DE19758946B4 - Photoinitiatormischungen, deren Verwendung und sie enthaltende photopolymerisierbare Zusammensetzungen - Google Patents

Info

Publication number

DE19758946B4

DE19758946B4 DE19758946A DE19758946A DE19758946B4 DE 19758946 B4 DE19758946 B4 DE 19758946B4 DE 19758946 A DE19758946 A DE 19758946A DE 19758946 A DE19758946 A DE 19758946A DE 19758946 B4 DE19758946 B4 DE 19758946B4

Authority

DE

Germany

Prior art keywords

phenyl

bis

methyl

hydroxy

photoinitiator

Prior art date

1996-03-04

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

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• 239000000203 mixture Substances 0.000 title claims abstract description 141
• 150000001875 compounds Chemical class 0.000 claims abstract description 81
• -1 (2-methyl-2-morpholino-propan-1-one) -9-octyl-carbazole Chemical compound 0.000 claims abstract description 45
• GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-UHFFFAOYSA-N 0.000 claims abstract description 22
• XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 claims abstract description 15
• RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims abstract description 11
• 239000012965 benzophenone Substances 0.000 claims abstract description 9
• KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 claims abstract description 8
• LJAGLTAHKHCSBP-UHFFFAOYSA-N CC1=C(C(=CC(=C1)C)C)C1=C(C=CC=C1)C(=O)C1=C(C=CC=C1)C1=C(C=C(C=C1C)C)C Chemical compound CC1=C(C(=CC(=C1)C)C)C1=C(C=CC=C1)C(=O)C1=C(C=CC=C1)C1=C(C=C(C=C1C)C)C LJAGLTAHKHCSBP-UHFFFAOYSA-N 0.000 claims abstract description 5
• BWPYBAJTDILQPY-UHFFFAOYSA-N Methoxyphenone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC(C)=C1 BWPYBAJTDILQPY-UHFFFAOYSA-N 0.000 claims abstract description 5
• WXPWZZHELZEVPO-UHFFFAOYSA-N (4-methylphenyl)-phenylmethanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 WXPWZZHELZEVPO-UHFFFAOYSA-N 0.000 claims abstract description 4
• NLQYBGASAMIPJJ-UHFFFAOYSA-N 2-hydroxy-1-[2-(2-hydroxyethoxy)phenyl]-2-methylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1OCCO NLQYBGASAMIPJJ-UHFFFAOYSA-N 0.000 claims abstract description 4
• QPXVRLXJHPTCPW-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-(4-propan-2-ylphenyl)propan-1-one Chemical compound CC(C)C1=CC=C(C(=O)C(C)(C)O)C=C1 QPXVRLXJHPTCPW-UHFFFAOYSA-N 0.000 claims abstract description 4
• JLZIXYIYQIKFHP-UHFFFAOYSA-N 2-methyl-1-(4-methylphenyl)-2-morpholin-4-ylpropane-1-thione Chemical compound C1=CC(C)=CC=C1C(=S)C(C)(C)N1CCOCC1 JLZIXYIYQIKFHP-UHFFFAOYSA-N 0.000 claims abstract description 4
• IZQPOHAUAILGKE-UHFFFAOYSA-N [2-(4-methylphenyl)sulfanylphenyl]-phenylmethanone Chemical compound C1=CC(C)=CC=C1SC1=CC=CC=C1C(=O)C1=CC=CC=C1 IZQPOHAUAILGKE-UHFFFAOYSA-N 0.000 claims abstract description 4
• KNVGEVSDKAHVAH-UHFFFAOYSA-N 2-benzyl-1-(3,4-dimethoxyphenyl)-2-morpholin-4-ylbutan-1-one Chemical compound C1COCCN1C(C(=O)C=1C=C(OC)C(OC)=CC=1)(CC)CC1=CC=CC=C1 KNVGEVSDKAHVAH-UHFFFAOYSA-N 0.000 claims abstract description 3
• BMFYCFSWWDXEPB-UHFFFAOYSA-N cyclohexyl(phenyl)methanone Chemical compound C=1C=CC=CC=1C(=O)C1CCCCC1 BMFYCFSWWDXEPB-UHFFFAOYSA-N 0.000 claims abstract 2
• QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 claims description 18
• 150000001412 amines Chemical class 0.000 claims description 11
• 239000006096 absorbing agent Substances 0.000 claims description 8
• NJCDRURWJZAMBM-UHFFFAOYSA-N 6-phenyl-1h-1,3,5-triazin-2-one Chemical class OC1=NC=NC(C=2C=CC=CC=2)=N1 NJCDRURWJZAMBM-UHFFFAOYSA-N 0.000 claims description 5
• RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical class CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims description 3
• XUKUURHRXDUEBC-KAYWLYCHSA-N Atorvastatin Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-KAYWLYCHSA-N 0.000 claims 1
• BZODUMLNVVCIGC-UHFFFAOYSA-N OCCOC1=CC=CC(C(C2=C(C3=CC=CC=C3)C(OCCO)=CC=C2)=O)=C1C1=CC=CC=C1 Chemical compound OCCOC1=CC=CC(C(C2=C(C3=CC=CC=C3)C(OCCO)=CC=C2)=O)=C1C1=CC=CC=C1 BZODUMLNVVCIGC-UHFFFAOYSA-N 0.000 claims 1
• DMOKFIORYMEUQH-UHFFFAOYSA-N [2-(2-hydroxyethoxy)phenyl]-phenylmethanone Chemical compound OCCOC1=CC=CC=C1C(=O)C1=CC=CC=C1 DMOKFIORYMEUQH-UHFFFAOYSA-N 0.000 abstract description 2
• 238000000576 coating method Methods 0.000 description 30
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 24
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 24
• 239000010410 layer Substances 0.000 description 23
• 238000001723 curing Methods 0.000 description 21
