JP5318367B2 - ジメチレンシクロへキサン化合物、その製造方法及びそれを備えた有機発光素子 - Google Patents
ジメチレンシクロへキサン化合物、その製造方法及びそれを備えた有機発光素子 Download PDFInfo
- Publication number
- JP5318367B2 JP5318367B2 JP2007126088A JP2007126088A JP5318367B2 JP 5318367 B2 JP5318367 B2 JP 5318367B2 JP 2007126088 A JP2007126088 A JP 2007126088A JP 2007126088 A JP2007126088 A JP 2007126088A JP 5318367 B2 JP5318367 B2 JP 5318367B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- substituted
- unsubstituted
- chemical formula
- light emitting
- Prior art date
- 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.)
- Active
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 118
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- -1 methylenecyclohexane compound Chemical class 0.000 claims description 84
- 239000000126 substance Substances 0.000 claims description 71
- 238000002347 injection Methods 0.000 claims description 59
- 239000007924 injection Substances 0.000 claims description 59
- 125000003118 aryl group Chemical group 0.000 claims description 51
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 32
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 30
- 125000001072 heteroaryl group Chemical group 0.000 claims description 29
- 125000003277 amino group Chemical group 0.000 claims description 28
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 26
- 230000005525 hole transport Effects 0.000 claims description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 26
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 23
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 19
- 230000000903 blocking effect Effects 0.000 claims description 14
- 125000000732 arylene group Chemical group 0.000 claims description 12
- 125000005843 halogen group Chemical group 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 125000005842 heteroatom Chemical group 0.000 claims description 7
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- WPHGSKGZRAQSGP-UHFFFAOYSA-N methylenecyclohexane Natural products C1CCCC2CC21 WPHGSKGZRAQSGP-UHFFFAOYSA-N 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 27
- 239000010410 layer Substances 0.000 description 125
- 229910052757 nitrogen Inorganic materials 0.000 description 22
- 125000001309 chloro group Chemical group Cl* 0.000 description 20
- 239000000463 material Substances 0.000 description 20
- 125000001246 bromo group Chemical group Br* 0.000 description 19
- 230000015572 biosynthetic process Effects 0.000 description 18
- 125000001424 substituent group Chemical group 0.000 description 17
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 16
- 239000002019 doping agent Substances 0.000 description 15
- 239000002904 solvent Substances 0.000 description 14
- 238000004528 spin coating Methods 0.000 description 14
- 238000003786 synthesis reaction Methods 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000000758 substrate Substances 0.000 description 11
- 238000001771 vacuum deposition Methods 0.000 description 11
- 125000000217 alkyl group Chemical group 0.000 description 10
- 125000002947 alkylene group Chemical group 0.000 description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 239000004305 biphenyl Substances 0.000 description 8
