JP2013519740A - エレクトロルミネッセンスポリマー、その調製方法、およびその使用 - Google Patents
エレクトロルミネッセンスポリマー、その調製方法、およびその使用 Download PDFInfo
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- JP2013519740A JP2013519740A JP2012552286A JP2012552286A JP2013519740A JP 2013519740 A JP2013519740 A JP 2013519740A JP 2012552286 A JP2012552286 A JP 2012552286A JP 2012552286 A JP2012552286 A JP 2012552286A JP 2013519740 A JP2013519740 A JP 2013519740A
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- 229920000642 polymer Polymers 0.000 title claims abstract description 148
- 238000000034 method Methods 0.000 title claims abstract description 16
- 238000002360 preparation method Methods 0.000 title abstract description 7
- 230000008569 process Effects 0.000 title abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 23
- -1 indenofluorene arylamine Chemical class 0.000 claims abstract description 22
- 238000009472 formulation Methods 0.000 claims abstract description 6
- 125000003118 aryl group Chemical group 0.000 claims description 51
- 150000001875 compounds Chemical class 0.000 claims description 33
- 150000003254 radicals Chemical class 0.000 claims description 26
- 229910052760 oxygen Inorganic materials 0.000 claims description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims description 19
- 238000006116 polymerization reaction Methods 0.000 claims description 19
- 229910052717 sulfur Inorganic materials 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 15
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 14
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 125000004122 cyclic group Chemical group 0.000 claims description 13
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 12
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 12
- 238000002347 injection Methods 0.000 claims description 12
- 239000007924 injection Substances 0.000 claims description 12
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims description 12
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims description 10
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims description 10
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 8
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 7
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 6
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 6
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 229910052787 antimony Inorganic materials 0.000 claims description 6
- 229910052785 arsenic Inorganic materials 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 229930192474 thiophene Natural products 0.000 claims description 6
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 5
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
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- 125000000524 functional group Chemical group 0.000 claims description 5
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- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 5
