JP2015508119A - ジベンゾシクロヘプタン構造単位を含むポリマー - Google Patents
ジベンゾシクロヘプタン構造単位を含むポリマー Download PDFInfo
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- JP2015508119A JP2015508119A JP2014558029A JP2014558029A JP2015508119A JP 2015508119 A JP2015508119 A JP 2015508119A JP 2014558029 A JP2014558029 A JP 2014558029A JP 2014558029 A JP2014558029 A JP 2014558029A JP 2015508119 A JP2015508119 A JP 2015508119A
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- 229920000642 polymer Polymers 0.000 title claims abstract description 115
- BKBBHXQBVJMMHW-UHFFFAOYSA-N 6,7-dihydro-5h-dibenzo[2,1-b:2',1'-e][7]annulene Chemical compound C1CCC2=CC=CC=C2C2=CC=CC=C21 BKBBHXQBVJMMHW-UHFFFAOYSA-N 0.000 title abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 30
- 238000009472 formulation Methods 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 34
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000002950 monocyclic group Chemical group 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 238000006116 polymerization reaction Methods 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 8
- -1 boronate ester Chemical class 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000003367 polycyclic group Chemical group 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 4
- 230000005669 field effect Effects 0.000 claims description 3
- 238000013086 organic photovoltaic Methods 0.000 claims description 3
- 108091008695 photoreceptors Proteins 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 239000010409 thin film Substances 0.000 claims description 3
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical group [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 20
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- 238000004770 highest occupied molecular orbital Methods 0.000 description 4
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- 239000000243 solution Substances 0.000 description 4
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- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 3
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 description 3
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- 239000002800 charge carrier Substances 0.000 description 3
- XXPBFNVKTVJZKF-UHFFFAOYSA-N dihydrophenanthrene Natural products C1=CC=C2CCC3=CC=CC=C3C2=C1 XXPBFNVKTVJZKF-UHFFFAOYSA-N 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000005693 optoelectronics Effects 0.000 description 3
- 229950000688 phenothiazine Drugs 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- 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 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical compound C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 description 2
- ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 1,2-dihydrophenazine Chemical compound C1=CC=C2N=C(C=CCC3)C3=NC2=C1 ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
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- 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 description 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 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 2
- 229920000265 Polyparaphenylene Polymers 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
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- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
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- 230000000903 blocking effect Effects 0.000 description 2
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- 238000000576 coating method Methods 0.000 description 2
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 2
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 2
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
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- 125000005842 heteroatom Chemical group 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- PJULCNAVAGQLAT-UHFFFAOYSA-N indeno[2,1-a]fluorene Chemical compound C1=CC=C2C=C3C4=CC5=CC=CC=C5C4=CC=C3C2=C1 PJULCNAVAGQLAT-UHFFFAOYSA-N 0.000 description 2
