JP7276652B2 - 光ラジカル硬化酸素阻害低減剤、光ラジカル硬化酸素阻害低減剤を含有する光ラジカル重合性組成物及び光ラジカル硬化酸素阻害低減剤を含有する塗膜並びにその硬化方法 - Google Patents
光ラジカル硬化酸素阻害低減剤、光ラジカル硬化酸素阻害低減剤を含有する光ラジカル重合性組成物及び光ラジカル硬化酸素阻害低減剤を含有する塗膜並びにその硬化方法 Download PDFInfo
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- JP7276652B2 JP7276652B2 JP2019075963A JP2019075963A JP7276652B2 JP 7276652 B2 JP7276652 B2 JP 7276652B2 JP 2019075963 A JP2019075963 A JP 2019075963A JP 2019075963 A JP2019075963 A JP 2019075963A JP 7276652 B2 JP7276652 B2 JP 7276652B2
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- bis
- anthracene
- photoradical
- curing
- coating film
- Prior art date
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- 239000001301 oxygen Substances 0.000 title claims description 125
- 229910052760 oxygen Inorganic materials 0.000 title claims description 125
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- 230000005764 inhibitory process Effects 0.000 title claims description 105
- 239000011248 coating agent Substances 0.000 title claims description 90
- 238000000576 coating method Methods 0.000 title claims description 90
- 239000000203 mixture Substances 0.000 title claims description 86
- 239000003638 chemical reducing agent Substances 0.000 title claims description 64
- 238000001723 curing Methods 0.000 title description 101
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 274
- -1 anthracene compound Chemical class 0.000 claims description 185
- 239000003505 polymerization initiator Substances 0.000 claims description 73
- 150000001875 compounds Chemical class 0.000 claims description 69
- 238000000034 method Methods 0.000 claims description 36
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- 125000004185 ester group Chemical group 0.000 claims description 19
- 239000003999 initiator Substances 0.000 claims description 19
- 238000010526 radical polymerization reaction Methods 0.000 claims description 16
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- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- ZWVHTXAYIKBMEE-UHFFFAOYSA-N 2-hydroxyacetophenone Chemical group OCC(=O)C1=CC=CC=C1 ZWVHTXAYIKBMEE-UHFFFAOYSA-N 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
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- HDIZHGVJEPKQKR-UHFFFAOYSA-N ethyl 2-[10-(2-ethoxy-2-oxoethoxy)anthracen-9-yl]oxyacetate Chemical compound C(C)OC(=O)COC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCC(=O)OCC HDIZHGVJEPKQKR-UHFFFAOYSA-N 0.000 description 14
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- 229910052757 nitrogen Inorganic materials 0.000 description 11
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
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- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 6
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
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- 239000003795 chemical substances by application Substances 0.000 description 5
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- 239000011261 inert gas Substances 0.000 description 5
- 239000012299 nitrogen atmosphere Substances 0.000 description 5
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- 238000000967 suction filtration Methods 0.000 description 5
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 5
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- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 4
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-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
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
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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 4
- 239000002253 acid Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
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- DAZHYNJTMCZVJA-UHFFFAOYSA-N butyl 9-[10-(9-butoxy-9-oxononoxy)-3-ethylanthracen-9-yl]oxynonanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC(=O)OCCCC)OCCCCCCCCC(=O)OCCCC DAZHYNJTMCZVJA-UHFFFAOYSA-N 0.000 description 1
- HVPOORBEOZOPOB-UHFFFAOYSA-N butyl 9-[10-(9-butoxy-9-oxononoxy)anthracen-9-yl]oxynonanoate Chemical compound C(CCC)OC(=O)CCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCC(=O)OCCCC HVPOORBEOZOPOB-UHFFFAOYSA-N 0.000 description 1
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- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical group C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 1
- JYWVQPBVBQZEPW-UHFFFAOYSA-N cyclohexylmethyl 2-chloroacetate Chemical compound ClCC(=O)OCC1CCCCC1 JYWVQPBVBQZEPW-UHFFFAOYSA-N 0.000 description 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
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- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
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- QIPFGFYXERNTNP-UHFFFAOYSA-N dodecyl 2-bromoacetate Chemical compound CCCCCCCCCCCCOC(=O)CBr QIPFGFYXERNTNP-UHFFFAOYSA-N 0.000 description 1
- NXCHIIAWZIHPAX-UHFFFAOYSA-N dodecyl 2-bromobutanoate Chemical compound CCCCCCCCCCCCOC(=O)C(Br)CC NXCHIIAWZIHPAX-UHFFFAOYSA-N 0.000 description 1
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- RXTSHIDRCASANN-UHFFFAOYSA-N dodecyl 2-bromopropanoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)Br RXTSHIDRCASANN-UHFFFAOYSA-N 0.000 description 1
- JPPYCWJDINILKY-UHFFFAOYSA-N dodecyl 2-chloroacetate Chemical compound CCCCCCCCCCCCOC(=O)CCl JPPYCWJDINILKY-UHFFFAOYSA-N 0.000 description 1
- RYGXUTLSVVTWHR-UHFFFAOYSA-N dodecyl 2-chlorobutanoate Chemical compound CCCCCCCCCCCCOC(=O)C(Cl)CC RYGXUTLSVVTWHR-UHFFFAOYSA-N 0.000 description 1
- IHWMNIVCLZDVCD-UHFFFAOYSA-N dodecyl 2-chloropentanoate Chemical compound CCCCCCCCCCCCOC(=O)C(Cl)CCC IHWMNIVCLZDVCD-UHFFFAOYSA-N 0.000 description 1
