KR20050044549A

KR20050044549A - 아실포스핀 및 이의 유도체의 멀티머 형태

아실포스핀 및 이의 유도체의 멀티머 형태 Download PDF

Info

Publication number: KR20050044549A
Authority: KR; South Korea
Prior art keywords: alkyl; substituted; phenyl; unsubstituted; lithium
Prior art date: 2001-11-20
Legal status : Withdrawn

Application number

KR1020047007699A

Other languages

English (en)

Korean (ko)

Inventor

볼프쟝-삐에르

후크게브하르트

Original Assignee

시바 스페셜티 케미칼스 홀딩 인크.

Priority date

2001-11-20

Filing date

2002-11-13

Publication date

2005-05-12

2002-11-13 Application filed by 시바 스페셜티 케미칼스 홀딩 인크. filed Critical 시바 스페셜티 케미칼스 홀딩 인크.

2005-05-12 Publication of KR20050044549A publication Critical patent/KR20050044549A/ko

Status Withdrawn legal-status Critical Current

Links

125000000217 alkyl group Chemical group 0.000 claims abstract description 181
-1 biphenylyl Chemical group 0.000 claims abstract description 146
150000001875 compounds Chemical class 0.000 claims abstract description 96
229910052760 oxygen Inorganic materials 0.000 claims abstract description 60
229910052717 sulfur Inorganic materials 0.000 claims abstract description 54
229910052736 halogen Inorganic materials 0.000 claims abstract description 40
125000003118 aryl group Chemical group 0.000 claims abstract description 19
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 19
125000005647 linker group Chemical group 0.000 claims abstract description 19
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 18
239000000126 substance Substances 0.000 claims abstract description 18
125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 12
125000004350 aryl cycloalkyl group Chemical group 0.000 claims abstract description 10
125000001624 naphthyl group Chemical group 0.000 claims abstract description 10
125000004070 6 membered heterocyclic group Chemical group 0.000 claims abstract description 8
125000003342 alkenyl group Chemical group 0.000 claims abstract description 7
125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 7
125000002373 5 membered heterocyclic group Chemical group 0.000 claims abstract description 6
239000000203 mixture Substances 0.000 claims description 105
238000000576 coating method Methods 0.000 claims description 96
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 81
229910052739 hydrogen Inorganic materials 0.000 claims description 66
239000001257 hydrogen Substances 0.000 claims description 64
150000002431 hydrogen Chemical class 0.000 claims description 43
150000002367 halogens Chemical group 0.000 claims description 37
238000000034 method Methods 0.000 claims description 36
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 34
125000002947 alkylene group Chemical group 0.000 claims description 24
239000000463 material Substances 0.000 claims description 24
239000000654 additive Substances 0.000 claims description 23
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 22
239000000976 ink Substances 0.000 claims description 22
125000003545 alkoxy group Chemical group 0.000 claims description 20
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 19
229910052799 carbon Inorganic materials 0.000 claims description 19
238000007639 printing Methods 0.000 claims description 18
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
239000013307 optical fiber Substances 0.000 claims description 17
239000000843 powder Substances 0.000 claims description 17
239000000758 substrate Substances 0.000 claims description 17
125000004430 oxygen atom Chemical group O* 0.000 claims description 14
230000003287 optical effect Effects 0.000 claims description 13
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 12
125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 11
235000010290 biphenyl Nutrition 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
239000004305 biphenyl Substances 0.000 claims description 9
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 8
239000002131 composite material Substances 0.000 claims description 7
239000003365 glass fiber Substances 0.000 claims description 7
125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 6
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
229910052731 fluorine Inorganic materials 0.000 claims description 6
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 6
125000004956 cyclohexylene group Chemical group 0.000 claims description 5
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 5
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 5
238000007650 screen-printing Methods 0.000 claims description 5
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 4
230000000996 additive effect Effects 0.000 claims description 4
ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 4
239000000853 adhesive Substances 0.000 claims description 3
230000001070 adhesive effect Effects 0.000 claims description 3
125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 3
239000011152 fibreglass Substances 0.000 claims description 3
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 3