- CECAIMUJVYQLKA-UHFFFAOYSA-N iridium 1-phenylisoquinoline Chemical compound [Ir].C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 CECAIMUJVYQLKA-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 125000001624 naphthyl group Chemical group 0.000 description 8
- 238000005160 1H NMR spectroscopy Methods 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 238000000151 deposition Methods 0.000 description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 5
- 125000004450 alkenylene group Chemical group 0.000 description 5
- 125000004419 alkynylene group Chemical group 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 4
- 235000010290 biphenyl Nutrition 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 125000004474 heteroalkylene group Chemical group 0.000 description 4
- 125000005549 heteroarylene group Chemical group 0.000 description 4
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical compound 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 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 229920000767 polyaniline Polymers 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 4
- 238000007740 vapor deposition Methods 0.000 description 4
- IBXMKLPFLZYRQZ-UHFFFAOYSA-N 1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1C=CC(=O)C=CC1=CC=CC=C1 IBXMKLPFLZYRQZ-UHFFFAOYSA-N 0.000 description 3
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000005036 alkoxyphenyl group Chemical group 0.000 description 3
- 125000005037 alkyl phenyl group Chemical group 0.000 description 3
- 125000004653 anthracenylene group Chemical group 0.000 description 3
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000003336 coronenyl group Chemical group C1(=CC2=CC=C3C=CC4=CC=C5C=CC6=CC=C1C1=C6C5=C4C3=C21)* 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 125000005059 halophenyl group Chemical group 0.000 description 3
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 125000004957 naphthylene group Chemical group 0.000 description 3
- 229940078552 o-xylene Drugs 0.000 description 3
- 230000037361 pathway Effects 0.000 description 3
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- ZGNPLWZYVAFUNZ-UHFFFAOYSA-N tert-butylphosphane Chemical compound CC(C)(C)P ZGNPLWZYVAFUNZ-UHFFFAOYSA-N 0.000 description 3
- VFUDMQLBKNMONU-UHFFFAOYSA-N 9-[4-(4-carbazol-9-ylphenyl)phenyl]carbazole Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 VFUDMQLBKNMONU-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical group CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 125000005566 carbazolylene group Chemical group 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- OANQELUUJGCUOQ-UHFFFAOYSA-N hexaphenylene Chemical group C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C2=C1 OANQELUUJGCUOQ-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- 125000001828 phenalenyl group Chemical group C1(C=CC2=CC=CC3=CC=CC1=C23)* 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 125000002098 pyridazinyl group Chemical group 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- 125000004627 thianthrenyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3SC12)* 0.000 description 2
- 125000005730 thiophenylene group Chemical group 0.000 description 2