- ZWBOULTZYRWSPZ-UHFFFAOYSA-N dodecyl 2-chloropropanoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)Cl ZWBOULTZYRWSPZ-UHFFFAOYSA-N 0.000 description 1
- MNGZVGSVVWRICW-UHFFFAOYSA-N dodecyl 2-iodoacetate Chemical compound ICC(=O)OCCCCCCCCCCCC MNGZVGSVVWRICW-UHFFFAOYSA-N 0.000 description 1
- ONSQNBFFXHKKST-UHFFFAOYSA-N dodecyl 2-iodobutanoate Chemical compound IC(C(=O)OCCCCCCCCCCCC)CC ONSQNBFFXHKKST-UHFFFAOYSA-N 0.000 description 1
- QLRVPVFBHMPQNY-UHFFFAOYSA-N dodecyl 2-iodopentanoate Chemical compound IC(C(=O)OCCCCCCCCCCCC)CCC QLRVPVFBHMPQNY-UHFFFAOYSA-N 0.000 description 1
- PFLGWCAGVNPGLF-UHFFFAOYSA-N dodecyl 2-iodopropanoate Chemical compound IC(C(=O)OCCCCCCCCCCCC)C PFLGWCAGVNPGLF-UHFFFAOYSA-N 0.000 description 1
- IGQKNAACKNTMFH-UHFFFAOYSA-N dodecyl 3-bromobutanoate Chemical compound BrC(CC(=O)OCCCCCCCCCCCC)C IGQKNAACKNTMFH-UHFFFAOYSA-N 0.000 description 1
- WDFZONVZFZVYAJ-UHFFFAOYSA-N dodecyl 3-bromopentanoate Chemical compound BrC(CC(=O)OCCCCCCCCCCCC)CC WDFZONVZFZVYAJ-UHFFFAOYSA-N 0.000 description 1
- VGSMBPAFUBNJNB-UHFFFAOYSA-N dodecyl 3-bromopropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCBr VGSMBPAFUBNJNB-UHFFFAOYSA-N 0.000 description 1
- AUFXSBSHIKABLE-UHFFFAOYSA-N dodecyl 3-chlorobutanoate Chemical compound CCCCCCCCCCCCOC(=O)CC(C)Cl AUFXSBSHIKABLE-UHFFFAOYSA-N 0.000 description 1
- ZANSUDXKLBNEQY-UHFFFAOYSA-N dodecyl 3-chloropentanoate Chemical compound CCCCCCCCCCCCOC(=O)CC(Cl)CC ZANSUDXKLBNEQY-UHFFFAOYSA-N 0.000 description 1
- NCUROSDPAOGNHW-UHFFFAOYSA-N dodecyl 3-chloropropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCCl NCUROSDPAOGNHW-UHFFFAOYSA-N 0.000 description 1
- XSFHWMVTPFCRBL-UHFFFAOYSA-N dodecyl 3-iodobutanoate Chemical compound IC(CC(=O)OCCCCCCCCCCCC)C XSFHWMVTPFCRBL-UHFFFAOYSA-N 0.000 description 1
- JKYXPZRGEGOZCV-UHFFFAOYSA-N dodecyl 3-iodopentanoate Chemical compound IC(CC(=O)OCCCCCCCCCCCC)CC JKYXPZRGEGOZCV-UHFFFAOYSA-N 0.000 description 1
- NYKLGAAAHRBJRW-UHFFFAOYSA-N dodecyl 3-iodopropanoate Chemical compound ICCC(=O)OCCCCCCCCCCCC NYKLGAAAHRBJRW-UHFFFAOYSA-N 0.000 description 1
- KNIFYGIJDIBWET-UHFFFAOYSA-N dodecyl 4-bromobutanoate Chemical compound CCCCCCCCCCCCOC(=O)CCCBr KNIFYGIJDIBWET-UHFFFAOYSA-N 0.000 description 1
- AXXZYAPWIRKGFS-UHFFFAOYSA-N dodecyl 4-bromopentanoate Chemical compound BrC(CCC(=O)OCCCCCCCCCCCC)C AXXZYAPWIRKGFS-UHFFFAOYSA-N 0.000 description 1
- AMCRHNDYMZXQRU-UHFFFAOYSA-N dodecyl 4-chlorobutanoate Chemical compound CCCCCCCCCCCCOC(=O)CCCCl AMCRHNDYMZXQRU-UHFFFAOYSA-N 0.000 description 1
- QLMPMDVEORXENM-UHFFFAOYSA-N dodecyl 4-chloropentanoate Chemical compound ClC(CCC(=O)OCCCCCCCCCCCC)C QLMPMDVEORXENM-UHFFFAOYSA-N 0.000 description 1
- HYNGTXPPWXXLCE-UHFFFAOYSA-N dodecyl 4-iodopentanoate Chemical compound IC(CCC(=O)OCCCCCCCCCCCC)C HYNGTXPPWXXLCE-UHFFFAOYSA-N 0.000 description 1
- CAOPRGQQYVKHLQ-UHFFFAOYSA-N dodecyl 5-bromopentanoate Chemical compound BrCCCCC(=O)OCCCCCCCCCCCC CAOPRGQQYVKHLQ-UHFFFAOYSA-N 0.000 description 1
- LVDVAYQNFNJKNW-UHFFFAOYSA-N dodecyl 5-chloropentanoate Chemical compound ClCCCCC(=O)OCCCCCCCCCCCC LVDVAYQNFNJKNW-UHFFFAOYSA-N 0.000 description 1
- SKQXYMZPTDGRHN-UHFFFAOYSA-N dodecyl 5-iodopentanoate Chemical compound ICCCCC(=O)OCCCCCCCCCCCC SKQXYMZPTDGRHN-UHFFFAOYSA-N 0.000 description 1
- 125000006575 electron-withdrawing group Chemical group 0.000 description 1
- 238000000295 emission spectrum Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- ILDKOMMXKZEPFK-UHFFFAOYSA-N ethyl 10-[10-(10-ethoxy-10-oxodecoxy)anthracen-9-yl]oxydecanoate Chemical compound C(C)OC(=O)CCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCC(=O)OCC ILDKOMMXKZEPFK-UHFFFAOYSA-N 0.000 description 1
- SXOKDSDQQAGMQR-UHFFFAOYSA-N ethyl 11-[10-(11-ethoxy-11-oxoundecoxy)anthracen-9-yl]oxyundecanoate Chemical compound C(C)OC(=O)CCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCC(=O)OCC SXOKDSDQQAGMQR-UHFFFAOYSA-N 0.000 description 1
- AIOOVYCRIBWOON-UHFFFAOYSA-N ethyl 12-[10-(12-ethoxy-12-oxododecoxy)anthracen-9-yl]oxydodecanoate Chemical compound C(C)OC(=O)CCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCC(=O)OCC AIOOVYCRIBWOON-UHFFFAOYSA-N 0.000 description 1
- ODVQQVIRHRNPBU-UHFFFAOYSA-N ethyl 13-[10-(13-ethoxy-13-oxotridecoxy)anthracen-9-yl]oxytridecanoate Chemical compound C(C)OC(=O)CCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCC(=O)OCC ODVQQVIRHRNPBU-UHFFFAOYSA-N 0.000 description 1
- CDDWCDAEWMWKHT-UHFFFAOYSA-N ethyl 14-[10-(14-ethoxy-14-oxotetradecoxy)anthracen-9-yl]oxytetradecanoate Chemical compound C(C)OC(=O)CCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCC(=O)OCC CDDWCDAEWMWKHT-UHFFFAOYSA-N 0.000 description 1
- CKFAYEKTSVNHCE-UHFFFAOYSA-N ethyl 15-[10-(15-ethoxy-15-oxopentadecoxy)anthracen-9-yl]oxypentadecanoate Chemical compound C(C)OC(=O)CCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCC(=O)OCC CKFAYEKTSVNHCE-UHFFFAOYSA-N 0.000 description 1
- AXICXMGPPWJAJH-UHFFFAOYSA-N ethyl 16-[10-(16-ethoxy-16-oxohexadecoxy)anthracen-9-yl]oxyhexadecanoate Chemical compound C(C)OC(=O)CCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCC(=O)OCC AXICXMGPPWJAJH-UHFFFAOYSA-N 0.000 description 1
- LPEGITHCSPKDFU-UHFFFAOYSA-N ethyl 17-[10-(17-ethoxy-17-oxoheptadecoxy)-3-ethylanthracen-9-yl]oxyheptadecanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCC(=O)OCC)OCCCCCCCCCCCCCCCCC(=O)OCC LPEGITHCSPKDFU-UHFFFAOYSA-N 0.000 description 1
- IRKSROWQVBCYNI-UHFFFAOYSA-N ethyl 17-[10-(17-ethoxy-17-oxoheptadecoxy)anthracen-9-yl]oxyheptadecanoate Chemical compound CCOC(=O)CCCCCCCCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCC(=O)OCC IRKSROWQVBCYNI-UHFFFAOYSA-N 0.000 description 1
