FR2573435A1 - Utilisation comme matieres colorantes pour un laser ultraviolet de 2,6-diphenyl-benzo- 1.2d; 4.5d' -bisoxazoles et de 2,6-diphenyl-benzo- 1.2d; 5.4d' -bisoxazoles substitues - Google Patents
Utilisation comme matieres colorantes pour un laser ultraviolet de 2,6-diphenyl-benzo- 1.2d; 4.5d' -bisoxazoles et de 2,6-diphenyl-benzo- 1.2d; 5.4d' -bisoxazoles substitues Download PDFInfo
- Publication number
- FR2573435A1 FR2573435A1 FR8514956A FR8514956A FR2573435A1 FR 2573435 A1 FR2573435 A1 FR 2573435A1 FR 8514956 A FR8514956 A FR 8514956A FR 8514956 A FR8514956 A FR 8514956A FR 2573435 A1 FR2573435 A1 FR 2573435A1
- Authority
- FR
- France
- Prior art keywords
- laser
- diphenyl
- bisoxazoles
- benzo
- substituted
- 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
- 238000004040 coloring Methods 0.000 title abstract description 11
- 239000000463 material Substances 0.000 title abstract description 4
- 238000005086 pumping Methods 0.000 abstract description 7
- 230000001976 improved effect Effects 0.000 abstract description 4
- -1 BUTYL Chemical group 0.000 abstract 1
- 239000000975 dye Substances 0.000 description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000001427 coherent effect Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 238000002189 fluorescence spectrum Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000990 laser dye Substances 0.000 description 2
- 238000006862 quantum yield reaction Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- DPYROBMRMXHROQ-UHFFFAOYSA-N 4,6-diaminobenzene-1,3-diol Chemical compound NC1=CC(N)=C(O)C=C1O DPYROBMRMXHROQ-UHFFFAOYSA-N 0.000 description 1
- AANMVENRNJYEMK-UHFFFAOYSA-N 4-propan-2-ylcyclohex-2-en-1-one Chemical compound CC(C)C1CCC(=O)C=C1 AANMVENRNJYEMK-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- FUWXCBQJKGNLNU-UHFFFAOYSA-N C1=CC=CC=C1.O1C=NC=C1 Chemical compound C1=CC=CC=C1.O1C=NC=C1 FUWXCBQJKGNLNU-UHFFFAOYSA-N 0.000 description 1
- 206010056740 Genital discharge Diseases 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000003935 benzaldehydes Chemical class 0.000 description 1
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzenecarboxaldehyde Natural products O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- 230000000763 evoking effect Effects 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- JEHCHYAKAXDFKV-UHFFFAOYSA-J lead tetraacetate Chemical compound CC(=O)O[Pb](OC(C)=O)(OC(C)=O)OC(C)=O JEHCHYAKAXDFKV-UHFFFAOYSA-J 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
- H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
- H01S3/14—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range characterised by the material used as the active medium
- H01S3/20—Liquids
- H01S3/213—Liquids including an organic dye
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
Landscapes
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- Optics & Photonics (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lasers (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19843442293 DE3442293A1 (de) | 1984-11-20 | 1984-11-20 | Verwendung von unsubstituierten und substituierten 2,6-diphenyl-benzo-(1.2d;4.5d')-bisoxazolen und 2,6-diphenyl-benzo-(1.2d;5.4d')-bisoxazolen als uv-laserfarbstoffe |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FR2573435A1 true FR2573435A1 (fr) | 1986-05-23 |
Family
ID=6250700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR8514956A Pending FR2573435A1 (fr) | 1984-11-20 | 1985-10-09 | Utilisation comme matieres colorantes pour un laser ultraviolet de 2,6-diphenyl-benzo- 1.2d; 4.5d' -bisoxazoles et de 2,6-diphenyl-benzo- 1.2d; 5.4d' -bisoxazoles substitues |
Country Status (3)
| Country | Link |
|---|---|
| DE (1) | DE3442293A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2573435A1 (enrdf_load_stackoverflow) |
| GB (1) | GB2170505B (enrdf_load_stackoverflow) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001049508A1 (fr) * | 2000-01-07 | 2001-07-12 | Mitsui Chemicals, Incorporated | Compose de benzbisazole et support d'enregistrement optique le contenant |
| CN105503847A (zh) * | 2016-01-15 | 2016-04-20 | 中国科学院兰州化学物理研究所 | 一种苯并二噁唑类化合物的合成方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3976656A (en) * | 1975-01-20 | 1976-08-24 | The United States Of America As Represented By The Secretary Of The Navy | 1,4-Bis(5-p-n-butoxyphenyloxazol-2-yl)benzene and the preparaion thereof |
-
1984
- 1984-11-20 DE DE19843442293 patent/DE3442293A1/de active Granted
-
1985
- 1985-10-09 FR FR8514956A patent/FR2573435A1/fr active Pending
- 1985-11-14 GB GB08528087A patent/GB2170505B/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3976656A (en) * | 1975-01-20 | 1976-08-24 | The United States Of America As Represented By The Secretary Of The Navy | 1,4-Bis(5-p-n-butoxyphenyloxazol-2-yl)benzene and the preparaion thereof |
Non-Patent Citations (3)
| Title |
|---|
| CHEMICAL ABSTRACTS, vol. 102, 1985, page 558, résumé no. 87182g, Columbus, Ohio, US; Z. GAO et al.: "Spectral and lasing properties of new UV laser dye DPDO series", & GUANGXUE XUEBAO 1984, 4(6), 485-8 * |
| CHEMICAL ABSTRACTS, vol. 102, 1985, page 611, résumé no. 122727n, Columbus, Ohio, US; M. RINKE: "Photophysical and laser properties of new organic laser dyes in the blue and ultraviolet spectral region", & KERNFORSCHUNGSZENT. KARLSRUHE, ÄBER.Ü KfK 1984, KfK 3810, 112 * |
| CHEMICAL ABSTRACTS, vol. 98, 1983, page 553, résumé no. 215514e, Columbus, Ohio, US; J. PAN et al.: "2,6-Disubstituted benzobisoxazoles", & GAODENG XUEXIAO HUAZUE XUEBAO 1982, (ZHUANKAN), 61-4 * |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3442293A1 (de) | 1986-05-22 |
| GB2170505B (en) | 1988-06-22 |
| GB8528087D0 (en) | 1985-12-18 |
| GB2170505A (en) | 1986-08-06 |
| DE3442293C2 (enrdf_load_stackoverflow) | 1991-04-25 |
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