FI71322C - Acylfosfinoxidfoereningar och deras anvaendning - Google Patents

Acylfosfinoxidfoereningar och deras anvaendning Download PDF

Info

Publication number: FI71322C
Authority: FI; Finland
Prior art keywords: compounds; acylphosphine; photoinitiators; group; curing
Prior art date: 1981-08-24

Application number

FI822872A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI71322B (fi

FI822872A0 (fi

FI822872L (fi

Inventor

Andreas Henne

Anton Hesse

Manfred Jacobi

Gunnar Schornick

Rudolf Vyvial

Klaus Holoch

Original Assignee

Basf Ag

Priority date (The priority date 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 date listed.)

1981-08-24

Filing date

1982-08-18

Publication date

1986-12-19

1982-08-18 Application filed by Basf Ag filed Critical Basf Ag

1982-08-18 Publication of FI822872A0 publication Critical patent/FI822872A0/fi

1983-02-25 Publication of FI822872L publication Critical patent/FI822872L/fi

1986-09-09 Application granted granted Critical

1986-09-09 Publication of FI71322B publication Critical patent/FI71322B/fi

1986-12-19 Publication of FI71322C publication Critical patent/FI71322C/fi

Links

150000001875 compounds Chemical class 0.000 claims description 35
-1 2,5-dimethylphenyl group Chemical group 0.000 claims description 31
238000000576 coating method Methods 0.000 claims description 7
239000000976 ink Substances 0.000 claims description 7
150000002148 esters Chemical class 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 claims description 4
229920006337 unsaturated polyester resin Polymers 0.000 claims description 4
239000004922 lacquer Substances 0.000 claims description 3
244000028419 Styrax benzoin Species 0.000 claims description 2
235000000126 Styrax benzoin Nutrition 0.000 claims description 2
235000008411 Sumatra benzointree Nutrition 0.000 claims description 2
229960002130 benzoin Drugs 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
239000003365 glass fiber Substances 0.000 claims description 2
235000019382 gum benzoic Nutrition 0.000 claims description 2
AYDPPJFUTOOTRP-UHFFFAOYSA-N naphthalene;sulfurochloridic acid Chemical class OS(Cl)(=O)=O.C1=CC=CC2=CC=CC=C21 AYDPPJFUTOOTRP-UHFFFAOYSA-N 0.000 claims description 2
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 2
150000003335 secondary amines Chemical class 0.000 claims description 2
150000003512 tertiary amines Chemical class 0.000 claims description 2
KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical group COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 claims 1
239000000945 filler Substances 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
239000000546 pharmaceutical excipient Substances 0.000 claims 1
239000004033 plastic Substances 0.000 claims 1
229920003023 plastic Polymers 0.000 claims 1
238000001723 curing Methods 0.000 description 20
239000002966 varnish Substances 0.000 description 13
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
239000000203 mixture Substances 0.000 description 10
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
239000011521 glass Substances 0.000 description 6
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000003999 initiator Substances 0.000 description 5
229920005989 resin Polymers 0.000 description 5
239000011347 resin Substances 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
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QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
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229910000073 phosphorus hydride Inorganic materials 0.000 description 4
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CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
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YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
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238000002360 preparation method Methods 0.000 description 3
238000012719 thermal polymerization Methods 0.000 description 3
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FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
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238000003848 UV Light-Curing Methods 0.000 description 2
150000001252 acrylic acid derivatives Chemical class 0.000 description 2
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VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 2
239000000178 monomer Substances 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920001225 polyester resin Polymers 0.000 description 2
239000004645 polyester resin Substances 0.000 description 2
239000003505 polymerization initiator Substances 0.000 description 2
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239000000523 sample Substances 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004408 titanium dioxide Substances 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
WNBXQARBPBWRFD-UHFFFAOYSA-N 1-chloro-2-(chloromethyl)naphthalene Chemical compound C1=CC=CC2=C(Cl)C(CCl)=CC=C21 WNBXQARBPBWRFD-UHFFFAOYSA-N 0.000 description 1
JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
UKRQMDIFLKHCRO-UHFFFAOYSA-N 2,4,6-trimethylbenzoyl chloride Chemical compound CC1=CC(C)=C(C(Cl)=O)C(C)=C1 UKRQMDIFLKHCRO-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
MPCHQYWZAVTABQ-UHFFFAOYSA-N 2-(chloromethyl)naphthalene Chemical compound C1=CC=CC2=CC(CCl)=CC=C21 MPCHQYWZAVTABQ-UHFFFAOYSA-N 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
DGUJJOYLOCXENZ-UHFFFAOYSA-N 4-[2-[4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenol Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C1=CC=C(O)C=C1 DGUJJOYLOCXENZ-UHFFFAOYSA-N 0.000 description 1
JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
LETNSRDDPGPXCR-UHFFFAOYSA-N CC1=C(C=C(C=C1)C)[PH2]=O Chemical compound CC1=C(C=C(C=C1)C)[PH2]=O LETNSRDDPGPXCR-UHFFFAOYSA-N 0.000 description 1
ANKIMFFAZPEJIK-UHFFFAOYSA-N ClC1=C(C(=O)P(C2=C(C=CC(=C2)C)C)(C2=C(C=CC(=C2)C)C)=O)C(=CC=C1)Cl.CC1=C(C(=O)P(C2=C(C(=CC=C2)C)C)(C2=C(C(=CC=C2)C)C)=O)C(=CC(=C1)C)C Chemical compound ClC1=C(C(=O)P(C2=C(C=CC(=C2)C)C)(C2=C(C=CC(=C2)C)C)=O)C(=CC=C1)Cl.CC1=C(C(=O)P(C2=C(C(=CC=C2)C)C)(C2=C(C(=CC=C2)C)C)=O)C(=CC(=C1)C)C ANKIMFFAZPEJIK-UHFFFAOYSA-N 0.000 description 1
241000195493 Cryptophyta Species 0.000 description 1
XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
239000004641 Diallyl-phthalate Substances 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000008365 aromatic ketones Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229960002887 deanol Drugs 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
239000012972 dimethylethanolamine Substances 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical class OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
IYSJRUFLTNCMAF-UHFFFAOYSA-N methoxy-bis(2-methylphenyl)phosphane Chemical compound C=1C=CC=C(C)C=1P(OC)C1=CC=CC=C1C IYSJRUFLTNCMAF-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
238000000465 moulding Methods 0.000 description 1
238000010137 moulding (plastic) Methods 0.000 description 1
KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
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125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000003678 scratch resistant effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000001993 wax Substances 0.000 description 1
238000004383 yellowing Methods 0.000 description 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
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/029—Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/53—Organo-phosphine oxides; Organo-phosphine thioxides
- C07F9/5337—Phosphine oxides or thioxides containing the structure -C(=X)-P(=X) or NC-P(=X) (X = O, S, Se)
- 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
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5397—Phosphine oxides
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/114—Initiator containing
- Y10S430/124—Carbonyl compound containing

