the compound represented by Formula 1 may be included in an organic solar cell or an organic transistor in addition to the organic light emitting device.
- intermediate compound 1a (10 g, 37.4 mmol), compound 1-1 (15.2 g, 37.4 mmol), and NaOtBu (7.2 g, 74.7 mmol) were added to xylene (200 mL), followed by stirring and refluxing. After this, bis (tri-tert-butylphosphine) palladium (0) (0.4 g, 0.7 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 1 (7.4 g).
- intermediate compound 2a (10 g, 23.8 mmol), compound 1-1 (9.7 g, 23.8 mmol), and NaOtBu (4.6 g, 47.6 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.2 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 2 (11.3 g).
- intermediate compound 3a (10 g, 24.6 mmol), compound 1-1 (10 g, 24.6 mmol), and NaOtBu (4.7 g, 49.3 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 3 (8 g).
- intermediate compound 4a (10 g, 28.8 mmol), compound 1-1 (11.7 g, 28.8 mmol), and NaOtBu (5.5 g, 57.7 mmol) were added to xylene (200 mL), followed by stirring and refluxing. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.6 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 4 (9.5 g).
- intermediate compound 5a (10 g, 25.6 mmol), compound 1-1 (10.4 g, 25.6 mmol), and NaOtBu (4.9 g, 51.2 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 5 (8 g).
- intermediate compound 6a (10 g, 26.3 mmol), compound 1-1 (10.7 g, 26.3 mmol), and NaOtBu (5.1 g, 52.7 mmol) were added to xylene (200 mL), followed by stirring and refluxing. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 6 (8.5 g).
- intermediate compound 7a (10 g, 26.3 mmol), compound 1-1 (10.7 g, 26.3 mmol), and NaOtBu (5 g, 52.5 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 7 (5.9 g).
- intermediate compound 8a (10 g, 23.6 mmol), compound 1-1 (9.6 g, 23.6 mmol), and NaOtBu (4.5 g, 47.3 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.2 g, 0.5 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 8 (6.6 g).
- intermediate compound 9a (10 g, 26.8 mmol), compound 1-1 (10.9 g, 26.8 mmol), and NaOtBu (5.2 g, 53.6 mmol) were added to xylene (200 mL), followed by stirring and refluxing. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 9 (10.4 g).
- intermediate compound 10a (10 g, 25.8 mmol), compound 1-1 (10.5 g, 25.8 mmol), and NaOtBu (5 g, 51.7 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 10 (8.8 g).
- intermediate compound 11a (10 g, 24.8 mmol), compound 1-1 (10.1 g, 24.8 mmol), and NaOtBu (4.8 g, 49.6 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 11 (6.1 g).
- intermediate compound 12a (10 g, 30.2 mmol), compound 1-1 (12.3 g, 30.2 mmol), and NaOtBu (5.8 g, 60.5 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.6 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 12 (8.7 g).
- intermediate compound 13a (10 g, 27 mmol), compound 1-1 (11 g, 27 mmol), and NaOtBu (5.2 g, 53.9 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 13 (8 g).
- intermediate compound 14a (10 g, 28 mmol), compound 1-1 (11.4 g, 28 mmol), and NaOtBu (5.4 g, 56.1 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.6 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 14 (7.7 g).
- intermediate compound 15a (10 g, 22.4 mmol), compound 1-1 (9.1 g, 22.4 mmol), and NaOtBu (4.3 g, 44.9 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.2 g, 0.4 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 15 (9.3 g).
- intermediate compound 16a (10 g, 31.5 mmol), compound 1-2 (12.8 g, 31.5 mmol), and NaOtBu (6 g, 62.9 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.6 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 16 (9.7 g).
- intermediate compound 17a (10 g, 25.4 mmol), compound 1-2 (10.3 g, 25.4 mmol), and NaOtBu (4.9 g, 50.8 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 17 (9.7 g).
- intermediate compound 18a (10 g, 27.9 mmol), compound 1-2 (11.4 g, 27.9 mmol), and NaOtBu (5.4 g, 55.9 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.6 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 18 (9.6 g).
