KR910009623A - 신규의 안트라센 유도체, 이를 함유하는 조성물 및 이를 사용하는 화확발광 광의 생성방법 - Google Patents
신규의 안트라센 유도체, 이를 함유하는 조성물 및 이를 사용하는 화확발광 광의 생성방법 Download PDFInfo
- Publication number
- KR910009623A KR910009623A KR1019900018606A KR900018606A KR910009623A KR 910009623 A KR910009623 A KR 910009623A KR 1019900018606 A KR1019900018606 A KR 1019900018606A KR 900018606 A KR900018606 A KR 900018606A KR 910009623 A KR910009623 A KR 910009623A
- Authority
- KR
- South Korea
- Prior art keywords
- bis
- composition
- compound
- chloroanthracene
- phosphor
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 15
- 150000001454 anthracenes Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 5
- -1 4-ethoxyphenyl Chemical group 0.000 claims 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- PBUQZKXKYSAJDO-UHFFFAOYSA-N 2-[(2-methylpropan-2-yl)oxycarbonyl]benzoic acid Chemical group CC(C)(C)OC(=O)C1=CC=CC=C1C(O)=O PBUQZKXKYSAJDO-UHFFFAOYSA-N 0.000 claims 1
- MMIPZTDLMULNHS-UHFFFAOYSA-N 2-bromo-9,10-bis(4-ethoxyphenyl)anthracene Chemical compound C1=CC(OCC)=CC=C1C(C1=CC=C(Br)C=C11)=C(C=CC=C2)C2=C1C1=CC=C(OCC)C=C1 MMIPZTDLMULNHS-UHFFFAOYSA-N 0.000 claims 1
- RFVZBUUPBPFZMH-UHFFFAOYSA-N 2-chloro-9,10-bis(4-ethoxyphenyl)anthracene Chemical compound C1=CC(OCC)=CC=C1C(C1=CC=C(Cl)C=C11)=C(C=CC=C2)C2=C1C1=CC=C(OCC)C=C1 RFVZBUUPBPFZMH-UHFFFAOYSA-N 0.000 claims 1
- WQCABUAKUBRKPS-UHFFFAOYSA-N 2-chloro-9,10-bis(4-fluorophenyl)anthracene Chemical compound C1=CC(F)=CC=C1C(C1=CC=C(Cl)C=C11)=C(C=CC=C2)C2=C1C1=CC=C(F)C=C1 WQCABUAKUBRKPS-UHFFFAOYSA-N 0.000 claims 1
- WJCKSZPBALUDCI-UHFFFAOYSA-N 2-chloro-9,10-bis(4-phenoxyphenyl)anthracene Chemical compound C=12C=CC=CC2=C(C=2C=CC(OC=3C=CC=CC=3)=CC=2)C2=CC(Cl)=CC=C2C=1C(C=C1)=CC=C1OC1=CC=CC=C1 WJCKSZPBALUDCI-UHFFFAOYSA-N 0.000 claims 1
- UYFIEORDWFQYIN-UHFFFAOYSA-N 2-fluoro-9,10-bis(4-fluorophenyl)anthracene Chemical compound C1=CC(F)=CC=C1C(C1=CC=C(F)C=C11)=C(C=CC=C2)C2=C1C1=CC=C(F)C=C1 UYFIEORDWFQYIN-UHFFFAOYSA-N 0.000 claims 1
- CLSYZYRGWDVENZ-UHFFFAOYSA-N 9,10-bis(3,4-dimethoxyphenyl)-2-fluoroanthracene Chemical compound C1=C(OC)C(OC)=CC=C1C(C1=CC=C(F)C=C11)=C(C=CC=C2)C2=C1C1=CC=C(OC)C(OC)=C1 CLSYZYRGWDVENZ-UHFFFAOYSA-N 0.000 claims 1
- 125000005011 alkyl ether group Chemical group 0.000 claims 1
- MQMJQPYOEGFMAZ-UHFFFAOYSA-N anthracene;styrene Chemical compound C=CC1=CC=CC=C1.C1=CC=CC2=CC3=CC=CC=C3C=C21 MQMJQPYOEGFMAZ-UHFFFAOYSA-N 0.000 claims 1
- TZZLVFUOAYMTHA-UHFFFAOYSA-N bis-(2,4,5-trichloro-6-(pentyloxycarbonyl)phenyl)oxalate Chemical group CCCCCOC(=O)C1=C(Cl)C(Cl)=CC(Cl)=C1OC(=O)C(=O)OC1=C(Cl)C=C(Cl)C(Cl)=C1C(=O)OCCCCC TZZLVFUOAYMTHA-UHFFFAOYSA-N 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 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 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/235—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring and to a carbon atom of a ring other than a six-membered aromatic ring
- C07C43/247—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring and to a carbon atom of a ring other than a six-membered aromatic ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
- C07C25/22—Polycyclic aromatic halogenated hydrocarbons with condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/29—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing halogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
- C09K11/07—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials having chemically interreactive components, e.g. reactive chemiluminescent compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/24—Anthracenes; Hydrogenated anthracenes
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Luminescent Compositions (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Physical Water Treatments (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (17)
- 다음 일반구조식을 갖는 화합물 :상기식에서, R은 플푸오르, 클로로, 브로모, 알콕시(C1-C4), 또는 페녹시이며, (R1)은 하나 또는 그 이상의 동일 또는 상이한 기로서, 알콕시(C1-C4), 페녹시, 플루오로, 또는 폴리알킬렌옥시 알킬 에테르기(C1-C4)로 부터 선택되며, n은 1-3이고, R이 클로로일 때, R1은 P-메톡시가 아닌것을 제외한다.
