JP6105040B2 - エレクトロルミネッセンス素子のための9,9’−スピロビキサンテン誘導体 - Google Patents
エレクトロルミネッセンス素子のための9,9’−スピロビキサンテン誘導体 Download PDFInfo
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- JP6105040B2 JP6105040B2 JP2015502119A JP2015502119A JP6105040B2 JP 6105040 B2 JP6105040 B2 JP 6105040B2 JP 2015502119 A JP2015502119 A JP 2015502119A JP 2015502119 A JP2015502119 A JP 2015502119A JP 6105040 B2 JP6105040 B2 JP 6105040B2
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- VKKRGFDLDAZZEW-UHFFFAOYSA-N 9,9'-spirobi[xanthene] Chemical class C12=CC=CC=C2OC2=CC=CC=C2C11C2=CC=CC=C2OC2=CC=CC=C21 VKKRGFDLDAZZEW-UHFFFAOYSA-N 0.000 title 1
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- -1 NR 3 Inorganic materials 0.000 claims description 24
- 125000001072 heteroaryl group Chemical group 0.000 claims description 23
- 229910052731 fluorine Inorganic materials 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 230000000903 blocking effect Effects 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 17
- 229910052794 bromium Inorganic materials 0.000 claims description 16
- 229910052801 chlorine Inorganic materials 0.000 claims description 16
- 229910052717 sulfur Inorganic materials 0.000 claims description 16
- 230000005525 hole transport Effects 0.000 claims description 15
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 12
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- 125000003545 alkoxy group Chemical group 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 12
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- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 6
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- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 claims description 6
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- 238000006068 polycondensation reaction Methods 0.000 claims description 3
- 150000003254 radicals Chemical class 0.000 claims description 3
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- HQALDKFFRYFTKP-UHFFFAOYSA-N 2-[4-[4-(2-benzyl-1-benzothiophen-3-yl)phenyl]-2-bromo-6-(3-methoxyphenyl)phenoxy]acetic acid Chemical compound COC1=CC=CC(C=2C(=C(Br)C=C(C=2)C=2C=CC(=CC=2)C=2C3=CC=CC=C3SC=2CC=2C=CC=CC=2)OCC(O)=O)=C1 HQALDKFFRYFTKP-UHFFFAOYSA-N 0.000 claims description 2
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- IYYZUPMFVPLQIF-ALWQSETLSA-N dibenzothiophene Chemical class C1=CC=CC=2[34S]C3=C(C=21)C=CC=C3 IYYZUPMFVPLQIF-ALWQSETLSA-N 0.000 claims description 2
