JP2016027040A - 環状アジン化合物、その製造方法、及びその用途 - Google Patents
環状アジン化合物、その製造方法、及びその用途 Download PDFInfo
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- JP2016027040A JP2016027040A JP2015133840A JP2015133840A JP2016027040A JP 2016027040 A JP2016027040 A JP 2016027040A JP 2015133840 A JP2015133840 A JP 2015133840A JP 2015133840 A JP2015133840 A JP 2015133840A JP 2016027040 A JP2016027040 A JP 2016027040A
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- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract description 20
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 12
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- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims description 79
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- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 10
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 10
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- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CAYQIZIAYYNFCS-UHFFFAOYSA-N (4-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=C(Cl)C=C1 CAYQIZIAYYNFCS-UHFFFAOYSA-N 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- RSQXKVWKJVUZDG-UHFFFAOYSA-N 9-bromophenanthrene Chemical compound C1=CC=C2C(Br)=CC3=CC=CC=C3C2=C1 RSQXKVWKJVUZDG-UHFFFAOYSA-N 0.000 description 4
- NBXPFOBBSGIVIG-UHFFFAOYSA-N C(C=C1)=CC=C1C1=NC(C2=CC=CC=C2)=NC(C2=CC(C(C=C3)=CC=C3C3=CC(C=CC=C4)=C4C4=CC=CC=C34)=CC(C3=CC=CN=C3)=C2)=N1 Chemical compound C(C=C1)=CC=C1C1=NC(C2=CC=CC=C2)=NC(C2=CC(C(C=C3)=CC=C3C3=CC(C=CC=C4)=C4C4=CC=CC=C34)=CC(C3=CC=CN=C3)=C2)=N1 NBXPFOBBSGIVIG-UHFFFAOYSA-N 0.000 description 4
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- USVZFSNDGFNNJT-UHFFFAOYSA-N cyclopenta-1,4-dien-1-yl(diphenyl)phosphane (2,3-dichlorocyclopenta-1,4-dien-1-yl)-diphenylphosphane iron(2+) Chemical compound [Fe++].c1cc[c-](c1)P(c1ccccc1)c1ccccc1.Clc1c(cc[c-]1Cl)P(c1ccccc1)c1ccccc1 USVZFSNDGFNNJT-UHFFFAOYSA-N 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- LCSNDSFWVKMJCT-UHFFFAOYSA-N dicyclohexyl-(2-phenylphenyl)phosphane Chemical group C1CCCCC1P(C=1C(=CC=CC=1)C=1C=CC=CC=1)C1CCCCC1 LCSNDSFWVKMJCT-UHFFFAOYSA-N 0.000 description 1
- CNXMDTWQWLGCPE-UHFFFAOYSA-N ditert-butyl-(2-phenylphenyl)phosphane Chemical group CC(C)(C)P(C(C)(C)C)C1=CC=CC=C1C1=CC=CC=C1 CNXMDTWQWLGCPE-UHFFFAOYSA-N 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 150000008376 fluorenones Chemical class 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
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- 150000007857 hydrazones Chemical class 0.000 description 1
