JP2013537517A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013537517A5 JP2013537517A5 JP2013518306A JP2013518306A JP2013537517A5 JP 2013537517 A5 JP2013537517 A5 JP 2013537517A5 JP 2013518306 A JP2013518306 A JP 2013518306A JP 2013518306 A JP2013518306 A JP 2013518306A JP 2013537517 A5 JP2013537517 A5 JP 2013537517A5
- Authority
- JP
- Japan
- Prior art keywords
- acid
- formula
- precursor
- conh
- reaction
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000011669 selenium Substances 0.000 claims description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 9
- 239000002243 precursor Substances 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- 239000003446 ligand Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001301 oxygen Chemical group 0.000 claims description 7
- 229910052711 selenium Inorganic materials 0.000 claims description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 239000011593 sulfur Chemical group 0.000 claims description 6
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 5
- 229910052714 tellurium Inorganic materials 0.000 claims description 5
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 5
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 4
- 150000008065 acid anhydrides Chemical class 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 230000010512 thermal transition Effects 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000005725 8-Hydroxyquinoline Substances 0.000 claims description 3
- 150000001449 anionic compounds Chemical class 0.000 claims description 3
- 125000000524 functional group Chemical group 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 150000002431 hydrogen Chemical group 0.000 claims description 3
- -1 inorganic acid salts Chemical class 0.000 claims description 3
- 229910001412 inorganic anion Inorganic materials 0.000 claims description 3
- 229960003540 oxyquinoline Drugs 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 125000000468 ketone group Chemical group 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 12
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims 8
- 229910017604 nitric acid Inorganic materials 0.000 claims 8
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims 4
- 239000004327 boric acid Substances 0.000 claims 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 4
- HDFRDWFLWVCOGP-UHFFFAOYSA-N carbonothioic O,S-acid Chemical compound OC(S)=O HDFRDWFLWVCOGP-UHFFFAOYSA-N 0.000 claims 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims 3
- 239000003960 organic solvent Substances 0.000 claims 3
- MVVGSPCXHRFDDR-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)phenol Chemical compound OC1=CC=CC=C1C1=NC2=CC=CC=C2S1 MVVGSPCXHRFDDR-UHFFFAOYSA-N 0.000 claims 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- SPVXKVOXSXTJOY-UHFFFAOYSA-N selane Chemical compound [SeH2] SPVXKVOXSXTJOY-UHFFFAOYSA-N 0.000 claims 2
- 229910000058 selane Inorganic materials 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- UKWMNFHGYXRSFQ-UHFFFAOYSA-N 5,7-dimethylquinolin-8-ol Chemical group C1=CC=NC2=C(O)C(C)=CC(C)=C21 UKWMNFHGYXRSFQ-UHFFFAOYSA-N 0.000 claims 1
- KESRRRLHHXXBRW-UHFFFAOYSA-N C1=CC=NC2=C3C(O)=CC=CC3=CC=C21 Chemical compound C1=CC=NC2=C3C(O)=CC=CC3=CC=C21 KESRRRLHHXXBRW-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 101710178035 Chorismate synthase 2 Proteins 0.000 claims 1
- 101710152694 Cysteine synthase 2 Proteins 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N cyclobenzothiazole Natural products C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 238000003384 imaging method Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 0 CC(*)C(*=**=I)=C(*=C)C(C(C(C)=*C)=NC)=*C Chemical compound CC(*)C(*=**=I)=C(*=C)C(C(C(C)=*C)=NC)=*C 0.000 description 1