- 229950000688 phenothiazine Drugs 0.000 claims description 5
- ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 1,2-dihydrophenazine Chemical compound C1=CC=C2N=C(C=CCC3)C3=NC2=C1 ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 0.000 claims description 4
- XXPBFNVKTVJZKF-UHFFFAOYSA-N 9,10-dihydrophenanthrene Chemical compound C1=CC=C2CCC3=CC=CC=C3C2=C1 XXPBFNVKTVJZKF-UHFFFAOYSA-N 0.000 claims description 4
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 claims description 4
- 230000005684 electric field Effects 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 4
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 4
- 230000007704 transition Effects 0.000 claims description 4
- FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical compound C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 claims description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 3
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 3
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 claims description 3
- SNFCXVRWFNAHQX-UHFFFAOYSA-N 9,9'-spirobi[fluorene] Chemical compound C12=CC=CC=C2C2=CC=CC=C2C21C1=CC=CC=C1C1=CC=CC=C21 SNFCXVRWFNAHQX-UHFFFAOYSA-N 0.000 claims description 3
- 239000005964 Acibenzolar-S-methyl Substances 0.000 claims description 3
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 3
- 230000005669 field effect Effects 0.000 claims description 3
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 claims description 3
- 125000002950 monocyclic group Chemical group 0.000 claims description 3
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 3
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 claims description 3
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 3
- 108091008695 photoreceptors Proteins 0.000 claims description 3
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 3
- 239000010409 thin film Substances 0.000 claims description 3
- 125000005259 triarylamine group Chemical group 0.000 claims description 3
- 125000004958 1,4-naphthylene group Chemical group 0.000 claims description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 2
- XDFUNRTWHPWCKO-UHFFFAOYSA-N 4,5,9,10-tetrahydropyrene Chemical compound C1CC2=CC=CC3=C2C2=C1C=CC=C2CC3 XDFUNRTWHPWCKO-UHFFFAOYSA-N 0.000 claims description 2
- WPCIUCNVWJNRCD-UHFFFAOYSA-N 4,5-dihydropyrene Chemical compound C1=CC=C2CCC3=CC=CC4=CC=C1C2=C34 WPCIUCNVWJNRCD-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 125000000732 arylene group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 2
- 150000002240 furans Chemical class 0.000 claims description 2
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 2
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims description 2
- 150000002926 oxygen Chemical class 0.000 claims description 2
- 150000002988 phenazines Chemical class 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims description 2
