JP5770289B2 - Oledのためのビカルバゾール化合物 - Google Patents
Oledのためのビカルバゾール化合物 Download PDFInfo
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- JP5770289B2 JP5770289B2 JP2013524828A JP2013524828A JP5770289B2 JP 5770289 B2 JP5770289 B2 JP 5770289B2 JP 2013524828 A JP2013524828 A JP 2013524828A JP 2013524828 A JP2013524828 A JP 2013524828A JP 5770289 B2 JP5770289 B2 JP 5770289B2
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- 0 CC(C(*)=C(C=C(c1cccc2c1cccc2)N)c1cccc2c1cccc2)N(c(cccc1)c1C1=C2)C1=CCC2c(cc1)cc(c2ccccc22)c1[n]2C1=CC2C=CC=CC2c2c1cccc2 Chemical compound CC(C(*)=C(C=C(c1cccc2c1cccc2)N)c1cccc2c1cccc2)N(c(cccc1)c1C1=C2)C1=CCC2c(cc1)cc(c2ccccc22)c1[n]2C1=CC2C=CC=CC2c2c1cccc2 0.000 description 11
- AIPOQSTYULGPTM-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-[n]2c(ccc(-c(cc3)cc(c4c5cccc4)c3[n]5-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)c3)c3c3ccccc23)ccc1 Chemical compound c(cc1)ccc1-c1cc(-[n]2c(ccc(-c(cc3)cc(c4c5cccc4)c3[n]5-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)c3)c3c3ccccc23)ccc1 AIPOQSTYULGPTM-UHFFFAOYSA-N 0.000 description 2
- ZIASFLJDTRVPQF-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-c2ccccc2)nc(-[n](c2ccccc2c2c3)c2ccc3-c(cc2)cc(c3c4cccc3)c2[n]4-c2cccc3c2[s]c2ccccc32)n1 Chemical compound c(cc1)ccc1-c1nc(-c2ccccc2)nc(-[n](c2ccccc2c2c3)c2ccc3-c(cc2)cc(c3c4cccc3)c2[n]4-c2cccc3c2[s]c2ccccc32)n1 ZIASFLJDTRVPQF-UHFFFAOYSA-N 0.000 description 2
- JOSRHFCDJNWEPC-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-c2ccccc2)nc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c(cc3)cc4c3[s]c3ccccc43)c3)c3c3c2cccc3)n1 Chemical compound c(cc1)ccc1-c1nc(-c2ccccc2)nc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c(cc3)cc4c3[s]c3ccccc43)c3)c3c3c2cccc3)n1 JOSRHFCDJNWEPC-UHFFFAOYSA-N 0.000 description 2
- LYOQBIUROGKZAJ-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-c2ccccc2)nc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c3ccc4[o]c(cccc5)c5c4c3)c3)c3c3c2cccc3)n1 Chemical compound c(cc1)ccc1-c1nc(-c2ccccc2)nc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c3ccc4[o]c(cccc5)c5c4c3)c3)c3c3c2cccc3)n1 LYOQBIUROGKZAJ-UHFFFAOYSA-N 0.000 description 2
- DGDPYDTWHOOWGP-UHFFFAOYSA-N c(cc1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4nc(-c5c(cccc6)c6ccc5)nc(-c5c(cccc6)c6ccc5)n4)c2)ccc1[n]3-c(cc1)cc2c1c1ccccc1cc2 Chemical compound c(cc1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4nc(-c5c(cccc6)c6ccc5)nc(-c5c(cccc6)c6ccc5)n4)c2)ccc1[n]3-c(cc1)cc2c1c1ccccc1cc2 DGDPYDTWHOOWGP-UHFFFAOYSA-N 0.000 description 2
- ATXBKQRWNHXAHJ-UHFFFAOYSA-N c(cc1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4nc(-c5c(cccc6)c6ccc5)nc(-c5c(cccc6)c6ccc5)n4)c2)ccc1[n]3-c1cc(c2ccccc2cc2)c2cc1 Chemical compound c(cc1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4nc(-c5c(cccc6)c6ccc5)nc(-c5c(cccc6)c6ccc5)n4)c2)ccc1[n]3-c1cc(c2ccccc2cc2)c2cc1 ATXBKQRWNHXAHJ-UHFFFAOYSA-N 0.000 description 2
- XKFOHQTWAHATHU-UHFFFAOYSA-N c(cc1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4nc(-c5cccc6c5cccc6)nc(-c5c(cccc6)c6ccc5)n4)c2)ccc1[n]3-c1cc2ccccc2c2ccccc12 Chemical compound c(cc1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4nc(-c5cccc6c5cccc6)nc(-c5c(cccc6)c6ccc5)n4)c2)ccc1[n]3-c1cc2ccccc2c2ccccc12 XKFOHQTWAHATHU-UHFFFAOYSA-N 0.000 description 2
- SFXIYFQQQCQJQI-UHFFFAOYSA-N c(cc1c2cc(-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4cc5ccccc5c5c4cccc5)cc(-c4cc(cccc5)c5c5c4cccc5)n3)ccc22)ccc1[n]2-c1ccc2[o]c(cccc3)c3c2c1 Chemical compound c(cc1c2cc(-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4cc5ccccc5c5c4cccc5)cc(-c4cc(cccc5)c5c5c4cccc5)n3)ccc22)ccc1[n]2-c1ccc2[o]c(cccc3)c3c2c1 SFXIYFQQQCQJQI-UHFFFAOYSA-N 0.000 description 2
- IJZPLALRIPSLSV-UHFFFAOYSA-N C(C(C=C1)c(cc2)cc(c3c4cccc3)c2[n]4-c2nc(-c3cc4c(cccc5)c5c(cccc5)c5c4cc3)cc(-c3cc4c(cccc5)c5c(cccc5)c5c4cc3)n2)c(c2ccccc22)c1[n]2-c(cc1)cc2c1c(cccc1)c1cc2 Chemical compound C(C(C=C1)c(cc2)cc(c3c4cccc3)c2[n]4-c2nc(-c3cc4c(cccc5)c5c(cccc5)c5c4cc3)cc(-c3cc4c(cccc5)c5c(cccc5)c5c4cc3)n2)c(c2ccccc22)c1[n]2-c(cc1)cc2c1c(cccc1)c1cc2 IJZPLALRIPSLSV-UHFFFAOYSA-N 0.000 description 1
- PGGQVINWSOBYDK-UHFFFAOYSA-N C(C(C=C1)c(cc2)cc(c3c4cccc3)c2[n]4-c2nc(-c3ccc(c4ccccc4c4c5cccc4)c5c3)cc(-c3cc4c(cccc5)c5c(cccc5)c5c4cc3)n2)c(c2ccccc22)c1[n]2-c1cc(cccc2)c2cc1 Chemical compound C(C(C=C1)c(cc2)cc(c3c4cccc3)c2[n]4-c2nc(-c3ccc(c4ccccc4c4c5cccc4)c5c3)cc(-c3cc4c(cccc5)c5c(cccc5)c5c4cc3)n2)c(c2ccccc22)c1[n]2-c1cc(cccc2)c2cc1 PGGQVINWSOBYDK-UHFFFAOYSA-N 0.000 description 1
- DQOJBOODRRMFOK-UHFFFAOYSA-N C(C(C=C1)c(cc2c3ccccc33)ccc2[n]3-c2ccccc2)c(c2ccccc22)c1[n]2-c1ccccc1 Chemical compound C(C(C=C1)c(cc2c3ccccc33)ccc2[n]3-c2ccccc2)c(c2ccccc22)c1[n]2-c1ccccc1 DQOJBOODRRMFOK-UHFFFAOYSA-N 0.000 description 1
- OTZHUVUDBQSTJX-HLWKLDSFSA-N C(C12)=CC=CC1=C(C=CC=C1)C1=C[C@@H]2c1nc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c3ccc4[s]c(cccc5)c5c4c3)c3)c3c3c2cccc3)nc(-c2c(cccc3)c3c(cccc3)c3c2)c1 Chemical compound C(C12)=CC=CC1=C(C=CC=C1)C1=C[C@@H]2c1nc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c3ccc4[s]c(cccc5)c5c4c3)c3)c3c3c2cccc3)nc(-c2c(cccc3)c3c(cccc3)c3c2)c1 OTZHUVUDBQSTJX-HLWKLDSFSA-N 0.000 description 1
- OKFZFXBCMQGGLA-UHFFFAOYSA-N C(C12)C=CC=C1c(cc(cc1)-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)c1N2c1cccc2c1[o]c1ccccc21 Chemical compound C(C12)C=CC=C1c(cc(cc1)-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)c1N2c1cccc2c1[o]c1ccccc21 OKFZFXBCMQGGLA-UHFFFAOYSA-N 0.000 description 1
