JPH0424397B2 - - Google Patents
Info
- Publication number
- JPH0424397B2 JPH0424397B2 JP63206503A JP20650388A JPH0424397B2 JP H0424397 B2 JPH0424397 B2 JP H0424397B2 JP 63206503 A JP63206503 A JP 63206503A JP 20650388 A JP20650388 A JP 20650388A JP H0424397 B2 JPH0424397 B2 JP H0424397B2
- Authority
- JP
- Japan
- Prior art keywords
- dye
- fluorescent
- collector
- formula
- dyes
- 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 - Lifetime
Links
- 238000002834 transmittance Methods 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000000975 dye Substances 0.000 description 15
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 230000003287 optical effect Effects 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000006862 quantum yield reaction Methods 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- STWCWAOCWOCVDY-UHFFFAOYSA-N CCOC(=O)C1=CC=C2C3=C4C(=CC=C3)C(=CC=C4C5=C2C1=CC=C5)C(=O)OCC Chemical compound CCOC(=O)C1=CC=C2C3=C4C(=CC=C3)C(=CC=C4C5=C2C1=CC=C5)C(=O)OCC STWCWAOCWOCVDY-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- JSQFXMIMWAKJQJ-UHFFFAOYSA-N [9-(2-carboxyphenyl)-6-(ethylamino)xanthen-3-ylidene]-diethylazanium;chloride Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(NCC)=CC=C2C=1C1=CC=CC=C1C(O)=O JSQFXMIMWAKJQJ-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229920001577 copolymer Polymers 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
- -1 dinonyl 3,9-perylene dicarboxylate Chemical compound 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000990 laser dye Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000004810 partition chromatography Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000003345 scintillation counting Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/40—Optical elements or arrangements
- H10F77/42—Optical elements or arrangements directly associated or integrated with photovoltaic cells, e.g. light-reflecting means or light-concentrating means
- H10F77/45—Wavelength conversion means, e.g. by using luminescent material, fluorescent concentrators or up-conversion arrangements
-
- 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/14—Perylene derivatives
-
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/52—PV systems with concentrators
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Luminescent Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2851513A DE2851513C3 (de) | 1978-11-29 | 1978-11-29 | Lichtsammelsystem |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6485282A JPS6485282A (en) | 1989-03-30 |
| JPH0424397B2 true JPH0424397B2 (enrdf_load_stackoverflow) | 1992-04-24 |
Family
ID=6055762
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15306879A Granted JPS5575480A (en) | 1978-11-29 | 1979-11-28 | Fluorescent collector |
| JP63206503A Granted JPS6485282A (en) | 1978-11-29 | 1988-08-22 | Fluorescent collector |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15306879A Granted JPS5575480A (en) | 1978-11-29 | 1979-11-28 | Fluorescent collector |
Country Status (2)
| Country | Link |
|---|---|
| JP (2) | JPS5575480A (enrdf_load_stackoverflow) |
| DE (1) | DE2851513C3 (enrdf_load_stackoverflow) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4379934A (en) * | 1980-01-19 | 1983-04-12 | Basf Aktiengesellschaft | Process for two-dimensionally concentrating light, and novel perylene-3,4,9,10-tetracarboxylic acid diimides |
