GB1425770A - Use of chlorinated bis-phenylethylnyl- anthracenes as fluorescers in chemiluminescent systems - Google Patents
Use of chlorinated bis-phenylethylnyl- anthracenes as fluorescers in chemiluminescent systemsInfo
- Publication number
- GB1425770A GB1425770A GB2142173A GB2142173A GB1425770A GB 1425770 A GB1425770 A GB 1425770A GB 2142173 A GB2142173 A GB 2142173A GB 2142173 A GB2142173 A GB 2142173A GB 1425770 A GB1425770 A GB 1425770A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- phenylethynyl
- anthracene
- hydroperoxide
- dichloro
- 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.)
- Expired
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 5
- -1 hexafluoro - 2 - propyl Chemical group 0.000 abstract 5
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 3
- 239000003085 diluting agent Substances 0.000 abstract 3
- DCCXNTCSVXAHAN-UHFFFAOYSA-N 1,5-dichloro-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=C(Cl)C=CC=C2C(C#CC=2C=CC=CC=2)=C2C(Cl)=CC=CC2=C1C#CC1=CC=CC=C1 DCCXNTCSVXAHAN-UHFFFAOYSA-N 0.000 abstract 1
- YONGNHJIWAYNLC-UHFFFAOYSA-N 1,8-dichloro-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=CC=CC(Cl)=C2C(C#CC=2C=CC=CC=2)=C2C(Cl)=CC=CC2=C1C#CC1=CC=CC=C1 YONGNHJIWAYNLC-UHFFFAOYSA-N 0.000 abstract 1
- IMMCAKJISYGPDQ-UHFFFAOYSA-N 1-chloro-9,10-bis(phenylethynyl)anthracene Chemical compound C12=CC=CC=C2C(C#CC=2C=CC=CC=2)=C2C(Cl)=CC=CC2=C1C#CC1=CC=CC=C1 IMMCAKJISYGPDQ-UHFFFAOYSA-N 0.000 abstract 1
- FNXCATDORZAEFA-UHFFFAOYSA-N 2,3-dichloro-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=CC=CC=C2C(C#CC=2C=CC=CC=2)=C2C=C(Cl)C(Cl)=CC2=C1C#CC1=CC=CC=C1 FNXCATDORZAEFA-UHFFFAOYSA-N 0.000 abstract 1
- YDYTTZZBQVZTPY-UHFFFAOYSA-N 2-chloro-9,10-bis(phenylethynyl)anthracene Chemical compound C=12C=CC=CC2=C(C#CC=2C=CC=CC=2)C2=CC(Cl)=CC=C2C=1C#CC1=CC=CC=C1 YDYTTZZBQVZTPY-UHFFFAOYSA-N 0.000 abstract 1
- KBIWITFMKHHGQY-UHFFFAOYSA-N 2-methyl-9,10-bis(2-phenylethynyl)anthracene Chemical compound C=12C=CC=CC2=C(C#CC=2C=CC=CC=2)C2=CC(C)=CC=C2C=1C#CC1=CC=CC=C1 KBIWITFMKHHGQY-UHFFFAOYSA-N 0.000 abstract 1
- ZHBOFZNNPZNWGB-UHFFFAOYSA-N 9,10-bis(phenylethynyl)anthracene Chemical compound C1=CC=CC=C1C#CC(C1=CC=CC=C11)=C(C=CC=C2)C2=C1C#CC1=CC=CC=C1 ZHBOFZNNPZNWGB-UHFFFAOYSA-N 0.000 abstract 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000005826 halohydrocarbons Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 235000006408 oxalic acid Nutrition 0.000 abstract 1
- 150000003901 oxalic acid esters Chemical class 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 229960001922 sodium perborate Drugs 0.000 abstract 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- WODGXFMUOLGZSY-UHFFFAOYSA-J tetrasodium phosphonatooxy phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OOP([O-])([O-])=O WODGXFMUOLGZSY-UHFFFAOYSA-J 0.000 abstract 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Luminescent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26188872A | 1972-06-12 | 1972-06-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1425770A true GB1425770A (en) | 1976-02-18 |
Family
ID=22995312
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2142173A Expired GB1425770A (en) | 1972-06-12 | 1973-05-04 | Use of chlorinated bis-phenylethylnyl- anthracenes as fluorescers in chemiluminescent systems |