- KACNHLCDADKTHA-UHFFFAOYSA-N ethyl 17-[3-chloro-10-(17-ethoxy-17-oxoheptadecoxy)anthracen-9-yl]oxyheptadecanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCC(=O)OCC)OCCCCCCCCCCCCCCCCC(=O)OCC KACNHLCDADKTHA-UHFFFAOYSA-N 0.000 description 1
- NXOBXCHQZNHWLE-UHFFFAOYSA-N ethyl 19-[10-(19-ethoxy-19-oxononadecoxy)anthracen-9-yl]oxynonadecanoate Chemical compound C(C)OC(=O)CCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCC(=O)OCC NXOBXCHQZNHWLE-UHFFFAOYSA-N 0.000 description 1
- ZQLZCMVHMDGNRP-UHFFFAOYSA-N ethyl 2-anthracen-1-yloxyacetate Chemical compound C1=CC=C2C=C3C(OCC(=O)OCC)=CC=CC3=CC2=C1 ZQLZCMVHMDGNRP-UHFFFAOYSA-N 0.000 description 1
- XIMFCGSNSKXPBO-UHFFFAOYSA-N ethyl 2-bromobutanoate Chemical compound CCOC(=O)C(Br)CC XIMFCGSNSKXPBO-UHFFFAOYSA-N 0.000 description 1
- ORSIRXYHFPHWTN-UHFFFAOYSA-N ethyl 2-bromopentanoate Chemical compound CCCC(Br)C(=O)OCC ORSIRXYHFPHWTN-UHFFFAOYSA-N 0.000 description 1
- ARFLASKVLJTEJD-UHFFFAOYSA-N ethyl 2-bromopropanoate Chemical compound CCOC(=O)C(C)Br ARFLASKVLJTEJD-UHFFFAOYSA-N 0.000 description 1
- QTEITWPJVHAOTN-UHFFFAOYSA-N ethyl 2-chlorobutanoate Chemical compound CCOC(=O)C(Cl)CC QTEITWPJVHAOTN-UHFFFAOYSA-N 0.000 description 1
- ZAOIIUSDMKVQJW-UHFFFAOYSA-N ethyl 2-chloropentanoate Chemical compound CCCC(Cl)C(=O)OCC ZAOIIUSDMKVQJW-UHFFFAOYSA-N 0.000 description 1
- BEKQSWCOHDSDPD-UHFFFAOYSA-N ethyl 2-iodobutanoate Chemical compound CCOC(=O)C(I)CC BEKQSWCOHDSDPD-UHFFFAOYSA-N 0.000 description 1
- RSWKYQKHEXVXOA-UHFFFAOYSA-N ethyl 2-iodopentanoate Chemical compound CCCC(I)C(=O)OCC RSWKYQKHEXVXOA-UHFFFAOYSA-N 0.000 description 1
- AVMMXNKUHBWIMU-UHFFFAOYSA-N ethyl 2-iodopropanoate Chemical compound CCOC(=O)C(C)I AVMMXNKUHBWIMU-UHFFFAOYSA-N 0.000 description 1
- UIAQMDXVKREEBF-UHFFFAOYSA-N ethyl 20-[10-(20-ethoxy-20-oxoicosoxy)anthracen-9-yl]oxyicosanoate Chemical compound CCOC(=O)CCCCCCCCCCCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCCCCC(=O)OCC UIAQMDXVKREEBF-UHFFFAOYSA-N 0.000 description 1
- QMIAPNMGNYYPIH-UHFFFAOYSA-N ethyl 21-[10-(21-ethoxy-21-oxohenicosoxy)-3-ethylanthracen-9-yl]oxyhenicosanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OCC)OCCCCCCCCCCCCCCCCCCCCC(=O)OCC QMIAPNMGNYYPIH-UHFFFAOYSA-N 0.000 description 1
- SMNAYDGQQKAKBN-UHFFFAOYSA-N ethyl 21-[10-(21-ethoxy-21-oxohenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound C(C)OC(=O)CCCCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCCCC(=O)OCC SMNAYDGQQKAKBN-UHFFFAOYSA-N 0.000 description 1
- DOQMLRPQQUSUEP-UHFFFAOYSA-N ethyl 21-[3-chloro-10-(21-ethoxy-21-oxohenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OCC)OCCCCCCCCCCCCCCCCCCCCC(=O)OCC DOQMLRPQQUSUEP-UHFFFAOYSA-N 0.000 description 1
- DTNQEYGPQSHXSO-UHFFFAOYSA-N ethyl 3-[10-(4-ethoxy-4-oxobutan-2-yl)oxy-3-pentylanthracen-9-yl]oxybutanoate Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OCC)C)OC(CC(=O)OCC)C DTNQEYGPQSHXSO-UHFFFAOYSA-N 0.000 description 1
- FADVBWPHECUXJN-UHFFFAOYSA-N ethyl 3-[3-chloro-10-(4-ethoxy-4-oxobutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OCC)C)OC(CC(=O)OCC)C FADVBWPHECUXJN-UHFFFAOYSA-N 0.000 description 1
- OPXQLUFLTHEZST-UHFFFAOYSA-N ethyl 3-bromobutanoate Chemical compound CCOC(=O)CC(C)Br OPXQLUFLTHEZST-UHFFFAOYSA-N 0.000 description 1
- VOEAEELHRMARKD-UHFFFAOYSA-N ethyl 3-bromopentanoate Chemical compound CCOC(=O)CC(Br)CC VOEAEELHRMARKD-UHFFFAOYSA-N 0.000 description 1
- FQTIYMRSUOADDK-UHFFFAOYSA-N ethyl 3-bromopropanoate Chemical compound CCOC(=O)CCBr FQTIYMRSUOADDK-UHFFFAOYSA-N 0.000 description 1
- ZSWGSCUZUONRDN-UHFFFAOYSA-N ethyl 3-chlorobutanoate Chemical compound CCOC(=O)CC(C)Cl ZSWGSCUZUONRDN-UHFFFAOYSA-N 0.000 description 1
- ZCLGVXACCAZJOX-UHFFFAOYSA-N ethyl 3-chloropropanoate Chemical compound CCOC(=O)CCCl ZCLGVXACCAZJOX-UHFFFAOYSA-N 0.000 description 1
- SWFYWWCVNZRJMK-UHFFFAOYSA-N ethyl 3-iodobutanoate Chemical compound CCOC(=O)CC(C)I SWFYWWCVNZRJMK-UHFFFAOYSA-N 0.000 description 1
- KZTNQOAFISZIEI-UHFFFAOYSA-N ethyl 3-iodopropanoate Chemical compound CCOC(=O)CCI KZTNQOAFISZIEI-UHFFFAOYSA-N 0.000 description 1
- XBPOBCXHALHJFP-UHFFFAOYSA-N ethyl 4-bromobutanoate Chemical compound CCOC(=O)CCCBr XBPOBCXHALHJFP-UHFFFAOYSA-N 0.000 description 1
- CTVCPHLFHPQRNF-UHFFFAOYSA-N ethyl 4-bromopentanoate Chemical compound CCOC(=O)CCC(C)Br CTVCPHLFHPQRNF-UHFFFAOYSA-N 0.000 description 1
- RLZFVPPGVAHZPE-UHFFFAOYSA-N ethyl 4-iodobutanoate Chemical compound CCOC(=O)CCCI RLZFVPPGVAHZPE-UHFFFAOYSA-N 0.000 description 1
- UDETXEIHHVHSTP-UHFFFAOYSA-N ethyl 5-[10-(5-ethoxy-5-oxopentoxy)-3-ethylanthracen-9-yl]oxypentanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OCC)OCCCCC(=O)OCC UDETXEIHHVHSTP-UHFFFAOYSA-N 0.000 description 1
- ASLDORZTLLRJKQ-UHFFFAOYSA-N ethyl 5-[10-(5-ethoxy-5-oxopentoxy)-3-pentylanthracen-9-yl]oxypentanoate Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OCC)OCCCCC(=O)OCC ASLDORZTLLRJKQ-UHFFFAOYSA-N 0.000 description 1
- QKXUYXLUCRMIPN-UHFFFAOYSA-N ethyl 5-[3-chloro-10-(5-ethoxy-5-oxopentoxy)anthracen-9-yl]oxypentanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OCC)OCCCCC(=O)OCC QKXUYXLUCRMIPN-UHFFFAOYSA-N 0.000 description 1
- BBQVIWHSSLDVFN-UHFFFAOYSA-N ethyl 6-[10-(6-ethoxy-6-oxohexoxy)anthracen-9-yl]oxyhexanoate Chemical compound C(C)OC(=O)CCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCC(=O)OCC BBQVIWHSSLDVFN-UHFFFAOYSA-N 0.000 description 1
- NVHYGTVXKGDSMC-UHFFFAOYSA-N ethyl 7-[10-(7-ethoxy-7-oxoheptoxy)anthracen-9-yl]oxyheptanoate Chemical compound CCOC(=O)CCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCC(=O)OCC NVHYGTVXKGDSMC-UHFFFAOYSA-N 0.000 description 1
- ADLOQUGCSVTDHK-UHFFFAOYSA-N ethyl 8-[10-(8-ethoxy-8-oxooctoxy)anthracen-9-yl]oxyoctanoate Chemical compound C(C)OC(=O)CCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCC(=O)OCC ADLOQUGCSVTDHK-UHFFFAOYSA-N 0.000 description 1