- UVPKKOGZTAPFOV-UHFFFAOYSA-N C(C1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4c(cccc5)c5ccc4)c2)=CC=CC1N3c1nc(-c2cc(cccc3)c3cc2)cc(-c2cc(cccc3)c3cc2)n1 Chemical compound C(C1c2c3ccc(-c(cc4)cc(c5ccccc55)c4[n]5-c4c(cccc5)c5ccc4)c2)=CC=CC1N3c1nc(-c2cc(cccc3)c3cc2)cc(-c2cc(cccc3)c3cc2)n1 UVPKKOGZTAPFOV-UHFFFAOYSA-N 0.000 description 1
- PRFCRNILMFCCRD-UHFFFAOYSA-N C(C1c2c3ccc(-c(cc4c5c6cccc5)ccc4[n]6-c4cc5c(cccc6)c6c(cccc6)c6c5cc4)c2)=CC=CC1N3c1nc(-c2ccc(c3ccccc3c3ccccc33)c3c2)cc(-c(cc2)cc3c2c(cccc2)c2c2c3cccc2)n1 Chemical compound C(C1c2c3ccc(-c(cc4c5c6cccc5)ccc4[n]6-c4cc5c(cccc6)c6c(cccc6)c6c5cc4)c2)=CC=CC1N3c1nc(-c2ccc(c3ccccc3c3ccccc33)c3c2)cc(-c(cc2)cc3c2c(cccc2)c2c2c3cccc2)n1 PRFCRNILMFCCRD-UHFFFAOYSA-N 0.000 description 1
- LQTDJVAXLOZIJS-UHFFFAOYSA-N C(C1c2cc(-c(cc3)cc(c4ccccc44)c3[n]4-c3c(c4ccccc4c4ccccc44)c4ccc3)ccc22)=CC=CC1N2c1nc(-c2cc(cccc3)c3c3ccccc23)cc(-c2cc(cccc3)c3c3c2cccc3)n1 Chemical compound C(C1c2cc(-c(cc3)cc(c4ccccc44)c3[n]4-c3c(c4ccccc4c4ccccc44)c4ccc3)ccc22)=CC=CC1N2c1nc(-c2cc(cccc3)c3c3ccccc23)cc(-c2cc(cccc3)c3c3c2cccc3)n1 LQTDJVAXLOZIJS-UHFFFAOYSA-N 0.000 description 1
- IHNYEOGXMOYLGV-UHFFFAOYSA-N CC1C=Cc2cc(-c3nc(-c4cc(cccc5)c5cc4)nc(-[n]4c(ccc(-c(cc5)cc(c6ccccc66)c5[n]6-c5cc(-c6ccccc6)cc(-c6ccccc6)c5)c5)c5c5c4cccc5)n3)ccc2C1 Chemical compound CC1C=Cc2cc(-c3nc(-c4cc(cccc5)c5cc4)nc(-[n]4c(ccc(-c(cc5)cc(c6ccccc66)c5[n]6-c5cc(-c6ccccc6)cc(-c6ccccc6)c5)c5)c5c5c4cccc5)n3)ccc2C1 IHNYEOGXMOYLGV-UHFFFAOYSA-N 0.000 description 1
- SZZQSDXTVDDHPQ-UHFFFAOYSA-N c(cc1)cc(c2c3ccc(-c(cc4)cc(c5c6cccc5)c4[n]6-c4nc(-c5cccc6c5cccc6)cc(-c5cccc6c5cccc6)n4)c2)c1[n]3-c(cc1)cc2c1c1ccccc1cc2 Chemical compound c(cc1)cc(c2c3ccc(-c(cc4)cc(c5c6cccc5)c4[n]6-c4nc(-c5cccc6c5cccc6)cc(-c5cccc6c5cccc6)n4)c2)c1[n]3-c(cc1)cc2c1c1ccccc1cc2 SZZQSDXTVDDHPQ-UHFFFAOYSA-N 0.000 description 1
- VTRMPSGEXUDPBQ-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-[n](c1ccccc11)c2c1c(-c(cc1c3c4cccc3)ccc1[n]4-c(cc1)cc3c1[s]c1c(-[n]4c5ccccc5c5ccccc45)nccc31)ccc2 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-[n](c1ccccc11)c2c1c(-c(cc1c3c4cccc3)ccc1[n]4-c(cc1)cc3c1[s]c1c(-[n]4c5ccccc5c5ccccc45)nccc31)ccc2 VTRMPSGEXUDPBQ-UHFFFAOYSA-N 0.000 description 1
- KVDBJSMLMOOJGT-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c(cc2c3c4cccc3)ccc2[n]4-c2nc(-c3cc(cccc4)c4cc3)cc(-c3cc(cccc4)c4cc3)n2)c2)c2c2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c(cc2c3c4cccc3)ccc2[n]4-c2nc(-c3cc(cccc4)c4cc3)cc(-c3cc(cccc4)c4cc3)n2)c2)c2c2ccccc12 KVDBJSMLMOOJGT-UHFFFAOYSA-N 0.000 description 1
- GYGMLPLYVBJTNE-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c(cc2c3ccccc33)ccc2[n]3-c2nc(-c3ccc(cccc4)c4c3)nc(-c3cc(cccc4)c4cc3)n2)c2)c2c2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c(cc2c3ccccc33)ccc2[n]3-c2nc(-c3ccc(cccc4)c4c3)nc(-c3cc(cccc4)c4cc3)n2)c2)c2c2ccccc12 GYGMLPLYVBJTNE-UHFFFAOYSA-N 0.000 description 1
- MQQZKBBRNKPIFV-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-[n]1c(ccc(-c(cc2c3c4cccc3)ccc2[n]4-c2nc(-c3cc(cccc4)c4cc3)nc(-c3cc(cccc4)c4cc3)n2)c2)c2c2ccccc12 Chemical compound c(cc1)ccc1-c(cc1)ccc1-[n]1c(ccc(-c(cc2c3c4cccc3)ccc2[n]4-c2nc(-c3cc(cccc4)c4cc3)nc(-c3cc(cccc4)c4cc3)n2)c2)c2c2ccccc12 MQQZKBBRNKPIFV-UHFFFAOYSA-N 0.000 description 1
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- LSOHNSTVOHZTTJ-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c3nc(-c4c(cccc5)c5c(cccc5)c5c4)cc(-c4cc(cccc5)c5c5c4cccc5)n3)c3)c3c3ccccc23)ccc1 Chemical compound c(cc1)ccc1-c1cc(-[n]2c(ccc(-c(cc3)cc(c4ccccc44)c3[n]4-c3nc(-c4c(cccc5)c5c(cccc5)c5c4)cc(-c4cc(cccc5)c5c5c4cccc5)n3)c3)c3c3ccccc23)ccc1 LSOHNSTVOHZTTJ-UHFFFAOYSA-N 0.000 description 1
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- QLHFRJVIAWAMHG-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c2ccccc2)cc(-[n]2c(ccc(-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4ccccc4)cc(-c4ccccc4)n3)c3)c3c3ccccc23)c1 Chemical compound c(cc1)ccc1-c1cc(-c2ccccc2)cc(-[n]2c(ccc(-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4ccccc4)cc(-c4ccccc4)n3)c3)c3c3ccccc23)c1 QLHFRJVIAWAMHG-UHFFFAOYSA-N 0.000 description 1
- IPDKNXCWEJKRKD-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c2ccccc2)nc(-[n](c(cccc2)c2c2c3)c2ccc3-c(cc2)cc(c3ccccc33)c2[n]3-c2cccc3c2[s]c2c3cccc2)n1 Chemical compound c(cc1)ccc1-c1cc(-c2ccccc2)nc(-[n](c(cccc2)c2c2c3)c2ccc3-c(cc2)cc(c3ccccc33)c2[n]3-c2cccc3c2[s]c2c3cccc2)n1 IPDKNXCWEJKRKD-UHFFFAOYSA-N 0.000 description 1
- TUNWIAZQVFDGAI-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c2ccccc2)nc(-[n](c2ccccc2c2c3)c2ccc3-c(cc2)cc(c3ccccc33)c2[n]3-c2cccc3c2cccc3)n1 Chemical compound c(cc1)ccc1-c1cc(-c2ccccc2)nc(-[n](c2ccccc2c2c3)c2ccc3-c(cc2)cc(c3ccccc33)c2[n]3-c2cccc3c2cccc3)n1 TUNWIAZQVFDGAI-UHFFFAOYSA-N 0.000 description 1
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- CHSXBPMWISXHFJ-UHFFFAOYSA-N c(cc1c2c3ccc(-c(cc4)cc(c5c6cccc5)c4[n]6-c4nc(-c5c(cccc6)c6c(cccc6)c6c5)cc(-c5cc(cccc6)c6c6c5cccc6)n4)c2)ccc1[n]3-c1cc(c2ccccc2cc2)c2cc1 Chemical compound c(cc1c2c3ccc(-c(cc4)cc(c5c6cccc5)c4[n]6-c4nc(-c5c(cccc6)c6c(cccc6)c6c5)cc(-c5cc(cccc6)c6c6c5cccc6)n4)c2)ccc1[n]3-c1cc(c2ccccc2cc2)c2cc1 CHSXBPMWISXHFJ-UHFFFAOYSA-N 0.000 description 1
