KR101627725B1 - 광경화형 화합물 - Google Patents
광경화형 화합물 Download PDFInfo
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- KR101627725B1 KR101627725B1 KR1020090008604A KR20090008604A KR101627725B1 KR 101627725 B1 KR101627725 B1 KR 101627725B1 KR 1020090008604 A KR1020090008604 A KR 1020090008604A KR 20090008604 A KR20090008604 A KR 20090008604A KR 101627725 B1 KR101627725 B1 KR 101627725B1
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 6
- 125000001424 substituent group Chemical group 0.000 claims description 87
- 239000001257 hydrogen Substances 0.000 claims description 53
- 229910052739 hydrogen Inorganic materials 0.000 claims description 53
- 150000002431 hydrogen Chemical class 0.000 claims description 43
- 239000000126 substance Substances 0.000 claims description 23
- 125000000732 arylene group Chemical group 0.000 claims description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 229910052710 silicon Inorganic materials 0.000 claims description 13
- 239000010703 silicon Substances 0.000 claims description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 230000003287 optical effect Effects 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 2
- 239000003063 flame retardant Substances 0.000 claims description 2
- 239000013308 plastic optical fiber Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 19
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 10
- -1 polyfunctional Chemical compound 0.000 abstract description 9
- 125000000217 alkyl group Chemical group 0.000 description 23
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 14
- 238000003786 synthesis reaction Methods 0.000 description 13
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 9
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 7
- 125000005649 substituted arylene group Chemical group 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 6
- BOCLKUCIZOXUEY-UHFFFAOYSA-N 4-[tris(4-hydroxyphenyl)methyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 BOCLKUCIZOXUEY-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 125000000547 substituted alkyl group Chemical group 0.000 description 4
- QASBHTCRFDZQAM-UHFFFAOYSA-N (2-isocyanato-2-methyl-3-prop-2-enoyloxypropyl) prop-2-enoate Chemical compound C=CC(=O)OCC(C)(COC(=O)C=C)N=C=O QASBHTCRFDZQAM-UHFFFAOYSA-N 0.000 description 3
- DPNXHTDWGGVXID-UHFFFAOYSA-N 2-isocyanatoethyl prop-2-enoate Chemical compound C=CC(=O)OCCN=C=O DPNXHTDWGGVXID-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 238000010526 radical polymerization reaction Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- VRVUKQWNRPNACD-UHFFFAOYSA-N 1-isocyanatopentane Chemical compound CCCCCN=C=O VRVUKQWNRPNACD-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- SXAMGRAIZSSWIH-UHFFFAOYSA-N 2-[3-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,2,4-oxadiazol-5-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NOC(=N1)CC(=O)N1CC2=C(CC1)NN=N2 SXAMGRAIZSSWIH-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- JEHFRMABGJJCPF-UHFFFAOYSA-N 2-methylprop-2-enoyl isocyanate Chemical class CC(=C)C(=O)N=C=O JEHFRMABGJJCPF-UHFFFAOYSA-N 0.000 description 1
- KLSLBUSXWBJMEC-UHFFFAOYSA-N 4-Propylphenol Chemical compound CCCC1=CC=C(O)C=C1 KLSLBUSXWBJMEC-UHFFFAOYSA-N 0.000 description 1
- DVJDHNJKCNMAED-UHFFFAOYSA-N 4-[1,1-bis(4-hydroxyphenyl)butyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(CCC)C1=CC=C(O)C=C1 DVJDHNJKCNMAED-UHFFFAOYSA-N 0.000 description 1
- BRPSWMCDEYMRPE-UHFFFAOYSA-N 4-[1,1-bis(4-hydroxyphenyl)ethyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(C)C1=CC=C(O)C=C1 BRPSWMCDEYMRPE-UHFFFAOYSA-N 0.000 description 1