- XOWIZHGUWJSHBR-UHFFFAOYSA-N CC(C)(C)[Zn] Chemical class CC(C)(C)[Zn] XOWIZHGUWJSHBR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PLP.391776 | 2010-07-07 | ||
| PL391776A PL222231B1 (pl) | 2010-07-07 | 2010-07-07 | Związki luminescencyjne, sposób wytwarzania związków luminescencyjnych oraz ich zastosowanie |
| PCT/PL2011/000070 WO2012005615A1 (en) | 2010-07-07 | 2011-07-06 | Luminescent compounds, method of preparation of luminescent compounds and applications thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013537517A JP2013537517A (ja) | 2013-10-03 |
| JP2013537517A5 true JP2013537517A5 (enExample) | 2016-02-04 |
Family
ID=44511446
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013518306A Pending JP2013537517A (ja) | 2010-07-07 | 2011-07-06 | 発光化合物、発光化合物の調製方法およびその用途 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9217104B2 (enExample) |
| EP (1) | EP2591065A1 (enExample) |
| JP (1) | JP2013537517A (enExample) |
| KR (1) | KR20130094297A (enExample) |
| CN (1) | CN103221509B (enExample) |
| BR (1) | BR112013000426A2 (enExample) |
| CA (1) | CA2804366A1 (enExample) |
| PL (1) | PL222231B1 (enExample) |
| WO (1) | WO2012005615A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9778510B2 (en) * | 2013-10-08 | 2017-10-03 | Samsung Electronics Co., Ltd. | Nanocrystal polymer composites and production methods thereof |
| EP3503234B1 (en) * | 2017-12-20 | 2020-11-04 | Novaled GmbH | Organic electronic device comprising an inverse coordination complex and a method for preparing the same |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4539507A (en) | 1983-03-25 | 1985-09-03 | Eastman Kodak Company | Organic electroluminescent devices having improved power conversion efficiencies |
| US4720432A (en) | 1987-02-11 | 1988-01-19 | Eastman Kodak Company | Electroluminescent device with organic luminescent medium |
| JPH0528678A (ja) | 1991-07-16 | 1993-02-05 | Canon Electron Inc | 記録再生装置のアクセス機構 |
| JP3585060B2 (ja) | 1995-05-10 | 2004-11-04 | ソニー株式会社 | 亜鉛複核錯体、その製造方法及び光学的素子 |
| JP3564859B2 (ja) * | 1996-04-01 | 2004-09-15 | 東洋インキ製造株式会社 | 有機エレクトロルミネッセンス素子用材料およびそれを使用した有機エレクトロルミネッセンス素子 |
| JP3760508B2 (ja) * | 1996-06-10 | 2006-03-29 | 東洋インキ製造株式会社 | 有機エレクトロルミネッセンス素子材料およびそれを用いた有機エレクトロルミネッセンス素子 |
| KR100373203B1 (ko) | 1999-03-31 | 2003-02-25 | 주식회사 엘지화학 | 새로운 큐마린계 착물 및 이를 이용한 유기 발광 소자 |
| US6790540B2 (en) | 2000-06-01 | 2004-09-14 | Nippon Steel Chemical Co., Ltd. | Organic electroluminescent element material and organic electroluminescent element |
| WO2004073030A2 (en) | 2003-02-06 | 2004-08-26 | Georgia Tech Research Corporation | Metal 8-hydroxyquinoline -functionalized polymers and related materials and methods of making and using the same |
| JP4328702B2 (ja) | 2003-12-01 | 2009-09-09 | キヤノン株式会社 | 有機ｅｌ素子 |
| JP4741920B2 (ja) | 2005-09-29 | 2011-08-10 | 富士フイルム株式会社 | 有機電界発光素子 |
| JP4478166B2 (ja) | 2006-11-09 | 2010-06-09 | 三星モバイルディスプレイ株式會社 | 有機金属錯体を含む有機膜を備えた有機発光素子 |
| KR100836020B1 (ko) | 2007-01-04 | 2008-06-09 | (주)그라쎌 | 전기발광용 유기금속 화합물 및 이를 발광재료로 채용하고있는 표시소자 |
| KR100850886B1 (ko) | 2007-09-07 | 2008-08-07 | (주)그라쎌 | 전기발광용 유기금속 화합물 및 이를 발광재료로 채용하고있는 표시소자 |
| KR100923566B1 (ko) | 2007-10-25 | 2009-10-27 | (주)그라쎌 | 신규한 적색 인광 화합물 및 이를 발광재료로서 채용하고있는 유기발광소자 |
| KR100910151B1 (ko) | 2007-11-22 | 2009-07-30 | (주)그라쎌 | 신규한 유기 발광 화합물 및 이를 발광재료로 채용하고있는 전기발광소자 |
| PL213271B1 (pl) | 2008-08-22 | 2013-02-28 | Politechnika Warszawska | Prekursory nanocząstek tlenku cynku i sposób wytwarzania prekursorów nanocząstek tlenku cynku |
-
2010
- 2010-07-07 PL PL391776A patent/PL222231B1/pl unknown