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Physics & Mathematics (AREA)
Polymers & Plastics (AREA)
Medicinal Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Molecular Biology (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Inorganic Chemistry (AREA)
Crystallography & Structural Chemistry (AREA)
Spectroscopy & Molecular Physics (AREA)
General Physics & Mathematics (AREA)
Polymerisation Methods In General (AREA)
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FI822872A 1981-08-24 1982-08-18 Acylfosfinoxidfoereningar och deras anvaendning FI71322C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3133419		1981-08-24
DE19813133419 DE3133419A1 (de)	1981-08-24	1981-08-24	Acylphosphinoxidverbindungen und ihre verwendung

Publications (4)

Publication Number	Publication Date
FI822872A0 FI822872A0 (fi)	1982-08-18
FI822872L FI822872L (fi)	1983-02-25
FI71322B FI71322B (fi)	1986-09-09
FI71322C true FI71322C (fi)	1986-12-19

Family

ID=6139980

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI822872A FI71322C (fi)	1981-08-24	1982-08-18	Acylfosfinoxidfoereningar och deras anvaendning

Country Status (9)

Country	Link
US (1)	US4447520A (no)
EP (1)	EP0073413B1 (no)
JP (1)	JPS5877890A (no)
CA (1)	CA1200559A (no)
DE (2)	DE3133419A1 (no)
DK (1)	DK158043C (no)
ES (1)	ES8400448A1 (no)
FI (1)	FI71322C (no)
NO (1)	NO164837C (no)