239000003094 microcapsule Substances 0.000 claims description 3
125000001422 pyrrolinyl group Chemical group 0.000 claims description 3
238000012360 testing method Methods 0.000 claims description 3
BNJMRELGMDUDDB-UHFFFAOYSA-N $l^{1}-sulfanylbenzene Chemical compound [S]C1=CC=CC=C1 BNJMRELGMDUDDB-UHFFFAOYSA-N 0.000 claims description 2
OMJKVIFSWSQTGQ-UHFFFAOYSA-N 6,7-bis(aziridin-1-yl)quinazoline-5,8-dione Chemical compound C1CN1C=1C(=O)C2=NC=NC=C2C(=O)C=1N1CC1 OMJKVIFSWSQTGQ-UHFFFAOYSA-N 0.000 claims description 2
125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 2
125000004419 alkynylene group Chemical group 0.000 claims description 2
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 2
125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims description 2
238000005538 encapsulation Methods 0.000 claims description 2
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims description 2
125000001153 fluoro group Chemical group F* 0.000 claims description 2
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 2
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
125000001064 morpholinomethyl group Chemical group [H]C([H])(*)N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
239000007844 bleaching agent Substances 0.000 claims 2
239000005548 dental material Substances 0.000 claims 1
230000001678 irradiating effect Effects 0.000 claims 1
125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
125000005843 halogen group Chemical group 0.000 abstract 1
125000005017 substituted alkenyl group Chemical group 0.000 abstract 1
239000011248 coating agent Substances 0.000 description 46
239000000049 pigment Substances 0.000 description 41
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 28
229910052744 lithium Inorganic materials 0.000 description 27
238000004519 manufacturing process Methods 0.000 description 27
238000006243 chemical reaction Methods 0.000 description 24
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 21
239000000460 chlorine Substances 0.000 description 20
238000001723 curing Methods 0.000 description 19
239000000178 monomer Substances 0.000 description 18
229920001577 copolymer Polymers 0.000 description 17
230000005855 radiation Effects 0.000 description 17
150000003254 radicals Chemical class 0.000 description 17
239000010410 layer Substances 0.000 description 16
239000000243 solution Substances 0.000 description 16
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
229920000642 polymer Polymers 0.000 description 15
230000008569 process Effects 0.000 description 15
239000002904 solvent Substances 0.000 description 15
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 14
229910052757 nitrogen Inorganic materials 0.000 description 14
238000002360 preparation method Methods 0.000 description 14
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 14
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
238000009472 formulation Methods 0.000 description 11
229920005862 polyol Polymers 0.000 description 11
229920005989 resin Polymers 0.000 description 11
239000011347 resin Substances 0.000 description 11
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
150000001252 acrylic acid derivatives Chemical class 0.000 description 10
150000001412 amines Chemical class 0.000 description 10
229910052751 metal Inorganic materials 0.000 description 10
239000002184 metal Substances 0.000 description 10
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 9
239000000975 dye Substances 0.000 description 9
239000000835 fiber Substances 0.000 description 9
229920002120 photoresistant polymer Polymers 0.000 description 9
229920000728 polyester Polymers 0.000 description 9
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 8
229910052801 chlorine Inorganic materials 0.000 description 8
125000002993 cycloalkylene group Chemical group 0.000 description 8
239000003085 diluting agent Substances 0.000 description 8
238000003384 imaging method Methods 0.000 description 8
239000007788 liquid Substances 0.000 description 8
150000003077 polyols Chemical class 0.000 description 8
239000000047 product Substances 0.000 description 8
239000007787 solid Substances 0.000 description 8
TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 7
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 7
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 7
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 7
125000001931 aliphatic group Chemical group 0.000 description 7
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
239000003795 chemical substances by application Substances 0.000 description 7
239000008199 coating composition Substances 0.000 description 7
239000006185 dispersion Substances 0.000 description 7
150000002148 esters Chemical class 0.000 description 7
239000003999 initiator Substances 0.000 description 7
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 7
239000000600 sorbitol Substances 0.000 description 7