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- QSTBBFJOXMCIHM-UHFFFAOYSA-N c(cc1c2cc(-c(cc3)cc(c4ccccc44)c3[n]4-c3nc(-c4cccc5c4cccc5)cc(-c4cccc5c4cccc5)n3)ccc22)ccc1[n]2-c1cc(c2ccccc2cc2)c2cc1 Chemical compound c(cc1c2cc(-c(cc3)cc(c4ccccc44)c3[n]4-c3nc(-c4cccc5c4cccc5)cc(-c4cccc5c4cccc5)n3)ccc22)ccc1[n]2-c1cc(c2ccccc2cc2)c2cc1 QSTBBFJOXMCIHM-UHFFFAOYSA-N 0.000 description 1
- NDEZILGENGYFLX-UHFFFAOYSA-N c(cc1c2cc(-c(cc3c4c5cccc4)ccc3[n]5-c3nc(-c4cc5ccccc5c5ccccc45)cc(-c4c(cccc5)c5c(cccc5)c5c4)n3)ccc22)ccc1[n]2-c1cccc2c1[o]c1ccccc21 Chemical compound c(cc1c2cc(-c(cc3c4c5cccc4)ccc3[n]5-c3nc(-c4cc5ccccc5c5ccccc45)cc(-c4c(cccc5)c5c(cccc5)c5c4)n3)ccc22)ccc1[n]2-c1cccc2c1[o]c1ccccc21 NDEZILGENGYFLX-UHFFFAOYSA-N 0.000 description 1
- CALKYZYFKCICHD-UHFFFAOYSA-N c(cc1c2cc(-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4c(cccc5)c5ccc4)nc(-c4c(cccc5)c5ccc4)n3)ccc22)ccc1[n]2-c(cc1)cc2c1c1ccccc1c1c2cccc1 Chemical compound c(cc1c2cc(-c(cc3c4ccccc44)ccc3[n]4-c3nc(-c4c(cccc5)c5ccc4)nc(-c4c(cccc5)c5ccc4)n3)ccc22)ccc1[n]2-c(cc1)cc2c1c1ccccc1c1c2cccc1 CALKYZYFKCICHD-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
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- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
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- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
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- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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Description
一般に、OLEDは、アノードとカソードとの間に配置され且つそれらと電気的に接続された少なくとも1つの有機層を含む。電流が流された場合、有機層(1又は複数)にアノードは正孔を注入し、カソードは電子を注入する。注入された正孔と電子はそれぞれ反対に帯電した電極に向かって移動する。電子と正孔が同じ分子上に局在する場合、励起エネルギー状態を有する局在化された電子−正孔対である「励起子」が形成される。励起子が発光機構によって緩和するときに光が発せられる。いくつかの場合には、励起子はエキシマー又はエキシプレックス上に局在化されうる。非放射機構、例えば、熱緩和も起こりうるが、通常は好ましくないと考えられる。
及び、Baldoら,“Very high-efficiency green organic light-emitting devices based on electrophosphorescence”, Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”)、これらを参照により全体を援用する。燐光は、米国特許第7,279,704号明細書の第5〜6欄に、より詳細に記載されており、これを参照により援用する。
有機発光デバイス中の具体的な層に有用として本明細書に記載した物質は、そのデバイス中に存在するその他の広範囲にわたる物質と組み合わせて用いることができる。例えば、本明細書に開示した発光ドーパントは、存在してもよい広い範囲のホスト、輸送層、阻止層、注入層、電極、及びその他の層と組み合わせて用いることができる。以下に記載乃至言及した物質は、本明細書に記載した化合物と組み合わせて有用でありうる物質の非限定例であり、当業者は組み合わせて有用でありうるその他の物質を特定するために文献を容易に参考にすることができる。
フタロシアニン又はポルフィリン誘導体;芳香族アミン誘導体;インドロカルバゾール誘導体;フルオロ炭化水素を含むポリマー;導電性ドーパントを伴うポリマー;導電性ポリマー、例えば、PEDOT/PSS;ホスホン酸及びシラン誘導体などの化合物から誘導される自己組織化モノマー;金属酸化物誘導体、例えば、MoOx;p型半導体有機化合物、例えば、1,4,5,8,9,12−ヘキサアザトリフェニレンヘキサカルボニトリル;金属錯体、及び架橋性化合物。
AcOH(92 mL)中の9H−カルバゾール(5.57 g, 33.3 mmol)及びKI(3.68 g, 22.2 mmol)の溶液を100℃で1時間加熱した。その溶液にKIO3(3.57 g, 16.7 mmol)を分割して添加し、得られた混合物をさらに2時間、100℃で撹拌した。その混合物を水(500 mL)に注ぎ、沈殿物を濾過によって集め、熱水で洗った。DCM中での再結晶を行い、6.8g(70%)の生成物を白色固体として得た。
THF(150 mL)中の3−ブロモ−9−フェニル−9H−カルバゾール(20.3 g, 63 mmol)の溶液に、47.25mL(75.8 mmol)のn−ブチルリチウム(ヘキサン中1.6 M)を添加した。その混合物を−78℃で1時間撹拌した。21mL(100 mmol)の2−イソプロポキシ−4,4,5,5−テトラメチル[1,3,2]−ジオキサボロランをその溶液に添加し、得られた混合物を室温まで温め、8時間撹拌した。その混合物を水に注ぎ、ジクロロメタンで抽出した。有機抽出物を食塩水で洗い、硫酸マグネシウム上で乾燥させた。溶媒をロータリーエバポレーションによって除去し、ヘキサン中で再結晶をして、19.3g(83%)の生成物を白色固体として得た。
ジオキサン(5 mL)中の3−ヨード−9H−カルバゾール(879 mg, 3.0 mmol)、Pd(PPh3)4(165 mg, 0.15 mmol)、9−フェニル−3−(4,4,5,5−テトラメチル−1,3,2−ジオキサボロラン−2−イル)−9H−カルバゾール(1.29 g, 4.5 mmol)、及びK3PO4(1.8 g, 18.0 mmol)の溶液を、アルゴン雰囲気下で48時間激しく撹拌しながら85℃に加熱した。その混合物を水に注ぎ、DCMで抽出した。有機抽出物を食塩水で洗い、MgSO4上で乾燥させた。溶媒をロータリーエバポレーションによって除去し、DMC中で再結晶をして、900mg(74%)の生成物を得た。
無水DMF(40 mL)中の水素化ナトリウム(100 mg, 3.0 mmol)及び3−(9−フェニル−9H−カルバゾール−3−イル)−9H−カルバゾール(816 mg, 2.0 mmol)の溶液をアルゴン雰囲気下で1時間、室温で撹拌し、その溶液に室温で2−クロロ−4,6−ジフェニル−1,3,5−トリアジン(448 mg, 1,67 mmol)を添加し、次に夜通し還流させた。その混合物を水に注ぎ、沈殿物を濾過によって集め、水、メタノール、及びDMCで洗い、800mg(75%)の黄色固体を得た。
全てのデバイス例は高真空(<10−7Torr)熱蒸着によって作製した。アノード電極は800Åのインジウムスズオキシド(ITO)である。カソードは10ÅのLiFとそれに続く1000ÅのAlからなっていた。全てのデバイスは作製後直ちに窒素グローブボックス(<1ppmのH2O及びO2)中で、エポキシ樹脂で封止したガラス蓋で密封し、水分捕捉剤をそのパッケージに組み込んだ。
Claims (13)
- Ar1、Ar2、及びAr3がさらに置換されている、請求項1に記載の化合物。
- Ar3が、フェニル、ピリジン、ナフタレン、ビフェニル、ターフェニル、フルオレン、ジベンゾフラン、ジベンゾチオフェン、フェナントレン、及びトリフェニレンからなる群から選択され;且つ、
Ar1、Ar2、及びAr3は独立に、さらに、水素、アルキル、アルコキシ、アミノ、アルケニル、アルキニル、アリール、及びヘテロアリールからなる群から選択される置換基で置換されているが、前記置換基はAr1、Ar2、及びAr3に直接縮合しているアリール又はヘテロアリールではない、請求項1に記載の化合物。 - Ar1及びAr2が独立に、ピリジン及びナフタレンからなる群から選択される、請求項1に記載の化合物。
- Ar3が、フェニル、ビフェニル、ジベンゾフラン、及びジベンゾチオフェンからなる群から選択される、請求項1に記載の化合物。
- R1、R2、R3、及びR4が水素である、請求項1に記載の化合物。
- 前記有機層が溶液加工法を用いて堆積されたものである、請求項8に記載のデバイス。
- 前記有機層が発光層であり、前記化合物がホストである、請求項8に記載のデバイス。
- 消費者製品である、請求項8に記載のデバイス。
- 有機発光デバイスである、請求項8に記載のデバイス。
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012023947A1 (en) * | 2010-08-20 | 2012-02-23 | Universal Display Corporation | Bicarbazole compounds for oleds |
US10147888B2 (en) | 2011-02-07 | 2018-12-04 | Idemitsu Kosan Co., Ltd. | Biscarbazole derivative and organic electroluminescent element using same |
EP2674429B1 (en) | 2011-02-07 | 2020-12-23 | Idemitsu Kosan Co., Ltd. | Biscarbazole derivative and organic electroluminescent element using same |
US9806270B2 (en) | 2011-03-25 | 2017-10-31 | Udc Ireland Limited | 4H-imidazo[1,2-a]imidazoles for electronic applications |
CN103518271B (zh) * | 2011-05-12 | 2016-06-29 | 东丽株式会社 | 发光元件材料和发光元件 |
KR101443756B1 (ko) * | 2011-05-26 | 2014-09-23 | 제일모직 주식회사 | 유기광전자소자용 화합물, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
KR101354638B1 (ko) | 2011-06-20 | 2014-01-22 | 제일모직주식회사 | 유기광전자소자용 재료, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
WO2013012298A1 (en) * | 2011-07-21 | 2013-01-24 | Rohm And Haas Electronic Materials Korea Ltd. | 9h-carbazole compounds and electroluminescent devices involving them |
KR20130011955A (ko) * | 2011-07-21 | 2013-01-30 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