- intermediate compound 19a (10 g, 41.5 mmol), compound 1-2 (16.9 g, 41.5 mmol), and NaOtBu (8 g, 83.1 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.4 g, 0.8 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 19 (8.4 g).
- intermediate compound 20a (10 g, 29.3 mmol), compound 1-2 (11.9 g, 29.3 mmol), and NaOtBu (5.6 g, 58.7 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.6 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 20 (8.8 g).
- intermediate compound 21a (10 g, 24.6 mmol), compound 1-2 (10 g, 24.6 mmol), and NaOtBu (4.7 g, 49.3 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 21 (7.8 g).
- intermediate compound 22a (10 g, 25.6 mmol), compound 1-2 (10.4 g, 25.6 mmol), and NaOtBu (4.9 g, 51.2 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 22 (5.8 g).
- intermediate compound 23a (10 g, 22.6 mmol), compound 1-2 (9.2 g, 22.6 mmol), and NaOtBu (4.3 g, 45.2 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.2 g, 0.5 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 23 (11 g).
- intermediate compound 24a (10 g, 33.7 mmol), compound 1-2 (13.7 g, 33.7 mmol), and NaOtBu (6.5 g, 67.4 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.7 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 24 (12.6 g).
- intermediate compound 25a (10 g, 22.3 mmol), compound 1-2 (9.1 g, 22.3 mmol), and NaOtBu (4.3 g, 44.5 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.2 g, 0.4 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 25 (8.9 g).
- intermediate compound 26a (10 g, 25.8 mmol), compound 1-2 (10.5 g, 25.8 mmol), and NaOtBu (5 g, 51.7 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 26 (7.4 g).
- intermediate compound 27a (10 g, 21.6 mmol), compound 1-2 (8.8 g, 21.6 mmol), and NaOtBu (4.2 g, 43.3 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.2 g, 0.4 mmol) was added. After 2 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 27 (8.5 g).
- intermediate compound 28a (10 g, 35.6 mmol), compound 1-2 (14.5 g, 35.6 mmol), and NaOtBu (6.8 g, 71.2 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.4 g, 0.7 mmol) was added. After 3 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 28 (10.9 g).
- intermediate compound 29a (10 g, 28 mmol), compound 1-2 (11.4 g, 28 mmol), and NaOtBu (5.4 g, 56.1 mmol) were added to xylene (200 mL), followed by stirring and refluxing. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.6 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 29 (7.5 g).
- intermediate compound 30a (10 g, 25.8 mmol), compound 1-2 (10.5 g, 25.8 mmol), and NaOtBu (5 g, 51.7 mmol) were added to xylene (200 mL) and stirred and refluxed. After this, bis (tri-tert-butylphosphine) palladium (0) (0.3 g, 0.5 mmol) was added. After 4 hours, the reaction was terminated, cooled to room temperature, and reduced pressure to remove the solvent. Thereafter, the compound was completely dissolved in chloroform again, washed twice with water, and the organic layer was separated, treated with anhydrous magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to obtain compound 30 (6.3 g).
- a glass substrate coated with a thin film of ITO (indium tin oxide) to a thickness of 1,000 ⁇ was put in distilled water dissolved in a detergent and washed with ultrasonic waves.
- ITO indium tin oxide
- a product made by Fischer Co. was used as a detergent, and distilled water secondarily filtered with a filter manufactured by Millipore Co. was used as distilled water.
- ultrasonic washing was performed with a solvent of isopropyl alcohol, acetone, and methanol, dried, and then transported to a plasma cleaner. Further, after cleaning the substrate for 5 minutes using oxygen plasma, the substrate was transported to a vacuum evaporator.
- the HI-1 compound was formed as a hole injection layer on the prepared ITO transparent electrode to a thickness of 1150 ⁇ , but the following compound A-1 was p-doping at a concentration of 1.5%.
- the following HT-1 compound was vacuum deposited on the hole injection layer to form a hole transport layer having a thickness of 800 ⁇ .
- the following EB-1 compound was vacuum deposited on the hole transport layer with a film thickness of 150 ⁇ to form an electron suppressing layer.
