JP2012124252A - 金属錯体を含む素子 - Google Patents
金属錯体を含む素子 Download PDFInfo
- Publication number
- JP2012124252A JP2012124252A JP2010272417A JP2010272417A JP2012124252A JP 2012124252 A JP2012124252 A JP 2012124252A JP 2010272417 A JP2010272417 A JP 2010272417A JP 2010272417 A JP2010272417 A JP 2010272417A JP 2012124252 A JP2012124252 A JP 2012124252A
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- Prior art keywords
- group
- substituent
- same
- different
- nitrogen atom
- Prior art date
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- Granted
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- 150000004696 coordination complex Chemical class 0.000 title claims abstract description 52
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 72
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 71
- 125000001424 substituent group Chemical group 0.000 claims abstract description 67
- 150000001923 cyclic compounds Chemical class 0.000 claims abstract description 55
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 21
- 229910052684 Cerium Inorganic materials 0.000 claims abstract description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 16
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 9
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 9
- 239000003446 ligand Substances 0.000 claims description 21
- 125000000623 heterocyclic group Chemical group 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 12
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 238000004020 luminiscence type Methods 0.000 abstract description 3
- -1 cerium ions Chemical class 0.000 description 330
- 239000010410 layer Substances 0.000 description 145
- 150000001875 compounds Chemical class 0.000 description 33
- 239000000463 material Substances 0.000 description 31
- 238000002347 injection Methods 0.000 description 30
- 239000007924 injection Substances 0.000 description 30
- 238000000034 method Methods 0.000 description 28
- 230000032258 transport Effects 0.000 description 24
- 150000002500 ions Chemical class 0.000 description 22
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- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- 125000002676 chrysenyl group Chemical group C1(=CC=CC=2C3=CC=C4C=CC=CC4=C3C=CC12)* 0.000 description 13
- 239000000758 substrate Substances 0.000 description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 10
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 10
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 10
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 10
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 10
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- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 9
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- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 9
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 8
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 8
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 7
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 7
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- 125000003118 aryl group Chemical group 0.000 description 7
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- 238000000576 coating method Methods 0.000 description 7
- 229920000547 conjugated polymer Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 6
- 230000005284 excitation Effects 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 125000000748 anthracen-2-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([H])=C([*])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 150000001721 carbon Chemical group 0.000 description 5
- 239000010408 film Substances 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 125000004430 oxygen atom Chemical group O* 0.000 description 5
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 5
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 5
- 125000006410 propenylene group Chemical group 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 4
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000003710 aryl alkyl group Chemical group 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 229920001940 conductive polymer Polymers 0.000 description 4