- 125000001425 triazolyl group Chemical group 0.000 description 2
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 2
- 238000005019 vapor deposition process Methods 0.000 description 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 description 1
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 1
- GRHFIPKABQYICC-UHFFFAOYSA-N 1,1'-biphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1.C1=CC=CC=C1C1=CC=CC=C1 GRHFIPKABQYICC-UHFFFAOYSA-N 0.000 description 1
- 125000005918 1,2-dimethylbutyl group Chemical group 0.000 description 1
- PWTFRUXTAFBWBW-UHFFFAOYSA-N 1,3-dibromo-5-(bromomethyl)benzene Chemical compound BrCC1=CC(Br)=CC(Br)=C1 PWTFRUXTAFBWBW-UHFFFAOYSA-N 0.000 description 1
- WYZFJRPOPFJGLI-UHFFFAOYSA-N 1,5-dibromo-5-methylcyclohexa-1,3-diene Chemical compound CC1(Br)CC(Br)=CC=C1 WYZFJRPOPFJGLI-UHFFFAOYSA-N 0.000 description 1
- YLRBJYMANQKEAW-UHFFFAOYSA-N 1-bromo-4-(bromomethyl)benzene Chemical compound BrCC1=CC=C(Br)C=C1 YLRBJYMANQKEAW-UHFFFAOYSA-N 0.000 description 1
- OGNSDRMLWYNUED-UHFFFAOYSA-N 1-cyclohexyl-4-[4-[4-(4-cyclohexylcyclohexyl)cyclohexyl]cyclohexyl]cyclohexane Chemical group C1CCCCC1C1CCC(C2CCC(CC2)C2CCC(CC2)C2CCC(CC2)C2CCCCC2)CC1 OGNSDRMLWYNUED-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- AWXGSYPUMWKTBR-UHFFFAOYSA-N 4-carbazol-9-yl-n,n-bis(4-carbazol-9-ylphenyl)aniline Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(N(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 AWXGSYPUMWKTBR-UHFFFAOYSA-N 0.000 description 1
- MAGFQRLKWCCTQJ-UHFFFAOYSA-N 4-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(C=C)C=C1 MAGFQRLKWCCTQJ-UHFFFAOYSA-N 0.000 description 1
- OSQXTXTYKAEHQV-WXUKJITCSA-N 4-methyl-n-[4-[(e)-2-[4-[4-[(e)-2-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]ethenyl]phenyl]phenyl]ethenyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(\C=C\C=2C=CC(=CC=2)C=2C=CC(\C=C\C=3C=CC(=CC=3)N(C=3C=CC(C)=CC=3)C=3C=CC(C)=CC=3)=CC=2)=CC=1)C1=CC=C(C)C=C1 OSQXTXTYKAEHQV-WXUKJITCSA-N 0.000 description 1
- DIVZFUBWFAOMCW-UHFFFAOYSA-N 4-n-(3-methylphenyl)-1-n,1-n-bis[4-(n-(3-methylphenyl)anilino)phenyl]-4-n-phenylbenzene-1,4-diamine Chemical compound CC1=CC=CC(N(C=2C=CC=CC=2)C=2C=CC(=CC=2)N(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C(C)C=CC=2)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C(C)C=CC=2)=C1 DIVZFUBWFAOMCW-UHFFFAOYSA-N 0.000 description 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
- HIHOEGPXVVKJPP-JTQLQIEISA-N 5-fluoro-2-[[(1s)-1-(5-fluoropyridin-2-yl)ethyl]amino]-6-[(5-methyl-1h-pyrazol-3-yl)amino]pyridine-3-carbonitrile Chemical compound N([C@@H](C)C=1N=CC(F)=CC=1)C(C(=CC=1F)C#N)=NC=1NC=1C=C(C)NN=1 HIHOEGPXVVKJPP-JTQLQIEISA-N 0.000 description 1
- VIJYEGDOKCKUOL-UHFFFAOYSA-N 9-phenylcarbazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2C2=CC=CC=C21 VIJYEGDOKCKUOL-UHFFFAOYSA-N 0.000 description 1
- 229910001148 Al-Li alloy Inorganic materials 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- 101000837344 Homo sapiens T-cell leukemia translocation-altered gene protein Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910018068 Li 2 O Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 244000097202 Rathbunia alamosensis Species 0.000 description 1