- QQUZHNPGWNIYMK-UHFFFAOYSA-N 4-[1,2,2-tris(4-hydroxyphenyl)ethenyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)=C(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 QQUZHNPGWNIYMK-UHFFFAOYSA-N 0.000 description 1
- UHUUGQDYCYKQTC-UHFFFAOYSA-N 4-[2,2,2-tris(4-hydroxyphenyl)ethyl]phenol Chemical compound C1=CC(O)=CC=C1CC(C=1C=CC(O)=CC=1)(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 UHUUGQDYCYKQTC-UHFFFAOYSA-N 0.000 description 1
- WFCQTAXSWSWIHS-UHFFFAOYSA-N 4-[bis(4-hydroxyphenyl)methyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 WFCQTAXSWSWIHS-UHFFFAOYSA-N 0.000 description 1
- OQEAEWQOPZQPSS-UHFFFAOYSA-N 4-isocyanatobutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCN=C=O OQEAEWQOPZQPSS-UHFFFAOYSA-N 0.000 description 1
- AIHRQGUYNQTCBQ-UHFFFAOYSA-N 4-tris(4-hydroxyphenyl)silylphenol Chemical compound C1=CC(O)=CC=C1[Si](C=1C=CC(O)=CC=1)(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 AIHRQGUYNQTCBQ-UHFFFAOYSA-N 0.000 description 1
- TVEXGJYMHHTVKP-UHFFFAOYSA-N 6-oxabicyclo[3.2.1]oct-3-en-7-one Chemical compound C1C2C(=O)OC1C=CC2 TVEXGJYMHHTVKP-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- HIRTXVQAFIFZMC-UHFFFAOYSA-N OC1=CC=C(C=C1)C1=C(C(=C(C(=C1C=C)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O Chemical compound OC1=CC=C(C=C1)C1=C(C(=C(C(=C1C=C)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O HIRTXVQAFIFZMC-UHFFFAOYSA-N 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- WUDNUHPRLBTKOJ-UHFFFAOYSA-N ethyl isocyanate Chemical compound CCN=C=O WUDNUHPRLBTKOJ-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- FOVRCVYQPBQVTL-UHFFFAOYSA-N isocyanatomethyl prop-2-enoate Chemical compound C=CC(=O)OCN=C=O FOVRCVYQPBQVTL-UHFFFAOYSA-N 0.000 description 1
- QHDRKFYEGYYIIK-UHFFFAOYSA-N isovaleronitrile Chemical compound CC(C)CC#N QHDRKFYEGYYIIK-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- YOSXAXYCARLZTR-UHFFFAOYSA-N prop-2-enoyl isocyanate Chemical class C=CC(=O)N=C=O YOSXAXYCARLZTR-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
- C07C271/42—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/48—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C235/34—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
- C08F220/36—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate containing oxygen in addition to the carboxy oxygen, e.g. 2-N-morpholinoethyl (meth)acrylate or 2-isocyanatoethyl (meth)acrylate
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (19)
- 하기 화학식 1로 표시되는 광경화형 화합물:[화학식 1]상기 화학식 1에서,A1는 탄소(C) 또는 규소(Si)이고,Ar1 내지 Ar3은 각각 독립적으로 C6 내지 C20의 치환 또는 비치환된 아릴렌이고,L1은 단일결합 및 C1 내지 C20의 알킬렌기로 이루어진 군에서 선택되고,R1은 수소, C1 내지 C5의 알킬기 및 하기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고,X1 내지 X3은 각각 독립적으로 수소, C1 내지 C5의 알킬기 및 하기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택된 하나일 수 있고, R1 및 X1 내지 X3 중 적어도 하나는 하기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고,a 내지 c는 각각 독립적으로 1 또는 2의 정수이고, a 내지 c가 2인 경우 각각의 X1 내지 X3은 동일하거나 서로 상이할 수 있고,[화학식 1-1]상기 화학식 1-1에서,Z는 단일결합, -O-, -COO- 및 -OCO-로 이루어진 군에서 선택되고,i는 1 내지 5의 정수이고,h는 0 내지 5의 정수이고,R100은 수소 또는 메틸기이고,단, A1이 탄소인 경우 화학식 1-1에서 Z는 -O-, -COO- 및 -OCO-로 이루어진 군에서 선택되고, h는 1 내지 5의 정수이고,[화학식 1-2]상기 화학식 1-2에서,p 및 q는 각각 독립적으로 1 내지 5의 정수이고,R101 내지 R103은 각각 독립적으로 수소 또는 메틸기이다.
- 제1항에 있어서,상기 화학식 1의 화합물은 화학식 1A로 표시되는 광경화형 화합물:[화학식 1A]상기 화학식 1A에서,A1는 탄소 또는 규소이고,L1은 단일결합 및 C1 내지 C20의 알킬렌기로 이루어진 군에서 선택되고,R1은 수소, C1 내지 C5의 알킬기 및 상기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고,R1, R4 내지 R6 및 X1 내지 X3은 각각 독립적으로 수소, C1 내지 C5의 알킬기 및 상기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고, 이 중 적어도 하나는 상기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고,a 내지 c는 각각 독립적으로 1 또는 2의 정수이고, a 내지 c가 2인 경우 각각의 X1 내지 X3은 동일하거나 서로 상이할 수 있다.
