GB1002212A - Improvements relating to photo-polymerization initiators - Google Patents
Improvements relating to photo-polymerization initiatorsInfo
- Publication number
- GB1002212A GB1002212A GB2663463A GB2663463A GB1002212A GB 1002212 A GB1002212 A GB 1002212A GB 2663463 A GB2663463 A GB 2663463A GB 2663463 A GB2663463 A GB 2663463A GB 1002212 A GB1002212 A GB 1002212A
- Authority
- GB
- United Kingdom
- Prior art keywords
- anthraquinone
- cellulose
- photopolymerizable
- acid chloride
- carboxylic acid
- 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
- 239000003505 polymerization initiator Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 8
- 229920002301 cellulose acetate Polymers 0.000 abstract 7
- 229920000642 polymer Polymers 0.000 abstract 7
- AZQWKYJCGOJGHM-UHFFFAOYSA-N para-benzoquinone Natural products O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 abstract 6
- 229920002678 cellulose Polymers 0.000 abstract 5
- 239000001913 cellulose Substances 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- IYKJEILNJZQJPU-UHFFFAOYSA-N acetic acid;butanedioic acid Chemical compound CC(O)=O.OC(=O)CCC(O)=O IYKJEILNJZQJPU-UHFFFAOYSA-N 0.000 abstract 4
- XOGPDSATLSAZEK-UHFFFAOYSA-N 2-Aminoanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(N)=CC=C3C(=O)C2=C1 XOGPDSATLSAZEK-UHFFFAOYSA-N 0.000 abstract 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 abstract 2
- DGJNWQJOASAMHY-UHFFFAOYSA-N 9,10-dioxoanthracene-2-carbonyl chloride Chemical compound C1=CC=C2C(=O)C3=CC(C(=O)Cl)=CC=C3C(=O)C2=C1 DGJNWQJOASAMHY-UHFFFAOYSA-N 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- 230000032050 esterification Effects 0.000 abstract 2
- 238000005886 esterification reaction Methods 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 239000008103 glucose Substances 0.000 abstract 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 abstract 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 2
- -1 organic dyestuffs Substances 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 2
- 229920001169 thermoplastic Polymers 0.000 abstract 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 2
- DSMFFOSDNKPHJP-ODZAUARKSA-N (z)-but-2-enedioic acid;propanoic acid Chemical compound CCC(O)=O.OC(=O)\C=C/C(O)=O DSMFFOSDNKPHJP-ODZAUARKSA-N 0.000 abstract 1
- LNURHOKVMJBWMO-UHFFFAOYSA-N 1,4-dichloro-9,10-dioxoanthracene-2-sulfonyl chloride Chemical compound ClC1=C(C=C(C=2C(C3=CC=CC=C3C(C1=2)=O)=O)Cl)S(=O)(=O)Cl LNURHOKVMJBWMO-UHFFFAOYSA-N 0.000 abstract 1
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 abstract 1
- LOVIUJLBPOAANA-UHFFFAOYSA-N 4-nitro-9,10-dioxoanthracene-1-sulfonyl chloride Chemical compound [N+](=O)([O-])C1=CC=C(C=2C(C3=CC=CC=C3C(C1=2)=O)=O)S(=O)(=O)Cl LOVIUJLBPOAANA-UHFFFAOYSA-N 0.000 abstract 1
- ZANJGNALLJAIQT-UHFFFAOYSA-N 8-nitro-9,10-dioxoanthracene-1-sulfonyl chloride Chemical compound [N+](=O)([O-])C1=CC=CC=2C(C3=CC=CC(=C3C(C1=2)=O)S(=O)(=O)Cl)=O ZANJGNALLJAIQT-UHFFFAOYSA-N 0.000 abstract 1
- LLSVGXGSYBLMNY-UHFFFAOYSA-N 9,10-dioxoanthracene-1-carbonyl chloride Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(=O)Cl LLSVGXGSYBLMNY-UHFFFAOYSA-N 0.000 abstract 1
- UDFCHANCMRCOQT-UHFFFAOYSA-N 9,10-dioxoanthracene-2-sulfonyl chloride Chemical compound C1=CC=C2C(=O)C3=CC(S(=O)(=O)Cl)=CC=C3C(=O)C2=C1 UDFCHANCMRCOQT-UHFFFAOYSA-N 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 abstract 1
- GAMPNQJDUFQVQO-UHFFFAOYSA-N acetic acid;phthalic acid Chemical compound CC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O GAMPNQJDUFQVQO-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 238000012644 addition polymerization Methods 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 230000009435 amidation Effects 0.000 abstract 1
- 238000007112 amidation reaction Methods 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 abstract 1
- 235000012216 bentonite Nutrition 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000001768 carboxy methyl cellulose Substances 0.000 abstract 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 abstract 1
- 239000000919 ceramic Substances 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 abstract 1
- 229910002804 graphite Inorganic materials 0.000 abstract 1
- 239000010439 graphite Substances 0.000 abstract 1
- 150000004820 halides Chemical group 0.000 abstract 1
- 239000003999 initiator Substances 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 229920005862 polyol Polymers 0.000 abstract 1
- 150000003077 polyols Chemical class 0.000 abstract 1
- 229920002689 polyvinyl acetate Polymers 0.000 abstract 1
- 239000011118 polyvinyl acetate Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000012744 reinforcing agent Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 abstract 1