- 125000006413 ring segment Chemical group 0.000 claims description 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 description 2
- 150000004756 silanes Chemical class 0.000 claims description 2
- 150000003457 sulfones Chemical class 0.000 claims description 2
- 150000003462 sulfoxides Chemical class 0.000 claims description 2
- GVIJJXMXTUZIOD-UHFFFAOYSA-N thianthrene Chemical compound C1=CC=C2SC3=CC=CC=C3SC2=C1 GVIJJXMXTUZIOD-UHFFFAOYSA-N 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 125000005730 thiophenylene group Chemical group 0.000 claims description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 claims 2
- RICKKZXCGCSLIU-UHFFFAOYSA-N 2-[2-[carboxymethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]ethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]acetic acid Chemical compound CC1=NC=C(CO)C(CN(CCN(CC(O)=O)CC=2C(=C(C)N=CC=2CO)O)CC(O)=O)=C1O RICKKZXCGCSLIU-UHFFFAOYSA-N 0.000 claims 1
- MZCJSUCRGWIKHH-UHFFFAOYSA-N 6,7-dihydrobenzo[d][1]benzoxepine Chemical compound O1CCC2=CC=CC=C2C2=CC=CC=C21 MZCJSUCRGWIKHH-UHFFFAOYSA-N 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- 125000005605 benzo group Chemical group 0.000 claims 1
- 238000004770 highest occupied molecular orbital Methods 0.000 claims 1
- NFBOHOGPQUYFRF-UHFFFAOYSA-N oxanthrene Chemical compound C1=CC=C2OC3=CC=CC=C3OC2=C1 NFBOHOGPQUYFRF-UHFFFAOYSA-N 0.000 claims 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims 1
- GJSGGHOYGKMUPT-UHFFFAOYSA-N phenoxathiine Chemical compound C1=CC=C2OC3=CC=CC=C3SC2=C1 GJSGGHOYGKMUPT-UHFFFAOYSA-N 0.000 claims 1
- 150000003003 phosphines Chemical class 0.000 claims 1
- 239000000463 material Substances 0.000 description 28
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 229920000547 conjugated polymer Polymers 0.000 description 12
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- 239000000412 dendrimer Substances 0.000 description 10
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 8
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
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- ICPSWZFVWAPUKF-UHFFFAOYSA-N 1,1'-spirobi[fluorene] Chemical compound C1=CC=C2C=C3C4(C=5C(C6=CC=CC=C6C=5)=CC=C4)C=CC=C3C2=C1 ICPSWZFVWAPUKF-UHFFFAOYSA-N 0.000 description 3
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- 238000011065 in-situ storage Methods 0.000 description 3
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
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- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
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- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
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- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
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- 238000012360 testing method Methods 0.000 description 2