- YNHMOMFPPOSBJC-UHFFFAOYSA-N ethyl 9-[10-(9-ethoxy-9-oxononoxy)-3-ethylanthracen-9-yl]oxynonanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC(=O)OCC)OCCCCCCCCC(=O)OCC YNHMOMFPPOSBJC-UHFFFAOYSA-N 0.000 description 1
- YVCKJANFYGVRRY-UHFFFAOYSA-N ethyl 9-[10-(9-ethoxy-9-oxononoxy)anthracen-9-yl]oxynonanoate Chemical compound C(C)OC(=O)CCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCC(=O)OCC YVCKJANFYGVRRY-UHFFFAOYSA-N 0.000 description 1
- JBHMSBCRGVUZLJ-UHFFFAOYSA-N ethyl 9-[3-chloro-10-(9-ethoxy-9-oxononoxy)anthracen-9-yl]oxynonanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC(=O)OCC)OCCCCCCCCC(=O)OCC JBHMSBCRGVUZLJ-UHFFFAOYSA-N 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 1
- MFFXVVHUKRKXCI-UHFFFAOYSA-N ethyl iodoacetate Chemical compound CCOC(=O)CI MFFXVVHUKRKXCI-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- SZZUXOYNCHATNT-UHFFFAOYSA-N heptyl 2-bromoacetate Chemical compound CCCCCCCOC(=O)CBr SZZUXOYNCHATNT-UHFFFAOYSA-N 0.000 description 1
- MTMOXPALHHFPIA-UHFFFAOYSA-N heptyl 2-bromobutanoate Chemical compound CCCCCCCOC(=O)C(Br)CC MTMOXPALHHFPIA-UHFFFAOYSA-N 0.000 description 1
- XOLHAEPYINTAFR-UHFFFAOYSA-N heptyl 2-bromopropanoate Chemical compound CCCCCCCOC(=O)C(C)Br XOLHAEPYINTAFR-UHFFFAOYSA-N 0.000 description 1
- JUFPTDUONWPUBM-UHFFFAOYSA-N heptyl 2-chloroacetate Chemical compound CCCCCCCOC(=O)CCl JUFPTDUONWPUBM-UHFFFAOYSA-N 0.000 description 1
- SLAXIYNQTGZROJ-UHFFFAOYSA-N heptyl 2-chlorobutanoate Chemical compound CCCCCCCOC(=O)C(Cl)CC SLAXIYNQTGZROJ-UHFFFAOYSA-N 0.000 description 1
- PEZLEBVYILJITE-UHFFFAOYSA-N heptyl 2-iodoacetate Chemical compound CCCCCCCOC(=O)CI PEZLEBVYILJITE-UHFFFAOYSA-N 0.000 description 1
- MJMGPPHJASAABA-UHFFFAOYSA-N heptyl 2-iodobutanoate Chemical compound IC(C(=O)OCCCCCCC)CC MJMGPPHJASAABA-UHFFFAOYSA-N 0.000 description 1
- WOIPKSCXWVRTBJ-UHFFFAOYSA-N heptyl 3-bromobutanoate Chemical compound BrC(CC(=O)OCCCCCCC)C WOIPKSCXWVRTBJ-UHFFFAOYSA-N 0.000 description 1
- IGXUKCXWWOJUDO-UHFFFAOYSA-N heptyl 3-bromopropanoate Chemical compound BrCCC(=O)OCCCCCCC IGXUKCXWWOJUDO-UHFFFAOYSA-N 0.000 description 1
- IVSMBZGOSOEERU-UHFFFAOYSA-N heptyl 3-chlorobutanoate Chemical compound CCCCCCCOC(=O)CC(C)Cl IVSMBZGOSOEERU-UHFFFAOYSA-N 0.000 description 1
- BQZQUWKYBJWQNL-UHFFFAOYSA-N heptyl 3-chloropropanoate Chemical compound CCCCCCCOC(=O)CCCl BQZQUWKYBJWQNL-UHFFFAOYSA-N 0.000 description 1
- PGEXRFROXDWODV-UHFFFAOYSA-N heptyl 3-iodobutanoate Chemical compound CCCCCCCOC(=O)CC(C)I PGEXRFROXDWODV-UHFFFAOYSA-N 0.000 description 1
- ZDAKXTNCFMGVCT-UHFFFAOYSA-N heptyl 3-iodopropanoate Chemical compound CCCCCCCOC(=O)CCI ZDAKXTNCFMGVCT-UHFFFAOYSA-N 0.000 description 1
- KBGUKTQUUYTJGR-UHFFFAOYSA-N heptyl 4-bromobutanoate Chemical compound BrCCCC(=O)OCCCCCCC KBGUKTQUUYTJGR-UHFFFAOYSA-N 0.000 description 1
- QQKBYADYMOAKDB-UHFFFAOYSA-N heptyl 4-chlorobutanoate Chemical compound CCCCCCCOC(=O)CCCCl QQKBYADYMOAKDB-UHFFFAOYSA-N 0.000 description 1
- HITZNAZHFYPTGD-UHFFFAOYSA-N heptyl 4-chloropentanoate Chemical compound ClC(CCC(=O)OCCCCCCC)C HITZNAZHFYPTGD-UHFFFAOYSA-N 0.000 description 1
- MODQUXCQFOWRKC-UHFFFAOYSA-N heptyl 4-iodobutanoate Chemical compound ICCCC(=O)OCCCCCCC MODQUXCQFOWRKC-UHFFFAOYSA-N 0.000 description 1
- BGNOKLIKAZVZLG-UHFFFAOYSA-N heptyl 4-iodopentanoate Chemical compound IC(CCC(=O)OCCCCCCC)C BGNOKLIKAZVZLG-UHFFFAOYSA-N 0.000 description 1
- PSTOZFWGSOOMNV-UHFFFAOYSA-N heptyl 5-chloropentanoate Chemical compound CCCCCCCOC(=O)CCCCCl PSTOZFWGSOOMNV-UHFFFAOYSA-N 0.000 description 1
- ISKUVJOZQJHYAC-UHFFFAOYSA-N heptyl 5-iodopentanoate Chemical compound ICCCCC(=O)OCCCCCCC ISKUVJOZQJHYAC-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- NNPJKFMGVZNJHG-UHFFFAOYSA-N hexyl 2-bromoacetate Chemical compound CCCCCCOC(=O)CBr NNPJKFMGVZNJHG-UHFFFAOYSA-N 0.000 description 1
- AXPPUDLSKDAEGB-UHFFFAOYSA-N hexyl 2-bromobutanoate Chemical compound CCCCCCOC(=O)C(Br)CC AXPPUDLSKDAEGB-UHFFFAOYSA-N 0.000 description 1
- CVIVDRZPZOBMDR-UHFFFAOYSA-N hexyl 2-bromopropanoate Chemical compound CCCCCCOC(=O)C(C)Br CVIVDRZPZOBMDR-UHFFFAOYSA-N 0.000 description 1
- OJGRZJILAIHWIY-UHFFFAOYSA-N hexyl 2-chloroacetate Chemical compound CCCCCCOC(=O)CCl OJGRZJILAIHWIY-UHFFFAOYSA-N 0.000 description 1
- GAONBEAFOOASRD-UHFFFAOYSA-N hexyl 2-chlorobutanoate Chemical compound CCCCCCOC(=O)C(Cl)CC GAONBEAFOOASRD-UHFFFAOYSA-N 0.000 description 1
- CKKHJCOIGGVMAZ-UHFFFAOYSA-N hexyl 2-chloropropanoate Chemical compound CCCCCCOC(=O)C(C)Cl CKKHJCOIGGVMAZ-UHFFFAOYSA-N 0.000 description 1
- XJOFYNWBVZSJJZ-UHFFFAOYSA-N hexyl 2-iodoacetate Chemical compound CCCCCCOC(=O)CI XJOFYNWBVZSJJZ-UHFFFAOYSA-N 0.000 description 1
- QTUOJRWHXIOFIU-UHFFFAOYSA-N hexyl 2-iodopropanoate Chemical compound IC(C(=O)OCCCCCC)C QTUOJRWHXIOFIU-UHFFFAOYSA-N 0.000 description 1
- RXOMKMSVAYQJGZ-UHFFFAOYSA-N hexyl 3-bromobutanoate Chemical compound BrC(CC(=O)OCCCCCC)C RXOMKMSVAYQJGZ-UHFFFAOYSA-N 0.000 description 1
- SKMQINQBZSMTFL-UHFFFAOYSA-N hexyl 3-bromopropanoate Chemical compound CCCCCCOC(=O)CCBr SKMQINQBZSMTFL-UHFFFAOYSA-N 0.000 description 1
- PYOAHWWMEFRKLM-UHFFFAOYSA-N hexyl 3-chloropropanoate Chemical compound CCCCCCOC(=O)CCCl PYOAHWWMEFRKLM-UHFFFAOYSA-N 0.000 description 1
- PNZVARIWXDPJLC-UHFFFAOYSA-N hexyl 3-iodopropanoate Chemical compound CCCCCCOC(=O)CCI PNZVARIWXDPJLC-UHFFFAOYSA-N 0.000 description 1
- NJJCFVMCDUBLGH-UHFFFAOYSA-N hexyl 4-chlorobutanoate Chemical compound CCCCCCOC(=O)CCCCl NJJCFVMCDUBLGH-UHFFFAOYSA-N 0.000 description 1
- JTQSDWPZGLKVIE-UHFFFAOYSA-N hexyl 4-iodobutanoate Chemical compound ICCCC(=O)OCCCCCC JTQSDWPZGLKVIE-UHFFFAOYSA-N 0.000 description 1
- UUAYKMOVVXBYOO-UHFFFAOYSA-N icosyl 2-bromoacetate Chemical compound BrCC(=O)OCCCCCCCCCCCCCCCCCCCC UUAYKMOVVXBYOO-UHFFFAOYSA-N 0.000 description 1