- 제1항에 있어서, 하기로 구성되는 군으로 부터 선택되는 화합물. 9,10-비스(4-에톡시페닐)-2-클로로안트라센; 9,10-비스(4-에톡시페닐)-2-클루오로안트라센; 9,10-비스(4-에톡시페닐)-2-브로모안트라센; 9,10-비스(4-에콕시페닐)-2-메톡안트라센; 9,10-비스(4-디메톡시페닐)-2-클로로안트라센; 9,10-비스(3,4-디메톡시페닐)-2-플루오로안트라센; 9,10-비스(4-플루오로페닐)-2-클로로안트라센; 9,10-비스(4-플루오로페닐)-2-플로오로안트라센; 9,10-비스(4-페녹시페닐)-2-클로로안트라센; 9,10-비스(4-모노에테르트리에틸렌글리콜옥시페닐)-2-클로로안트라센;
- 3. 제1항에 있어서, R 과 R1이 모두 플루오로인 화합물.
- 제1항에 있어서, R이 클로로이며, R1이 페녹시인 화합물.
- 제1항의 화합물을 함유하는, 과산화수소와 반응되어 화학 발광 광(光)을 제공하기에 적합한 조성물.
- 제2항의 화합물을 함유하는, 과산화수소와 반응되어 화학 발광 광(光)을 제공하기에 적합한 조성물.
- 제5항에 있어서, R과 R1이 모두 플루오로인 조성물.
- 제5항에 있어서, R이 클로로이고, R1이 페녹시인 조성물.
- 제5항에 있어서, 상기 화합물을 위한 용매를 첨가함을 특징으로 하는 조성물.
- 제5항에 있어서, 옥살레이트 화합물을 첨가함을 특징으로 하는 조성물.
- 제10항에 있어서, 상기 옥살레이트는 치환된 카브알콕시페닐 옥살레이트인 조성물.
- 제11항에 있어서, 상기 옥살레이트는 비스(2,4,5-트리클로로-6-카르보펜톡시페닐)옥살레이트인 조성물.
- 제9항에 있어서, 상기 용매는 t-부틸프탈레이트인 조성물.
- 제10항의 조성물에 과산화수소 용액을 첨가하는 것으로 구성되는 화학발광 광(光)의 생성방법.
- 어느 한 형광체만에 의해 방출되는 색과 다른 화학발광 광(光)을 제공하기 위하여 과산화 수소와 반응되기에 적합한, 상기의 여러가지 색을 생성할 만한 농도의 두 형광체의 혼합물로 구성되는 조성물.
- 제15항에 있어서, 한 형광체는 제1항의 화합물이고 다른 형광체는 9,10-비스(페닐에틸렌) 안트라센인 조성물.