- 125000004956 cyclohexylene group Chemical group 0.000 description 4
- 238000000295 emission spectrum Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 125000002883 imidazolyl group Chemical group 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical group [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 4
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Chemical compound [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 125000003226 pyrazolyl group Chemical group 0.000 description 4
- 125000004076 pyridyl group Chemical group 0.000 description 4
- 238000004544 sputter deposition Methods 0.000 description 4
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 4
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 4
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
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- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
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- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 3
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- 125000002078 anthracen-1-yl 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 description 3
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- AFVFQIVMOAPDHO-UHFFFAOYSA-N methanesulfonic acid Substances CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
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- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229920000292 Polyquinoline Polymers 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
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- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000010405 anode material Substances 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000007611 bar coating method Methods 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
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- 239000007853 buffer solution Substances 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
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- 125000004744 butyloxycarbonyl group Chemical group 0.000 description 1
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- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
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- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
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- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 1
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- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
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- 125000005935 hexyloxycarbonyl group Chemical group 0.000 description 1
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- 150000003949 imides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
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- YZASAXHKAQYPEH-UHFFFAOYSA-N indium silver Chemical compound [Ag].[In] YZASAXHKAQYPEH-UHFFFAOYSA-N 0.000 description 1
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- 230000002687 intercalation Effects 0.000 description 1
- 238000009830 intercalation Methods 0.000 description 1
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- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- GCICAPWZNUIIDV-UHFFFAOYSA-N lithium magnesium Chemical compound [Li].[Mg] GCICAPWZNUIIDV-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- SJCKRGFTWFGHGZ-UHFFFAOYSA-N magnesium silver Chemical compound [Mg].[Ag] SJCKRGFTWFGHGZ-UHFFFAOYSA-N 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- HXZSFRJGDPGVNY-UHFFFAOYSA-N methyl(oxido)phosphanium Chemical group C[PH2]=O HXZSFRJGDPGVNY-UHFFFAOYSA-N 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- DCZNSJVFOQPSRV-UHFFFAOYSA-N n,n-diphenyl-4-[4-(n-phenylanilino)phenyl]aniline Chemical class C1=CC=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 DCZNSJVFOQPSRV-UHFFFAOYSA-N 0.000 description 1
- ZHDORMMHAKXTPT-UHFFFAOYSA-N n-benzoylbenzamide Chemical group C=1C=CC=CC=1C(=O)NC(=O)C1=CC=CC=C1 ZHDORMMHAKXTPT-UHFFFAOYSA-N 0.000 description 1
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- 239000004800 polyvinyl chloride Substances 0.000 description 1