- XQVTYVFZIZDZCZ-UHFFFAOYSA-N icosyl 2-bromobutanoate Chemical compound BrC(C(=O)OCCCCCCCCCCCCCCCCCCCC)CC XQVTYVFZIZDZCZ-UHFFFAOYSA-N 0.000 description 1
- APJSKKDKJJVZMQ-UHFFFAOYSA-N icosyl 2-bromopentanoate Chemical compound BrC(C(=O)OCCCCCCCCCCCCCCCCCCCC)CCC APJSKKDKJJVZMQ-UHFFFAOYSA-N 0.000 description 1
- ALWGFAOCGUWQGH-UHFFFAOYSA-N icosyl 2-bromopropanoate Chemical compound CCCCCCCCCCCCCCCCCCCCOC(=O)C(C)Br ALWGFAOCGUWQGH-UHFFFAOYSA-N 0.000 description 1
- UPMIEOMATULYDQ-UHFFFAOYSA-N icosyl 2-chloroacetate Chemical compound CCCCCCCCCCCCCCCCCCCCOC(=O)CCl UPMIEOMATULYDQ-UHFFFAOYSA-N 0.000 description 1
- IVDLDTRPYGXBNL-UHFFFAOYSA-N icosyl 2-chlorobutanoate Chemical compound ClC(C(=O)OCCCCCCCCCCCCCCCCCCCC)CC IVDLDTRPYGXBNL-UHFFFAOYSA-N 0.000 description 1
- UXUGUUHGRRRMOA-UHFFFAOYSA-N icosyl 2-chloropentanoate Chemical compound ClC(C(=O)OCCCCCCCCCCCCCCCCCCCC)CCC UXUGUUHGRRRMOA-UHFFFAOYSA-N 0.000 description 1
- TXDGKOFXKLXGKY-UHFFFAOYSA-N icosyl 2-chloropropanoate Chemical compound ClC(C(=O)OCCCCCCCCCCCCCCCCCCCC)C TXDGKOFXKLXGKY-UHFFFAOYSA-N 0.000 description 1
- DBTHNHTYOBUAEW-UHFFFAOYSA-N icosyl 2-iodoacetate Chemical compound ICC(=O)OCCCCCCCCCCCCCCCCCCCC DBTHNHTYOBUAEW-UHFFFAOYSA-N 0.000 description 1
- YMVCCIKORGQCJI-UHFFFAOYSA-N icosyl 2-iodobutanoate Chemical compound IC(C(=O)OCCCCCCCCCCCCCCCCCCCC)CC YMVCCIKORGQCJI-UHFFFAOYSA-N 0.000 description 1
- OSDUUEZKNWEAHM-UHFFFAOYSA-N icosyl 2-iodopentanoate Chemical compound IC(C(=O)OCCCCCCCCCCCCCCCCCCCC)CCC OSDUUEZKNWEAHM-UHFFFAOYSA-N 0.000 description 1
- MQGZZEPLPMMKTK-UHFFFAOYSA-N icosyl 2-iodopropanoate Chemical compound IC(C(=O)OCCCCCCCCCCCCCCCCCCCC)C MQGZZEPLPMMKTK-UHFFFAOYSA-N 0.000 description 1
- USGBAWUBPLJLKV-UHFFFAOYSA-N icosyl 3-bromobutanoate Chemical compound BrC(CC(=O)OCCCCCCCCCCCCCCCCCCCC)C USGBAWUBPLJLKV-UHFFFAOYSA-N 0.000 description 1
- RYXYSAIGXSUPMA-UHFFFAOYSA-N icosyl 3-bromopentanoate Chemical compound BrC(CC(=O)OCCCCCCCCCCCCCCCCCCCC)CC RYXYSAIGXSUPMA-UHFFFAOYSA-N 0.000 description 1
- MYADFYITMHCAJU-UHFFFAOYSA-N icosyl 3-bromopropanoate Chemical compound BrCCC(=O)OCCCCCCCCCCCCCCCCCCCC MYADFYITMHCAJU-UHFFFAOYSA-N 0.000 description 1
- GPMWAFONUZGZAZ-UHFFFAOYSA-N icosyl 3-chlorobutanoate Chemical compound ClC(CC(=O)OCCCCCCCCCCCCCCCCCCCC)C GPMWAFONUZGZAZ-UHFFFAOYSA-N 0.000 description 1
- XGBHRCADTLHURD-UHFFFAOYSA-N icosyl 3-chloropentanoate Chemical compound ClC(CC(=O)OCCCCCCCCCCCCCCCCCCCC)CC XGBHRCADTLHURD-UHFFFAOYSA-N 0.000 description 1
- GFHHGGVYMBELJF-UHFFFAOYSA-N icosyl 3-chloropropanoate Chemical compound ClCCC(=O)OCCCCCCCCCCCCCCCCCCCC GFHHGGVYMBELJF-UHFFFAOYSA-N 0.000 description 1
- CUPUSFMXACEKPZ-UHFFFAOYSA-N icosyl 3-iodobutanoate Chemical compound IC(CC(=O)OCCCCCCCCCCCCCCCCCCCC)C CUPUSFMXACEKPZ-UHFFFAOYSA-N 0.000 description 1
- DIIBPQULEVCZFX-UHFFFAOYSA-N icosyl 3-iodopentanoate Chemical compound IC(CC(=O)OCCCCCCCCCCCCCCCCCCCC)CC DIIBPQULEVCZFX-UHFFFAOYSA-N 0.000 description 1
- ALSQPZACQQPOIA-UHFFFAOYSA-N icosyl 3-iodopropanoate Chemical compound ICCC(=O)OCCCCCCCCCCCCCCCCCCCC ALSQPZACQQPOIA-UHFFFAOYSA-N 0.000 description 1
- OWKWTEMNTFWGFQ-UHFFFAOYSA-N icosyl 4-bromobutanoate Chemical compound BrCCCC(=O)OCCCCCCCCCCCCCCCCCCCC OWKWTEMNTFWGFQ-UHFFFAOYSA-N 0.000 description 1
- ONHGAVODVZGSRN-UHFFFAOYSA-N icosyl 4-bromopentanoate Chemical compound BrC(CCC(=O)OCCCCCCCCCCCCCCCCCCCC)C ONHGAVODVZGSRN-UHFFFAOYSA-N 0.000 description 1
- RROXGHSGTRLUSS-UHFFFAOYSA-N icosyl 4-chlorobutanoate Chemical compound CCCCCCCCCCCCCCCCCCCCOC(=O)CCCCl RROXGHSGTRLUSS-UHFFFAOYSA-N 0.000 description 1
- KBMYIKQMUSXHPE-UHFFFAOYSA-N icosyl 4-chloropentanoate Chemical compound ClC(CCC(=O)OCCCCCCCCCCCCCCCCCCCC)C KBMYIKQMUSXHPE-UHFFFAOYSA-N 0.000 description 1
- PKQPFWJHCLZBHC-UHFFFAOYSA-N icosyl 4-iodobutanoate Chemical compound ICCCC(=O)OCCCCCCCCCCCCCCCCCCCC PKQPFWJHCLZBHC-UHFFFAOYSA-N 0.000 description 1
- MWYBOPYKUZFKDP-UHFFFAOYSA-N icosyl 4-iodopentanoate Chemical compound IC(CCC(=O)OCCCCCCCCCCCCCCCCCCCC)C MWYBOPYKUZFKDP-UHFFFAOYSA-N 0.000 description 1
- JQILNLQJXTYYMT-UHFFFAOYSA-N icosyl 5-bromopentanoate Chemical compound BrCCCCC(=O)OCCCCCCCCCCCCCCCCCCCC JQILNLQJXTYYMT-UHFFFAOYSA-N 0.000 description 1
- PPPRJMFBRGJKJJ-UHFFFAOYSA-N icosyl 5-chloropentanoate Chemical compound ClCCCCC(=O)OCCCCCCCCCCCCCCCCCCCC PPPRJMFBRGJKJJ-UHFFFAOYSA-N 0.000 description 1
- AYHZGWMHNNGUND-UHFFFAOYSA-N icosyl 5-iodopentanoate Chemical compound ICCCCC(=O)OCCCCCCCCCCCCCCCCCCCC AYHZGWMHNNGUND-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229940119545 isobornyl methacrylate Drugs 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- ALWCFWKIDQONBL-UHFFFAOYSA-N methyl 10-[10-(10-methoxy-10-oxodecoxy)anthracen-9-yl]oxydecanoate Chemical compound COC(=O)CCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCC(=O)OC ALWCFWKIDQONBL-UHFFFAOYSA-N 0.000 description 1
- KNMQDQZWKKMBCZ-UHFFFAOYSA-N methyl 11-[10-(11-methoxy-11-oxoundecoxy)anthracen-9-yl]oxyundecanoate Chemical compound COC(=O)CCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCC(=O)OC KNMQDQZWKKMBCZ-UHFFFAOYSA-N 0.000 description 1
- RHOZVZFCXJQZPM-UHFFFAOYSA-N methyl 12-[10-(12-methoxy-12-oxododecoxy)anthracen-9-yl]oxydodecanoate Chemical compound COC(=O)CCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCC(=O)OC RHOZVZFCXJQZPM-UHFFFAOYSA-N 0.000 description 1
- OSVICUKKWUISQC-UHFFFAOYSA-N methyl 13-[10-(13-methoxy-13-oxotridecoxy)anthracen-9-yl]oxytridecanoate Chemical compound COC(=O)CCCCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCC(=O)OC OSVICUKKWUISQC-UHFFFAOYSA-N 0.000 description 1
- NFYKWBOWTNHGLA-UHFFFAOYSA-N methyl 14-[10-(14-methoxy-14-oxotetradecoxy)anthracen-9-yl]oxytetradecanoate Chemical compound COC(=O)CCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCC(=O)OC NFYKWBOWTNHGLA-UHFFFAOYSA-N 0.000 description 1