- 제15항에 있어서, 한 형광체는 제1항의 화합물이고 다른 형광체는 페리렌 디카르복시이미드인 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE8901272A BE1003403A7 (fr) | 1989-11-28 | 1989-11-28 | Solution chimiluminescente a base d'anthracene substitue. |
BE08901272 | 1989-11-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910009623A true KR910009623A (ko) | 1991-06-28 |
Family
ID=3884410
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900018606A KR910009623A (ko) | 1989-11-28 | 1990-11-16 | 신규의 안트라센 유도체, 이를 함유하는 조성물 및 이를 사용하는 화확발광 광의 생성방법 |
Country Status (16)
Country | Link |
---|---|
US (1) | US5232635A (ko) |
EP (1) | EP0429821B1 (ko) |
JP (1) | JPH03178942A (ko) |
KR (1) | KR910009623A (ko) |
AT (1) | ATE174318T1 (ko) |
BE (1) | BE1003403A7 (ko) |
CA (1) | CA2030883A1 (ko) |
DE (1) | DE69032818T2 (ko) |
ES (1) | ES2126550T3 (ko) |
FI (1) | FI905837A (ko) |
GR (1) | GR3029468T3 (ko) |
HK (1) | HK1014531A1 (ko) |
IL (1) | IL96002A0 (ko) |
MX (1) | MX23463A (ko) |
NO (1) | NO905101L (ko) |
PT (1) | PT95994A (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010103124A (ko) * | 2001-10-22 | 2001-11-23 | 박균하 | 안트라센 화합물 및 이를 포함하는 화학발광 조성물 |
Families Citing this family (28)
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JPH0453894A (ja) * | 1990-06-20 | 1992-02-21 | Nippon Kagaku Hakko Kk | 赤色化学発光体 |
DE4131810A1 (de) * | 1991-07-11 | 1993-01-14 | Windmoeller & Hoelscher | Verfahren zum herstellen, befuellen und verschliessen von saecken |
US5281367A (en) * | 1993-06-28 | 1994-01-25 | Jame Fine Chemicals, Inc. | Two-component chemiluminescent composition |
US5683316A (en) * | 1995-11-28 | 1997-11-04 | Campbell; Daniel Scott | Illuminated sports ball |
US6012820A (en) | 1998-01-13 | 2000-01-11 | 3M Innovative Properties Compnay | Lighted hand-holdable novelty article |
US6082876A (en) | 1998-01-13 | 2000-07-04 | 3M Innovative Properties Company | Hand-holdable toy light tube with color changing film |
KR20010034064A (ko) | 1998-01-13 | 2001-04-25 | 스프레이그 로버트 월터 | 색상전이필름 글리터 |
US6455140B1 (en) | 1999-01-13 | 2002-09-24 | 3M Innovative Properties Company | Visible mirror film glitter |
DE29903497U1 (de) * | 1999-02-26 | 2000-07-06 | Bundesdruckerei Gmbh | Sicherheitsdokument mit Chemolumineszenzeigenschaften |
US7028687B1 (en) | 1999-08-26 | 2006-04-18 | Precious Life, Llc | Escape hood |
US6860614B1 (en) | 2000-11-15 | 2005-03-01 | Fred J. Pinciaro | Chemiluminescent jewelry and accessories |
US6884447B2 (en) | 2001-06-04 | 2005-04-26 | Brad Baker | Confectionery with body, handle and container |
KR100441498B1 (ko) * | 2001-08-28 | 2004-07-23 | (주)아로마뉴텍 | 단위 형광체들을 포함하는 화학발광용 중합체 형광체와 그제조방법 및 상기 중합체 형광체를 포함하는 화학발광조성물 |
AU2002366600A1 (en) * | 2001-12-07 | 2003-06-23 | Earl W. Sullivan Iii | Harness for lighted sport article |
KR100439312B1 (ko) * | 2002-04-18 | 2004-07-07 | 주식회사 알지비케미컬 | 디페닐안트라센 단위 형광체들을 포함하는 청색화학발광용 고분자형광체와 그 제조방법 및 상기고분자형광체를 포함하는 화학발광 조성물 |
US7252893B2 (en) | 2004-02-17 | 2007-08-07 | Eastman Kodak Company | Anthracene derivative host having ranges of dopants |
US20070134513A1 (en) * | 2005-12-13 | 2007-06-14 | Binney & Smith | Chemiluminescent system |
US20080128666A1 (en) * | 2005-12-13 | 2008-06-05 | Crayola, Llc | Chemiluminescent system |
CN101240165B (zh) * | 2007-02-07 | 2012-05-02 | 天津天龙化学发光管有限公司 | 一种草酸酯化学发光体系 |
KR101427588B1 (ko) * | 2007-06-14 | 2014-08-08 | 삼성디스플레이 주식회사 | 액정조성물과 이를 포함하는 액정표시장치 |
KR100974125B1 (ko) | 2008-05-14 | 2010-08-04 | 주식회사 두산 | 비대칭 안트라센 유도체의 제조 및 이를 이용한 유기전계발광 소자 |
EP2445987B1 (en) * | 2009-06-24 | 2018-05-02 | Cyalume Technologies, Inc | Blue/violet diphenylanthracene chemiluminescent fluorescers |
WO2012058139A1 (en) * | 2010-10-24 | 2012-05-03 | Cyalume Technologies, Inc. | Combined thermal and chemiluminescent reaction system |