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- 238000007689 inspection Methods 0.000 claims description 2
- 125000004437 phosphorous atom Chemical group 0.000 claims description 2
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- 239000004332 silver Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 238000001931 thermography Methods 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000002061 vacuum sublimation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 150000007964 xanthones Polymers 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
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Description
Xは、出現毎に同一であるか異なり、CR1もしくはNであるか;または二個の隣接するXは、S、OもしくはNR1であり、その結果、五員環を形成するか;または二個の隣接するXは、以下の式(2)、(3)もしくは(4)の基であり、
ここで、ArもしくはLが基Xに結合するならば、Xは、Cであり;
Vは、出現毎に同一であるか異なり、C(R1)2、NR1、OまたはSであり;
Zは、出現毎に同一であるか異なり、CR1もしくはNであり;
Arは、出現毎に同一であるか異なり、1以上の基R2により置換されてよい5〜40個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造であり;ここで、基Arとこの場合にCである隣接する基Xは、単結合またはC(R2)2、NR2、OもしくはSから選ばれる二価基により互いにブリッジしてもよく;
Lは、出現毎に同一であるか異なり、単結合または二価基であり;
R1、R2は、出現毎に同一であるか異なり、H、D、F、Cl、Br、I、CN、NO2、N(Ar1)2、N(R3)2、C(=O)Ar1、C(=O)R3、P(=O)(Ar1)2、P(Ar1)2、B(Ar1)2、Si(Ar1)3、Si(R3)3、1〜40個のC原子を有する直鎖アルキル、アルコキシもしくはチオアルキル基、3〜40個のC原子を有する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キル基、2〜40個のC原子を有するアルケニルもしくはアルキニル基(夫々は、1以上の基R3により置換されてよく、1以上の隣接しないCH2基は、R3C=CR3、C≡C、Si(R3)2、C=O、C=S、C=NR3、P(=O)(R3)、SO、SO2、NR3、O、SもしくはCONR3で置き代えられてよく、ここで、1以上のH原子は、D、F、Cl、Br、I、CNもしくはNO2で置き代えられてよい。)または、各場合に、1以上の基R3により置換されてよい5〜60個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造、1以上の基R3で置換されてよい5〜60個の芳香族環原子を有するアリールオキシもしくはヘテロアリールオキシ基より成る群から選ばれ;ここで、2個以上の隣接する置換基R1もしくはR2は、1以上の基R3で置換されてよいモノ環状あるいはポリ環状の脂肪族、芳香族もしくは複素環式芳香族環構造を随意に形成してもよく;
Ar1は、出現毎に同一であるか異なり、1以上の非芳香族基R3により置換されてよい5〜30個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造であり;ここで、同じN原子もしくはP原子に結合する二個の基Ar1は、また、単結合またはN(R3)、C(R3)2、OもしくはSから選ばれるブリッジにより互いにブリッジされてよく;
R3は、出現毎に同一であるか異なり、H、D、F、Cl、Br、I、CN、NO2、N(R4)2、C(=O)R4、P(=O)(R4)2、1〜40個のC原子を有する直鎖アルキル、アルコキシもしくはチオアルキル基、3〜40個のC原子を有する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キル基、2〜40個のC原子を有するアルケニルもしくはアルキニル基(夫々は、1以上の基R4により置換されてよく、1以上の隣接しないCH2基は、R4C=CR4、C≡C、Si(R4)2、C=O、C=S、C=NR4、P(=O)(R4)、SO、SO2、NR4、O、SもしくはCONR4で置き代えられてよく、ここで、1以上のH原子は、D、F、Cl、Br、I、CNもしくはNO2で置き代えられてよい。)または、各場合に、1以上の基R4により置換されてよい5〜60個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造、1以上の基R4で置換されてよい5〜60個の芳香族環原子を有するアリールオキシもしくはヘテロアリールオキシ基またはこれらの構造の組み合わせより成る群から選ばれ;ここで、2個以上の隣接する置換基R3は、1以上の基R4で置換されてよいモノ環状あるいはポリ環状の脂肪族環構造を随意に形成してもよく;