US20140217393A1 (en) * | 2011-09-09 | 2014-08-07 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence element |
EP2776443B1 (en) | 2011-11-10 | 2016-02-03 | Basf Se | 4h-imidazo[1,2-a]imidazoles for electronic applications |
JP2013116975A (ja) * | 2011-12-02 | 2013-06-13 | Kyushu Univ | 遅延蛍光材料、有機発光素子および化合物 |
KR20130062583A (ko) * | 2011-12-05 | 2013-06-13 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
WO2013102992A1 (ja) * | 2012-01-05 | 2013-07-11 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料とそれを用いた素子 |
KR102012047B1 (ko) | 2012-01-06 | 2019-08-19 | 유니버셜 디스플레이 코포레이션 | 효율이 큰 인광 물질 |
JPWO2013105206A1 (ja) | 2012-01-10 | 2015-05-11 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料及びそれを用いた素子 |
JP2015155378A (ja) * | 2012-04-18 | 2015-08-27 | 保土谷化学工業株式会社 | トリフェニレン環構造を有する化合物および有機エレクトロルミネッセンス素子 |
KR102004387B1 (ko) * | 2012-04-18 | 2019-07-26 | 에스에프씨 주식회사 | 이형고리 화합물 및 이를 포함하는 유기전계발광소자 |
US9985232B2 (en) | 2012-05-17 | 2018-05-29 | Idemitsu Kosan Co., Ltd. | Biscarbazole derivative host materials for OLED emissive region |
KR20150030660A (ko) * | 2012-06-14 | 2015-03-20 | 유니버셜 디스플레이 코포레이션 | Oled 발광 영역을 위한 비스카바졸 유도체 호스트 물질 및 적색 에미터 |
KR101431645B1 (ko) * | 2012-06-26 | 2014-08-20 | 롬엔드하스전자재료코리아유한회사 | 발광층 및 이를 포함하는 유기 전계 발광 소자 |
KR102026824B1 (ko) * | 2012-06-27 | 2019-10-01 | 삼성디스플레이 주식회사 | 신규한 축합환 화합물 및 이를 포함하는 유기 발광 소자 |
WO2014007564A1 (ko) * | 2012-07-04 | 2014-01-09 | 제일모직 주식회사 | 유기발광소자용 조성물, 이를 포함하는 유기발광층 및 유기발광소자 |
JP6189431B2 (ja) * | 2012-07-04 | 2017-08-30 | サムスン エスディアイ カンパニー, リミテッドSamsung Sdi Co., Ltd. | 有機光電子素子用化合物、これを含む有機発光素子および前記有機発光素子を含む表示装置 |
WO2014009317A1 (en) | 2012-07-10 | 2014-01-16 | Basf Se | Benzimidazo[1,2-a]benzimidazole derivatives for electronic applications |
KR102102580B1 (ko) * | 2012-07-20 | 2020-04-22 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 소자 |
KR101497138B1 (ko) | 2012-08-21 | 2015-02-27 | 제일모직 주식회사 | 유기광전자소자 및 이를 포함하는 표시장치 |
WO2014030666A1 (ja) | 2012-08-24 | 2014-02-27 | コニカミノルタ株式会社 | 透明電極、電子デバイス、および透明電極の製造方法 |
WO2014042405A1 (en) * | 2012-09-11 | 2014-03-20 | Rohm And Haas Electronic Materials Korea Ltd. | A novel combination of a host compound and a dopant compound and an organic electroluminescence device comprising the same |
US20140131665A1 (en) * | 2012-11-12 | 2014-05-15 | Universal Display Corporation | Organic Electroluminescent Device With Delayed Fluorescence |
JP6314599B2 (ja) | 2013-03-29 | 2018-04-25 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス用化合物、有機エレクトロルミネッセンス素子、それを具備した照明装置及び表示装置 |
WO2014157494A1 (ja) | 2013-03-29 | 2014-10-02 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子用材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
WO2014177518A1 (en) | 2013-04-29 | 2014-11-06 | Basf Se | Transition metal complexes with carbene ligands and the use thereof in oleds |
KR102145885B1 (ko) | 2013-06-05 | 2020-08-20 | 삼성디스플레이 주식회사 | 헤테로고리 화합물 및 이를 포함한 유기 발광 소자 |
KR101686078B1 (ko) * | 2013-08-12 | 2016-12-13 | 제일모직 주식회사 | 조성물, 유기 광전자 소자 및 표시 장치 |
US10074806B2 (en) * | 2013-08-20 | 2018-09-11 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR101649683B1 (ko) * | 2013-09-06 | 2016-08-19 | 제일모직 주식회사 | 유기광전자소자용 조성물, 유기 광전자 소자 및 표시 장치 |
KR102171124B1 (ko) * | 2013-10-15 | 2020-10-28 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
KR102191108B1 (ko) * | 2013-10-18 | 2020-12-15 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 소자 |
CN103664909B (zh) * | 2013-12-10 | 2015-02-25 | 京东方科技集团股份有限公司 | 联咔唑类衍生物及制备方法、应用和有机发光器件 |
WO2016000803A1 (de) * | 2014-06-30 | 2016-01-07 | Merck Patent Gmbh | Metallkomplexe |
KR20160004466A (ko) * | 2014-07-02 | 2016-01-13 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
US10297762B2 (en) | 2014-07-09 | 2019-05-21 | Universal Display Corporation | Organic electroluminescent materials and devices |
JP6780925B2 (ja) | 2014-07-25 | 2020-11-04 | 株式会社半導体エネルギー研究所 | 発光素子、発光装置、電子機器及び照明装置 |
WO2016016791A1 (en) | 2014-07-28 | 2016-02-04 | Idemitsu Kosan Co., Ltd (Ikc) | 2,9-functionalized benzimidazolo[1,2-a]benzimidazoles as hosts for organic light emitting diodes (oleds) |
TWI663173B (zh) | 2014-08-08 | 2019-06-21 | 愛爾蘭商Udc愛爾蘭責任有限公司 | 電致發光咪唑并喹噁啉碳烯金屬錯合物 |
US10749113B2 (en) * | 2014-09-29 | 2020-08-18 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10361375B2 (en) | 2014-10-06 | 2019-07-23 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR20160052443A (ko) * | 2014-11-04 | 2016-05-12 | 롬엔드하스전자재료코리아유한회사 | 도판트 화합물 및 호스트 화합물의 신규한 조합 및 이를 포함하는 유기 전계 발광 소자 |
WO2016079169A1 (en) | 2014-11-18 | 2016-05-26 | Basf Se | Pt- or pd-carbene complexes for use in organic light emitting diodes |
JP5831654B1 (ja) | 2015-02-13 | 2015-12-09 | コニカミノルタ株式会社 | 芳香族複素環誘導体、それを用いた有機エレクトロルミネッセンス素子、照明装置及び表示装置 |
KR101929860B1 (ko) * | 2015-05-15 | 2018-12-17 | 삼성에스디아이 주식회사 | 유기광전자소자 및 표시장치 |
CN106328816B (zh) * | 2015-06-16 | 2018-11-13 | 昆山国显光电有限公司 | 一种有机电致发光器件及其制备方法 |
US11522140B2 (en) | 2015-08-17 | 2022-12-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10651392B2 (en) | 2015-09-30 | 2020-05-12 | Samsung Electronics Co., Ltd. | Organic light-emitting device |
JP2019023163A (ja) * | 2015-10-21 | 2019-02-14 | 出光興産株式会社 | 新規化合物、有機エレクトロルミネッセンス素子用材料、有機エレクトロルミネッセンス素子及び電子機器 |
KR102507371B1 (ko) * | 2015-12-03 | 2023-03-08 | 솔루스첨단소재 주식회사 | 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자 |