- QXPNVMIMEYZTBC-UHFFFAOYSA-N methyl 15-[10-(15-methoxy-15-oxopentadecoxy)anthracen-9-yl]oxypentadecanoate Chemical compound COC(=O)CCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCC(=O)OC QXPNVMIMEYZTBC-UHFFFAOYSA-N 0.000 description 1
- IZALINGHQCLCKM-UHFFFAOYSA-N methyl 16-[10-(16-methoxy-16-oxohexadecoxy)anthracen-9-yl]oxyhexadecanoate Chemical compound COC(=O)CCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCC(=O)OC IZALINGHQCLCKM-UHFFFAOYSA-N 0.000 description 1
- TZZJRHGQNVGAHG-UHFFFAOYSA-N methyl 17-[10-(17-methoxy-17-oxoheptadecoxy)anthracen-9-yl]oxyheptadecanoate Chemical compound COC(=O)CCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCC(=O)OC TZZJRHGQNVGAHG-UHFFFAOYSA-N 0.000 description 1
- VTGLYJIKKJHPJC-UHFFFAOYSA-N methyl 17-[3-chloro-10-(17-methoxy-17-oxoheptadecoxy)anthracen-9-yl]oxyheptadecanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCC(=O)OC)OCCCCCCCCCCCCCCCCC(=O)OC VTGLYJIKKJHPJC-UHFFFAOYSA-N 0.000 description 1
- XONDKQSEDVEBGK-UHFFFAOYSA-N methyl 17-[3-ethyl-10-(17-methoxy-17-oxoheptadecoxy)anthracen-9-yl]oxyheptadecanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCC(=O)OC)OCCCCCCCCCCCCCCCCC(=O)OC XONDKQSEDVEBGK-UHFFFAOYSA-N 0.000 description 1
- IVZQKIVVFMGAMC-UHFFFAOYSA-N methyl 18-[10-(18-methoxy-18-oxooctadecoxy)anthracen-9-yl]oxyoctadecanoate Chemical compound COC(=O)CCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCC(=O)OC IVZQKIVVFMGAMC-UHFFFAOYSA-N 0.000 description 1
- AUWSEGKPYKLXEE-UHFFFAOYSA-N methyl 19-[10-(19-methoxy-19-oxononadecoxy)anthracen-9-yl]oxynonadecanoate Chemical compound COC(=O)CCCCCCCCCCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCCCC(=O)OC AUWSEGKPYKLXEE-UHFFFAOYSA-N 0.000 description 1
- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 1
- UFQQDNMQADCHGH-UHFFFAOYSA-N methyl 2-bromobutanoate Chemical compound CCC(Br)C(=O)OC UFQQDNMQADCHGH-UHFFFAOYSA-N 0.000 description 1
- MGMWQSVSOGNGPL-UHFFFAOYSA-N methyl 2-bromopentanoate Chemical compound CCCC(Br)C(=O)OC MGMWQSVSOGNGPL-UHFFFAOYSA-N 0.000 description 1
- ACEONLNNWKIPTM-UHFFFAOYSA-N methyl 2-bromopropanoate Chemical compound COC(=O)C(C)Br ACEONLNNWKIPTM-UHFFFAOYSA-N 0.000 description 1
- QABLOFMHHSOFRJ-UHFFFAOYSA-N methyl 2-chloroacetate Chemical compound COC(=O)CCl QABLOFMHHSOFRJ-UHFFFAOYSA-N 0.000 description 1
- DFJFGBSFTBCENV-UHFFFAOYSA-N methyl 2-chloropentanoate Chemical compound CCCC(Cl)C(=O)OC DFJFGBSFTBCENV-UHFFFAOYSA-N 0.000 description 1
- YDGMIJCIBXSCQR-UHFFFAOYSA-N methyl 2-iodoacetate Chemical compound COC(=O)CI YDGMIJCIBXSCQR-UHFFFAOYSA-N 0.000 description 1
- BALADIHEPAEKQJ-UHFFFAOYSA-N methyl 2-iodopropanoate Chemical compound COC(=O)C(C)I BALADIHEPAEKQJ-UHFFFAOYSA-N 0.000 description 1
- YJIAXQUTJZRQJG-UHFFFAOYSA-N methyl 20-[10-(20-methoxy-20-oxoicosoxy)anthracen-9-yl]oxyicosanoate Chemical compound COC(=O)CCCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCCC(=O)OC YJIAXQUTJZRQJG-UHFFFAOYSA-N 0.000 description 1
- WSYYTBJCJFHTRZ-UHFFFAOYSA-N methyl 21-[10-(21-methoxy-21-oxohenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound COC(=O)CCCCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCCCC(=O)OC WSYYTBJCJFHTRZ-UHFFFAOYSA-N 0.000 description 1
- QSCGYHAZQXYILF-UHFFFAOYSA-N methyl 3-[10-(4-methoxy-4-oxobutan-2-yl)oxy-3-pentylanthracen-9-yl]oxybutanoate Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OC)C)OC(CC(=O)OC)C QSCGYHAZQXYILF-UHFFFAOYSA-N 0.000 description 1
- NXNZNWCOGABLFK-UHFFFAOYSA-N methyl 3-[3-chloro-10-(4-methoxy-4-oxobutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OC)C)OC(CC(=O)OC)C NXNZNWCOGABLFK-UHFFFAOYSA-N 0.000 description 1
- WJYBMWHJTZBYSO-UHFFFAOYSA-N methyl 3-bromobutanoate Chemical compound COC(=O)CC(C)Br WJYBMWHJTZBYSO-UHFFFAOYSA-N 0.000 description 1
- PCQPIVKTPFWWHW-UHFFFAOYSA-N methyl 3-bromopentanoate Chemical compound CCC(Br)CC(=O)OC PCQPIVKTPFWWHW-UHFFFAOYSA-N 0.000 description 1
- KQEVIFKPZOGBMZ-UHFFFAOYSA-N methyl 3-bromopropanoate Chemical compound COC(=O)CCBr KQEVIFKPZOGBMZ-UHFFFAOYSA-N 0.000 description 1
- HDQHWBXUKZBPDN-UHFFFAOYSA-N methyl 3-chlorobutanoate Chemical compound COC(=O)CC(C)Cl HDQHWBXUKZBPDN-UHFFFAOYSA-N 0.000 description 1
- HBUFAVOUAAGAOA-UHFFFAOYSA-N methyl 3-iodobutanoate Chemical compound COC(=O)CC(C)I HBUFAVOUAAGAOA-UHFFFAOYSA-N 0.000 description 1
- ZZUYIRISBMWFMV-UHFFFAOYSA-N methyl 4-chlorobutanoate Chemical compound COC(=O)CCCCl ZZUYIRISBMWFMV-UHFFFAOYSA-N 0.000 description 1
- HUEAHYURPVGTBN-UHFFFAOYSA-N methyl 5-[3-chloro-10-(5-methoxy-5-oxopentoxy)anthracen-9-yl]oxypentanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC)OCCCCC(=O)OC HUEAHYURPVGTBN-UHFFFAOYSA-N 0.000 description 1
- WPSOYRVWDJGLCW-UHFFFAOYSA-N methyl 5-[3-ethyl-10-(5-methoxy-5-oxopentoxy)anthracen-9-yl]oxypentanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC)OCCCCC(=O)OC WPSOYRVWDJGLCW-UHFFFAOYSA-N 0.000 description 1
- RAVVJKCSZXAIQP-UHFFFAOYSA-N methyl 5-bromopentanoate Chemical compound COC(=O)CCCCBr RAVVJKCSZXAIQP-UHFFFAOYSA-N 0.000 description 1
- DWOZSQFTZLQQMU-UHFFFAOYSA-N methyl 6-[10-(6-methoxy-6-oxohexoxy)anthracen-9-yl]oxyhexanoate Chemical compound COC(=O)CCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCC(=O)OC DWOZSQFTZLQQMU-UHFFFAOYSA-N 0.000 description 1
- ZHRZXBOHTRKBMF-UHFFFAOYSA-N methyl 7-[10-(7-methoxy-7-oxoheptoxy)anthracen-9-yl]oxyheptanoate Chemical compound COC(=O)CCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCC(=O)OC ZHRZXBOHTRKBMF-UHFFFAOYSA-N 0.000 description 1
- HFBZMJHHOPZXSI-UHFFFAOYSA-N methyl 8-[10-(8-methoxy-8-oxooctoxy)anthracen-9-yl]oxyoctanoate Chemical compound COC(=O)CCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCC(=O)OC HFBZMJHHOPZXSI-UHFFFAOYSA-N 0.000 description 1