238000003756 stirring Methods 0.000 description 7
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
125000003860 C1-C20 alkoxy group Chemical group 0.000 description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 6
238000005481 NMR spectroscopy Methods 0.000 description 6
229910003849 O-Si Inorganic materials 0.000 description 6
229910003872 O—Si Inorganic materials 0.000 description 6
XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 6
125000004450 alkenylene group Chemical group 0.000 description 6
229910052786 argon Inorganic materials 0.000 description 6
125000000732 arylene group Chemical group 0.000 description 6
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical group C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 6
239000012965 benzophenone Substances 0.000 description 6
239000011230 binding agent Substances 0.000 description 6
229910052794 bromium Inorganic materials 0.000 description 6
150000001735 carboxylic acids Chemical class 0.000 description 6
239000007859 condensation product Substances 0.000 description 6
150000002009 diols Chemical class 0.000 description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
PWFZLKWEXYJYQO-UHFFFAOYSA-N lithium;phenylphosphanyl-(2,4,6-trimethylphenyl)methanone Chemical compound [Li].CC1=CC(C)=CC(C)=C1C(=O)PC1=CC=CC=C1 PWFZLKWEXYJYQO-UHFFFAOYSA-N 0.000 description 6
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 6
229910052753 mercury Inorganic materials 0.000 description 6
239000003960 organic solvent Substances 0.000 description 6
238000007254 oxidation reaction Methods 0.000 description 6
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 6
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 6
238000000016 photochemical curing Methods 0.000 description 6
229920003023 plastic Polymers 0.000 description 6
239000004033 plastic Substances 0.000 description 6
229920000570 polyether Polymers 0.000 description 6
229920001296 polysiloxane Polymers 0.000 description 6
229920002635 polyurethane Polymers 0.000 description 6
239000004814 polyurethane Substances 0.000 description 6
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 5
239000005977 Ethylene Substances 0.000 description 5
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 5
239000006096 absorbing agent Substances 0.000 description 5
150000004056 anthraquinones Chemical class 0.000 description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
125000005724 cycloalkenylene group Chemical group 0.000 description 5
238000010438 heat treatment Methods 0.000 description 5
235000013980 iron oxide Nutrition 0.000 description 5
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 5
239000011159 matrix material Substances 0.000 description 5
239000002609 medium Substances 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 5
238000007645 offset printing Methods 0.000 description 5
230000003647 oxidation Effects 0.000 description 5
239000001301 oxygen Substances 0.000 description 5
239000003973 paint Substances 0.000 description 5
229920000647 polyepoxide Polymers 0.000 description 5
239000007858 starting material Substances 0.000 description 5
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 4
KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 4
VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 4
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
239000004952 Polyamide Substances 0.000 description 4
239000004721 Polyphenylene oxide Substances 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 4
150000001266 acyl halides Chemical class 0.000 description 4
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 description 4
125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
239000006227 byproduct Substances 0.000 description 4
239000006229 carbon black Substances 0.000 description 4
238000004040 coloring Methods 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 4
238000010894 electron beam technology Methods 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000011737 fluorine Substances 0.000 description 4
239000007789 gas Substances 0.000 description 4
239000011521 glass Substances 0.000 description 4
235000011187 glycerol Nutrition 0.000 description 4
125000002768 hydroxyalkyl group Chemical group 0.000 description 4
239000011976 maleic acid Substances 0.000 description 4
229920002647 polyamide Polymers 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
229920001187 thermosetting polymer Polymers 0.000 description 4
YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 4
239000004408 titanium dioxide Substances 0.000 description 4
HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 4
229920006337 unsaturated polyester resin Polymers 0.000 description 4
239000002023 wood Substances 0.000 description 4
235000014692 zinc oxide Nutrition 0.000 description 4
239000011787 zinc oxide Substances 0.000 description 4
125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
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