• 229910052739 hydrogen Inorganic materials 0.000 description 21
• 239000000758 substrate Substances 0.000 description 21
• 239000001257 hydrogen Substances 0.000 description 19
• 239000000843 powder Substances 0.000 description 19
• 239000011248 coating agent Substances 0.000 description 18
• 238000004519 manufacturing process Methods 0.000 description 18
• 238000000034 method Methods 0.000 description 18
• 229920001577 copolymer Polymers 0.000 description 17
• 239000003973 paint Substances 0.000 description 17
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 15
• 125000000217 alkyl group Chemical group 0.000 description 15
• 239000000463 material Substances 0.000 description 15
• 239000002904 solvent Substances 0.000 description 15
• PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
• 150000002431 hydrogen Chemical class 0.000 description 14
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 14
• 229920000642 polymer Polymers 0.000 description 13
• 238000007639 printing Methods 0.000 description 13
• 150000001252 acrylic acid derivatives Chemical class 0.000 description 12
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 12
• GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 11
• 239000000178 monomer Substances 0.000 description 11
• 229920005862 polyol Polymers 0.000 description 11
• 238000002360 preparation method Methods 0.000 description 11
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
• 239000007788 liquid Substances 0.000 description 10
• QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 10
• 229920000728 polyester Polymers 0.000 description 10
• 239000000243 solution Substances 0.000 description 10
• 239000000654 additive Substances 0.000 description 9
• 229910052753 mercury Inorganic materials 0.000 description 9
• 238000002156 mixing Methods 0.000 description 9
• 150000003077 polyols Chemical class 0.000 description 9
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 8
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
• 150000002148 esters Chemical class 0.000 description 8
• 229910052736 halogen Inorganic materials 0.000 description 8
• 150000002367 halogens Chemical class 0.000 description 8
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
• 229910052751 metal Inorganic materials 0.000 description 8
• 239000002184 metal Substances 0.000 description 8
• 229910052757 nitrogen Inorganic materials 0.000 description 8
• 239000002023 wood Substances 0.000 description 8
• 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
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
• QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 7
• 229920002120 photoresistant polymer Polymers 0.000 description 7
• 229920005989 resin Polymers 0.000 description 7
• 239000011347 resin Substances 0.000 description 7
• 239000000600 sorbitol Substances 0.000 description 7
• ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 6
• 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 6
• NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
• XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
• 239000011230 binding agent Substances 0.000 description 6
• 239000007376 cm-medium Substances 0.000 description 6
• 238000009472 formulation Methods 0.000 description 6
• 239000000976 ink Substances 0.000 description 6
• XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
• 239000003960 organic solvent Substances 0.000 description 6
• 229920000647 polyepoxide Polymers 0.000 description 6
• 229920002635 polyurethane Polymers 0.000 description 6
• 239000004814 polyurethane Substances 0.000 description 6
• 239000007787 solid Substances 0.000 description 6
• CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
• NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
• 229910052782 aluminium Inorganic materials 0.000 description 5
• 150000001735 carboxylic acids Chemical class 0.000 description 5
• 239000003795 chemical substances by application Substances 0.000 description 5
• 239000002131 composite material Substances 0.000 description 5
• 239000007859 condensation product Substances 0.000 description 5
• 239000006185 dispersion Substances 0.000 description 5
• 239000000975 dye Substances 0.000 description 5
• 239000003999 initiator Substances 0.000 description 5
• 238000000016 photochemical curing Methods 0.000 description 5
• 229920003023 plastic Polymers 0.000 description 5
• 239000004033 plastic Substances 0.000 description 5
• 229920000570 polyether Polymers 0.000 description 5