- 235000009776 Rathbunia alamosensis Nutrition 0.000 description 1
- 229910006404 SnO 2 Inorganic materials 0.000 description 1
- 102100028692 T-cell leukemia translocation-altered gene protein Human genes 0.000 description 1
- 229910052771 Terbium Inorganic materials 0.000 description 1
- 229910052775 Thulium Inorganic materials 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- JHYLKGDXMUDNEO-UHFFFAOYSA-N [Mg].[In] Chemical compound [Mg].[In] JHYLKGDXMUDNEO-UHFFFAOYSA-N 0.000 description 1
- 125000004054 acenaphthylenyl group Chemical group C1(=CC2=CC=CC3=CC=CC1=C23)* 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 1
- 125000005577 anthracene group Chemical group 0.000 description 1
- 125000003943 azolyl group Chemical group 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Inorganic materials [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 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 1
- 229910052796 boron Inorganic materials 0.000 description 1
- KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical group CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 1
- 125000005569 butenylene group Chemical group 0.000 description 1
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Inorganic materials [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- MIOPJNTWMNEORI-UHFFFAOYSA-N camphorsulfonic acid Chemical compound C1CC2(CS(O)(=O)=O)C(=O)CC1C2(C)C MIOPJNTWMNEORI-UHFFFAOYSA-N 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000002676 chrysenyl group Chemical group C1(=CC=CC=2C3=CC=C4C=CC=CC4=C3C=CC12)* 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004802 cyanophenyl group Chemical group 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- DCZFGQYXRKMVFG-UHFFFAOYSA-N cyclohexane-1,4-dione Chemical compound O=C1CCC(=O)CC1 DCZFGQYXRKMVFG-UHFFFAOYSA-N 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- VCJZTATVUDMNLU-UHFFFAOYSA-N dibromomethylbenzene Chemical compound BrC(Br)C1=CC=CC=C1 VCJZTATVUDMNLU-UHFFFAOYSA-N 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
- 125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- 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
- 125000002192 heptalenyl group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Inorganic materials [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 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
- 238000005259 measurement Methods 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- HTISDHGSRIQJEV-UHFFFAOYSA-N octacyclo[36.4.0.02,7.08,13.014,19.020,25.026,31.032,37]dotetraconta-1(42),2,4,6,8,10,12,14,16,18,20,22,24,26,28,30,32,34,36,38,40-henicosaene Chemical group C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C2=C1 HTISDHGSRIQJEV-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 125000005564 oxazolylene group Chemical group 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 125000003933 pentacenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C12)* 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- JQQSUOJIMKJQHS-UHFFFAOYSA-N pentaphenyl group Chemical group C1=CC=CC2=CC3=CC=C4C=C5C=CC=CC5=CC4=C3C=C12 JQQSUOJIMKJQHS-UHFFFAOYSA-N 0.000 description 1