KR20170074170A (ko) | 2015-12-21 | 2017-06-29 | 유디씨 아일랜드 리미티드 | 삼각형 리간드를 갖는 전이 금속 착체 및 oled에서의 이의 용도 |
JP6788314B2 (ja) * | 2016-01-06 | 2020-11-25 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子の製造方法、表示装置及び照明装置 |
KR102592185B1 (ko) * | 2016-04-06 | 2023-10-20 | 솔루스첨단소재 주식회사 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
KR102061246B1 (ko) | 2016-09-28 | 2020-02-20 | 삼성에스디아이 주식회사 | 유기 광전자 소자용 화합물, 유기 광전자 소자용 조성물, 유기 광전자 소자 및 표시 장치 |
US10680188B2 (en) * | 2016-11-11 | 2020-06-09 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR20180058200A (ko) * | 2016-11-23 | 2018-05-31 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 소자 |
KR102078302B1 (ko) * | 2016-11-29 | 2020-02-18 | 주식회사 엘지화학 | 유기 발광 소자 |
KR102616441B1 (ko) | 2016-12-23 | 2023-12-26 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 유기 화합물, 발광 소자, 발광 장치, 전자 기기, 및 조명 장치 |
CN115275032A (zh) | 2016-12-28 | 2022-11-01 | 株式会社半导体能源研究所 | 发光元件、有机化合物、发光装置、电子设备及照明装置 |
KR101915712B1 (ko) | 2017-03-24 | 2018-11-06 | 희성소재 (주) | 유기 발광 소자 및 유기 발광 소자의 유기물층용 조성물 |
KR101943428B1 (ko) | 2017-03-24 | 2019-01-30 | 엘티소재주식회사 | 유기 발광 소자 및 유기 발광 소자의 유기물층용 조성물 |
US10968226B2 (en) | 2017-06-23 | 2021-04-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
TWI787279B (zh) | 2017-06-23 | 2022-12-21 | 日商半導體能源研究所股份有限公司 | 有機化合物、發光元件、發光裝置、電子裝置及照明設備 |
JP7159173B2 (ja) * | 2017-09-11 | 2022-10-24 | 保土谷化学工業株式会社 | ピリミジン環構造を有する化合物および有機エレクトロルミネッセンス素子 |
US11706977B2 (en) | 2018-01-11 | 2023-07-18 | Samsung Electronics Co., Ltd. | Heterocyclic compound, composition including the same, and organic light-emitting device including the heterocyclic compound |
CN111032645B (zh) * | 2018-01-22 | 2023-03-10 | 株式会社Lg化学 | 多环化合物及包含其的有机发光器件 |
US11459348B2 (en) * | 2018-04-02 | 2022-10-04 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound |
KR20190115422A (ko) | 2018-04-02 | 2019-10-11 | 삼성전자주식회사 | 유기금속 화합물, 이를 포함한 유기 발광 소자 및 이를 포함한 진단용 조성물 |
KR102290359B1 (ko) * | 2018-12-11 | 2021-08-19 | 엘티소재주식회사 | 헤테로고리 화합물, 이를 포함하는 유기 발광 소자, 이의 제조 방법 및 유기물층용 조성물 |
KR20210063747A (ko) | 2019-11-25 | 2021-06-02 | 삼성전자주식회사 | 유기금속 화합물, 이를 포함한 유기 발광 소자 및 이를 포함한 진단용 조성물 |
Family Cites Families (151)
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 |
GB8909011D0 (en) | 1989-04-20 | 1989-06-07 | Friend Richard H | Electroluminescent devices |
US5061569A (en) | 1990-07-26 | 1991-10-29 | Eastman Kodak Company | Electroluminescent device with organic electroluminescent medium |
DE69412567T2 (de) | 1993-11-01 | 1999-02-04 | Hodogaya Chemical Co Ltd | Aminverbindung und sie enthaltende Elektrolumineszenzvorrichtung |
US5707745A (en) | 1994-12-13 | 1998-01-13 | The Trustees Of Princeton University | Multicolor organic light emitting devices |
US5703436A (en) | 1994-12-13 | 1997-12-30 | The Trustees Of Princeton University | Transparent contacts for organic devices |
US6939625B2 (en) | 1996-06-25 | 2005-09-06 | Nôrthwestern University | Organic light-emitting diodes and methods for assembly and enhanced charge injection |
US5844363A (en) | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
US6091195A (en) | 1997-02-03 | 2000-07-18 | The Trustees Of Princeton University | Displays having mesa pixel configuration |
US5834893A (en) | 1996-12-23 | 1998-11-10 | The Trustees Of Princeton University | High efficiency organic light emitting devices with light directing structures |
US6013982A (en) | 1996-12-23 | 2000-01-11 | The Trustees Of Princeton University | Multicolor display devices |
US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
US6337102B1 (en) | 1997-11-17 | 2002-01-08 | The Trustees Of Princeton University | Low pressure vapor phase deposition of organic thin films |
US6087196A (en) | 1998-01-30 | 2000-07-11 | The Trustees Of Princeton University | Fabrication of organic semiconductor devices using ink jet printing |
US6528187B1 (en) | 1998-09-08 | 2003-03-04 | Fuji Photo Film Co., Ltd. | Material for luminescence element and luminescence element using the same |
US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
US6830828B2 (en) * | 1998-09-14 | 2004-12-14 | The Trustees Of Princeton University | Organometallic complexes as phosphorescent emitters in organic LEDs |
US6294398B1 (en) | 1999-11-23 | 2001-09-25 | The Trustees Of Princeton University | Method for patterning devices |
US6458475B1 (en) | 1999-11-24 | 2002-10-01 | The Trustee Of Princeton University | Organic light emitting diode having a blue phosphorescent molecule as an emitter |
KR100377321B1 (ko) | 1999-12-31 | 2003-03-26 | 주식회사 엘지화학 | 피-형 반도체 성질을 갖는 유기 화합물을 포함하는 전기소자 |
US20020121638A1 (en) | 2000-06-30 | 2002-09-05 | Vladimir Grushin | Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds |
JP2002050860A (ja) | 2000-08-04 | 2002-02-15 | Toray Eng Co Ltd | 実装方法および実装装置 |
CN100505375C (zh) | 2000-08-11 | 2009-06-24 | 普林斯顿大学理事会 | 有机金属化合物和发射转换有机电致磷光 |
US6579630B2 (en) | 2000-12-07 | 2003-06-17 | Canon Kabushiki Kaisha | Deuterated semiconducting organic compounds used for opto-electronic devices |
US6720090B2 (en) * | 2001-01-02 | 2004-04-13 | Eastman Kodak Company | Organic light emitting diode devices with improved luminance efficiency |
JP3812730B2 (ja) | 2001-02-01 | 2006-08-23 | 富士写真フイルム株式会社 | 遷移金属錯体及び発光素子 |
JP4307000B2 (ja) | 2001-03-08 | 2009-08-05 | キヤノン株式会社 | 金属配位化合物、電界発光素子及び表示装置 |
JP4493915B2 (ja) * | 2001-05-16 | 2010-06-30 | ザ、トラスティーズ オブ プリンストン ユニバーシティ | 高効率多色電界リン光oled |