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- 239000011591 potassium Substances 0.000 description 1
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- 239000002244 precipitate Substances 0.000 description 1
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- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
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- SKRWFPLZQAAQSU-UHFFFAOYSA-N stibanylidynetin;hydrate Chemical compound O.[Sn].[Sb] SKRWFPLZQAAQSU-UHFFFAOYSA-N 0.000 description 1
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- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- Plural Heterocyclic Compounds (AREA)
Abstract
Description
[2]A1、R1又はR2が、置換基として1つ以上の窒素原子含有ヘテロシクリル基を有する上記[1]に記載の素子。
[3]窒素原子含有環式化合物が下記式(2)で表される、上記[1]又は[2]に記載の素子。
[4]上記式(2)において、m+pが3〜6の整数である上記[3]に記載の素子。
[5]上記式(2)において、pが0である上記[3]又は[4]に記載の素子。
[6]窒素原子含有環式化合物が下記式(3)で表される、上記[1]〜[5]のいずれか1項に記載の素子。
[7]上記金属錯体が、下記組成式(11)で表される金属錯体である[6]に記載の素子。
[8]上記素子が電界発光素子である上記[1]〜[7]のいずれか1項に記載の素子。
[9]下記組成式(4)で表される金属錯体。
[10]下記式(5)で表される窒素原子含有環式化合物。
このようなイミド基としては、例えば、N−スクシンイミド基、N−フタルイミド基、及びベンゾフェノンイミド基が挙げられ、好ましくは、N−フタルイミド基である。
本発明の素子に用いられる金属錯体は、例えば、窒素原子含有環式化合物と金属塩(例えば、塩化セリウム(III)又はトリフルオロメタンスルホン酸セリウム(III))とを、溶媒(例えば、メタノール又はアセトニトリル)中で室温下混合させ、得られた沈殿を回収するか又は得られた溶液の溶媒を留去することで、容易に得ることができる。
本発明の素子は、セリウムと、上記窒素原子含有環式化合物との金属錯体を含有する。
発光素子は、通常、陽極及び陰極からなる電極間に、発光する機能を有する層、すなわち発光層が含まれている。また、発光効率及び耐久性を向上させるために、発光する機能以外の機能を有する公知の層を一つ以上含んでいてもよい。このような層としては、例えば、電荷輸送層、電荷阻止層、電荷注入層及びバッファ層が挙げられる。なお、本発明の素子が発光素子の場合において、発光層、電荷輸送層、電荷阻止層、電荷注入層、バッファ層等の層は、各々、一層からなるものでも二層以上からなるものでもよい。上記金属錯体は、上記層のうちの1層以上に含まれていることが好ましく、発光層に含まれていることが好ましい。
a)陽極/発光層/陰極
b)陽極/正孔輸送層/発光層/陰極
c)陽極/発光層/電子輸送層/陰極
d)陽極/発光層/正孔阻止層/陰極
e)陽極/正孔輸送層/発光層/電子輸送層/陰極
f)陽極/電荷注入層/発光層/陰極
g)陽極/発光層/電荷注入層/陰極
h)陽極/電荷注入層/発光層/電荷注入層/陰極
i)陽極/電荷注入層/正孔輸送層/発光層/陰極
j)陽極/正孔輸送層/発光層/電荷注入層/陰極
k)陽極/電荷注入層/正孔輸送層/発光層/電荷注入層/陰極
l)陽極/電荷注入層/発光層/電子輸送層/陰極
m)陽極/発光層/電子輸送層/電荷注入層/陰極
n)陽極/電荷注入層/発光層/電子輸送層/電荷注入層/陰極
o)陽極/電荷注入層/正孔輸送層/発光層/電子輸送層/陰極
p)陽極/正孔輸送層/発光層/電子輸送層/電荷注入層/陰極
q)陽極/電荷注入層/正孔輸送層/発光層/電子輸送層/電荷注入層/陰極
(ここで、「/」は各層が隣接して積層されていることを示す。なお、発光層、正孔輸送層、電子輸送層は、それぞれ独立に2層以上用いてもよい。)
続いて本発明の素子が光電変換素子の場合について以下説明する。
<窒素原子含有環式化合物(A−13)の合成例>
<金属錯体(B−2)の合成例>
スパッタリング法にて150nmの厚みでITO膜を形成したガラス基板に、ポリ(2−ヒドロキシエチルメタクリレート)(重量平均分子量 Mw 20000以下)に、金属錯体(B−2)を50重量%混合し、スピンコート法にて成膜した。厚さは120nmであった。成膜された膜を60℃にて20分乾燥させた後、フッ化リチウムを約0.5nm、更にアルミニウムを約80nm蒸着して陰極とし、電界発光素子を作製した。得られた素子に電圧を印加したところ黄緑色の発光が観測された。
Claims (10)
- セリウムと、下記式(1)で表される窒素原子含有環式化合物との金属錯体を含有する素子。
- A1、R1又はR2が、置換基として1つ以上の窒素原子含有ヘテロシクリル基を有する請求項1に記載の素子。
- 窒素原子含有環式化合物が下記式(2)で表される、請求項1又は2に記載の素子。
- 上記式(2)において、m+pが3〜6の整数である請求項3に記載の素子。
- 上記式(2)において、pが0である請求項3又は4に記載の素子。
- 窒素原子含有環式化合物が下記式(3)で表される、請求項1〜5のいずれか1項に記載の素子。
- 上記金属錯体が、下記組成式(11)で表される金属錯体である請求項6に記載の素子。
- 上記素子が電界発光素子である請求項1〜7のいずれか1項に記載の素子。
- 下記組成式(4)で表される金属錯体。
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WO2012157631A1 (ja) * | 2011-05-18 | 2012-11-22 | 住友化学株式会社 | 脂肪族アミン配位セリウム錯体及び該錯体を含む素子 |
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JPH05504361A (ja) * | 1991-01-24 | 1993-07-08 | ゲールベ ソシエテ アノニム | 新規窒素含有マクロ環状リガンド、調製方法、多金属錯体、及び診断用組成物 |
JPH07224050A (ja) * | 1993-12-30 | 1995-08-22 | Guerbet Sa | ポリアミノ酸化リガンド類及びそれらの金属錯体 |
JP2005187546A (ja) * | 2003-12-24 | 2005-07-14 | Kansai Tlo Kk | 有機ラジカル配位子を有する希土類錯体を含有する発光材料 |
JP2005272430A (ja) * | 2004-03-23 | 2005-10-06 | Minerva Light Laboratory | マイクロ波加熱による錯体発光素子材料、その製造方法および発光素子 |
JP2007177252A (ja) * | 1998-12-25 | 2007-07-12 | Konica Minolta Holdings Inc | エレクトロルミネッセンス材料、エレクトロルミネッセンス素子及び色変換フィルター |
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JPH05504361A (ja) * | 1991-01-24 | 1993-07-08 | ゲールベ ソシエテ アノニム | 新規窒素含有マクロ環状リガンド、調製方法、多金属錯体、及び診断用組成物 |
JPH07224050A (ja) * | 1993-12-30 | 1995-08-22 | Guerbet Sa | ポリアミノ酸化リガンド類及びそれらの金属錯体 |
JP2007177252A (ja) * | 1998-12-25 | 2007-07-12 | Konica Minolta Holdings Inc | エレクトロルミネッセンス材料、エレクトロルミネッセンス素子及び色変換フィルター |
JP2005187546A (ja) * | 2003-12-24 | 2005-07-14 | Kansai Tlo Kk | 有機ラジカル配位子を有する希土類錯体を含有する発光材料 |
JP2005272430A (ja) * | 2004-03-23 | 2005-10-06 | Minerva Light Laboratory | マイクロ波加熱による錯体発光素子材料、その製造方法および発光素子 |
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WO2012157631A1 (ja) * | 2011-05-18 | 2012-11-22 | 住友化学株式会社 | 脂肪族アミン配位セリウム錯体及び該錯体を含む素子 |
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