- MHAUGLFOVCQYNR-UHFFFAOYSA-N pentaphenylene Chemical group C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C3=CC=CC=C3C2=C1 MHAUGLFOVCQYNR-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 1
- 150000005041 phenanthrolines Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001388 picenyl group Chemical group C1(=CC=CC2=CC=C3C4=CC=C5C=CC=CC5=C4C=CC3=C21)* 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 125000006410 propenylene group Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 125000005550 pyrazinylene group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 125000005548 pyrenylene group Chemical group 0.000 description 1
- 125000005551 pyridylene group Chemical group 0.000 description 1
- 125000005576 pyrimidinylene group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 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 description 1
- 125000005559 triazolylene group Chemical group 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000003960 triphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C3=CC=CC=C3C12)* 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/72—Spiro hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/86—Carbazoles; Hydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/93—Spiro compounds
- C07C2603/94—Spiro compounds containing "free" spiro atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/14—Carrier transporting layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/17—Carrier injection layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Electroluminescent Light Sources (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Description
下記反応式2の反応経路によって化学式5の化合物を合成した。
1,3−ジブロモトルエン(4mmol、1.0g)、NBS(N−bromosuccinimide、6mmol、1.07g)、過酸化ベンゾイル(0.4mmol、96mg)をベンゼン100mlに入れて5時間還流させた後、カラムクロマトグラフィーと再結晶とを通じて精製し、真空乾燥して、1,3−ジブロモ−5−ブロモメチル−ベンゼン(881mg、収率=67%)を得た。さらに、トリエチルホスファイト[P(OCH2CH3)3](20mmol、3.5g)と混合して、12時間還流状態で攪拌した。溶媒を減圧除去した後、室温に冷却して中間体A(2.15g、87%)の化合物を得た。
<中間体Bの合成>
前記中間体A(10mmol、3.86g)とシクロヘキサン−1,4−ジオン(4.5mmol、0.5g)とをテトラヒドロフラン(THF、300ml)溶媒に溶解させた後、t−BuOK(カリウムターシャリーブトオキサイド、11mmol、1.25g)を添加して60℃で一晩中反応させた後、放置して上澄液のみ取って、溶媒を除去した後、メタノール(100ml)を添加してろ過した後、再びメタノールで洗浄した。次いで、シリカゲル管クロマトグラフィー(CHCl3)で分離精製して2.2g(収率83%)の中間体Bを得た。
<化学式5の化合物の合成>
前記中間体B(10mmol、5.76g)をo−キシレン(200ml)溶媒に溶解させた後、カルバゾール(60mmol、10g)、Pd2(dba)3(トリ(ジベンジリデンアセトン)ジパラジウム(0))(4.0mmol、3.7g)、P(t−Bu)3(t−ブチルホスフィン;tri−tert−butyl phosphine、3.0mmol、0.6g)、t−ブトキシドナトリウム(60mmol、5.8g)を添加した後、還流温度で24時間攪拌した。常温まで冷却させた後、溶媒を除去してシリカゲル管クロマトグラフィーで分離精製した後、再結晶して化学式5の白い固体パウダー4.1g(収率45%)の化合物5を得た。
<合成例2>
下記反応式3の反応経路によって化学式7の化合物を合成した。
4−ブロモベンジルブロマイド(40mmol、10g)をトリエチルホスファイト[P(OCH2CH3)3](80mmol、13.3g)と混合して、185℃で6時間攪拌した。溶媒を減圧除去した後、室温に冷却して、白い固体パウダー(11.8g、96%)を得た。
<中間体Dの合成>
前記中間体C(100mmol、31.6g)をテトラヒドロフラン(THF、300ml)溶媒に溶解させた後、t−BuOK(110mmol、12.5g)を添加して50℃で1時間反応させた後、1,4−シクロヘキサンジオン(40mmol、5g)を滴下して70℃で一晩中反応させ、エタノール(20ml)を添加して真空で乾燥させた後、塩化メチレン200mlを添加した。これから得た有機層を水200mlで2回洗浄した後、無水硫酸マグネシウムを入れて乾燥させた後、ろ過して溶媒部分のみを乾燥させた。次いで、シリカゲル管クロマトグラフィーで分離精製して9.7g(収率58%)の中間体Dを得た。
<化学式7の化合物の合成>
得られた前記中間体D(10.6mmol、4.45g)をo−キシレン(80ml)溶媒に溶解させた後、化学式11の化合物(14.9mmol、6.62g)に、Pd2(dba)3(トリ(ジベンジリデンアセトン)ジパラジウム(0))(0.54mmol、0.5g)、t−ブチルホスフィン(P(t−Bu)3、0.41mmol、0.083g)、NaO−t−Bu(t−ブトキシドナトリウム、30mmol、2.88g)を添加した後、常温で4時間攪拌した。反応が終わった後にジクロロメタン100mlを添加し、水100mLで2回洗浄して有機層を得て無水硫酸マグネシウムで乾燥させた後、溶媒を蒸発させて生成物を得た後、シリカゲル管クロマトグラフィーで分離精製した後、再結晶して3.7g(収率55%)の化学式7の化合物を得た。
