JP2008056658A5 - - Google Patents

Info

Publication number

JP2008056658A5

JP2008056658A5 JP2007118218A JP2007118218A JP2008056658A5 JP 2008056658 A5 JP2008056658 A5 JP 2008056658A5 JP 2007118218 A JP2007118218 A JP 2007118218A JP 2007118218 A JP2007118218 A JP 2007118218A JP 2008056658 A5 JP2008056658 A5 JP 2008056658A5

Authority

JP

Japan

Prior art keywords

light emitting

organic light

emitting device

compound

substituted

Prior art date

2007-04-27

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

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• 150000001875 compounds Chemical class 0.000 claims description 22
• 150000002391 heterocyclic compounds Chemical class 0.000 claims description 13
• 229910052757 nitrogen Inorganic materials 0.000 claims description 8
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
• 125000001424 substituent group Chemical group 0.000 claims description 5
• 125000003118 aryl group Chemical group 0.000 claims description 4
• 125000004432 carbon atom Chemical group C* 0.000 claims description 4
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
• 125000001769 aryl amino group Chemical group 0.000 claims description 2
• 125000002619 bicyclic group Chemical group 0.000 claims description 2
• 150000002894 organic compounds Chemical class 0.000 claims 2
• 229960001716 benzalkonium Drugs 0.000 claims 1
• CYDRXTMLKJDRQH-UHFFFAOYSA-N benzododecinium Chemical compound CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 CYDRXTMLKJDRQH-UHFFFAOYSA-N 0.000 claims 1
• 239000007772 electrode material Substances 0.000 claims 1
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
• 238000005160 1H NMR spectroscopy Methods 0.000 description 8
• 238000001228 spectrum Methods 0.000 description 8
• 238000000103 photoluminescence spectrum Methods 0.000 description 7
• 239000000463 material Substances 0.000 description 6
• 238000010586 diagram Methods 0.000 description 4
• 125000000623 heterocyclic group Chemical group 0.000 description 4
• 125000003277 amino group Chemical group 0.000 description 3
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
• 125000003342 alkenyl group Chemical group 0.000 description 2
• 125000000217 alkyl group Chemical group 0.000 description 2
• 125000000304 alkynyl group Chemical group 0.000 description 2
• 125000003710 aryl alkyl group Chemical group 0.000 description 2
• 125000004093 cyano group Chemical group *C#N 0.000 description 2
• 230000006866 deterioration Effects 0.000 description 2
• 125000005843 halogen group Chemical group 0.000 description 2
• 125000003367 polycyclic group Chemical group 0.000 description 2
• OJRUSAPKCPIVBY-KQYNXXCUSA-N C1=NC2=C(N=C(N=C2N1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(CP(=O)(O)O)O)O)O)I)N Chemical compound C1=NC2=C(N=C(N=C2N1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(CP(=O)(O)O)O)O)O)I)N OJRUSAPKCPIVBY-KQYNXXCUSA-N 0.000 description 1
• LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 1
• 229910052799 carbon Inorganic materials 0.000 description 1
• 230000000052 comparative effect Effects 0.000 description 1
• 229940125758 compound 15 Drugs 0.000 description 1
• 238000005401 electroluminescence Methods 0.000 description 1
• 238000000295 emission spectrum Methods 0.000 description 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
• 239000000203 mixture Substances 0.000 description 1