JP4996794B2

JP4996794B2 - 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子

炭化水素化合物、有機電界発光素子用材料および有機電界発光素子

Info

Publication number: JP4996794B2
Authority: JP; Japan
Prior art keywords: group; carbon atoms; branched; linear; compound
Prior art date: 2000-08-10
Legal status : Expired - Lifetime

Application number

JP2001243306A

Other languages

English (en)

Japanese (ja)

Other versions

JP2002154993A5 (enrdf_load_stackoverflow

JP2002154993A (ja

Inventor

努石田

武彦島村

良満田辺

由之戸谷

正勝中塚

Current Assignee

Mitsui Chemicals Inc

Original Assignee

Mitsui Chemicals Inc

Priority date

2000-08-10

Filing date

2001-08-10

Publication date

2012-08-08

2001-08-10 Application filed by Mitsui Chemicals Inc filed Critical Mitsui Chemicals Inc

2001-08-10 Priority to JP2001243306A priority Critical patent/JP4996794B2/ja

2002-05-28 Publication of JP2002154993A publication Critical patent/JP2002154993A/ja

2008-08-28 Publication of JP2002154993A5 publication Critical patent/JP2002154993A5/ja

2012-08-08 Application granted granted Critical

2012-08-08 Publication of JP4996794B2 publication Critical patent/JP4996794B2/ja

2021-08-10 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

150000002430 hydrocarbons Chemical class 0.000 title claims description 46
238000005401 electroluminescence Methods 0.000 title claims description 21
239000000463 material Substances 0.000 title claims description 20
150000001875 compounds Chemical class 0.000 claims description 552
-1 anthracene-9,10-diyl group Chemical group 0.000 claims description 366
125000004432 carbon atom Chemical group C* 0.000 claims description 203
125000006165 cyclic alkyl group Chemical group 0.000 claims description 88
125000005843 halogen group Chemical group 0.000 claims description 78
125000003118 aryl group Chemical group 0.000 claims description 76
125000004122 cyclic group Chemical group 0.000 claims description 74
125000003545 alkoxy group Chemical group 0.000 claims description 72
238000002347 injection Methods 0.000 claims description 62
239000007924 injection Substances 0.000 claims description 62
125000003277 amino group Chemical group 0.000 claims description 58
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 53
125000003710 aryl alkyl group Chemical group 0.000 claims description 52
125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 20
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 16
125000002524 organometallic group Chemical group 0.000 claims description 12
125000001424 substituent group Chemical group 0.000 claims description 12
125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims description 11
229910052799 carbon Inorganic materials 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 8
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
238000006467 substitution reaction Methods 0.000 claims description 7
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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 23
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GISRWBROCYNDME-PELMWDNLSA-N F[C@H]1[C@H]([C@H](NC1=O)COC1=NC=CC2=CC(=C(C=C12)OC)C(=O)N)C Chemical compound F[C@H]1[C@H]([C@H](NC1=O)COC1=NC=CC2=CC(=C(C=C12)OC)C(=O)N)C GISRWBROCYNDME-PELMWDNLSA-N 0.000 description 5
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YNHIGQDRGKUECZ-UHFFFAOYSA-N dichloropalladium;triphenylphosphanium Chemical compound Cl[Pd]Cl.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-N 0.000 description 3
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QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
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FCNCGHJSNVOIKE-UHFFFAOYSA-N 9,10-diphenylanthracene Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 FCNCGHJSNVOIKE-UHFFFAOYSA-N 0.000 description 2
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MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
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ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 2
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125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 2
239000004327 boric acid Substances 0.000 description 2
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