- WWBBOHZRNAKMAM-UHFFFAOYSA-N methyl 9-[10-(9-methoxy-9-oxononoxy)anthracen-9-yl]oxynonanoate Chemical compound COC(=O)CCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCC(=O)OC WWBBOHZRNAKMAM-UHFFFAOYSA-N 0.000 description 1
- MQMRUJYUHNQGAY-UHFFFAOYSA-N methyl 9-[3-chloro-10-(9-methoxy-9-oxononoxy)anthracen-9-yl]oxynonanoate Chemical compound COC(=O)CCCCCCCCOC1=C2C=CC(=CC2=C(C3=CC=CC=C31)OCCCCCCCCC(=O)OC)Cl MQMRUJYUHNQGAY-UHFFFAOYSA-N 0.000 description 1
- OVLPSJMQQJNOLP-UHFFFAOYSA-N methyl 9-[3-ethyl-10-(9-methoxy-9-oxononoxy)anthracen-9-yl]oxynonanoate Chemical compound CCC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC(=O)OC)OCCCCCCCCC(=O)OC OVLPSJMQQJNOLP-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- QLPMKRZYJPNIRP-UHFFFAOYSA-M methyl(trioctyl)azanium;bromide Chemical compound [Br-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC QLPMKRZYJPNIRP-UHFFFAOYSA-M 0.000 description 1
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- QTJPCBIGWQXEBW-UHFFFAOYSA-N nonadecyl 2-bromoacetate Chemical compound BrCC(=O)OCCCCCCCCCCCCCCCCCCC QTJPCBIGWQXEBW-UHFFFAOYSA-N 0.000 description 1
- DGMPZWPISULYBC-UHFFFAOYSA-N nonadecyl 2-bromopentanoate Chemical compound BrC(C(=O)OCCCCCCCCCCCCCCCCCCC)CCC DGMPZWPISULYBC-UHFFFAOYSA-N 0.000 description 1
- AKLPSRZIGMGYCM-UHFFFAOYSA-N nonadecyl 2-bromopropanoate Chemical compound BrC(C(=O)OCCCCCCCCCCCCCCCCCCC)C AKLPSRZIGMGYCM-UHFFFAOYSA-N 0.000 description 1
- MKQZIZBPFKYZPZ-UHFFFAOYSA-N nonadecyl 2-chloroacetate Chemical compound ClCC(=O)OCCCCCCCCCCCCCCCCCCC MKQZIZBPFKYZPZ-UHFFFAOYSA-N 0.000 description 1
- WIXXMRKRIHDWTI-UHFFFAOYSA-N nonadecyl 2-chlorobutanoate Chemical compound ClC(C(=O)OCCCCCCCCCCCCCCCCCCC)CC WIXXMRKRIHDWTI-UHFFFAOYSA-N 0.000 description 1
- CVJDLIQGTKTSAQ-UHFFFAOYSA-N nonadecyl 2-chloropentanoate Chemical compound ClC(C(=O)OCCCCCCCCCCCCCCCCCCC)CCC CVJDLIQGTKTSAQ-UHFFFAOYSA-N 0.000 description 1
- NLUMLXMKLGROBG-UHFFFAOYSA-N nonadecyl 2-chloropropanoate Chemical compound ClC(C(=O)OCCCCCCCCCCCCCCCCCCC)C NLUMLXMKLGROBG-UHFFFAOYSA-N 0.000 description 1
- QQEGWZGIPXRZCQ-UHFFFAOYSA-N nonadecyl 2-iodoacetate Chemical compound ICC(=O)OCCCCCCCCCCCCCCCCCCC QQEGWZGIPXRZCQ-UHFFFAOYSA-N 0.000 description 1
- MQRLYVBDCBERID-UHFFFAOYSA-N nonadecyl 2-iodobutanoate Chemical compound IC(C(=O)OCCCCCCCCCCCCCCCCCCC)CC MQRLYVBDCBERID-UHFFFAOYSA-N 0.000 description 1
- MEBLHYCOMGSQPJ-UHFFFAOYSA-N nonadecyl 2-iodopentanoate Chemical compound IC(C(=O)OCCCCCCCCCCCCCCCCCCC)CCC MEBLHYCOMGSQPJ-UHFFFAOYSA-N 0.000 description 1
- IYZNSXNYFORUQO-UHFFFAOYSA-N nonadecyl 2-iodopropanoate Chemical compound IC(C(=O)OCCCCCCCCCCCCCCCCCCC)C IYZNSXNYFORUQO-UHFFFAOYSA-N 0.000 description 1
- QPXWXNHHYRYGIK-UHFFFAOYSA-N nonadecyl 3-bromobutanoate Chemical compound BrC(CC(=O)OCCCCCCCCCCCCCCCCCCC)C QPXWXNHHYRYGIK-UHFFFAOYSA-N 0.000 description 1
- YJSRGTMCKICNNT-UHFFFAOYSA-N nonadecyl 3-bromopentanoate Chemical compound BrC(CC(=O)OCCCCCCCCCCCCCCCCCCC)CC YJSRGTMCKICNNT-UHFFFAOYSA-N 0.000 description 1
- YUCMQARIIIBDIQ-UHFFFAOYSA-N nonadecyl 3-bromopropanoate Chemical compound BrCCC(=O)OCCCCCCCCCCCCCCCCCCC YUCMQARIIIBDIQ-UHFFFAOYSA-N 0.000 description 1
- FDOKPKFHTNCUQN-UHFFFAOYSA-N nonadecyl 3-chlorobutanoate Chemical compound CCCCCCCCCCCCCCCCCCCOC(=O)CC(C)Cl FDOKPKFHTNCUQN-UHFFFAOYSA-N 0.000 description 1
- HJEPCGFDHNSSIX-UHFFFAOYSA-N nonadecyl 3-chloropropanoate Chemical compound ClCCC(=O)OCCCCCCCCCCCCCCCCCCC HJEPCGFDHNSSIX-UHFFFAOYSA-N 0.000 description 1
- KVKCKUDIPWNHLP-UHFFFAOYSA-N nonadecyl 3-iodobutanoate Chemical compound IC(CC(=O)OCCCCCCCCCCCCCCCCCCC)C KVKCKUDIPWNHLP-UHFFFAOYSA-N 0.000 description 1
- AOSBBGCQKDJLJH-UHFFFAOYSA-N nonadecyl 3-iodopropanoate Chemical compound ICCC(=O)OCCCCCCCCCCCCCCCCCCC AOSBBGCQKDJLJH-UHFFFAOYSA-N 0.000 description 1
- WLPHHABBPTZALM-UHFFFAOYSA-N nonadecyl 4-bromobutanoate Chemical compound BrCCCC(=O)OCCCCCCCCCCCCCCCCCCC WLPHHABBPTZALM-UHFFFAOYSA-N 0.000 description 1
- JVCUNXCVIVIURE-UHFFFAOYSA-N nonadecyl 4-bromopentanoate Chemical compound BrC(CCC(=O)OCCCCCCCCCCCCCCCCCCC)C JVCUNXCVIVIURE-UHFFFAOYSA-N 0.000 description 1
- OTYFZOJNSXOYDL-UHFFFAOYSA-N nonadecyl 4-chlorobutanoate Chemical compound CCCCCCCCCCCCCCCCCCCOC(=O)CCCCl OTYFZOJNSXOYDL-UHFFFAOYSA-N 0.000 description 1
- LYYYYHPJAQOBHK-UHFFFAOYSA-N nonadecyl 4-chloropentanoate Chemical compound ClC(CCC(=O)OCCCCCCCCCCCCCCCCCCC)C LYYYYHPJAQOBHK-UHFFFAOYSA-N 0.000 description 1
- DMADGQUAVSICHI-UHFFFAOYSA-N nonadecyl 4-iodobutanoate Chemical compound CCCCCCCCCCCCCCCCCCCOC(=O)CCCI DMADGQUAVSICHI-UHFFFAOYSA-N 0.000 description 1
- VREFRVOMTRAAPS-UHFFFAOYSA-N nonadecyl 4-iodopentanoate Chemical compound CCCCCCCCCCCCCCCCCCCOC(=O)CCC(C)I VREFRVOMTRAAPS-UHFFFAOYSA-N 0.000 description 1
- QLBCJWLCBGRINH-UHFFFAOYSA-N nonadecyl 5-bromopentanoate Chemical compound BrCCCCC(=O)OCCCCCCCCCCCCCCCCCCC QLBCJWLCBGRINH-UHFFFAOYSA-N 0.000 description 1
- LQOAIQMDQLUEOU-UHFFFAOYSA-N nonadecyl 5-chloropentanoate Chemical compound ClCCCCC(=O)OCCCCCCCCCCCCCCCCCCC LQOAIQMDQLUEOU-UHFFFAOYSA-N 0.000 description 1
- CQHLQAHODWNWNU-UHFFFAOYSA-N nonadecyl 5-iodopentanoate Chemical compound ICCCCC(=O)OCCCCCCCCCCCCCCCCCCC CQHLQAHODWNWNU-UHFFFAOYSA-N 0.000 description 1
- CTAPFXJABKRLIA-UHFFFAOYSA-N nonyl 2-bromoacetate Chemical compound CCCCCCCCCOC(=O)CBr CTAPFXJABKRLIA-UHFFFAOYSA-N 0.000 description 1
- QLHKAJYBOHBZQL-UHFFFAOYSA-N nonyl 2-bromobutanoate Chemical compound CCCCCCCCCOC(=O)C(Br)CC QLHKAJYBOHBZQL-UHFFFAOYSA-N 0.000 description 1
- XKPZGCFEEXQCRL-UHFFFAOYSA-N nonyl 2-bromopentanoate Chemical compound CCCCCCCCCOC(=O)C(CCC)Br XKPZGCFEEXQCRL-UHFFFAOYSA-N 0.000 description 1