- SFLXUZPXEWWQNH-UHFFFAOYSA-K tetrabutylazanium;tribromide Chemical compound [Br-].[Br-].[Br-].CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC SFLXUZPXEWWQNH-UHFFFAOYSA-K 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- HQDYNFWTFJFEPR-UHFFFAOYSA-N 1,2,3,3a-tetrahydropyrene Chemical compound C1=C2CCCC(C=C3)C2=C2C3=CC=CC2=C1 HQDYNFWTFJFEPR-UHFFFAOYSA-N 0.000 description 1
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- UUSUFQUCLACDTA-UHFFFAOYSA-N 1,2-dihydropyrene Chemical compound C1=CC=C2C=CC3=CCCC4=CC=C1C2=C43 UUSUFQUCLACDTA-UHFFFAOYSA-N 0.000 description 1
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- 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
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Abstract
【選択図】 なし
Description
Ar1、Ar2、Ar3は、出現する毎に、同一または異なり、5〜24個の芳香環原子を有する、C6〜C24アリールまたはC2〜C23ヘテロアリール基であり、これらは1つ以上のラジカルR1によって置換されていてもよく;
Yは、出現する毎に、N、P、P=O、PF2、P=S、As、As=O、As=S、Sb、Sb=OまたはSb=Sであり;
Ar4、Ar5は、出現する毎に、同一または異なり、5〜40個の芳香環原子を有する、芳香族環またはヘテロ芳香族環系であり、1つ以上のラジカルR1によって置換されていてもよく;
R1は、出現する毎に、同一または異なり、H、F、Cl、Br、I、CN、NO2、Si(R2)3、1〜40個のC原子を有する直鎖状のアルキル、アルコキシもしくはチオアルコキシ基、または3〜40個のC原子を有する分岐状もしくは環状のアルキル、アルコキシもしくはチオアルコキシ基(これらの各々は、1つ以上のラジカルR2によって置換されていてもよく、ここで、1つ以上の非隣接CH2基は、−R2C=CR2−、−C≡C−、Si(R2)2、Ge(R2)2、Sn(R2)2、C=O、C=S、C=Se、C=NR2、−O−、−S−もしくは−CONR2−によって置きかえられていてもよく、1つ以上のH原子は、F、Cl、Br、I、CNもしくはNO2によって置きかえられていてもよい)、あるいは5〜40個の芳香環原子を有する芳香族またはヘテロ芳香族環系(これらは、1つ以上のラジカルR2によって置換されていてもよい)、あるいは5〜40個の芳香環原子を有するアリールオキシまたはヘテロアリールオキシ基(これらは、1つ以上のラジカルR2によって置換されていてもよい)、あるいはこれらの系の組合せであり;ここで、2つ以上の置換基R1は、単環もしくは多環の、脂肪族、芳香族またはヘテロ芳香族環系を互いに形成していてもよく;
R2は、出現する毎に、同一または異なり、H、1〜20個のC原子を有する脂肪族炭化水素ラジカルまたは6〜20個のC原子を有する芳香族炭化水素ラジカルであり;
X1は、出現する毎に、同一または異なり、Ar1およびAr2と共に環系を形成する架橋であり、B(R1)、C(R1)2、Si(R1)2、C=O、C=NR1、C=C(R1)2、O、S、S=O、SO2、N(R1)、P(R1)、P(=O)R1、P(=S)R1またはこれらの基の2つ、3つもしくは4つの組合せから選択され;
X2、X3は、出現する毎に、同一または異なり、Ar2およびAr3と共に環系を形成する架橋であり、B(R1)、C(R1)2、Si(R1)2、C=O、C=NR1、C=C(R1)2、O、S、S=O、SO2、N(R1)、P(R1)、P(=O)R1、P(=S)R1またはこれらの基の2つ、3つもしくは4つの組合せから選択され;
n、oは、出現する毎に、同一または異なり、0または1であり、ただし、その合計(n+o)=1であり;
破線は、ポリマー中にあり得る結合を表す。
グループ1:ポリマーの正孔注入特性および/または正孔輸送特性に影響する単位、
グループ2:ポリマーの電子注入特性および/または電子輸送特性に影響する単位、
グループ3:グループ1およびグループ2の個々の単位の組合せを有する単位、
グループ4:電場蛍光(electrofluorescence)ではなく、電場燐光(electrophosphorescence)を得ることができる程度まで、発光特性を修飾する単位、
グループ5:いわゆる一重項状態から三重項状態への移行(transfer)を改善する単位、
グループ6:得られるポリマーの発光色に影響する単位、
グループ7:典型的には主鎖として使用する単位、
グループ8:得られるポリマーのフィルム状での形態学的特性および/またはレオロジー特性に影響する単位。
(A)スズキ重合、
(B)ヤマモト重合、
(C)スティル(STILLE)重合、
(D)ヘック(HECK)重合、
(E)ネギシ重合、
(F)ソノガシラ重合、
(G)ヒヤマ重合、および
(H)ハートウィッグ−ブッフバルト(HARTWIG−BUCHWALD)重合
である。
例2
N,N’−[4,4’ジブロモフェニル)−9−アミノ−2−ブロモベンゾインデノフルオレン4
例3〜6:
ポリマーの調製
本発明によるポリマーP1およびP2と、比較用ポリマーC1およびC2とを、下記のモノマーを使用して、WO03/048225A2に依拠したスズキカップリングによって合成する(パーセントデータ=mol%)。
PLEDデバイスの作製
ポリマー有機発光ダイオード(PLED)を、ここまでに何度も文献中で(例えばWO2004/037887A2中で)説明したように作製する。例示的な用語で本発明を説明するため、PLEDは、スピンコーティングにより、ポリマーP1およびP2と、比較用ポリマーC1およびC2とを用いて作製する。典型的なデバイスは、図1に示した構造を有する。
Claims (15)
- 0.01〜100mol%の1つ以上の式(1)の構造単位を含むポリマー:
Ar1、Ar2、Ar3は、出現する毎に、同一または異なり、5〜24個の芳香環原子を有する、C6〜C24アリールまたはC2〜C23ヘテロアリール基であり、これらは1つ以上のラジカルR1によって置換されていてもよく;
Yは、出現する毎に、N、P、P=O、PF2、P=S、As、As=O、As=S、Sb、Sb=OまたはSb=Sであり;
Ar4、Ar5は、出現する毎に、同一または異なり、5〜40個の芳香環原子を有する、芳香族またはヘテロ芳香族環系であり、1つ以上のラジカルR1によって置換されていてもよく;