- 238000007641 inkjet printing Methods 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 2
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- RDOWQLZANAYVLL-UHFFFAOYSA-N phenanthridine Chemical compound C1=CC=C2C3=CC=CC=C3C=NC2=C1 RDOWQLZANAYVLL-UHFFFAOYSA-N 0.000 description 2
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- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
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Classifications
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Abstract
Description
1.より広いバンドギャップを有し、その結果、広い色彩空間をもつ表示用途を達成することができる材料が必要とされる。ポリマー中のより広いバンドギャップは、これらが赤色のみならず緑色三重項発光のためのホスト材料として使用することを追加的に可能とする。
R1、R2は、出現毎に、同一であるか異なり、H、D、F、OH、N(R3)2、1〜40個のC原子を有する直鎖、分岐あるいは環状アルキル、アルコキシもしくはチオアルコキシ基であって、1以上のH原子は、Fで置き代えられてよく、ここで、さらに、1以上の非隣接のCH2基は、O、S、Si(R3)2、Ge(R3)2、BR3、NR3、PR3、CO、C=S、C=Se、C=NR3、PO(R3)、PS(R3)、R3C=CR3、C≡C、SO、SO2、COO、O(CO)OもしくはCONR2で置き代えられてよく、またはモノあるいはポリ環式の芳香族もしくは複素環式芳香族環構造であることができ;
R3は、出現毎に、同一であるか異なり、H、F、1〜40個のC原子を有する直鎖、分岐あるいは環状アルキル、アルコキシもしくはチオアルコキシ基であって、1以上のH原子は、Fで置き代えられてよく、ここで、さらに、1以上の非隣接のCH2基は、O、CO、COOもしくはO(CO)Oで置き代えられてよく、またはモノあるいはポリ環式の芳香族もしくは複素環式芳香族環構造であることができ;
m、nは、互いに独立して、出現毎に、同一であるか異なり、0、1、2または3、好ましくは、0または1、特に、好ましくは、0であり;
破線は、ポリマー中の隣接する構造単位ヘの結合である。
芳香族環構造は、モノ環状もしくはポリ環状であってよく、すなわち、それらは一個の環(たとえば、フェニル)または複数の環を含んでもよく、縮合(たとえば、ナフチル)、共有結合(たとえば、ビフェニル)または縮合と連結環の組み合わせを含んでもよい。
群1:ポリマーの正孔注入および/または正孔輸送特性に作用する単位。
したがって、本発明は、素子自体と本発明によるポリマーの対応する素子での使用の両者に関する。
モノマーの調製
本発明によるポリマー合成のためのモノマー化合物を、先行技術に記載の方法により調製することができ、当業者は、進歩性もなく特定の場合に対してこの方法を適用することができるであろう。
ポリマーの調製
本発明による比較ポリマーV1とポリマーP1を、次のモノマー(パーセントデータ=モル%)を用いて、WO 03/048225 A2からの一般的な手順にしたがい、スズキカップリングにより合成する。
ポリマー有機発光ダイオード(PLED)の製造は、特許文献(たとえば、WO 2004/037887 A2)に何度も既に記載されてきた。本発明を実例により説明するために、PLEDは、比較例のポリマーV1と本発明によるポリマーP1が、スピンコーティングを使用して製造される。
Claims (13)
- 一以上の式(I)の構造単位を含むポリマー。
R1、R2は、出現毎に、同一であるか異なり、H、D、F、OH、N(R3)2、1〜40個のC原子を有する直鎖、分岐あるいは環状アルキル、アルコキシもしくはチオアルコキシ基であって、1以上のH原子は、Fで置き代えられてよく、ここで、さらに、1以上の非隣接のCH2基は、O、S、Si(R3)2、Ge(R3)2、BR3、NR3、PR3、CO、C=S、C=Se、C=NR3、PO(R3)、PS(R3)、R3C=CR3、C≡C、SO、SO2、COO、O(CO)OもしくはCONR2で置き代えられてよく、またはモノあるいはポリ環式の芳香族もしくは複素環式芳香族環構造であることができ;
R3は、出現毎に、同一であるか異なり、H、F、1〜40個のC原子を有する直鎖、分岐あるいは環状アルキル、アルコキシもしくはチオアルコキシ基であって、1以上のH原子は、Fで置き代えられてよく、ここで、さらに、1以上の非隣接のCH2基は、O、CO、COOもしくはO(CO)Oで置き代えられてよく、またはモノあるいはポリ環式の芳香族もしくは複素環式芳香族環構造であることができ;
m,nは、互いに独立して、出現毎に、同一であるか異なり、0、1、2または3、好ましくは、0または1、特に、好ましくは、0であり;
破線は、ポリマー中の隣接する構造単位ヘの結合である。) - 1,000〜2,000,000g/molの範囲の分子量Mwを有することを特徴とする、請求項1〜3何れか1項記載のポリマー。
- ポリマー中の式(I)の構造単位の割合が、1〜95モル%であることを特徴とする、請求項1〜4何れか1項記載のポリマー。
- ポリマーは、また、式(I)の構造単位とは異なる少なくとも一つのさらなる構造単位を含むことを特徴とする、請求項1〜5何れか1項記載のポリマー。
- Xは、互いに独立して、同一であるか異なり、ハロゲン、O-トシレート、O-トリフレート、O-スルホネート、ボロン酸エステル、部分的にフッ素化されたシリル基、ジアゾニウム基および有機錫化合物から選ばれることを特徴とする、請求項7記載の化合物。
- 請求項1〜6何れか1項記載の少なくとも一つのポリマーと、さらに、ポリマー状、オリゴマー状、樹状および低分子量物質のクラスから選ばれる一以上の化合物を含む混合物。
- 請求項1〜6何れか1項記載の少なくとも一つのポリマーと、少なくとも一つの溶媒を含む調合物。
- 請求項1〜6何れか1項記載のポリマーまたは請求項9記載の混合物の有機電子素子での使用。
- 有機電子素子であって、一以上の活性層を含み、これら活性層の少なくとも一つは、請求項1〜6何れか1項記載のポリマーまたは請求項9記載の混合物を含む、有機電子素子。
- 有機電子素子は、有機エレクトロルミネッセンス素子(OLED)、有機発光電子化学電池(OLEC)、有機集積回路(O-IC)、有機電界効果トランジスタ(O-FET)、有機薄膜トランジスタ(O-TFT)、有機太陽電池(O-SC)、有機レーザーダイオード(O-laser)、有機光電池もしくは対応する素子(OPV)または有機光受容器(OPC)であって、好ましくは、有機エレクトロルミネッセンス素子(OLED)であることを特徴とする、請求項12記載の有機電子素子。
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PCT/EP2013/000232 WO2013124029A2 (de) | 2012-02-22 | 2013-01-26 | Polymere enthaltend dibenzocycloheptan-struktureinheiten |
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US10295338B2 (en) * | 2013-07-12 | 2019-05-21 | Magic Leap, Inc. | Method and system for generating map data from an image |
CN105934836A (zh) * | 2013-12-09 | 2016-09-07 | 日产化学工业株式会社 | 有机薄膜太阳能电池的阳极缓冲层用组合物及有机薄膜太阳能电池 |
KR102384224B1 (ko) | 2014-12-30 | 2022-04-08 | 삼성전자주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
CN114685288B (zh) * | 2020-12-25 | 2024-02-02 | 广州华睿光电材料有限公司 | 多环芳胺类有机化合物及其用途 |
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WO2013124029A3 (de) | 2013-12-05 |
EP2817350A2 (de) | 2014-12-31 |
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