JP4310077B2 (ja) | 2001-06-19 | 2009-08-05 | キヤノン株式会社 | 金属配位化合物及び有機発光素子 |
WO2003001616A2 (en) | 2001-06-20 | 2003-01-03 | Showa Denko K.K. | Light emitting material and organic light-emitting device |
JP2003133075A (ja) * | 2001-07-25 | 2003-05-09 | Toray Ind Inc | 発光素子 |
US7071615B2 (en) | 2001-08-20 | 2006-07-04 | Universal Display Corporation | Transparent electrodes |
US7250226B2 (en) | 2001-08-31 | 2007-07-31 | Nippon Hoso Kyokai | Phosphorescent compound, a phosphorescent composition and an organic light-emitting device |
US7431968B1 (en) | 2001-09-04 | 2008-10-07 | The Trustees Of Princeton University | Process and apparatus for organic vapor jet deposition |
US6835469B2 (en) | 2001-10-17 | 2004-12-28 | The University Of Southern California | Phosphorescent compounds and devices comprising the same |
US7166368B2 (en) | 2001-11-07 | 2007-01-23 | E. I. Du Pont De Nemours And Company | Electroluminescent platinum compounds and devices made with such compounds |
US6863997B2 (en) | 2001-12-28 | 2005-03-08 | The Trustees Of Princeton University | White light emitting OLEDs from combined monomer and aggregate emission |
KR100691543B1 (ko) | 2002-01-18 | 2007-03-09 | 주식회사 엘지화학 | 새로운 전자 수송용 물질 및 이를 이용한 유기 발광 소자 |
US6878975B2 (en) | 2002-02-08 | 2005-04-12 | Agilent Technologies, Inc. | Polarization field enhanced tunnel structures |
US20030230980A1 (en) | 2002-06-18 | 2003-12-18 | Forrest Stephen R | Very low voltage, high efficiency phosphorescent oled in a p-i-n structure |
US7189989B2 (en) | 2002-08-22 | 2007-03-13 | Fuji Photo Film Co., Ltd. | Light emitting element |
EP1550707B1 (en) | 2002-08-27 | 2016-03-23 | UDC Ireland Limited | Organometallic complexes, organic el devices, and organic el displays |
US6687266B1 (en) | 2002-11-08 | 2004-02-03 | Universal Display Corporation | Organic light emitting materials and devices |
JP4707082B2 (ja) * | 2002-11-26 | 2011-06-22 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子および表示装置 |
JP4365199B2 (ja) | 2002-12-27 | 2009-11-18 | 富士フイルム株式会社 | 有機電界発光素子 |
JP4365196B2 (ja) | 2002-12-27 | 2009-11-18 | 富士フイルム株式会社 | 有機電界発光素子 |
EP3109238B1 (en) | 2003-03-24 | 2019-09-18 | University of Southern California | Phenyl-pyrazole complexes of iridium |
US7090928B2 (en) | 2003-04-01 | 2006-08-15 | The University Of Southern California | Binuclear compounds |
WO2004093207A2 (de) | 2003-04-15 | 2004-10-28 | Covion Organic Semiconductors Gmbh | Mischungen von organischen zur emission befähigten halbleitern und matrixmaterialien, deren verwendung und elektronikbauteile enthaltend diese mischungen |
US7029765B2 (en) | 2003-04-22 | 2006-04-18 | Universal Display Corporation | Organic light emitting devices having reduced pixel shrinkage |
KR101032355B1 (ko) | 2003-05-29 | 2011-05-03 | 신닛테츠가가쿠 가부시키가이샤 | 유기 전계 발광 소자 |
JP2005011610A (ja) | 2003-06-18 | 2005-01-13 | Nippon Steel Chem Co Ltd | 有機電界発光素子 |
US20050025993A1 (en) | 2003-07-25 | 2005-02-03 | Thompson Mark E. | Materials and structures for enhancing the performance of organic light emitting devices |
TWI390006B (zh) | 2003-08-07 | 2013-03-21 | Nippon Steel Chemical Co | Organic EL materials with aluminum clamps |
DE10338550A1 (de) | 2003-08-19 | 2005-03-31 | Basf Ag | Übergangsmetallkomplexe mit Carbenliganden als Emitter für organische Licht-emittierende Dioden (OLEDs) |
US20060269780A1 (en) | 2003-09-25 | 2006-11-30 | Takayuki Fukumatsu | Organic electroluminescent device |
JP4822687B2 (ja) | 2003-11-21 | 2011-11-24 | 富士フイルム株式会社 | 有機電界発光素子 |
US7332232B2 (en) | 2004-02-03 | 2008-02-19 | Universal Display Corporation | OLEDs utilizing multidentate ligand systems |
EP2533610B1 (en) | 2004-03-11 | 2015-04-29 | Mitsubishi Chemical Corporation | Composition for Charge-Transport Film and Ionic Compound, Charge-Transport Film and Organic Electroluminescence Device Using the Same, and Production Method of the Organic Electruminescence Device and Production Method of the Charge-Transport Film |
TW200531592A (en) | 2004-03-15 | 2005-09-16 | Nippon Steel Chemical Co | Organic electroluminescent device |
JP4869565B2 (ja) | 2004-04-23 | 2012-02-08 | 富士フイルム株式会社 | 有機電界発光素子 |
US7393599B2 (en) | 2004-05-18 | 2008-07-01 | The University Of Southern California | Luminescent compounds with carbene ligands |
US7445855B2 (en) | 2004-05-18 | 2008-11-04 | The University Of Southern California | Cationic metal-carbene complexes |
US7279704B2 (en) | 2004-05-18 | 2007-10-09 | The University Of Southern California | Complexes with tridentate ligands |
US7491823B2 (en) | 2004-05-18 | 2009-02-17 | The University Of Southern California | Luminescent compounds with carbene ligands |
US7154114B2 (en) | 2004-05-18 | 2006-12-26 | Universal Display Corporation | Cyclometallated iridium carbene complexes for use as hosts |
US7534505B2 (en) | 2004-05-18 | 2009-05-19 | The University Of Southern California | Organometallic compounds for use in electroluminescent devices |
WO2005123873A1 (ja) | 2004-06-17 | 2005-12-29 | Konica Minolta Holdings, Inc. | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
EP1893718B1 (en) | 2004-06-28 | 2018-10-03 | UDC Ireland Limited | Electroluminescent metal complexes with triazoles and benotriazoles |
US20060008670A1 (en) | 2004-07-06 | 2006-01-12 | Chun Lin | Organic light emitting materials and devices |