R1は、出現する毎に、同一または異なり、H、F、Cl、Br、I、CN、NO2、Si(R2)3、1〜40個のC原子を有する直鎖状のアルキル、アルコキシもしくはチオアルコキシ基または3〜40個のC原子を有する分岐状もしくは環状のアルキル、アルコキシもしくはチオアルコキシ基(これらの各々は、1つ以上のラジカルR2によって置換されていてもよい)(ここで、1つ以上の非隣接CH2基は、−R2C=CR2−、−C≡C−、Si(R2)2、Ge(R2)2、Sn(R2)2、C=O、C=S、C=Se、C=NR2、−O−、−S−もしくは−CONR2−によって置きかえられていてもよく、1つ以上のH原子は、F、Cl、Br、I、CNもしくはNO2によって置きかえられていてもよい)、あるいは5〜40個の芳香環原子を有する芳香族またはヘテロ芳香族環系(これらは、1つ以上のラジカルR2によって置換されていてもよい)、あるいは5〜40個の芳香環原子を有するアリールオキシまたはヘテロアリールオキシ基(これらは、1つ以上のラジカルR2によって置換されていてもよい)、あるいはこれらの系の組合せであり;ここで、2つ以上の置換基R1は、単環もしくは多環の、脂肪族、芳香族またはヘテロ芳香族環系を互いに形成していてもよく;
R2は、出現する毎に、同一または異なり、H、1〜20個のC原子を有する脂肪族炭化水素ラジカルまたは6〜20個のC原子を有する芳香族炭化水素ラジカルであり;
X1は、出現する毎に、同一または異なり、Ar1およびAr2と共に環系を形成する架橋であり、B(R1)、C(R1)2、Si(R1)2、C=O、C=NR1、C=C(R1)2、O、S、S=O、SO2、N(R1)、P(R1)、P(=O)R1、P(=S)R1またはこれらの基の2つ、3つもしくは4つの組合せから選択され;
X2、X3は、出現する毎に、同一または異なり、Ar2およびAr3と共に環系を形成する架橋であり、B(R1)、C(R1)2、Si(R1)2、C=O、C=NR1、C=C(R1)2、O、S、S=O、SO2、N(R1)、P(R1)、P(=O)R1、P(=S)R1またはこれらの基の2つ、3つもしくは4つの組合せから選択され;
n、oは、出現する毎に、同一または異なり、0または1であり、ただし、その合計(n+o)=1であり;
破線は、前記ポリマー中にあり得る結合を表す。 - 請求項1に記載のポリマーであって、前記式(1)の単位に加えて、さらなる構造単位を含むことを特徴とするポリマー。
- 請求項2に記載のポリマーであって、前記さらなる構造単位は、正孔注入および/または正孔輸送特性を有し、トリアリールアミン、ベンジジン、テトラアリール−パラ−フェニレンジアミン、トリアリールホスフィン、フェノチアジン、フェノキサジン、ジヒドロフェナジン、チアントレン、ジベンゾ−パラ−ジオキシン、フェノキサチイン、カルバゾール、アズレン、チオフェン、ピロールおよびフラン誘導体、ならびにさらに、高いHOMOを有するO、SまたはN含有ヘテロ環化合物の群から選択されることを特徴とするポリマー。
- 請求項2または3に記載のポリマーであって、前記さらなる構造単位は、電子注入および/または電子輸送特性を有し、ピリジン、ピリミジン、ピリダジン、ピラジン、オキサジアゾール、キノリン、キノキサリン、アントラセン、ベンゾアントラセン、ピレン、ペリレン、ベンゾイミダゾール、トリアジン、ケトン、ホスフィンオキシドおよびフェナジン誘導体、またトリアリールボランおよびさらに、低いLUMOを有するO、SまたはN含有ヘテロ環化合物の群から選択されることを特徴とするポリマー。
- 請求項2〜4の1項以上に記載のポリマーであって、さらなる構造要素は、電場蛍光の代わりに電場燐光を得ることができる程度にまで発光特性を修飾することを特徴とするポリマー。
- 請求項2〜5の1項以上に記載のポリマーであって、さらなる構造要素は、一重項状態から三重項状態への移行を改善し、カルバゾールおよび架橋されたカルバゾール二量体単位、ケトン、ホスフィンオキシド、スルホキシド、スルホンならびにシラン誘導体のクラスから選択されることを特徴とするポリマー。
- 請求項2〜6の1項以上に記載のポリマーであって、さらなる構造要素は、前記ポリマーの発光色に影響し、1,4−フェニレン、1,4−ナフチレン、1,4−もしくは9,10−アントリレン、1,6−、2,7−もしくは4,9−ピレニレン、3,9−もしくは3,10−ペリレニレン、4,4’−ビフェニリレン、4,4’’−テルフェニリレン、4,4’−ビ−1,1’−ナフチリレン、4,4‘−トラニレン、4,4’−スチルベニレン、4,4’’−ビススチリルアリーレン、ベンゾチアジアゾールおよび対応する酸素誘導体、キノキサリン、フェノチアジン、フェノキサジン、ジヒドロフェナジン、ビス(チオフェニル)アリーレン、オリゴ(チオフェニレン)、フェナジン、ルブレン、ペンタセンならびにペリレン誘導体のクラスから選択されることを特徴とするポリマー。
- 請求項2〜7の1項以上に記載のポリマーであって、さらなる構造要素は、典型的には主鎖として使用され、4,5−ジヒドロピレン、4,5,9,10−テトラヒドロピレン、フルオレン、9,9‘−スピロビフルオレン、フェナントレン、9,10−ジヒドロフェナントレン、5,7−ジヒドロジベンゾオキセピンならびにcis−およびtrans−インデノフルオレン誘導体のクラスから選択されることを特徴とするポリマー。
- 請求項1〜8の1項以上に記載のポリマーの調製方法であって、前記ポリマーを、スズキ重合、ヤマモト重合、スティル重合またはハートウィッグ−ブッフバルト重合によって調製することを特徴とするポリマーの調製方法。
- 請求項10に記載の式(8)、(9)および(10)の化合物であって、前記官能基は、Cl、Br、I、O−トシラート、O−トリフラート、O−SO2R2、B(OR2)2およびSn(R2)3から選択され、ここでR2は、出現する毎に、同一または異なり、H、1〜20個のC原子を有する脂肪族または芳香族炭化水素ラジカルであり、前記ラジカルR2の2つ以上は互いに環系を形成していてもよいことを特徴とする化合物。
- 請求項1〜8の1項以上に記載の1種以上のポリマーと、さらなるポリマー物質、オリゴマー物質、樹状物質および/または低分子量物質との混合物(ブレンド)。
- 1種以上の溶媒中に、請求項1〜8の1項以上に記載の1種以上のポリマーを含む、または請求項12に記載のブレンドを含む溶液および配合物。
- 1種以上の活性層を有する有機電子デバイスであって、前記活性層の少なくとも1つが、請求項1〜8の1項以上に記載の1種以上のポリマーまたは請求項12に記載のブレンドを含むことを特徴とする有機電子デバイス。