R4は、出現毎に同一であるか異なり、H、D、F、CN、1〜20個のC原子を有する脂肪族炭化水素基、5〜30個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造であって、ここで、1以上のH原子は、D、F、Cl、Br、IもしくはCNで置き代えられてよく、ここで、2個以上の隣接する置換基R4は、モノ-あるいはポリ環状の脂肪族環構造を互いに形成してもよく;
mは、出現毎に同一であるか異なり、0または1であり;
nは、1、2、3、4または5であり;
ただし、n=0に対しては、CN、N(Ar1)2、C(=O)Ar1、P(=O)(Ar1)2、P(Ar1)2、B(Ar1)2、Si(Ar1)3、Si(R3)3または各場合に1以上の基R3により置換されてよい5〜60個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造より成る群から選ばれる少なくとも一つの置換基R1が存在し;
n=0であり、そして、四個の置換基R1が、出現毎に同一であるか異なり、各場合に、窒素原子を介して骨格に結合する随意に置換されたカルバゾールもしくはジフェニルアミンである式(1)の化合物は、本発明から除外される。
Aは、出現毎に同一であるか異なり、CR4もしくはNであり、ただし、一、二もしくは三個の基Aは、Nであり;
Ar2は、出現毎に同一であるか異なり、1以上の基R4により置換されてよい5〜16個のC原子を有する二価の芳香族もしくは複素環式芳香族環構造である。
Eは、C(R3)2、NR3、OまたはSより成る基から選ばれ;
Gは、出現毎に同一であるか異なり、NR3、OまたはSより成る基から選ばれる。
b)ハロゲン置換スピロ-9-9-ビキサンテンのスズキ、ネギシ、ヤマモト、グリニャール-クロス、スチル、ヘックカップリング等のC−Cカップリング、ブッフバルトまたはウルマンカップリング等のC−Nカップリング、シリル化、リン酸エステル化、ボロン酸エステル化、重縮合における反応。
と組み合わせて、有機エレクトロルミネッセンス素子のために知られたすべての材料を使用することができる。
以下の合成を、別段の指定がない限り、無水溶媒中で保護ガス雰囲気下で実施する。溶媒及び試薬をALDRICH又はABCRから購入することができる。商業的に入手できない出発材料の場合に示される番号は、対応するCAS番号である。
本発明によるOLEDと先行技術にしたがうOLEDが、WO 2004/058911にしたがう一般的プロセスにより製造されるが、ここに記載される状況(層の厚さの変化、材料)に適合される。
Claims (8)
- 式(5a)〜(5u)の一つの化合物:
R 1 は、出現毎に同一であるか異なり、H、D、F、Cl、Br、I、CN、NO2、N(Ar1)2、N(R3)2、C(=O)Ar1、C(=O)R3、P(=O)(Ar1)2、P(Ar1)2、B(Ar1)2、Si(Ar1)3、Si(R3)3、1〜40個のC原子を有する直鎖アルキル、アルコキシもしくはチオアルキル基、3〜40個のC原子を有する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キル基、2〜40個のC原子を有するアルケニルもしくはアルキニル基(夫々は、1以上の基R3により置換されてよく、1以上の隣接しないCH2基は、R3C=CR3、C≡C、Si(R3)2、C=O、C=S、C=NR3、P(=O)(R3)、SO、SO2、NR3、O、SもしくはCONR3で置き代えられてよく、ここで、1以上のH原子は、D、F、Cl、Br、I、CNもしくはNO2で置き代えられてよい。)または、各場合に、1以上の基R3により置換されてよい5〜60個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造、1以上の基R3で置換されてよい5〜60個の芳香族環原子を有するアリールオキシもしくはヘテロアリールオキシ基より成る群から選ばれ;
Ar1は、出現毎に同一であるか異なり、1以上の非芳香族基R3により置換されてよい5〜30個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造であり;ここで、同じN原子もしくはP原子に結合する二個の基Ar1は、また、単結合またはN(R3)、C(R3)2、OもしくはSから選ばれるブリッジにより互いにブリッジされてよく;
R3は、出現毎に同一であるか異なり、H、D、F、Cl、Br、I、CN、NO2、N(R4)2、C(=O)R4、P(=O)(R4)2、1〜40個のC原子を有する直鎖アルキル、アルコキシもしくはチオアルキル基、3〜40個のC原子を有する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キル基、2〜40個のC原子を有するアルケニルもしくはアルキニル基(夫々は、1以上の基R4により置換されてよく、1以上の隣接しないCH2基は、R4C=CR4、C≡C、Si(R4)2、C=O、C=S、C=NR4、P(=O)(R4)、SO、SO2、NR4、O、SもしくはCONR4で置き代えられてよく、ここで、1以上のH原子は、D、F、Cl、Br、I、CNもしくはNO2で置き代えられてよい。)または、各場合に、1以上の基R4により置換されてよい5〜60個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造、1以上の基R4で置換されてよい5〜60個の芳香族環原子を有するアリールオキシもしくはヘテロアリールオキシ基またはこれらの構造の組み合わせより成る群から選ばれ;ここで、2個以上の隣接する置換基R3は、1以上の基R4で置換されてよいモノ環状あるいはポリ環状の脂肪族環構造を随意に形成してもよく;