<合成例3>
下記反応式4の反応経路によって化学式8の化合物を合成した。
<実施例1>
前記化学式7の化合物を単独で発光層のホストとして使用して、次のような構造を持つ有機発光素子を製作した。
アノードは、15Ω/cm2(1000Å)ITOガラス基板を、50mm×500mm×0.7mmサイズに切断して、アセトン、イソプロピルアルコールと純水中で各15分間超音波洗浄した後、15分間UVオゾン洗浄して使用した。これを基板1とする。前記基板1の上部にα−NPDを真空蒸着して750Åの正孔輸送層を形成した。前記正孔輸送層の上部に、ホスト及びゲスト化合物(Ir(piq)3;トリス(1−フェニルイソキノリン)イリジウム(III))を真空蒸着して350Å厚さの発光層を形成した。この後、前記発光層の上部にBalqを50Å、Alq3化合物を180Åの厚さに真空蒸着して電子輸送層を形成した。前記電子輸送層の上部にLiF 10Å(電子注入層)とAl 2000Å(カソード)とを順次に真空蒸着して、図1Aに図示されたような有機発光素子を製造した。
前記化学式7の化合物を発光層のホストとして使用して、次のような構造を持つ有機発光素子を製作した。
アノードは、15Ω/cm2(1000Å)ITOガラス基板を50mm×500mm×0.7mmサイズに切断して、アセトン、イソプロピルアルコールと純水中で各15分間超音波洗浄した後、15分間UVオゾン洗浄して使用した。これを基板1とする。前記基板1の上部にPEDOT(ポリ(3,4−エチレンジオキシチオフェン))を一般環境で110℃で5分間熱処理をし、再び窒素雰囲気及び200℃で10分間熱処理して、500Åの正孔輸送層を形成した。前記正孔輸送層の上部に、ホストとゲスト化合物との混合液{ホスト(化合物7)とゲスト化合物(赤色ドープ剤=Ir(piq)3との混合比は5質量%(すなわち、ドープ剤/ホスト=0.05)であり、この混合物を含有する溶液(混合液)の濃度が1質量%となるように、溶媒にジクロロメタン使用して混合液を調整した。}をスピンコーティングした後、110℃で30分間熱処理して550Åの厚さの発光層を形成した。以後、前記発光層の上部にBalqを50Å、Alq3化合物を180Åの厚さに真空蒸着して電子輸送層を形成した。前記電子輸送層の上部にLiF 10Å(電子注入層)とAl 2000Å(カソード)とを順次に真空蒸着して、図1Aに図示されたような有機発光素子を製造した。
前記実施例1で、発光層のホスト化合物として前記化学式7の化合物の代りに化学式8の化合物を使用したことを除いては、前記実施例1と同じ過程を行って有機発光素子を製造した。
前記実施例2で、発光層のホスト化合物として前記化学式7の化合物の代りに化学式8の化合物を使用したことを除いては、前記実施例2と同じ過程を行って有機発光素子を製造した。
前記化学式7及び8の化合物と前記実施例1〜実施例4で得られた有機電界発光素子について、PR650(Spectroscan)Source Measurement Unit.)を利用して、駆動電圧、色純度、発光効率、最高輝度、電流密度、ELピーク波長をそれぞれ評価して、下記表1及び2に表した。
Claims (7)
- 下記化学式3、4、4Cまたは4Bの化合物のジメチレンシクロへキサン化合物:
前記Z’及びZ”は、互いに独立的に、置換または非置換のC1−C20アルキル基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基、置換または非置換のC5−C20シクロアルキル基または置換または非置換のC5−C30ヘテロシクロアルキル基を表し、
L1−L4は、C 2 −C 30 ヘテロアリール基であり、
前記Z’及びZ”は、互いに独立的に、置換または非置換のC1−C20アルキル基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基、置換または非置換のC5−C20シクロアルキル基または置換または非置換のC5−C30ヘテロシクロアルキル基を表し、
L1−L4は、C 2 −C 30 ヘテロアリール基であり、
R9、R10、R11、R12、R13、R14、R15、R16は、互いに独立的に、水素原子、ハロゲン原子、シアノ基、ヒドロキシル基、アミノ基、置換または非置換のC1−C20アルキル基、置換または非置換のC1−C20アルコキシ基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基または化学式−N(Z’)(Z”)を持つ置換されたアミノ基であり、
前記Z’及びZ”は、互いに独立的に、置換または非置換のC1−C20アルキル基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基、置換または非置換のC5−C20シクロアルキル基または置換または非置換のC5−C30ヘテロシクロアルキル基を表し、
前記Z’及びZ”は、互いに独立的に、置換または非置換のC1−C20アルキル基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基、置換または非置換のC5−C20シクロアルキル基または置換または非置換のC5−C30ヘテロシクロアルキル基を表し、
L1−L4は、C 6 −C 30 アリール基であり、
R9、R10、R11、R12、R13、R14、R15、R16は、互いに独立的に、水素原子、ハロゲン原子、シアノ基、ヒドロキシル基、アミノ基、置換または非置換のC1−C20アルキル基、置換または非置換のC1−C20アルコキシ基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基または化学式−N(Z’)(Z”)を持つ置換されたアミノ基であり、
前記Z’及びZ”は、互いに独立的に、置換または非置換のC1−C20アルキル基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基、置換または非置換のC5−C20シクロアルキル基または置換または非置換のC5−C30ヘテロシクロアルキル基を表す。 - 前記化学式3、4、4Cまたは4Bの化合物は、下記化学式5ないし8の化合物で表示されることを特徴とする請求項1に記載のジメチレンシクロへキサン化合物:
- 下記化学式1aで表示される化合物と、下記化学式1bで表示される化合物及び/または下記化学式1cで表示される化合物とを反応させて、下記化学式1dで表示される化合物を形成する工程と、
前記化学式1dで表示される化合物を化学式L1−Q1で表示される化合物、L2−Q2で表示される化合物、L3−Q3で表示される化合物及びL4−Q4で表示される化合物からなる群から選択された二以上と反応させて、請求項1に記載の化学式3、4、4Cまたは4Bで表示される化合物を形成する工程と、を含むことを特徴とするジメチレンシクロへキサン化合物の製造方法:
R1、R2、R3、R4、R5、R6、R7、R8は、互いに独立的に、水素原子、ハロゲン原子、シアノ基、ヒドロキシル基、アミノ基、置換または非置換のC1−C20アルキル基、置換または非置換のC1−C20アルコキシ基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基または化学式−N(Z’)(Z”)を持つ置換されたアミノ基であり、