- 請求項14に記載の有機電子デバイスであって、有機もしくはポリマー有機発光ダイオード(OLED、PLED)、有機集積回路(O−IC)、有機電界効果トランジスタ(OFET)、有機薄膜トランジスタ(OTFT)、有機太陽電池(O−SC)、有機レーザーダイオード(O−レーザー)、有機光電変換(OPV)素子もしくはデバイス、または有機光受容体(OPC)であることを特徴とする有機電子デバイス。
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---|---|---|---|---|
WO2020065920A1 (ja) * | 2018-09-28 | 2020-04-02 | 日立化成株式会社 | 有機エレクトロニクス材料及び有機エレクトロニクス素子 |
CN111051293A (zh) * | 2017-09-08 | 2020-04-21 | 默克专利有限公司 | 用于电子器件的材料 |
JP2020533324A (ja) * | 2017-09-08 | 2020-11-19 | メルク パテント ゲーエムベーハー | 電子デバイス用材料 |
Families Citing this family (15)
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DE102009041289A1 (de) * | 2009-09-16 | 2011-03-17 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
EP2610936A1 (en) * | 2011-12-28 | 2013-07-03 | Solvay Sa | Crosslinkable compositions comprising addition polymerizable monomers |
US9353122B2 (en) | 2013-02-15 | 2016-05-31 | Kala Pharmaceuticals, Inc. | Therapeutic compounds and uses thereof |
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US9890173B2 (en) | 2013-11-01 | 2018-02-13 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
AU2014342042B2 (en) | 2013-11-01 | 2017-08-17 | KALA BIO, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
CN105924629A (zh) * | 2016-06-27 | 2016-09-07 | 华南理工大学 | 一种基于萘并茚芴单元的共轭聚合物及其制备方法与应用 |
US10392399B2 (en) | 2016-09-08 | 2019-08-27 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
US10253036B2 (en) | 2016-09-08 | 2019-04-09 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
EP3509421A4 (en) | 2016-09-08 | 2020-05-20 | Kala Pharmaceuticals, Inc. | CRYSTALLINE FORMS OF THERAPEUTIC COMPOUNDS AND USES THEREOF |
CN108424344B (zh) * | 2018-04-11 | 2021-07-02 | 华南协同创新研究院 | 含菲的五元并环单元的单体和聚合物及其制备方法与应用 |
EP3582280B1 (en) * | 2018-06-14 | 2024-03-20 | Novaled GmbH | Organic material for an electronic optoelectronic device and electronic device comprising the organic material |
US20210253785A1 (en) * | 2018-07-03 | 2021-08-19 | Hodogaya Chemical Co., Ltd. | High molecular weight triarylamine compound comprising terphenyl structure in molecular main chain and organic electroluminescent element comprising said high molecular weight compound |
CN114106295B (zh) * | 2020-12-29 | 2023-06-16 | 广东聚华印刷显示技术有限公司 | 可交联型聚合物及其制备方法和应用 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007534814A (ja) * | 2004-04-26 | 2007-11-29 | メルク パテント ゲーエムベーハー | 平面アリールアミン単位を含むエレクトロルミネセンスポリマー、その調製および使用 |
JP2008545630A (ja) * | 2005-05-20 | 2008-12-18 | メルク パテント ゲーエムベーハー | 有機電子素子のための化合物 |
JP2009505995A (ja) * | 2005-08-26 | 2009-02-12 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネセンスデバイスのための新規材料 |
JP2009536981A (ja) * | 2006-05-12 | 2009-10-22 | メルク パテント ゲーエムベーハー | インデノフルオレンポリマー系有機半導体材料 |
JP2011505439A (ja) * | 2007-11-21 | 2011-02-24 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 共役コポリマー |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4505146B2 (ja) | 1999-02-04 | 2010-07-21 | ダウ グローバル テクノロジーズ インコーポレイティド | フルオレンコポリマーおよびそれから作られる素子 |
GB0104177D0 (en) | 2001-02-20 | 2001-04-11 | Isis Innovation | Aryl-aryl dendrimers |