US7504657B2 (en) | 2004-07-23 | 2009-03-17 | Konica Minolta Holdings, Inc. | Organic electroluminescent element, display and illuminator |
KR100721565B1 (ko) * | 2004-11-17 | 2007-05-23 | 삼성에스디아이 주식회사 | 저분자 유기 전계 발광 소자 및 그의 제조 방법 |
DE102004057072A1 (de) | 2004-11-25 | 2006-06-01 | Basf Ag | Verwendung von Übergangsmetall-Carbenkomplexen in organischen Licht-emittierenden Dioden (OLEDs) |
WO2006061759A2 (en) * | 2004-12-08 | 2006-06-15 | Koninklijke Philips Electronics N.V. | 9 , 9 ' - and 2 , 2 ' -substituted 3 , 3 ' -bicarbazolyl derivatives for use in semiconducting materials as a host matrix for phosphorescent emitters |
US8362463B2 (en) | 2004-12-30 | 2013-01-29 | E. I. Du Pont De Nemours And Company | Organometallic complexes |
US8377571B2 (en) | 2005-02-04 | 2013-02-19 | Konica Minolta Holdings, Inc. | Material for organic electroluminescence element, organic electroluminescence element, display device and lighting device |
KR100803125B1 (ko) | 2005-03-08 | 2008-02-14 | 엘지전자 주식회사 | 적색 인광 화합물 및 이를 사용한 유기전계발광소자 |
WO2006098120A1 (ja) | 2005-03-16 | 2006-09-21 | Konica Minolta Holdings, Inc. | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子 |
DE102005014284A1 (de) | 2005-03-24 | 2006-09-28 | Basf Ag | Verwendung von Verbindungen, welche aromatische oder heteroaromatische über Carbonyl-Gruppen enthaltende Gruppen verbundene Ringe enthalten, als Matrixmaterialien in organischen Leuchtdioden |
JPWO2006103874A1 (ja) | 2005-03-29 | 2008-09-04 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
JP5157442B2 (ja) | 2005-04-18 | 2013-03-06 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
US7807275B2 (en) | 2005-04-21 | 2010-10-05 | Universal Display Corporation | Non-blocked phosphorescent OLEDs |
JP4533796B2 (ja) | 2005-05-06 | 2010-09-01 | 富士フイルム株式会社 | 有機電界発光素子 |
US8007927B2 (en) | 2007-12-28 | 2011-08-30 | Universal Display Corporation | Dibenzothiophene-containing materials in phosphorescent light emitting diodes |
US9051344B2 (en) | 2005-05-06 | 2015-06-09 | Universal Display Corporation | Stability OLED materials and devices |
KR101634423B1 (ko) * | 2005-05-31 | 2016-06-28 | 유니버셜 디스플레이 코포레이션 | 인광 발광 다이오드에서의 트리페닐렌 호스트 |
US8709614B2 (en) | 2005-06-07 | 2014-04-29 | Nippon Steel & Sumikin Chemical Co., Ltd. | Organic metal complex and its use in organic electroluminescent device |
JP5324217B2 (ja) | 2005-06-27 | 2013-10-23 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性ポリマー組成物 |
JP5076891B2 (ja) | 2005-07-01 | 2012-11-21 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
WO2007028417A1 (en) | 2005-09-07 | 2007-03-15 | Technische Universität Braunschweig | Triplett emitter having condensed five-membered rings |
JP4887731B2 (ja) | 2005-10-26 | 2012-02-29 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
JPWO2007063796A1 (ja) | 2005-12-01 | 2009-05-07 | 新日鐵化学株式会社 | 有機電界発光素子 |
WO2007063754A1 (ja) | 2005-12-01 | 2007-06-07 | Nippon Steel Chemical Co., Ltd. | 有機電界発光素子用化合物及び有機電界発光素子 |
US7915415B2 (en) | 2006-02-10 | 2011-03-29 | Universal Display Corporation | Metal complexes of cyclometallated imidazo[1,2-f]phenanthridine and diimidazo[1,2-a:1′,2′-c]quinazoline ligands and isoelectronic and benzannulated analogs thereof |
JP4823730B2 (ja) | 2006-03-20 | 2011-11-24 | 新日鐵化学株式会社 | 発光層化合物及び有機電界発光素子 |
JP5055818B2 (ja) * | 2006-04-19 | 2012-10-24 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
KR101453109B1 (ko) | 2006-04-26 | 2014-10-27 | 이데미쓰 고산 가부시키가이샤 | 방향족 아민 유도체 및 그들을 이용한 유기 전기 발광 소자 |
JP5432523B2 (ja) | 2006-05-11 | 2014-03-05 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
EP2034538B1 (en) | 2006-06-02 | 2013-10-09 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescence element, and organic electroluminescence element using the material |
EP2055701A1 (en) | 2006-08-23 | 2009-05-06 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivatives and organic electroluminescent devices made by using the same |
JP5589251B2 (ja) | 2006-09-21 | 2014-09-17 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子材料 |
KR100955993B1 (ko) | 2006-11-09 | 2010-05-04 | 신닛테츠가가쿠 가부시키가이샤 | 유기 전계 발광 소자용 화합물 및 유기 전계 발광 소자 |
KR20120135325A (ko) | 2006-11-24 | 2012-12-12 | 이데미쓰 고산 가부시키가이샤 | 방향족 아민 유도체 및 그것을 이용한 유기 전기발광 소자 |
JP2008135498A (ja) * | 2006-11-28 | 2008-06-12 | Toray Ind Inc | 発光素子 |
US8119255B2 (en) | 2006-12-08 | 2012-02-21 | Universal Display Corporation | Cross-linkable iridium complexes and organic light-emitting devices using the same |
CN101631793B (zh) | 2007-02-23 | 2013-12-25 | 巴斯夫欧洲公司 | 电致发光的苯并三唑金属络合物 |
JP5399236B2 (ja) * | 2007-03-26 | 2014-01-29 | 新日鉄住金化学株式会社 | 有機電界発光素子用化合物及び有機電界発光素子 |
US8512877B2 (en) | 2007-03-29 | 2013-08-20 | Dongwoo Fine-Chem | Naphthyl carbazole derivatives, KL host material, the organic light emitting device employing the same, the display device and the illumination device employing the same |
US7989091B2 (en) | 2007-04-26 | 2011-08-02 | Basf Se | Silanes containing phenothiazine-S-oxide or phenothiazine-S,S-dioxide groups and the use thereof in OLEDs |
WO2008156879A1 (en) | 2007-06-20 | 2008-12-24 | Universal Display Corporation | Blue phosphorescent imidazophenanthridine materials |
WO2009000673A2 (en) | 2007-06-22 | 2008-12-31 | Basf Se | Light emitting cu(i) complexes |
KR101577465B1 (ko) | 2007-07-05 | 2015-12-14 | 바스프 에스이 | 카르벤 전이 금속 착체 이미터, 및 디실릴카르바졸, 디실릴디벤조푸란, 디실릴디벤조티오펜, 디실릴디벤조포스폴, 디실릴디벤조티오펜 s-옥사이드 및 디실릴디벤조티오펜 s,s-디옥사이드로부터 선택된 1종 이상의 화합물을 포함하는 유기 발광 다이오드 |