• 150000003254 radicals Chemical class 0.000 description 5
• 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 5
• 229920006337 unsaturated polyester resin Polymers 0.000 description 5
• 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 4
• 125000006710 (C2-C12) alkenyl group Chemical group 0.000 description 4
• ZCILGMFPJBRCNO-UHFFFAOYSA-N 4-phenyl-2H-benzotriazol-5-ol Chemical compound OC1=CC=C2NN=NC2=C1C1=CC=CC=C1 ZCILGMFPJBRCNO-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
• OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
• 238000007792 addition Methods 0.000 description 4
• XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
• 125000003118 aryl group Chemical group 0.000 description 4
• 229910052799 carbon Inorganic materials 0.000 description 4
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
• JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
• 150000002009 diols Chemical class 0.000 description 4
• 238000001035 drying Methods 0.000 description 4
• 230000000694 effects Effects 0.000 description 4
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
• 239000003365 glass fiber Substances 0.000 description 4
• 239000004922 lacquer Substances 0.000 description 4
• VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
• 239000011976 maleic acid Substances 0.000 description 4
• 238000002844 melting Methods 0.000 description 4
• 230000008018 melting Effects 0.000 description 4
• 150000002734 metacrylic acid derivatives Chemical class 0.000 description 4
• 229910001507 metal halide Inorganic materials 0.000 description 4
• 150000005309 metal halides Chemical class 0.000 description 4
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
• UJRDRFZCRQNLJM-UHFFFAOYSA-N methyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OC)=CC(N2N=C3C=CC=CC3=N2)=C1O UJRDRFZCRQNLJM-UHFFFAOYSA-N 0.000 description 4
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• YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
• VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
• 229920006305 unsaturated polyester Polymers 0.000 description 4
• 238000004383 yellowing Methods 0.000 description 4
• HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 3
• HUCQPHINKBNKRU-UHFFFAOYSA-N (4-methylphenyl)phosphane Chemical compound CC1=CC=C(P)C=C1 HUCQPHINKBNKRU-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
• KJARFYRANUVAFH-UHFFFAOYSA-N 2-hydroxy-3-(2-hydroxyethoxy)-2-methyl-1-phenylpropan-1-one Chemical compound OCCOCC(O)(C)C(=O)C1=CC=CC=C1 KJARFYRANUVAFH-UHFFFAOYSA-N 0.000 description 3
• NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
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• MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
• 239000004721 Polyphenylene oxide Substances 0.000 description 3
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• DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 3
• XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
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• GDSRTQXJZWRHLR-UHFFFAOYSA-N [(4-methylphenyl)-(2,4,6-trimethylbenzoyl)phosphanyl]-(2,4,6-trimethylphenyl)methanone Chemical compound C1=CC(C)=CC=C1P(C(=O)C=1C(=CC(C)=CC=1C)C)C(=O)C1=C(C)C=C(C)C=C1C GDSRTQXJZWRHLR-UHFFFAOYSA-N 0.000 description 3
• 150000003926 acrylamides Chemical class 0.000 description 3
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• UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
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• 238000010438 heat treatment Methods 0.000 description 3
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• 229910052760 oxygen Inorganic materials 0.000 description 3
• WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
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• HQEPZWYPQQKFLU-UHFFFAOYSA-N (2,6-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC(O)=C1C(=O)C1=CC=CC=C1 HQEPZWYPQQKFLU-UHFFFAOYSA-N 0.000 description 2
• GOZHNJTXLALKRL-UHFFFAOYSA-N (5-benzoyl-2,4-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(O)=C(C(=O)C=2C=CC=CC=2)C=C1C(=O)C1=CC=CC=C1 GOZHNJTXLALKRL-UHFFFAOYSA-N 0.000 description 2
• 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 2
• 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 2
• 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 2
• MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 2
• MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
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