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EP2649981B1 (de)	2012-04-11	2018-11-21	Ivoclar Vivadent AG	Polymerisierbare Zusammensetzungen mit hoher Polymerisationstiefe
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JP6671485B2 (ja) *	2016-09-07	2020-03-25	富士フイルム株式会社	光重合開始剤、重合性組成物、インクジェット記録方法、並びに、アシルホスフィンオキシド化合物
DE102017103084A1 (de)	2017-02-15	2018-08-16	Voco Gmbh	Dentaler Kompositblock zur Herstellung permanenter indirekter Restaurationen im CAD/CAM Verfahren
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1981
- 1981-08-24 DE DE19813133419 patent/DE3133419A1/de not_active Withdrawn
1982
- 1982-08-11 CA CA000409201A patent/CA1200559A/en not_active Expired
- 1982-08-18 EP EP82107509A patent/EP0073413B1/de not_active Expired
- 1982-08-18 FI FI822872A patent/FI71322C/fi not_active IP Right Cessation
- 1982-08-18 DE DE8282107509T patent/DE3261467D1/de not_active Expired
- 1982-08-19 US US06/409,555 patent/US4447520A/en not_active Expired - Lifetime
- 1982-08-23 JP JP57144896A patent/JPS5877890A/ja active Granted
- 1982-08-23 DK DK376982A patent/DK158043C/da not_active IP Right Cessation
- 1982-08-23 ES ES515178A patent/ES8400448A1/es not_active Expired
- 1982-08-23 NO NO822860A patent/NO164837C/no unknown

Also Published As

Publication number	Publication date
DK158043B (da)	1990-03-19
JPS5877890A (ja)	1983-05-11
EP0073413A2 (de)	1983-03-09
DE3133419A1 (de)	1983-03-10
US4447520A (en)	1984-05-08
FI71322B (fi)	1986-09-09
CA1200559A (en)	1986-02-11
NO822860L (no)	1983-02-25
NO164837C (no)	1990-11-21
DE3261467D1 (en)	1985-01-17
ES515178A0 (es)	1983-11-01
ES8400448A1 (es)	1983-11-01
FI822872A0 (fi)	1982-08-18
JPH0457677B2 (no)	1992-09-14
DK158043C (da)	1990-08-13
NO164837B (no)	1990-08-13
FI822872L (fi)	1983-02-25
DK376982A (da)	1983-02-25
EP0073413A3 (en)	1983-04-06
EP0073413B1 (de)	1984-12-05

Legal Events

Date	Code	Title	Description
1998-08-18	MM	Patent lapsed
2004-08-31	MM	Patent lapsed	Owner name: BASF AKTIENGESELLSCHAFT

Publication	Publication Date	Title
FI71322C (fi)	1986-12-19	Acylfosfinoxidfoereningar och deras anvaendning
FI68241B (fi)	1985-04-30	Fotopolymeriserbar massa
FI98817C (fi)	1997-08-25	Koreaktiivisia fotoinitiaattoreita
JP4451137B2 (ja)	2010-04-14	配合可能な光開始剤
CN107001400B (zh)	2019-08-27	多官能酰基氧化膦光引发剂
US4134813A (en)	1979-01-16	Photopolymerizable composition and its use
BR9806940B1 (pt)	2010-12-14	Ésteres fenilglioxÁlicos nço-volÁteis, composiÇÕes fotopolimerizÁveis, uso das mesmas e processo para fotopolimerizaÇço.
WO2000000869A1 (en)	2000-01-06	Photopolymerizable thermosetting resin compositions
CZ223695A3 (en)	1996-03-13	Alkoxyphenyl group substituted bisacylphosphine oxides
JPH0357916B2 (no)	1991-09-03
JPH029597B2 (no)	1990-03-02
TW200406425A (en)	2004-05-01	Improvement in the storage stability of photoinitiators
JPS6084305A (ja)	1985-05-13	光重合可能な混合物
ITMI990376A1 (it)	2000-08-24	Composizione fotoinduribil3e pigmentata
US4950795A (en)	1990-08-21	Oligomeric benzil ketals and their use as photoinitiators
US3988228A (en)	1976-10-26	Photopolymerizable polymeric compositions containing halogen containing aromatic ketones
EP1698646B1 (en)	2007-11-21	Photocurable composition and photocurable compound
JP6828467B2 (ja)	2021-02-10	活性エネルギー線重合開始剤、活性エネルギー線硬化性組成物、硬化物及びベンゾインチオエーテル化合物
US4082821A (en)	1978-04-04	1-oxo-2-(phosphona)-1,2-diphenylethanes
JP6900684B2 (ja)	2021-07-07	硫黄原子含有化合物、活性エネルギー線重合開始剤、活性エネルギー線硬化性組成物、硬化物およびベンゾインチオエーテル化合物
US5095044A (en)	1992-03-10	Oligomeric benzil ketals and their use as photoinitiators
US3966574A (en)	1976-06-29	Ultraviolet polymerization coatings suitable for food packaging using FDA approved dyes as photosensitizers
FI58927B (fi)	1981-01-30	Anvaendning av monacetaler av aromatiska 1,2-diketoner saosom fotosensibilisatorer
JPS61174202A (ja)	1986-08-05	水溶性の感光性樹脂の製造方法
KR19980063821A (ko)	1998-10-07	신규 α-아미노아세토페논 광개시제