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- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- SJCKRGFTWFGHGZ-UHFFFAOYSA-N magnesium silver Chemical group [Mg].[Ag] SJCKRGFTWFGHGZ-UHFFFAOYSA-N 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical group 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 1
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- GPRIERYVMZVKTC-UHFFFAOYSA-N p-quaterphenyl Chemical group C1=CC=CC=C1C1=CC=C(C=2C=CC(=CC=2)C=2C=CC=CC=2)C=C1 GPRIERYVMZVKTC-UHFFFAOYSA-N 0.000 description 1
- PBDBXAQKXCXZCJ-UHFFFAOYSA-L palladium(2+);2,2,2-trifluoroacetate Chemical compound [Pd+2].[O-]C(=O)C(F)(F)F.[O-]C(=O)C(F)(F)F PBDBXAQKXCXZCJ-UHFFFAOYSA-L 0.000 description 1
- PENAXHPKEVTBLF-UHFFFAOYSA-L palladium(2+);prop-1-ene;dichloride Chemical class [Pd+]Cl.[Pd+]Cl.[CH2-]C=C.[CH2-]C=C PENAXHPKEVTBLF-UHFFFAOYSA-L 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- JKDRQYIYVJVOPF-FDGPNNRMSA-L palladium(ii) acetylacetonate Chemical compound [Pd+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O JKDRQYIYVJVOPF-FDGPNNRMSA-L 0.000 description 1
- GPNDARIEYHPYAY-UHFFFAOYSA-N palladium(ii) nitrate Chemical compound [Pd+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O GPNDARIEYHPYAY-UHFFFAOYSA-N 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000007686 potassium Nutrition 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- 125000005551 pyridylene group Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 125000006836 terphenylene group Chemical group 0.000 description 1
- ZGNPLWZYVAFUNZ-UHFFFAOYSA-N tert-butylphosphane Chemical compound CC(C)(C)P ZGNPLWZYVAFUNZ-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 229940062627 tribasic potassium phosphate Drugs 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 1
- 125000002827 triflate group Chemical group FC(S(=O)(=O)O*)(F)F 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- KAAYGTMPJQOOGY-UHFFFAOYSA-N tris(2,5-dimethylphenyl)phosphane Chemical compound CC1=CC=C(C)C(P(C=2C(=CC=C(C)C=2)C)C=2C(=CC=C(C)C=2)C)=C1 KAAYGTMPJQOOGY-UHFFFAOYSA-N 0.000 description 1
- DLQYXUGCCKQSRJ-UHFFFAOYSA-N tris(furan-2-yl)phosphane Chemical compound C1=COC(P(C=2OC=CC=2)C=2OC=CC=2)=C1 DLQYXUGCCKQSRJ-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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Abstract
Description
なお、一般式(1)の各置換基については、有機EL素子の素子寿命の点で、下記の場合が好ましい。
(一般式(1)中、Ar1は、お互い同じであって、炭素数1〜4のアルキル基、フッ素原子、フェニル基、又はピリジル基で置換されていてもよい炭素数6〜10の芳香族炭素水素基を表す。Ar2は、炭素数1〜4のアルキル基、又はフッ素原子で置換されていてもよい炭素数10〜17の縮環芳香族炭化水素基を表す。Ar3は、炭素数1〜4のアルキル基、又はフッ素で置換されていてもよい炭素数6〜17の芳香族炭化水素基、又は炭素数1〜4のアルキル基、又はフッ素原子で置換されていてもよい炭素数4〜9の6環のみで構成される複素芳香族基を表す。Xは、炭素数1〜4のアルキル基、又はフッ素原子で置換されていてもよいフェニレン基、アザフェニレン基、又はジアザフェニレン基を表す。Yは、CH、又は窒素原子を表す。pは、1〜3の整数を表す。qは、0〜3の整数を表す。)
以下、一般式(1)で表される化合物について説明する。
反応式(1)〜(4)中、Zは、脱離基を表し、特に限定するものではないが、例えば、塩素原子、臭素原子、トリフルオロメタンスルホニル基(トリフラート基)、又はヨウ素原子が挙げられる。このうち、反応収率がよい点で、臭素原子、又は塩素原子が好ましく、選択性が良い点で、塩素原子がより好ましい。