- 하기 화학식 2로 표시되는 광경화형 화합물:[화학식 2]상기 화학식 2에서,A2는 탄소 또는 규소이고,Ar4 내지 Ar7은 각각 독립적으로 C6 내지 C20의 치환 또는 비치환된 아릴렌이고,X4 내지 X7은 각각 독립적으로 수소, C1 내지 C5의 알킬기 및 하기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고, X4 내지 X7 중 적어도 하나는 하기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고,d 내지 g는 각각 독립적으로 1 또는 2의 정수이고, d 내지 g가 2인 경우 각각의 X4 내지 X7은 동일하거나 서로 상이할 수 있고,[화학식 1-1]상기 화학식 1-1에서,Z는 단일결합, -O-, -COO- 및 -OCO-로 이루어진 군에서 선택되고,i는 1 내지 5의 정수이고,h는 0 내지 5의 정수이고,R100은 수소 또는 메틸기이고, 단 Z가 -O-, -COO- 또는 -OCO-인 경우 h는 0은 아니고,[화학식 1-2]상기 화학식 1-2에서,p 및 q는 각각 독립적으로 1 내지 5의 정수이고,R101 내지 R103은 각각 독립적으로 수소 또는 메틸기이다.
- 제3항에 있어서,상기 화학식 2의 화합물은 화학식 2A로 표시되는 광경화형 화합물:[화학식 2A]상기 화학식 2A에서,A2는 탄소 또는 규소이고,R7 내지 R10 및 X4 내지 X7은 각각 독립적으로 수소, C1 내지 C5의 알킬기 및 상기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고, 이 중 적어도 하나는 상기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되고,d 내지 g는 각각 독립적으로 1 또는 2의 정수이고, d 내지 g가 2인 경우 각각의 X4 내지 X7은 동일하거나 서로 상이할 수 있다.
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- 제1항에 있어서,상기 화학식 1의 R1 및 X1 내지 X3 중 적어도 세 개는 상기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되는 광경화형 화합물.
- 제3항에 있어서,상기 화학식 2의 X4 내지 X7 중 적어도 세 개는 상기 화학식 1-1 또는 1-2로 표시되는 치환기로 이루어진 군에서 선택되는 광경화형 화합물.
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- 제1항 내지 제4항, 제13항 및 제14항중 어느 하나의 항에 있어서,상기 광경화형 화합물은 광경화 도료, 잉크 조성물, 도광판, 절연층, 광학 필터, 난연 수지 또는 플라스틱 광섬유에 사용되는 것인 광경화형 화합물..
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KR20100089389A (ko) * | 2009-02-03 | 2010-08-12 | 삼성전자주식회사 | 점착 조성물 및 이로부터 제조되는 점착 필름 |
CN104245796B (zh) * | 2012-04-03 | 2016-08-31 | 巴斯夫欧洲公司 | 有色带电的倍半硅氧烷 |
SG11201505710UA (en) | 2013-01-28 | 2015-08-28 | Nippon Soda Co | Coating agent |
CN103342793B (zh) * | 2013-05-31 | 2015-08-05 | 成都彭州立源高分子材料有限公司 | 一种有机氟硅杂化光敏树脂及其合成方法 |
JP6197020B2 (ja) * | 2015-12-17 | 2017-09-13 | 三井化学株式会社 | 光硬化性樹脂組成物、表示素子シール剤、液晶シール剤及び液晶表示パネルとその製造方法 |
KR102020891B1 (ko) * | 2016-04-25 | 2019-09-11 | 삼성전자 주식회사 | 점착필름, 이를 포함하는 광학부재 및 이를 포함하는 광학표시장치 |
WO2018016634A1 (ja) * | 2016-07-21 | 2018-01-25 | 三菱瓦斯化学株式会社 | 化合物、樹脂及び組成物、並びにレジストパターン形成方法及び回路パターン形成方法 |
CN107629082B (zh) * | 2017-09-29 | 2019-11-22 | 西南石油大学 | 一种新型含硅苯并噁嗪及其制备方法 |
US12034015B2 (en) | 2018-05-25 | 2024-07-09 | Meta Platforms Technologies, Llc | Programmable pixel array |
US11888002B2 (en) | 2018-12-17 | 2024-01-30 | Meta Platforms Technologies, Llc | Dynamically programmable image sensor |
US11962928B2 (en) | 2018-12-17 | 2024-04-16 | Meta Platforms Technologies, Llc | Programmable pixel array |
US11718580B2 (en) | 2019-05-08 | 2023-08-08 | Meta Platforms Technologies, Llc | Fluorene derivatized monomers and polymers for volume Bragg gratings |
US12108141B2 (en) | 2019-08-05 | 2024-10-01 | Meta Platforms Technologies, Llc | Dynamically programmable image sensor |
US11935291B2 (en) | 2019-10-30 | 2024-03-19 | Meta Platforms Technologies, Llc | Distributed sensor system |
US11948089B2 (en) | 2019-11-07 | 2024-04-02 | Meta Platforms Technologies, Llc | Sparse image sensing and processing |
