GB1543978A - Pyrazoline compounds - Google Patents
Pyrazoline compoundsInfo
- Publication number
- GB1543978A GB1543978A GB1906876A GB1906876A GB1543978A GB 1543978 A GB1543978 A GB 1543978A GB 1906876 A GB1906876 A GB 1906876A GB 1906876 A GB1906876 A GB 1906876A GB 1543978 A GB1543978 A GB 1543978A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- image
- compounds
- pyrazoline compounds
- emission
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Luminescent Compositions (AREA)
- Measurement Of Radiation (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Pyrazoline compounds of the formula I are prepared by reacting a phenyl vinyl ketone of the formula <IMAGE> or a dimethylaminopropiophenone hydrochloride of the formula <IMAGE> with a phenylhydrazine of the formula <IMAGE> The meaning of the individual symbols is evident from Claim 1. The compounds with the said substituents in the 2',6' position and/or in the 2'',6'' position have the following properties: unusually large Stokes' shifts without alteration in the frequency range and the intensity of the fluorescence emission, high quantum yield of emission and no overlap between the absorption region and the fluorescence region. They can be used for radiation conversion, in particular for optical brightening and scintillation measurement. <IMAGE>
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19752531495 DE2531495C2 (en) | 1975-07-15 | 1975-07-15 | Pyrazoline compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1543978A true GB1543978A (en) | 1979-04-11 |
Family
ID=5951528
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1906876A Expired GB1543978A (en) | 1975-07-15 | 1976-05-10 | Pyrazoline compounds |
Country Status (4)
Country | Link |
---|---|
JP (1) | JPS5210272A (en) |
CH (1) | CH624940A5 (en) |
DE (1) | DE2531495C2 (en) |
GB (1) | GB1543978A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2643359B1 (en) * | 1989-01-31 | 1993-12-10 | Centre Nal Recherc Scientifique | PROCESS FOR MANUFACTURING SPARKLING OPTICAL FIBERS AND OPTICAL FIBERS OBTAINED |
DE4023860A1 (en) * | 1990-07-27 | 1992-01-30 | Kernforschungsz Karlsruhe | New sterically hindered di:phenyl pyrazoline cpds. - are used as scintillator having large strokes shift, good quantum yield and decay time |
DE4023859A1 (en) * | 1990-07-27 | 1992-01-30 | Kernforschungsz Karlsruhe | New sterically hindered phenyl mesityl pyrazoline cpds. - are used as scintillator having large strokes shift, good quantum yield and decay time |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1902459A1 (en) * | 1969-01-18 | 1970-08-20 | Basf Ag | Optically brightened fibre fleeces |
BE788658R (en) * | 1971-09-09 | 1973-03-12 | Hoechst Ag | 3- (3 ', 4'-DICHLORO-6'-ALKYLPHENYL) -DELTA2-PYRAZOLINES, THEIR PREPARATION AND THEIR USE AS BRIGHTENING AGENTS |
-
1975
- 1975-07-15 DE DE19752531495 patent/DE2531495C2/en not_active Expired
-
1976
- 1976-05-10 GB GB1906876A patent/GB1543978A/en not_active Expired
- 1976-07-06 CH CH867176A patent/CH624940A5/en not_active IP Right Cessation
- 1976-07-09 JP JP51081883A patent/JPS5210272A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
CH624940A5 (en) | 1981-08-31 |
JPS5210272A (en) | 1977-01-26 |
JPS6160068B2 (en) | 1986-12-19 |
DE2531495C2 (en) | 1985-01-17 |
DE2531495A1 (en) | 1977-01-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TR20770A (en) | PRIMIDIN-BUTANOL TUEREVLER, THEIR PREPARATION AND USE OF PLANT BUEYUEMES AS A REGULATOR | |
GB1543978A (en) | Pyrazoline compounds | |
GB1095784A (en) | Benzothioxanthene dyestuffs and processes for their manufacture | |
GB1068182A (en) | Photographic materials containing organic monohydrazone compounds | |
GB1471847A (en) | Dibenzofuran derivatives | |
GB1067244A (en) | Benzonaphthindolizine-dione-carboxyarylamide pigments | |
ES440216A1 (en) | Stilbene compounds | |
GB1104729A (en) | Colour couplers for cyan | |
SE7500446L (en) | ||
GB1095035A (en) | Dyes of the phthaloperinone series | |
GB1114323A (en) | Silver halide light-sensitive materials | |
SE7612961L (en) | TIENAMYCIN DERIVATIVES | |
NO151892C (en) | PROCEDURE FOR THE PREPARATION OF BASIC SUBSTITUTED PHENYL ACETONITRILS. | |
ES355253A1 (en) | Water-insoluble anthraquinone dyestuffs | |
SE7701732L (en) | 1,2,3-OXADIAZOLAMIDER | |
GB1063891A (en) | Method for preparation of benzodiazepinones | |
SE7701834L (en) | 4-HYDROXY-2-QUINOLINONE-3-CARBOXYLIC ACID ESTERS | |
GB2013187A (en) | Fungicidal phenypyrol derivatives | |
JPS52100472A (en) | 11thiazolyll55 acylimidazolidinone compound | |
SE7700962L (en) | ORGANIC ASSOCIATIONS, THEIR PREPARATION AND USE | |
GB1099756A (en) | Anthraquinone dyestuffs | |
GB1094045A (en) | Phthalazine derivatives | |
ES418462A1 (en) | Disazo pigmetn | |
GB1482047A (en) | Bicyclohexane derivatives for use in the synthesis of prostaglandins | |
GB1353133A (en) | Bisstyryltriazoles their use for the optical brightening of organic materials and process for their manufacture |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19950510 |