-
2011
- 2011-07-06 US US13/808,907 patent/US9217104B2/en not_active Expired - Fee Related
- 2011-07-06 CN CN201180042983.XA patent/CN103221509B/zh not_active Expired - Fee Related
- 2011-07-06 CA CA2804366A patent/CA2804366A1/en not_active Abandoned
- 2011-07-06 EP EP11748764.5A patent/EP2591065A1/en not_active Withdrawn
- 2011-07-06 KR KR1020137002799A patent/KR20130094297A/ko not_active Withdrawn
- 2011-07-06 BR BR112013000426A patent/BR112013000426A2/pt not_active IP Right Cessation
- 2011-07-06 JP JP2013518306A patent/JP2013537517A/ja active Pending
- 2011-07-06 WO PCT/PL2011/000070 patent/WO2012005615A1/en not_active Ceased
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Chen et al. | Chiral coordination polymers with SHG-active and luminescence: an unusual homochiral 3D MOF constructed from achiral components | |
| JP2010513494A5 (enExample) | ||
| Liang et al. | A new family of 3d–4f heterometallic tetrazole-based coordination frameworks: in situ tetrazole ligand synthesis, structure, luminescence, and magnetic properties | |
| Breault et al. | Influence of solvent on aromatic interactions in metal tris-bipyridine complexes | |
| Vittal et al. | Interconvertible supramolecular transformations | |
| Xu et al. | Homochiral cluster-organic frameworks constructed from enantiopure lactate derivatives | |
| Yang et al. | Unusual polymeric ZnII/CdII complexes with 2, 6-diaminopurine by synergistic coordination of nucleobases and polycarboxylate anions: binding behavior, self-assembled pattern of the nucleobase, and luminscent properties | |
| Kammoun et al. | A supramolecular double sulfate salt with a lamellar type: crystal structure and thermal behavior | |
| Palanisami et al. | Non-covalently aggregated zinc and cadmium complexes derived from substituted aromatic carboxylic acids: Synthesis, spectroscopy, and structural studies | |
| Rana et al. | 1D coordination polymers formed by tetranuclear lead (II) building blocks with carboxylate ligands: In situ isomerization of itaconic acid | |
| CN100347177C (zh) | 经由有机金属化合物制备有机中间产物的方法 | |
| Jin et al. | Five binary supramolecular organic salts constructed from 2-aminoheterocyclic compounds and carboxylic acid derivatives through strong and weak non-covalent interactions | |
| CN101602512B (zh) | 一种磷酸锆晶体材料及制备方法 | |
| Hou et al. | Genuine supramolecular isomers based on Y-shaped pyridinedicarboxylate ligands with distinct topology: 2D 63 layer, kgd layer to 3D rtl net | |
| Yang et al. | Syntheses, crystal structures and optical properties of six homochiral coordination networks based on phenyl acid-amino acids | |
| Yong et al. | Hydrothermal syntheses, crystal structures and properties of novel quinone biradical and mixed-valence copper coordination polymer with semiquinone radical ligand generated in situ | |
| Zhou | Three novel Cd (II) and Zn (II) coordination polymers with O-, N-donor ligands: syntheses, structures, and photoluminescence properties | |
| JP5358184B2 (ja) | 活性炭素原子のルイス酸触媒によるハロゲン化 | |
| Mameri et al. | Coordination Cluster Analogues of the High‐Spin [Mn19] System with Functionalized 2, 6‐Bis (hydroxymethyl) phenol Ligands | |
| Cheng et al. | A left-handed 21 helix with triple chiral components: Synthesis, luminescence and SHG response | |
| Lan et al. | Construction of three new coordination polymers based on 5-ethyltetrazole (ET) generated via in situ cycloaddition reaction | |
| Ji et al. | Structural assemblies of four Cd (II) coordination polymers based on 5-methylisophthalic acid | |
| WO2009099169A1 (ja) | ケージド化合物 | |
| JP5092140B2 (ja) | 非対称型ビス（ターピリジン）化合物の合成方法 | |
| CN103221509B (zh) | 发光化合物、发光化合物的制备方法和其应用 |