前記Z’及びZ”は、互いに独立的に、置換または非置換のC1−C20アルキル基、置換または非置換のC6−C30アリール基、置換または非置換のC2−C30ヘテロアリール基、置換または非置換のC5−C20シクロアルキル基または置換または非置換のC5−C30ヘテロシクロアルキル基を表し、
X1及びX2は、互いに独立的に、単結合、置換または非置換のC6−C30アリーレン基を表し、
n1及びn2は、互いに独立的に、0ないし1の整数であり、
Ar1’とAr2’とは、互いに独立的に、置換あるいは非置換されたC6−C30アリール基、C2−C30ヘテロアリール基、C4−C30シクロアルキル基あるいはC2−C30シクロヘテロアルキル基を表し、
Ha1及びHa2は、互いに独立的に、ハロゲン元素を表し、
m1及びm2は、互いに独立的に、0ないし5の整数を表し、ただし、m1とm2のうち少なくともいずれか一つは2以上の整数を表し、
前記化学式のL1−Q1 〜L4−Q4 が、
(i)下記の構造で表される基、または、
- 第1電極と、第2電極と、前記第1電極と前記第2電極との間にある少なくとも一層の有機膜と、を含む有機発光素子であり、前記有機膜が請求項1または2に記載のジメチレンシクロへキサン化合物を含むことを特徴とする有機発光素子。
- 前記有機膜は、正孔注入層、正孔輸送層または発光層であることを特徴とする請求項4に記載の有機発光素子。
- 前記第1電極と第2電極との間に正孔注入層、正孔輸送層、電子阻止層、正孔阻止層、電子輸送層及び電子注入層からなる群から選択された一層以上の層をさらに含むことを特徴とする請求項4に記載の有機発光素子。
- 前記素子は、第1電極/正孔注入層/発光層/電子輸送層/電子注入層/第2電極、第1電極/正孔注入層/正孔輸送層/発光層/電子輸送層/電子注入層/第2電極または第1電極/正孔注入層/正孔輸送層/発光層/正孔阻止層/電子輸送層/電子注入層/第2電極の構造を持つことを特徴とする請求項4〜6のいずれかに記載の有機発光素子。
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2006-0041970 | 2006-05-10 | ||
KR20060041970 | 2006-05-10 | ||
KR1020060129657A KR101372850B1 (ko) | 2006-05-10 | 2006-12-18 | 디메틸렌사이클로헥산 화합물, 이의 제조 방법 및 이를구비한 유기 발광 소자 |
KR10-2006-0129657 | 2006-12-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2007302671A JP2007302671A (ja) | 2007-11-22 |
JP5318367B2 true JP5318367B2 (ja) | 2013-10-16 |
Family
ID=38685510
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007126088A Active JP5318367B2 (ja) | 2006-05-10 | 2007-05-10 | ジメチレンシクロへキサン化合物、その製造方法及びそれを備えた有機発光素子 |
Country Status (2)
Country | Link |
---|---|
US (1) | US7879463B2 (ja) |
JP (1) | JP5318367B2 (ja) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101156425B1 (ko) * | 2005-07-28 | 2012-06-18 | 삼성모바일디스플레이주식회사 | 디메틸렌사이클로헥산 화합물, 이의 제조 방법 및 이를구비한 유기 발광 소자 |
JP5105820B2 (ja) * | 2006-10-12 | 2012-12-26 | 国立大学法人九州大学 | カルバゾール誘導体及びこれを用いた有機固体レーザー材料 |
KR101097316B1 (ko) * | 2009-10-12 | 2011-12-23 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
JP5597973B2 (ja) * | 2009-11-13 | 2014-10-01 | Dic株式会社 | トランス‐1,4−シクロヘキシレン構造を有する化合物の製造方法 |
CN108558595B (zh) * | 2018-05-22 | 2021-02-02 | 南京林业大学 | 一种对苯撑乙烯桥联三聚茚衍生物及其制备方法 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4356429A (en) * | 1980-07-17 | 1982-10-26 | Eastman Kodak Company | Organic electroluminescent cell |
JP3575104B2 (ja) * | 1995-03-24 | 2004-10-13 | 東洋インキ製造株式会社 | 正孔輸送材料およびその用途 |
EP0765106B1 (en) * | 1995-09-25 | 2002-11-27 | Toyo Ink Manufacturing Co., Ltd. | Light-emitting material for organic electroluminescence device, and organic electroluminescence device for which the light-emitting material is adapted |
JP3588978B2 (ja) | 1997-06-12 | 2004-11-17 | 凸版印刷株式会社 | 有機薄膜el素子 |
JP2973981B2 (ja) * | 1997-07-14 | 1999-11-08 | 日本電気株式会社 | 有機エレクトロルミネッセンス素子 |
JP3697038B2 (ja) * | 1997-09-25 | 2005-09-21 | キヤノン株式会社 | 電子写真感光体、該電子写真感光体を有するプロセスカ−トリッジ及び電子写真装置 |
JPH11329734A (ja) | 1998-03-10 | 1999-11-30 | Mitsubishi Chemical Corp | 有機電界発光素子 |
US20010043043A1 (en) * | 2000-01-07 | 2001-11-22 | Megumi Aoyama | Organic electroluminescent display panel and organic electroluminescent device used therefor |
JP2003186214A (ja) | 2001-12-21 | 2003-07-03 | Canon Inc | 電子写真感光体、該電子写真感光体を有するプロセスカートリッジ及び電子写真装置 |
