KR20250004127A - 유기 화합물, 발광 소자, 발광 장치, 전자 기기, 및 조명 장치 - Google Patents

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Publication number

KR20250004127A

KR20250004127A KR1020247040854A KR20247040854A KR20250004127A KR 20250004127 A KR20250004127 A KR 20250004127A KR 1020247040854 A KR1020247040854 A KR 1020247040854A KR 20247040854 A KR20247040854 A KR 20247040854A KR 20250004127 A KR20250004127 A KR 20250004127A

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KR

South Korea

Prior art keywords

light

substituted

unsubstituted

carbon atoms

abbreviation

Prior art date

2017-06-22

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• 125000003118 aryl group Chemical group 0.000 claims abstract description 48
• 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 47
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 24
• 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 23
• 239000001257 hydrogen Substances 0.000 claims abstract description 23
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 23
• 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 23
• 229910052760 oxygen Inorganic materials 0.000 claims abstract description 23
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 20
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• 229910052717 sulfur Chemical group 0.000 claims abstract description 19
• 239000011593 sulfur Chemical group 0.000 claims abstract description 19
• 239000000758 substrate Substances 0.000 claims description 125
• 230000005525 hole transport Effects 0.000 claims description 57
• TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical group C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 claims description 14
• IYYZUPMFVPLQIF-ALWQSETLSA-N dibenzothiophene Chemical group C1=CC=CC=2[34S]C3=C(C=21)C=CC=C3 IYYZUPMFVPLQIF-ALWQSETLSA-N 0.000 claims description 12
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• 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 10
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• OICJTSLHQGDCTQ-UHFFFAOYSA-N [1]benzothiolo[3,2-d]pyrimidine Chemical group N1=CN=C2C3=CC=CC=C3SC2=C1 OICJTSLHQGDCTQ-UHFFFAOYSA-N 0.000 abstract description 22
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• 125000005595 acetylacetonate group Chemical group 0.000 description 13
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• LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 10
• DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 description 9
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• YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 8
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• PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
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• 150000001768 cations Chemical class 0.000 description 7
• ZQASITYRQOCACA-UHFFFAOYSA-N dicyclohexyl-[2-(2-methyl-1,3-dioxolan-2-yl)phenyl]phosphane Chemical compound C=1C=CC=C(P(C2CCCCC2)C2CCCCC2)C=1C1(C)OCCO1 ZQASITYRQOCACA-UHFFFAOYSA-N 0.000 description 7
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• XJJZDHLZRNRKHD-UHFFFAOYSA-N 8-chloro-4-(3-dibenzothiophen-4-ylphenyl)-[1]benzofuro[3,2-d]pyrimidine Chemical compound ClC=1C=CC2=C(C=1)C=1N=CN=C(C=1O2)C1=CC(=CC=C1)C1=CC=CC2=C1SC1=C2C=CC=C1 XJJZDHLZRNRKHD-UHFFFAOYSA-N 0.000 description 6
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