- 239000004416 thermosoftening plastic Substances 0.000 abstract 1
- 239000004408 titanium dioxide Substances 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
- C08B15/05—Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur
- C08B15/06—Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur containing nitrogen, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B3/00—Preparation of cellulose esters of organic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US208091A US3149975A (en) | 1962-07-06 | 1962-07-06 | Photopolymerizable compositions and elements |
| US208090A US3314939A (en) | 1962-07-06 | 1962-07-06 | Photoinitiating compounds prepared by esterifying cellulosic material with substituted anthraquinones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1002212A true GB1002212A (en) | 1965-08-25 |
Family
ID=26902897
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2663463A Expired GB1002212A (en) | 1962-07-06 | 1963-07-04 | Improvements relating to photo-polymerization initiators |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE634562A (enrdf_load_stackoverflow) |
| CH (1) | CH447611A (enrdf_load_stackoverflow) |
| DE (1) | DE1280558B (enrdf_load_stackoverflow) |
| FR (1) | FR1367059A (enrdf_load_stackoverflow) |
| GB (1) | GB1002212A (enrdf_load_stackoverflow) |
| NL (1) | NL294759A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2140575A (en) * | 1983-05-18 | 1984-11-28 | Grace W R & Co | Compressible printing plate |
| WO1997017378A1 (en) * | 1995-11-06 | 1997-05-15 | Coates Brothers Plc | Photoinitiator |
| US5735983A (en) * | 1993-08-25 | 1998-04-07 | Polyfibron Technologies, Inc. | Method for manufacturing a printing plate |
-
1963
- 1963-07-01 NL NL294759D patent/NL294759A/xx unknown
- 1963-07-03 DE DE1963P0032130 patent/DE1280558B/de active Pending
- 1963-07-04 GB GB2663463A patent/GB1002212A/en not_active Expired
- 1963-07-05 FR FR940539A patent/FR1367059A/fr not_active Expired
- 1963-07-05 CH CH837463A patent/CH447611A/de unknown
- 1963-07-05 BE BE634562D patent/BE634562A/xx unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2140575A (en) * | 1983-05-18 | 1984-11-28 | Grace W R & Co | Compressible printing plate |
| US4582777A (en) * | 1983-05-18 | 1986-04-15 | W. R. Grace & Co. | Compressible printing plate |
| US5735983A (en) * | 1993-08-25 | 1998-04-07 | Polyfibron Technologies, Inc. | Method for manufacturing a printing plate |
| WO1997017378A1 (en) * | 1995-11-06 | 1997-05-15 | Coates Brothers Plc | Photoinitiator |
| US6296986B1 (en) | 1995-11-06 | 2001-10-02 | Coates Brothers Plc | Photoinitiator |
Also Published As
| Publication number | Publication date |
|---|---|
| BE634562A (enrdf_load_stackoverflow) | 1964-01-06 |
| CH447611A (de) | 1967-11-30 |
| NL294759A (enrdf_load_stackoverflow) | 1965-04-26 |
| DE1280558B (de) | 1968-10-17 |
| FR1367059A (fr) | 1964-07-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4249011A (en) | Poly(ethylenically unsaturated alkoxy) heterocyclic compounds | |
| US11667730B2 (en) | Oxime ester compound and photopolymerization initiator containing the same | |
| KR101418735B1 (ko) | 옥심에스테르 화합물 및 상기 화합물을 함유하는 광중합 개시제 | |
| US4937173A (en) | Radiation curable liquid resin composition containing microparticles | |
| JPS6281345A (ja) | 共重合性光開始剤 | |
| CA1057997A (en) | Radiation curable composition containing prepolymer with bonded hydroxyalkyl ester and halo substituted anhydride | |
| CN105086602A (zh) | 光固化热固化树脂组合物油墨、用途及使用其的线路板 | |
| KR20150082113A (ko) | 알칼리 현상성 감광성 조성물 | |
| US3149975A (en) | Photopolymerizable compositions and elements | |
| GB1002212A (en) | Improvements relating to photo-polymerization initiators | |
| EP0182642B1 (en) | Ethylenically unsaturated polyesters | |
| JPS5965090A (ja) | １０−フエニル−１，３，９−トリアザアントラセン及び該化合物を含有する光重合可能な混合物 | |
| GB940135A (en) | Improvements relating to photo-polymerizable compositions | |
| JPS5911096B2 (ja) | 樹脂凸版用感光性組成物 | |
| JPS5941444B2 (ja) | 光重合性組成物 | |
| JPH0151821B2 (enrdf_load_stackoverflow) | ||
| JPS58103519A (ja) | 硬化性樹脂組成物 | |
| EP0030969B1 (en) | Poly(ethylenically unsaturated alkoxy)heterocyclic compounds and crosslinked polymeric coatings | |
| US4165267A (en) | Photo-polymerizable systems containing 2-haloacetophenone derivatives as photosensitizing agents | |
| US4425208A (en) | Compositions and process | |
| JP4592544B2 (ja) | 感光性樹脂組成物及びフォトレジストフィルム | |
| US4518473A (en) | Compositions and process | |
| GB1055197A (en) | Improvements relating to photopolymerizable compositions | |
| JPH10259202A (ja) | サイクロデキストリンの（メタ）アクリル酸エステルの製法及びサイクロデキストリンの（メタ）アクリル酸エステル | |
| JPH03259905A (ja) | ウレタンアクリレートを用いた樹脂組成物及び印刷インキ組成物 |