R4は、出現毎に同一であるか異なり、H、D、F、CN、1〜20個のC原子を有する脂肪族炭化水素基、5〜30個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造であって、ここで、1以上のH原子は、D、F、Cl、Br、IもしくはCNで置き代えられてよく、ここで、2個以上の隣接する置換基R4は、モノ-あるいはポリ環状の脂肪族環構造を互いに形成してもよく;
ただし、CN、N(Ar1)2、C(=O)Ar1、P(=O)(Ar1)2 、B(Ar1)2、Si(Ar1)3、Si(R3)3または各場合に1以上の基R3により置換されてよい5〜60個の芳香族環原子を有する芳香族もしくは複素環式芳香族環構造より成る群から選ばれる少なくとも一つの置換基R1が存在する。 - R 1 が芳香族もしくは複素環式芳香族環構造であるならば、これは、出現毎に同一であるか異なり、ベンゼン、オルト-、メタ-もしくはパラ-ビフェニル、オルト-、メタ-、パラ-もしくは分岐テルフェニル、オルト-、メタ-、パラ-もしくは分岐クアテルフェニル、1-,2,-ナフチル、ピロール、フラン、チオフェン、インドール、ベンゾフラン、ベンゾチオフェン、カルバゾール、ジベンゾフラン、ジベンゾチオフェン、ピリジン、ピリミジン、ピラジン、ピリダジン、トリアジン、アントラセン、フェナントレン、ピレン、ベンズアントラセンもしくは二もしくは三個のこれらの組み合わせから選ばれ、それぞれ1以上の基R3により置換されてよいことを特徴とする、請求項1記載の化合物。
- 電子輸送材料としてまたは燐光エミッターのためのマトリックス材料として使用されるならば、化合物は、少なくとも一つの基-C(=O)Ar1もしくは-P(=O)(Ar1)2または電子欠損複素環式芳香族環構造で置換され、ここで、少なくとも一つの置換基R 1 は、式(13)〜(16)の構造から選ばれ、
mは、0または1であり;
Aは、出現毎に同一であるか異なり、CR4もしくはNであり、ただし、一、二もしくは三個の基Aは、Nであり;
Ar2は、出現毎に同一であるか異なり、1以上の基R4により置換されてよい5〜16個のC原子を有する二価の芳香族もしくは複素環式芳香族環構造であることを特徴とする、請求項1または2記載の化合物。 - 正孔輸送材料として、正孔注入材料として、電子もしくは励起子ブロック材料としてまたは燐光エミッターのためのマトリックス材料として使用されるならば、化合物は、それぞれ1以上の基R3基により置換されてよい少なくとも一つのトリアリールアミン誘導体、カルバゾール誘導体、インデノカルバゾール誘導体、インドロカルバゾール誘導体、アザカルバゾール誘導体、インドール誘導体、フラン誘導体、ベンゾフラン誘導体、ジベンゾフラン誘導体、チオフェン誘導体、ベンゾチオフェン誘導体もしくはジベンゾチオフェン誘導体により置換されるか、または、少なくとも一つの置換基R 1 は、-N(Ar1)2であり、ここで、これらの基は、以下の式(35)〜(49)の基から選ばれ、
Eは、C(R3)2、NR3、OまたはSより成る基から選ばれ;
Gは、出現毎に同一であるか異なり、NR3、OまたはSより成るから選ばれることを特徴とする請求項1〜3何れか1項記載の化合物。 - 以下の反応工程を含む、請求項1〜4何れか1項記載の化合物の製造方法:
a)ハロゲン置換スピロ-9-9-ビキサンテンの合成;および
b)ハロゲン置換スピロ-9-9-ビキサンテンのC−Cカップリング、C−Nカップリング、シリル化、リン酸エステル化、ボロン酸エステル化、重縮合における反応。 - 請求項1〜4何れか1項記載の化合物の、電子素子での使用。
- 請求項1〜4何れか1項記載の少なくとも一つの化合物を含む電子素子であって、ここで、電子素子は、有機エレクトロルミネッセンス素子、有機集積回路、有機電界効果トランジスタ、有機薄膜トランジスタ、有機発光トランジスタ、有機太陽電池、染料増感性有機太陽電池、有機光学検査器、有機光受容器、有機電場消光素子、発光電子化学電池、有機レーザーダイオードおよび「有機プラスモン発光素子」より成る群から選ばれる、電子素子。
- 請求項1〜4何れか1項記載の化合物が、蛍光もしくは燐光エミッターのためのマトリックス材料としておよび/または蛍光エミッターとしておよび/または電子ブロック層もしくは励起子ブロック層中でおよび/または正孔輸送中でおよび/または正孔ブロック層中でおよび/または電子輸送層中で、使用されることを特徴とする、請求項7記載の有機エレクトロルミネッセンス素子である電子素子。
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US9929354B2 (en) | 2018-03-27 |
KR102139456B1 (ko) | 2020-07-30 |
US20150045529A1 (en) | 2015-02-12 |
EP2828266A1 (de) | 2015-01-28 |
US20160329507A1 (en) | 2016-11-10 |
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