JP2003270811A (ja) * | 2002-03-19 | 2003-09-25 | Kyocera Mita Corp | 電子写真感光体および画像形成装置 |
JP3960131B2 (ja) * | 2002-06-05 | 2007-08-15 | 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、及びそれを用いた有機エレクトロルミネッセンス素子および表示装置 |
JP4311707B2 (ja) * | 2002-08-28 | 2009-08-12 | キヤノン株式会社 | 有機発光素子 |
JP4082297B2 (ja) * | 2003-07-29 | 2008-04-30 | 三菱化学株式会社 | 有機化合物、電荷輸送材料、有機電界発光素子材料および有機電界発光素子 |
KR101156425B1 (ko) * | 2005-07-28 | 2012-06-18 | 삼성모바일디스플레이주식회사 | 디메틸렌사이클로헥산 화합물, 이의 제조 방법 및 이를구비한 유기 발광 소자 |
-
2007
- 2007-05-10 US US11/798,171 patent/US7879463B2/en active Active
- 2007-05-10 JP JP2007126088A patent/JP5318367B2/ja active Active
Also Published As
Publication number | Publication date |
---|---|
JP2007302671A (ja) | 2007-11-22 |
US20070264526A1 (en) | 2007-11-15 |
US7879463B2 (en) | 2011-02-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100846590B1 (ko) | 실란일아민계 화합물, 이의 제조 방법 및 이를 포함한유기막을 구비한 유기 발광 소자 | |
EP1862524B1 (en) | Organic light emitting device and flat panel display device comprising the same | |
KR101320382B1 (ko) | 유기 발광 화합물 및 이를 구비한 유기 발광 소자 | |
KR101430589B1 (ko) | 유기발광화합물 및 이를 이용한 유기 광소자 | |
JP5160046B2 (ja) | アミノスチリル化合物、その製造方法及びそれを備えた有機発光素子 | |
JP5449643B2 (ja) | オルガノシロキサン化合物及びこれを含む有機発光素子 | |
KR101256205B1 (ko) | 유기발광화합물 및 이를 구비한 유기발광소자 | |
KR101193183B1 (ko) | 헤테로고리 화합물 및 이를 이용한 유기 발광 소자 | |
US20100298607A1 (en) | Cyclopentaphenanthrene-based compound and organic electroluminescent device using the same | |
JP5588789B2 (ja) | ヘテロアリールアミン化合物及びそれを用いた有機発光素子 | |
EP2298737B1 (en) | Indole compounds and organic light-emitting device including the same | |
KR20080047210A (ko) | 유기 발광 화합물 및 이를 구비한 유기 발광 소자 | |
KR20100006072A (ko) | 유기 발광 화합물 및 이를 구비한 유기 발광 소자 | |
US7824780B2 (en) | Imidazopyrimidine-based compound and organic light-emitting device employing organic layer including the same | |
EP2293650A1 (en) | Dipyrrolo[a,h]pyrenes for organic light-emitting devices | |
KR101356654B1 (ko) | 유기 발광 화합물 및 이를 구비한 유기 발광 소자 | |
KR101473306B1 (ko) | 사이클로펜타페난트렌계 화합물 및 이를 이용한 유기 전계발광 소자 | |
JP5318367B2 (ja) | ジメチレンシクロへキサン化合物、その製造方法及びそれを備えた有機発光素子 | |
JP5216823B2 (ja) | ヘテロ環化合物及び有機発光素子 | |
JP5306583B2 (ja) | シクロヘキサン誘導体、その製造方法、及びそれを具備した有機発光素子 | |
KR101372850B1 (ko) | 디메틸렌사이클로헥산 화합물, 이의 제조 방법 및 이를구비한 유기 발광 소자 | |
KR101606559B1 (ko) | 방향족 복소환 화합물 및 이를 포함한 유기막을 구비한 유기 발광 소자 | |
KR101621801B1 (ko) | 방향족 복소환 화합물 및 이를 포함한 유기막을 구비한 유기 발광 소자 | |
KR20200004248A (ko) | 다환 화합물 및 이를 포함하는 유기 발광 소자 | |
KR20090128889A (ko) | 유기 발광 화합물 및 이를 구비한 유기 발광 소자 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20081201 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20100303 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120710 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20120912 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20121010 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20121107 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130312 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130610 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130625 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130710 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5318367 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |