JP2008159577A5 - - Google Patents

Info

Publication number

JP2008159577A5

JP2008159577A5 JP2007299480A JP2007299480A JP2008159577A5 JP 2008159577 A5 JP2008159577 A5 JP 2008159577A5 JP 2007299480 A JP2007299480 A JP 2007299480A JP 2007299480 A JP2007299480 A JP 2007299480A JP 2008159577 A5 JP2008159577 A5 JP 2008159577A5

Authority

JP

Japan

Prior art keywords

light

emitting layer

emitting element

host material

phenyl

Prior art date

2007-11-19

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
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• 239000000463 material Substances 0.000 claims 28
• 150000001454 anthracenes Chemical group 0.000 claims 6
• -1 aromatic amine compound Chemical class 0.000 claims 4
• 238000000295 emission spectrum Methods 0.000 claims 4
• 150000002894 organic compounds Chemical class 0.000 claims 4
• IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical group C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 claims 3
• UWRZIZXBOLBCON-VOTSOKGWSA-N (e)-2-phenylethenamine Chemical class N\C=C\C1=CC=CC=C1 UWRZIZXBOLBCON-VOTSOKGWSA-N 0.000 claims 2
• UQVFZEYHQJJGPD-UHFFFAOYSA-N 9-[4-(10-phenylanthracen-9-yl)phenyl]carbazole Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=CC=C2)C2=C1C1=CC=C(N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 UQVFZEYHQJJGPD-UHFFFAOYSA-N 0.000 claims 2
• CRWAGLGPZJUQQK-UHFFFAOYSA-N n-(4-carbazol-9-ylphenyl)-4-[2-[4-(n-(4-carbazol-9-ylphenyl)anilino)phenyl]ethenyl]-n-phenylaniline Chemical compound C=1C=C(N(C=2C=CC=CC=2)C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=CC=1C=CC(C=C1)=CC=C1N(C=1C=CC(=CC=1)N1C2=CC=CC=C2C2=CC=CC=C21)C1=CC=CC=C1 CRWAGLGPZJUQQK-UHFFFAOYSA-N 0.000 claims 2
• 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 claims 2
• 150000003518 tetracenes Chemical class 0.000 claims 2
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
• ZULHHMJFLPUTMR-UHFFFAOYSA-N 2-[2,6-bis[2-(6-methoxy-4,4,10,10-tetramethyl-1-azatricyclo[7.3.1.05,13]trideca-5,7,9(13)-trien-7-yl)ethenyl]pyran-4-ylidene]propanedinitrile Chemical compound CC1(C)CCN2CCC(C)(C)C3=C2C1=CC(C=CC=1OC(=CC(C=1)=C(C#N)C#N)C=CC=1C(=C2C(C)(C)CCN4C2=C(C(CC4)(C)C)C=1)OC)=C3OC ZULHHMJFLPUTMR-UHFFFAOYSA-N 0.000 claims 1
• MRUWJENAYHTDQG-UHFFFAOYSA-N 4H-pyran Chemical group C1C=COC=C1 MRUWJENAYHTDQG-UHFFFAOYSA-N 0.000 claims 1
• 150000000531 4H-pyrans Chemical class 0.000 claims 1
• 125000003277 amino group Chemical group 0.000 claims 1
• 150000004696 coordination complex Chemical class 0.000 claims 1
• 239000000203 mixture Substances 0.000 claims 1
• AJNJGJDDJIBTBP-UHFFFAOYSA-N n-(9,10-diphenylanthracen-2-yl)-n,9-diphenylcarbazol-3-amine Chemical compound C1=CC=CC=C1N(C=1C=C2C(C=3C=CC=CC=3)=C3C=CC=CC3=C(C=3C=CC=CC=3)C2=CC=1)C1=CC=C(N(C=2C=CC=CC=2)C=2C3=CC=CC=2)C3=C1 AJNJGJDDJIBTBP-UHFFFAOYSA-N 0.000 claims 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 238000001228 spectrum Methods 0.000 claims 1
• 239000000758 substrate Substances 0.000 claims 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 claims 1