Country Status (13)
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0096749A1 (en) * | 1982-06-16 | 1983-12-28 | American Cyanamid Company | Enhanced aqueous chemiluminescent systems |
| EP0107008A1 (en) * | 1982-10-25 | 1984-05-02 | American Cyanamid Company | 9,10-bis(phenylethynyl)-anthracenes |
| CN102781904A (zh) * | 2009-10-13 | 2012-11-14 | 克禄美科技股份有限公司 | 包含支链草酸酯的化学光产生制剂及装置 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GR72790B (enrdf_load_stackoverflow) * | 1977-12-19 | 1983-12-05 | American Cyanamid Co | |
| US4401585A (en) * | 1982-01-21 | 1983-08-30 | American Cyanamid Company | Bis(p-alkylphenylethynyl)anthracene |
| US4678608A (en) * | 1985-04-15 | 1987-07-07 | American Cyanamid Company | Chemiluminescent composition |
| ES2488408T3 (es) * | 2004-04-27 | 2014-08-27 | Lumica Corporation | Composiciones quimioluminiscentes |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL6712108A (enrdf_load_stackoverflow) * | 1965-09-08 | 1968-03-08 | ||
| NL152290B (nl) * | 1965-09-08 | 1977-02-15 | American Cyanamid Co | Werkwijze ter bereiding van chemiluminescerende mengsels. |
| BE686610A (enrdf_load_stackoverflow) * | 1966-09-08 | 1967-03-08 |
-
1973
- 1973-04-30 CA CA169,875A patent/CA1015555A/en not_active Expired
- 1973-05-04 GB GB2142173A patent/GB1425770A/en not_active Expired
- 1973-05-04 AU AU55269/73A patent/AU475513B2/en not_active Expired
- 1973-05-17 AR AR248075A patent/AR197335A1/es active
- 1973-06-08 SE SE7308192A patent/SE386908B/xx unknown
- 1973-06-11 IT IT50692/73A patent/IT985420B/it active
- 1973-06-11 JP JP6488973A patent/JPS5347798B2/ja not_active Expired
- 1973-06-12 NL NLAANVRAGE7308133,A patent/NL176688C/xx active Search and Examination
- 1973-06-12 FR FR7321274A patent/FR2187871B1/fr not_active Expired
- 1973-06-12 BR BR4371/73A patent/BR7304371D0/pt unknown
- 1973-06-12 BE BE132162A patent/BE800790A/xx not_active IP Right Cessation
- 1973-06-12 DE DE2329779A patent/DE2329779C3/de not_active Expired
-
1979
- 1979-09-13 HK HK651/79A patent/HK65179A/xx unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0096749A1 (en) * | 1982-06-16 | 1983-12-28 | American Cyanamid Company | Enhanced aqueous chemiluminescent systems |
| EP0107008A1 (en) * | 1982-10-25 | 1984-05-02 | American Cyanamid Company | 9,10-bis(phenylethynyl)-anthracenes |
| CN102781904A (zh) * | 2009-10-13 | 2012-11-14 | 克禄美科技股份有限公司 | 包含支链草酸酯的化学光产生制剂及装置 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4951185A (enrdf_load_stackoverflow) | 1974-05-17 |
| AR197335A1 (es) | 1974-03-29 |
| FR2187871B1 (enrdf_load_stackoverflow) | 1977-12-30 |
| NL7308133A (enrdf_load_stackoverflow) | 1973-12-14 |
| HK65179A (en) | 1979-09-21 |
| DE2329779A1 (de) | 1974-01-03 |
| DE2329779B2 (de) | 1981-03-12 |
| CA1015555A (en) | 1977-08-16 |
| BR7304371D0 (pt) | 1974-09-05 |
| DE2329779C3 (de) | 1982-02-18 |
| AU5526973A (en) | 1974-11-07 |
| NL176688C (nl) | 1985-05-17 |
| BE800790A (fr) | 1973-12-12 |
| AU475513B2 (en) | 1976-08-26 |
| FR2187871A1 (enrdf_load_stackoverflow) | 1974-01-18 |
| JPS5347798B2 (enrdf_load_stackoverflow) | 1978-12-23 |
| SE386908B (sv) | 1976-08-23 |
| IT985420B (it) | 1974-11-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PE20 | Patent expired after termination of 20 years |
Effective date: 19930503 |