- the following RH-1 compound and the following Dp-7 compound were vacuum-deposited at a weight ratio of 98:2 on the EB-1 deposition film to form a red light emitting layer having a thickness of 400 ⁇ .
- a hole blocking layer was formed by vacuum depositing the following HB-1 compound with a thickness of 30 ⁇ on the emission layer. Subsequently, the following ET-1 compound and the following LiQ compound were vacuum-deposited at a weight ratio of 2:1 on the hole blocking layer to form an electron injection and transport layer with a thickness of 300 ⁇ . Lithium fluoride (LiF) at a thickness of 12 ⁇ and aluminum at a thickness of 1,000 ⁇ were sequentially deposited on the electron injection and transport layer to form a negative electrode.
- LiF lithium fluoride
- the deposition rate of organic material was maintained at 0.4 to 0.7 ⁇ /sec
- the deposition rate of lithium fluoride at the cathode was 0.3 ⁇ /sec
- the deposition rate of aluminum was 2 ⁇ /sec
- the vacuum degree during deposition was 2X10 -7
- an organic light emitting device was manufactured.
- An organic light-emitting device was manufactured in the same manner as in Comparative Example 1, except that the compounds of Compounds 1 to 30 synthesized above were used instead of RH-1 in the organic light-emitting device of Comparative Example 1.
- An organic light-emitting device was manufactured in the same manner as in Comparative Example 1, except that the following compounds C-1 to C-8 were used instead of RH-1 in the organic light-emitting device of Comparative Example 1.
- the lifetime T95 refers to the time it takes for the luminance to decrease from initial luminance (6000 nit) to 95%.
- the red organic light-emitting device of Comparative Example 1 uses a material that has been widely used in the past, and has a structure using compound EB-1 as an electron blocking layer and compounds RH-1/Dp-7 as a red light emitting layer.
- an organic light-emitting device was manufactured using C-1 to C-8 instead of RH-1.
- substrate 2 anode
- hole transport layer 4 light emitting layer
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Abstract
La présente invention concerne un nouveau composé et un dispositif électroluminescent organique l'utilisant.
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KR20150124902A (ko) * | 2014-04-29 | 2015-11-06 | 롬엔드하스전자재료코리아유한회사 | 복수종의 호스트 재료 및 이를 포함하는 유기 전계 발광 소자 |
KR20170086277A (ko) * | 2016-01-18 | 2017-07-26 | 에스에프씨 주식회사 | 유기발광 화합물 및 이를 포함하는 유기발광소자 |
CN107686484A (zh) * | 2016-08-05 | 2018-02-13 | 南京高光半导体材料有限公司 | 有机电致发光化合物和使用该化合物的有机电致发光器件 |
KR20180032471A (ko) * | 2016-09-22 | 2018-03-30 | 삼성에스디아이 주식회사 | 유기 화합물, 유기 광전자 소자 및 표시 장치 |
US20190140193A1 (en) * | 2017-11-07 | 2019-05-09 | Universal Display Corporation | Organic electroluminescent materials and devices |
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2020
- 2020-08-13 WO PCT/KR2020/010789 patent/WO2021034017A1/fr active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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KR20150124902A (ko) * | 2014-04-29 | 2015-11-06 | 롬엔드하스전자재료코리아유한회사 | 복수종의 호스트 재료 및 이를 포함하는 유기 전계 발광 소자 |
KR20170086277A (ko) * | 2016-01-18 | 2017-07-26 | 에스에프씨 주식회사 | 유기발광 화합물 및 이를 포함하는 유기발광소자 |
CN107686484A (zh) * | 2016-08-05 | 2018-02-13 | 南京高光半导体材料有限公司 | 有机电致发光化合物和使用该化合物的有机电致发光器件 |
KR20180032471A (ko) * | 2016-09-22 | 2018-03-30 | 삼성에스디아이 주식회사 | 유기 화합물, 유기 광전자 소자 및 표시 장치 |
US20190140193A1 (en) * | 2017-11-07 | 2019-05-09 | Universal Display Corporation | Organic electroluminescent materials and devices |
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