US11780819B2 (en) * | 2019-11-27 | 2023-10-10 | Meta Platforms Technologies, Llc | Aromatic substituted alkane-core monomers and polymers thereof for volume Bragg gratings |
US20210155584A1 (en) * | 2019-11-27 | 2021-05-27 | Facebook Technologies, Llc | Aromatic substituted methane-core monomers and polymers thereof for volume bragg gratings |
US20210155581A1 (en) * | 2019-11-27 | 2021-05-27 | Facebook Technologies, Llc | Aromatic substituted ethane-core monomers and polymers thereof for volume bragg gratings |
US11825228B2 (en) | 2020-05-20 | 2023-11-21 | Meta Platforms Technologies, Llc | Programmable pixel array having multiple power domains |
US11879024B1 (en) | 2020-07-14 | 2024-01-23 | Meta Platforms Technologies, Llc | Soft mold formulations for surface relief grating fabrication with imprinting lithography |
US12075175B1 (en) | 2020-09-08 | 2024-08-27 | Meta Platforms Technologies, Llc | Programmable smart sensor with adaptive readout |
CN115703901B (zh) * | 2021-08-10 | 2024-05-07 | 中国石油天然气股份有限公司 | 一种abs树脂加工助剂及其制备方法、abs树脂复合加工助剂 |
US12244936B2 (en) | 2022-01-26 | 2025-03-04 | Meta Platforms Technologies, Llc | On-sensor image processor utilizing contextual data |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070111136A1 (en) | 2003-08-28 | 2007-05-17 | Masahiro Miyasaka | Photosensitive resin composition, photosensitive element employing it, resist pattern forming method, process for manufacturing printed circuit board and method for removing photocured product |
Family Cites Families (6)
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JP4433145B2 (ja) | 2003-02-12 | 2010-03-17 | 日東電工株式会社 | 光学部材用粘着剤組成物、光学部材用粘着剤層、粘着型光学部材および画像表示装置 |
US20040254257A1 (en) | 2003-06-10 | 2004-12-16 | Laginess Thomas J. | Coating composition curable with ultraviolet radiation |
US7297374B1 (en) | 2004-12-29 | 2007-11-20 | 3M Innovative Properties Company | Single- and multi-photon polymerizable pre-ceramic polymeric compositions |
KR100907982B1 (ko) | 2006-12-27 | 2009-07-16 | 제일모직주식회사 | 점착필름 형성용 조성물에 의한 반도체 패키지용 점착필름을 포함하는 다이싱 다이본드 필름 |
KR100964642B1 (ko) * | 2008-02-22 | 2010-06-21 | 에스화인켐 주식회사 | 고굴절, 고탄성의 프리즘 시트와 이를 위한 조성물 및 그제조 방법 |
US8344041B2 (en) * | 2008-04-01 | 2013-01-01 | University Of Kansas | Monomer for dental compositions |
-
2009
- 2009-02-03 KR KR1020090008604A patent/KR101627725B1/ko active Active
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-
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070111136A1 (en) | 2003-08-28 | 2007-05-17 | Masahiro Miyasaka | Photosensitive resin composition, photosensitive element employing it, resist pattern forming method, process for manufacturing printed circuit board and method for removing photocured product |
Non-Patent Citations (2)
Title |
---|
AADR 학회 발표(2008)* |
논문 Macromolecules (Vol. 37, 2004) |
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