反応式(1’)の反応に使用できるパラジウム触媒、ホスフィン配位子、塩基、又は溶媒は、前述した反応式(1)〜(4)と同様のものが挙げられる。
化合物(3)は、例えば、特開2008−280330号公報[0061]〜[0076]又は特開2001−335516号公報[0047]〜[0082]に開示されている方法を用いて製造することができる。
反応式(1)で用いるパラジウム触媒の量は、いわゆる触媒量であれば特に制限はないが、収率がよい点で、化合物(2)の1モルに対して、0.1〜0.01倍モル(パラジウム原子換算)であることが好ましい。
反応式(3’)で得られた化合物(6)は、単離した後に精製を行っても、単離をせずに次工程に進んでもよい。化合物(6)は、反応式(3’)の終了後に通常の処理をすることで得られる。必要に応じて、再結晶、カラムクロマトグラフィー、又は昇華等で精製してもよい。
(i)陽極/発光層/陰極
(ii)陽極/正孔輸送層/発光層/陰極
(iii)陽極/発光層/電子輸送層/陰極
(iv)陽極/正孔輸送層/発光層/電子輸送層/陰極
(v)陽極/陽極バッファー層/正孔輸送層/発光層/電子輸送層/陰極バッファー層/陰極
本発明の有機電界発光素子における発光層には、従来公知の発光材料を用いることができる。発光層を形成する方法としては、例えば蒸着法、スピンコート法、キャスト法、LB法などの公知の方法により薄膜を形成する方法がある。
2.正孔注入層
3.電荷発生層
4.正孔輸送層
5.発光層
6.電子輸送層
7.電子注入層
8.陰極層
素子評価に用いた化合物の構造式及びその略称を以下に示す。
合成実施例−3
合成実施例−4
合成実験例−5
合成実施例−6
基板には、2mm幅の酸化インジウム−スズ(ITO)膜がストライプ状にパターンされたITO透明電極付きガラス基板を用いた。この基板をイソプロピルアルコールで洗浄した後、オゾン紫外線洗浄にて表面処理を行った。洗浄後の基板に、真空蒸着法で各層の真空蒸着を行い、断面図を図1に示すような発光面積4mm2有機電界発光素子を作製した。
素子実施例−1において、化合物A−10の代わりに2−[5−(9−フェナントリル)−4’−(2−ピリジル)ビフェニル−3−イル]−4,6−ジフェニル−1,3,5−トリアジン(ETL−1)を用いた以外は、素子実施例−1と同じ方法で有機電界発光素子を作製した。
素子実施例−1において、HILを65nm、HTLを10nm、EML−1とEML−2を95:5(重量比)の割合で20nm、化合物A−10の代わりに本発明の合成実施例−2で合成した4,6−ジフェニル−2−[4’−(9−フェナントレニル)−3−(3−ピリジル)ビフェニル−5−イル]−1,3,5−トリアジン(化合物A−3)を用いた以外は、素子実施例−1と同じ方法で有機電界発光素子を作製した。
素子実施例−2において、化合物A−3の代わりにETL−2を用いた以外は、素子実施例−2と同じ方法で有機電界発光素子を作製した。
素子実施例−2において、化合物A−3の代わりにETL−3を用いた以外は、素子実施例−2と同じ方法で有機電界発光素子を作製した。
Claims (10)
- 一般式(1)で表される環状アジン化合物。
- Ar1が、フェニル基、p−トリル基、m−トリル基、p−ビフェニル基、m−ビフェニル基、1−ナフチル基、又は2−ナフチル基である請求項1に記載の環状アジン化合物。
- Ar2が、ナフチル基、アントラセニル基、ピレニル基、フェナントレニル基、又はフルオランテニル基である請求項1又は請求項2に記載の環状アジン化合物。
- Ar2が、ナフチル基、アントラセニル基、ピレニル基、又はフェナントレニル基である請求項1又は請求項2に記載の環状アジン化合物。
- Ar3が、フェニル基、トリル基、ジメチルフェニル基、ナフチル基、アントラセニル基、ピレニル基、フェナントレニル基、フルオランテニル基、ピリジル基、ピリミジル基、ピラジル基、キノリル基、又はイソキノリル基である請求項1乃至請求項4のいずれか一項に記載の環状アジン化合物。
- Xが、フェニレン基である請求項1乃至請求項5のいずれか一項に記載の環状アジン化合物。
- Yが窒素原子である請求項1乃至請求項6のいずれか一項に記載の環状アジン化合物。
- 一般式(2)
で表される化合物と、一般式(3)
で表される化合物とを、塩基及びパラジウム触媒の存在下、又は塩基、パラジウム触媒、及びアルカリ金属塩の存在下でカップリング反応させることを特徴とする、請求項1に記載の一般式(1)
で表される環状アジン化合物の製造方法。 - 一般式(4)
で表される化合物と、一般式(5)
で表される化合物とを、塩基及びパラジウム触媒の存在下、又は塩基、パラジウム触媒、及びアルカリ金属塩の存在下でカップリング反応させることを特徴とする、請求項1に記載の一般式(1)
で表される環状アジン化合物の製造方法。
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JP2018145166A (ja) * | 2016-03-29 | 2018-09-20 | 東ソー株式会社 | トリアジン化合物及びそれを含有する有機電界発光素子 |
JP2019001732A (ja) * | 2017-06-13 | 2019-01-10 | 東ソー株式会社 | 1,2−置換フェニル基を有するトリアジン化合物及びその用途 |
JP2020147543A (ja) * | 2019-03-15 | 2020-09-17 | 東ソー株式会社 | 2’−アリールビフェニリル基を有するトリアジン化合物 |
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KR102101473B1 (ko) | 2017-07-10 | 2020-04-16 | 주식회사 엘지화학 | 헤테로 고리 화합물 및 이를 포함하는 유기 발광 소자 |
EP3527557A1 (en) * | 2018-02-16 | 2019-08-21 | Novaled GmbH | N-heteroarylene compounds |
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