DE10109027A1 (de) | 2001-02-24 | 2002-09-05 | Covion Organic Semiconductors | Rhodium- und Iridium-Komplexe |
JP4438042B2 (ja) | 2001-03-08 | 2010-03-24 | キヤノン株式会社 | 金属配位化合物、電界発光素子及び表示装置 |
DE50207293D1 (de) | 2001-03-10 | 2006-08-03 | Merck Patent Gmbh | Lösung und dispersionen organischer halbleiter |
CN1216928C (zh) | 2001-03-24 | 2005-08-31 | 科文有机半导体有限公司 | 含有螺二芴单元和氟单元的共轭聚合物及其应用 |
DE10116962A1 (de) | 2001-04-05 | 2002-10-10 | Covion Organic Semiconductors | Rhodium- und Iridium-Komplexe |
DE10141624A1 (de) | 2001-08-24 | 2003-03-06 | Covion Organic Semiconductors | Lösungen polymerer Halbleiter |
US7250226B2 (en) * | 2001-08-31 | 2007-07-31 | Nippon Hoso Kyokai | Phosphorescent compound, a phosphorescent composition and an organic light-emitting device |
DE10143353A1 (de) | 2001-09-04 | 2003-03-20 | Covion Organic Semiconductors | Konjugierte Polymere enthaltend Spirobifluoren-Einheiten und deren Verwendung |
DE10159946A1 (de) | 2001-12-06 | 2003-06-18 | Covion Organic Semiconductors | Prozess zur Herstellung von Aryl-Aryl gekoppelten Verbindungen |
DE10238903A1 (de) | 2002-08-24 | 2004-03-04 | Covion Organic Semiconductors Gmbh | Rhodium- und Iridium-Komplexe |
DE10249723A1 (de) | 2002-10-25 | 2004-05-06 | Covion Organic Semiconductors Gmbh | Arylamin-Einheiten enthaltende konjugierte Polymere, deren Darstellung und Verwendung |
GB0226010D0 (en) | 2002-11-08 | 2002-12-18 | Cambridge Display Tech Ltd | Polymers for use in organic electroluminescent devices |
DE10304819A1 (de) | 2003-02-06 | 2004-08-19 | Covion Organic Semiconductors Gmbh | Carbazol-enthaltende konjugierte Polymere und Blends, deren Darstellung und Verwendung |
US7049392B2 (en) * | 2003-02-12 | 2006-05-23 | E. I. Du Pont De Nemour And Company | Electroluminescent copolymers with multi-functional monomers and methods for use thereof |
JP4424307B2 (ja) * | 2003-04-18 | 2010-03-03 | 日立化成工業株式会社 | 枝分れ構造を有するポリキノリン共重合体およびこれを用いた有機エレクトロルミネセンス素子 |
DE10328627A1 (de) | 2003-06-26 | 2005-02-17 | Covion Organic Semiconductors Gmbh | Neue Materialien für die Elektrolumineszenz |
DE10337346A1 (de) | 2003-08-12 | 2005-03-31 | Covion Organic Semiconductors Gmbh | Konjugierte Polymere enthaltend Dihydrophenanthren-Einheiten und deren Verwendung |
DE10337077A1 (de) | 2003-08-12 | 2005-03-10 | Covion Organic Semiconductors | Konjugierte Copolymere, deren Darstellung und Verwendung |
JPWO2005026144A1 (ja) | 2003-09-12 | 2006-11-16 | 住友化学株式会社 | デンドリマー化合物及びそれを用いた有機発光素子 |
DE10343606A1 (de) | 2003-09-20 | 2005-04-14 | Covion Organic Semiconductors Gmbh | Weiß emittierende Copolymere, deren Darstellung und Verwendung |
JP4847327B2 (ja) | 2003-09-20 | 2011-12-28 | メルク パテント ゲーエムベーハー | 共役ポリマー、その調製と使用 |
EP2366752B1 (de) | 2003-10-22 | 2016-07-20 | Merck Patent GmbH | Neue materialien für die elektrolumineszenz und deren verwendung |
DE10350606A1 (de) | 2003-10-30 | 2005-06-09 | Covion Organic Semiconductors Gmbh | Verfahren zur Herstellung heteroleptischer, ortho-metallierter Organometall-Verbindungen |