US8779655B2 (en) | 2007-07-07 | 2014-07-15 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
US8330350B2 (en) | 2007-07-07 | 2012-12-11 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
KR20100057593A (ko) | 2007-07-07 | 2010-05-31 | 이데미쓰 고산 가부시키가이샤 | 유기 el 소자 및 유기 el 재료 함유 용액 |
WO2009008311A1 (ja) | 2007-07-07 | 2009-01-15 | Idemitsu Kosan Co., Ltd. | クリセン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
KR20100044200A (ko) | 2007-07-07 | 2010-04-29 | 이데미쓰 고산 가부시키가이샤 | 나프탈렌 유도체, 유기 el 소자용 재료 및 그것을 사용한 유기 el 소자 |
US20090045731A1 (en) | 2007-07-07 | 2009-02-19 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
KR101453128B1 (ko) | 2007-07-10 | 2014-10-27 | 이데미쓰 고산 가부시키가이샤 | 유기 전기발광 소자용 재료 및 그것을 이용한 유기 전기발광 소자 |
US8080658B2 (en) | 2007-07-10 | 2011-12-20 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescent element and organic electroluminescent element employing the same |
JP2010534739A (ja) | 2007-07-27 | 2010-11-11 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 無機ナノ粒子を含有する導電性ポリマーの水性分散体 |
CN101687837A (zh) * | 2007-08-06 | 2010-03-31 | 出光兴产株式会社 | 芳族胺衍生物以及使用该衍生物的有机电致发光元件 |
JP6009144B2 (ja) | 2007-08-08 | 2016-10-19 | ユニバーサル ディスプレイ コーポレイション | トリフェニレン基を含むベンゾ縮合チオフェンまたはベンゾ縮合フラン化合物 |
JP2009040728A (ja) | 2007-08-09 | 2009-02-26 | Canon Inc | 有機金属錯体及びこれを用いた有機発光素子 |
JP2011500648A (ja) | 2007-10-17 | 2011-01-06 | ビーエーエスエフ ソシエタス・ヨーロピア | 架橋カルベンリガンドを有する遷移金属錯体およびoledにおけるその使用 |
US20090101870A1 (en) | 2007-10-22 | 2009-04-23 | E. I. Du Pont De Nemours And Company | Electron transport bi-layers and devices made with such bi-layers |
US7914908B2 (en) | 2007-11-02 | 2011-03-29 | Global Oled Technology Llc | Organic electroluminescent device having an azatriphenylene derivative |
DE102007053771A1 (de) | 2007-11-12 | 2009-05-14 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
JPWO2009063833A1 (ja) | 2007-11-15 | 2011-03-31 | 出光興産株式会社 | ベンゾクリセン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
CN101874316B (zh) | 2007-11-22 | 2012-09-05 | 出光兴产株式会社 | 有机el元件以及含有机el材料的溶液 |
EP2221896A4 (en) | 2007-11-22 | 2012-04-18 | Idemitsu Kosan Co | ORGANIC EL ELEMENT |
WO2009073245A1 (en) | 2007-12-06 | 2009-06-11 | Universal Display Corporation | Light-emitting organometallic complexes |
US8221905B2 (en) | 2007-12-28 | 2012-07-17 | Universal Display Corporation | Carbazole-containing materials in phosphorescent light emitting diodes |
CN101970448B (zh) | 2008-02-12 | 2016-05-11 | 巴斯夫欧洲公司 | 具有二苯并[f,h]喹*啉的电致发光金属络合物 |
EP2796448B1 (en) * | 2008-08-22 | 2018-04-25 | Lg Chem, Ltd. | Material for organic electronic device and organic electronic device using the same |
US8247575B2 (en) * | 2009-03-20 | 2012-08-21 | Semiconductor Energy Laboratory Co., Ltd. | Carbazole derivative with heteroaromatic ring, and light-emitting element, light-emitting device, and electronic device using carbazole derivative with heteroaromatic ring |
DE102009023155A1 (de) * | 2009-05-29 | 2010-12-02 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
KR101431644B1 (ko) * | 2009-08-10 | 2014-08-21 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 발광 화합물 및 이를 포함하는 유기 전계 발광 소자 |
KR101506999B1 (ko) * | 2009-11-03 | 2015-03-31 | 제일모직 주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
US8828561B2 (en) * | 2009-11-03 | 2014-09-09 | Cheil Industries, Inc. | Compound for organic photoelectric device and organic photoelectric device including the same |
KR20110066494A (ko) * | 2009-12-11 | 2011-06-17 | 다우어드밴스드디스플레이머티리얼 유한회사 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
JP5562970B2 (ja) | 2010-04-20 | 2014-07-30 | 出光興産株式会社 | ビスカルバゾール誘導体、有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子 |
KR20110122051A (ko) * | 2010-05-03 | 2011-11-09 | 제일모직주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
JP5821635B2 (ja) * | 2010-06-24 | 2015-11-24 | 東レ株式会社 | 発光素子材料および発光素子 |
KR101432599B1 (ko) | 2010-08-04 | 2014-08-21 | 제일모직주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
WO2012023947A1 (en) * | 2010-08-20 | 2012-02-23 | Universal Display Corporation | Bicarbazole compounds for oleds |
KR101354638B1 (ko) * | 2011-06-20 | 2014-01-22 | 제일모직주식회사 | 유기광전자소자용 재료, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
JP2013116975A (ja) | 2011-12-02 | 2013-06-13 | Kyushu Univ | 遅延蛍光材料、有機発光素子および化合物 |
US9130174B2 (en) * | 2012-02-29 | 2015-09-08 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescence device and organic electroluminescence device |
JP2014072417A (ja) * | 2012-09-28 | 2014-04-21 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子用材料及び有機エレクトロルミネッセンス素子 |
US20140131665A1 (en) * | 2012-11-12 | 2014-05-15 | Universal Display Corporation | Organic Electroluminescent Device With Delayed Fluorescence |
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US20170170409A1 (en) | 2017-06-15 |
WO2012023947A1 (en) | 2012-02-23 |
US20130140549A1 (en) | 2013-06-06 |
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DE112010005815T5 (de) | 2013-06-06 |
US11289659B2 (en) | 2022-03-29 |
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KR20130108265A (ko) | 2013-10-02 |
TWI530496B (zh) | 2016-04-21 |
US20220216421A1 (en) | 2022-07-07 |
KR102004629B1 (ko) | 2019-07-26 |
US20190081246A1 (en) | 2019-03-14 |
DE112010005815B4 (de) | 2020-12-10 |
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US9954180B2 (en) | 2018-04-24 |
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