US20130168620A1 (en) | 2011-12-30 | 2013-07-04 | Maggilume, LLC | Chemiluminescent system |
CN110785867B (zh) | 2017-04-26 | 2023-05-02 | Oti照明公司 | 用于图案化表面上覆层的方法和包括图案化覆层的装置 |
US11751415B2 (en) | 2018-02-02 | 2023-09-05 | Oti Lumionics Inc. | Materials for forming a nucleation-inhibiting coating and devices incorporating same |
JP7390739B2 (ja) | 2019-03-07 | 2023-12-04 | オーティーアイ ルミオニクス インコーポレーテッド | 核生成抑制コーティングを形成するための材料およびそれを組み込んだデバイス |
US11985841B2 (en) | 2020-12-07 | 2024-05-14 | Oti Lumionics Inc. | Patterning a conductive deposited layer using a nucleation inhibiting coating and an underlying metallic coating |
Family Cites Families (8)
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US3637784A (en) * | 1965-09-08 | 1972-01-25 | American Cyanamid Co | Novel aromatic peroxy esters |
US3749679A (en) * | 1971-03-15 | 1973-07-31 | American Cyanamid Co | Carboalkoxy substituted bis-phenyl oxalates as superior chemiluminescent materials |
US3775336A (en) * | 1971-09-07 | 1973-11-27 | American Cyanamid Co | High intensity chemiluminescent system with weakly basic salt-type catalyst |
US3888786A (en) * | 1972-06-12 | 1975-06-10 | American Cyanamid Co | Chlorinated bis(phenylethynyl)anthracenes as fluorescers in chemiluminescent systems |
US4859369A (en) * | 1984-09-24 | 1989-08-22 | American Cyanamid Company | Use of water-soluble polymers in aqueous chemical light formulations |
US4678608A (en) * | 1985-04-15 | 1987-07-07 | American Cyanamid Company | Chemiluminescent composition |
US4717511A (en) * | 1985-12-26 | 1988-01-05 | American Cyanamid Company | Chemiluminescent composition |
US4751616A (en) * | 1987-01-07 | 1988-06-14 | American Cyanamid Company | Double reverse chemiluminescent lighting device |
-
1989
- 1989-11-28 BE BE8901272A patent/BE1003403A7/fr not_active IP Right Cessation
-
1990
- 1990-10-15 DE DE69032818T patent/DE69032818T2/de not_active Expired - Fee Related
- 1990-10-15 IL IL96002A patent/IL96002A0/xx unknown
- 1990-10-15 ES ES90119708T patent/ES2126550T3/es not_active Expired - Lifetime
- 1990-10-15 AT AT90119708T patent/ATE174318T1/de not_active IP Right Cessation
- 1990-10-15 EP EP90119708A patent/EP0429821B1/en not_active Expired - Lifetime
- 1990-10-26 US US07/603,494 patent/US5232635A/en not_active Expired - Lifetime
- 1990-11-16 KR KR1019900018606A patent/KR910009623A/ko not_active Application Discontinuation
- 1990-11-26 PT PT95994A patent/PT95994A/pt not_active Application Discontinuation
- 1990-11-26 NO NO90905101A patent/NO905101L/no unknown
- 1990-11-26 CA CA002030883A patent/CA2030883A1/en not_active Abandoned
- 1990-11-26 MX MX2346390A patent/MX23463A/es unknown
- 1990-11-26 JP JP2318145A patent/JPH03178942A/ja active Pending
- 1990-11-27 FI FI905837A patent/FI905837A/fi not_active IP Right Cessation
-
1998
- 1998-12-23 HK HK98115094A patent/HK1014531A1/xx not_active IP Right Cessation
-
1999
- 1999-02-23 GR GR990400564T patent/GR3029468T3/el unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010103124A (ko) * | 2001-10-22 | 2001-11-23 | 박균하 | 안트라센 화합물 및 이를 포함하는 화학발광 조성물 |
Also Published As
Publication number | Publication date |
---|---|
EP0429821A2 (en) | 1991-06-05 |
CA2030883A1 (en) | 1991-05-29 |
FI905837A (fi) | 1991-05-29 |
PT95994A (pt) | 1991-09-13 |
US5232635A (en) | 1993-08-03 |
GR3029468T3 (en) | 1999-05-28 |
NO905101D0 (no) | 1990-11-26 |
ES2126550T3 (es) | 1999-04-01 |
ATE174318T1 (de) | 1998-12-15 |
BE1003403A7 (fr) | 1992-03-17 |
FI905837A0 (fi) | 1990-11-27 |
JPH03178942A (ja) | 1991-08-02 |
DE69032818T2 (de) | 1999-04-29 |
MX23463A (es) | 1993-09-01 |
IL96002A0 (en) | 1991-07-18 |
HK1014531A1 (en) | 1999-09-30 |
DE69032818D1 (de) | 1999-01-21 |
EP0429821A3 (en) | 1993-01-13 |
NO905101L (no) | 1991-05-29 |
EP0429821B1 (en) | 1998-12-09 |
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