DE102004009355A1 (de) | 2004-02-26 | 2005-09-15 | Covion Organic Semiconductors Gmbh | Verfahren zur Vernetzung organischer Halbleiter |
KR101346907B1 (ko) | 2005-04-14 | 2014-01-02 | 메르크 파텐트 게엠베하 | 유기 전자 소자용 화합물 |
KR100812178B1 (ko) * | 2006-01-27 | 2008-03-12 | (주)그라쎌 | 플루오렌기를 함유하는 전기발광화합물 및 이를 발광재료로채용하고 있는 표시소자 |
DE102006031990A1 (de) * | 2006-07-11 | 2008-01-17 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
JP2009043896A (ja) * | 2007-08-08 | 2009-02-26 | Canon Inc | 有機発光素子及びディスプレイ |
EP3182479B1 (en) * | 2008-02-15 | 2018-10-03 | Mitsubishi Chemical Corporation | Conjugated polymer for organic electroluminescence element |
-
2010
- 2010-02-12 DE DE102010007938A patent/DE102010007938A1/de active Pending
-
2011
- 2011-01-18 US US13/578,439 patent/US9534077B2/en active Active
- 2011-01-18 JP JP2012552286A patent/JP5726905B2/ja active Active
- 2011-01-18 WO PCT/EP2011/000190 patent/WO2011098205A1/de active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007534814A (ja) * | 2004-04-26 | 2007-11-29 | メルク パテント ゲーエムベーハー | 平面アリールアミン単位を含むエレクトロルミネセンスポリマー、その調製および使用 |
JP2008545630A (ja) * | 2005-05-20 | 2008-12-18 | メルク パテント ゲーエムベーハー | 有機電子素子のための化合物 |
JP2009505995A (ja) * | 2005-08-26 | 2009-02-12 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネセンスデバイスのための新規材料 |
JP2009536981A (ja) * | 2006-05-12 | 2009-10-22 | メルク パテント ゲーエムベーハー | インデノフルオレンポリマー系有機半導体材料 |
JP2011505439A (ja) * | 2007-11-21 | 2011-02-24 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 共役コポリマー |
Non-Patent Citations (1)
Title |
---|
JPN6014022731; 'Synthesis and two-photon properties of a multipolarchromophore containing indenofluorenyl units' Tetrahedron Letters 50, 2009, p182-185 * |
Cited By (12)
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JP2020533324A (ja) * | 2017-09-08 | 2020-11-19 | メルク パテント ゲーエムベーハー | 電子デバイス用材料 |
JP2020533325A (ja) * | 2017-09-08 | 2020-11-19 | メルク パテント ゲーエムベーハー | 電子デバイス用材料 |
JP7250773B2 (ja) | 2017-09-08 | 2023-04-03 | メルク パテント ゲーエムベーハー | 電子デバイス用材料 |
JP7286625B2 (ja) | 2017-09-08 | 2023-06-05 | メルク パテント ゲーエムベーハー | 電子デバイス用材料 |
CN111051293B (zh) * | 2017-09-08 | 2024-02-13 | 默克专利有限公司 | 用于电子器件的材料 |
WO2020065920A1 (ja) * | 2018-09-28 | 2020-04-02 | 日立化成株式会社 | 有機エレクトロニクス材料及び有機エレクトロニクス素子 |
CN112771686A (zh) * | 2018-09-28 | 2021-05-07 | 昭和电工材料株式会社 | 有机电子材料和有机电子元件 |
KR20210056367A (ko) * | 2018-09-28 | 2021-05-18 | 쇼와덴코머티리얼즈가부시끼가이샤 | 유기 일렉트로닉스 재료 및 유기 일렉트로닉스 소자 |
JPWO2020065920A1 (ja) * | 2018-09-28 | 2021-09-24 | 昭和電工マテリアルズ株式会社 | 有機エレクトロニクス材料及び有機エレクトロニクス素子 |
JP7226452B2 (ja) | 2018-09-28 | 2023-02-21 | 株式会社レゾナック | 有機エレクトロニクス材料及び有機エレクトロニクス素子 |
KR102537755B1 (ko) * | 2018-09-28 | 2023-05-26 | 가부시끼가이샤 레조낙 | 유기 일렉트로닉스 재료 및 유기 일렉트로닉스 소자 |
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JP5726905B2 (ja) | 2015-06-03 |
US9534077B2 (en) | 2017-01-03 |
US20120305852A1 (en) | 2012-12-06 |
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