| DE3017185A1 (de) * | 1980-05-05 | 1981-11-19 | Hoechst Ag, 6000 Frankfurt | Perylen-3,4,9,10-tetracarbonsaeuremonoanhydridmonoimide, verfahren zur herstellung solcher verbindungen und ihre verwendung |
| DE3032546A1 (de) * | 1980-08-29 | 1982-05-06 | Basf Ag, 6700 Ludwigshafen | Verfahren zur flaechenmaessigen konzentrierung von licht |
| JPS5763377A (en) * | 1980-10-03 | 1982-04-16 | Mitsui Toatsu Chem Inc | Liquid crystal composition for color display |
| US4378302A (en) * | 1980-12-16 | 1983-03-29 | General Electric Company | Red perylene dichroic dye containing liquid crystal formulations |
| JPS581775A (ja) * | 1981-06-26 | 1983-01-07 | Mitsubishi Chem Ind Ltd | 液晶組成物 |
| US4561221A (en) * | 1981-09-17 | 1985-12-31 | Mckee Frederick B | Windows |
| WO1983001103A1 (en) * | 1981-09-17 | 1983-03-31 | Frederick Brian Mckee | Improvement in or relating to windows |
| DE3149620A1 (de) * | 1981-12-15 | 1983-07-21 | Bayer Ag, 5090 Leverkusen | Lichtsammelsysteme unter verwendung von halogenierten perylenderivaten als lichtwandler |
| DE3236241A1 (de) * | 1982-09-30 | 1984-04-05 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von lichtsammlern |
| DE3400991A1 (de) * | 1984-01-13 | 1985-07-18 | Basf Ag, 6700 Ludwigshafen | Verfahren zum flaechenmaessigen konzentrieren von licht und neue farbstoffe |
| US4597891A (en) * | 1984-06-04 | 1986-07-01 | Polaroid Corporation | Liquid crystal compositions and devices and novel compounds |
| WO2012094409A2 (en) | 2011-01-05 | 2012-07-12 | Nitto Denko Corporation | Wavelength conversion perylene diester chromophores and luminescent films |
| CN103562323B (zh) | 2011-09-26 | 2016-01-20 | 日东电工株式会社 | 用于提高的日光采集效率的高荧光且光稳定性生色团 |
| TW201317327A (zh) * | 2011-10-05 | 2013-05-01 | Nitto Denko Corp | 波長轉換膜、其形成方法以及其使用方法 |
| US20140311566A1 (en) * | 2011-11-04 | 2014-10-23 | Nitto Denko Corporation | Microstructured wavelength conversion films for enhanced solar harvesting efficiency |
| CN103339221B (zh) | 2011-12-06 | 2015-11-25 | 日东电工株式会社 | 作为太阳能模组系统所用封装的提高日光采集效率的波长转换材料 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2139690A1 (de) * | 1971-08-07 | 1973-02-15 | Basf Ag | Polychlorperylentetracarbonsaeurediimide |
| DE2139688A1 (de) * | 1971-08-07 | 1973-02-15 | Basf Ag | Farbstoffe zum faerben von kunststoffen |
| DE2147024A1 (de) * | 1971-09-21 | 1973-03-29 | Basf Ag | Farbstoffe der perylentetracarbonsaeurediimidreihe |
| DE2210170A1 (de) * | 1972-03-03 | 1973-09-06 | Basf Ag | Farbstoff der perylentetracarbonsaeurediimidreihe |
| DE2451784A1 (de) * | 1974-10-31 | 1976-05-13 | Basf Ag | Farbstoffe der perylen-3,4,9-10- tetracarbonsaeurediimid-reihe |
| DE2451781C2 (de) * | 1974-10-31 | 1976-08-19 | Basf Ag, 6700 Ludwigshafen | Perylen-SASMO-tetracarbonsäurebisimidfarbstoff |
| DE2620115C2 (de) * | 1976-05-06 | 1983-08-25 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V., 8000 München | Vorrichtung zur Umwandlung von Lichtenergie in elektrische Energie |
-
1978
- 1978-11-29 DE DE2851513A patent/DE2851513C3/de not_active Expired - Lifetime
-
1979
- 1979-11-28 JP JP15306879A patent/JPS5575480A/ja active Granted
-
1988
- 1988-08-22 JP JP63206503A patent/JPS6485282A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5575480A (en) | 1980-06-06 |
| JPS6485282A (en) | 1989-03-30 |
| DE2851513C2 (de) | 1986-10-30 |
| JPH0113512B2 (enrdf_load_stackoverflow) | 1989-03-07 |
| DE2851513A1 (de) | 1980-06-12 |
| DE2851513C3 (de) | 1993-11-18 |
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