- RYJOCSXNXWJISS-UHFFFAOYSA-N nonyl 2-bromopropanoate Chemical compound CCCCCCCCCOC(=O)C(C)Br RYJOCSXNXWJISS-UHFFFAOYSA-N 0.000 description 1
- OKWGMWNSHCOYJE-UHFFFAOYSA-N nonyl 2-chloroacetate Chemical compound CCCCCCCCCOC(=O)CCl OKWGMWNSHCOYJE-UHFFFAOYSA-N 0.000 description 1
- GRCVTYDSCRHGAC-UHFFFAOYSA-N nonyl 2-chlorobutanoate Chemical compound CCCCCCCCCOC(=O)C(Cl)CC GRCVTYDSCRHGAC-UHFFFAOYSA-N 0.000 description 1
- FZEGCCPYOGFPTL-UHFFFAOYSA-N nonyl 2-chloropentanoate Chemical compound ClC(C(=O)OCCCCCCCCC)CCC FZEGCCPYOGFPTL-UHFFFAOYSA-N 0.000 description 1
- OPUKQARDQCGBBY-UHFFFAOYSA-N nonyl 2-chloropropanoate Chemical compound CCCCCCCCCOC(=O)C(C)Cl OPUKQARDQCGBBY-UHFFFAOYSA-N 0.000 description 1
- IKPAMRQMGGQHLX-UHFFFAOYSA-N nonyl 2-iodoacetate Chemical compound CCCCCCCCCOC(=O)CI IKPAMRQMGGQHLX-UHFFFAOYSA-N 0.000 description 1
- BSJHWPATJWCTFS-UHFFFAOYSA-N nonyl 2-iodobutanoate Chemical compound IC(C(=O)OCCCCCCCCC)CC BSJHWPATJWCTFS-UHFFFAOYSA-N 0.000 description 1
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- HSZYJUHRYVAQET-UHFFFAOYSA-N nonyl 3-chlorobutanoate Chemical compound CCCCCCCCCOC(=O)CC(C)Cl HSZYJUHRYVAQET-UHFFFAOYSA-N 0.000 description 1
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- BTAWHIFCKWTSPU-UHFFFAOYSA-N nonyl 4-bromopentanoate Chemical compound BrC(CCC(=O)OCCCCCCCCC)C BTAWHIFCKWTSPU-UHFFFAOYSA-N 0.000 description 1
- JOHFUSYZUPEZNG-UHFFFAOYSA-N nonyl 4-chlorobutanoate Chemical compound CCCCCCCCCOC(=O)CCCCl JOHFUSYZUPEZNG-UHFFFAOYSA-N 0.000 description 1
- YIIQMLXUDMSQKM-UHFFFAOYSA-N nonyl 4-iodobutanoate Chemical compound ICCCC(=O)OCCCCCCCCC YIIQMLXUDMSQKM-UHFFFAOYSA-N 0.000 description 1
- ZZYSKZVVWOPSDZ-UHFFFAOYSA-N nonyl 5-bromopentanoate Chemical compound CCCCCCCCCOC(=O)CCCCBr ZZYSKZVVWOPSDZ-UHFFFAOYSA-N 0.000 description 1
- ZMLMYLLZBXHXHL-UHFFFAOYSA-N nonyl 5-chloropentanoate Chemical compound CCCCCCCCCOC(=O)CCCCCl ZMLMYLLZBXHXHL-UHFFFAOYSA-N 0.000 description 1
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- 229920001778 nylon Polymers 0.000 description 1
- ZBNUZMDEFBLZIJ-UHFFFAOYSA-N octyl 2-bromoacetate Chemical compound CCCCCCCCOC(=O)CBr ZBNUZMDEFBLZIJ-UHFFFAOYSA-N 0.000 description 1
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- QEQGUSNDCRXKBX-UHFFFAOYSA-N octyl 2-bromopentanoate Chemical compound CCCCCCCCOC(=O)C(Br)CCC QEQGUSNDCRXKBX-UHFFFAOYSA-N 0.000 description 1
- NNXMXUSTTDFBDE-UHFFFAOYSA-N octyl 2-chloroacetate Chemical compound CCCCCCCCOC(=O)CCl NNXMXUSTTDFBDE-UHFFFAOYSA-N 0.000 description 1
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- BGMYDZVCAOVIPM-UHFFFAOYSA-N octyl 2-chloropropanoate Chemical compound CCCCCCCCOC(=O)C(C)Cl BGMYDZVCAOVIPM-UHFFFAOYSA-N 0.000 description 1
- PTMGITASNQPNJJ-UHFFFAOYSA-N octyl 2-iodoacetate Chemical compound CCCCCCCCOC(=O)CI PTMGITASNQPNJJ-UHFFFAOYSA-N 0.000 description 1
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- YKLCSWKJXHAYKL-UHFFFAOYSA-N octyl 2-iodopentanoate Chemical compound IC(C(=O)OCCCCCCCC)CCC YKLCSWKJXHAYKL-UHFFFAOYSA-N 0.000 description 1
- BRWVXMCQZYVULC-UHFFFAOYSA-N octyl 2-iodopropanoate Chemical compound IC(C(=O)OCCCCCCCC)C BRWVXMCQZYVULC-UHFFFAOYSA-N 0.000 description 1
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- CESJLSXZSBTNSQ-UHFFFAOYSA-N octyl 3-bromopentanoate Chemical compound BrC(CC(=O)OCCCCCCCC)CC CESJLSXZSBTNSQ-UHFFFAOYSA-N 0.000 description 1
- RTGDICWSTDGLNC-UHFFFAOYSA-N octyl 3-bromopropanoate Chemical compound CCCCCCCCOC(=O)CCBr RTGDICWSTDGLNC-UHFFFAOYSA-N 0.000 description 1
- KGTJTJMGWKRVOB-UHFFFAOYSA-N octyl 3-chlorobutanoate Chemical compound CCCCCCCCOC(=O)CC(C)Cl KGTJTJMGWKRVOB-UHFFFAOYSA-N 0.000 description 1
- IASGPKRWWNGEIJ-UHFFFAOYSA-N octyl 3-chloropentanoate Chemical compound ClC(CC(=O)OCCCCCCCC)CC IASGPKRWWNGEIJ-UHFFFAOYSA-N 0.000 description 1
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- IOVIPPSZMYGEKH-UHFFFAOYSA-N octyl 3-iodobutanoate Chemical compound IC(CC(=O)OCCCCCCCC)C IOVIPPSZMYGEKH-UHFFFAOYSA-N 0.000 description 1
- RXHJZXOIXVWTCZ-UHFFFAOYSA-N octyl 3-iodopentanoate Chemical compound IC(CC(=O)OCCCCCCCC)CC RXHJZXOIXVWTCZ-UHFFFAOYSA-N 0.000 description 1
- IBTOBYKVXQPQGO-UHFFFAOYSA-N octyl 3-iodopropanoate Chemical compound CCCCCCCCOC(=O)CCI IBTOBYKVXQPQGO-UHFFFAOYSA-N 0.000 description 1
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- HSBMJYJLRGJAES-UHFFFAOYSA-N tert-butyl 9-[10-[9-[(2-methylpropan-2-yl)oxy]-9-oxononoxy]anthracen-9-yl]oxynonanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCC(=O)OC(C)(C)C HSBMJYJLRGJAES-UHFFFAOYSA-N 0.000 description 1
- LNIGCTKUWFUPDI-UHFFFAOYSA-N tert-butyl 9-[3-chloro-10-[9-[(2-methylpropan-2-yl)oxy]-9-oxononoxy]anthracen-9-yl]oxynonanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC(=O)OC(C)(C)C)OCCCCCCCCC(=O)OC(C)(C)C LNIGCTKUWFUPDI-UHFFFAOYSA-N 0.000 description 1
- AWFGCLNLCLWLKV-UHFFFAOYSA-N tert-butyl 9-[3-ethyl-10-[9-[(2-methylpropan-2-yl)oxy]-9-oxononoxy]anthracen-9-yl]oxynonanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC(=O)OC(C)(C)C)OCCCCCCCCC(=O)OC(C)(C)C AWFGCLNLCLWLKV-UHFFFAOYSA-N 0.000 description 1
- SCSLUABEVMLYEA-UHFFFAOYSA-N tert-butyl pentanoate Chemical compound CCCCC(=O)OC(C)(C)C SCSLUABEVMLYEA-UHFFFAOYSA-N 0.000 description 1
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
- YMBCJWGVCUEGHA-UHFFFAOYSA-M tetraethylammonium chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC YMBCJWGVCUEGHA-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- DDFYFBUWEBINLX-UHFFFAOYSA-M tetramethylammonium bromide Chemical compound [Br-].C[N+](C)(C)C DDFYFBUWEBINLX-UHFFFAOYSA-M 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- BGQMOFGZRJUORO-UHFFFAOYSA-M tetrapropylammonium bromide Chemical compound [Br-].CCC[N+](CCC)(CCC)CCC BGQMOFGZRJUORO-UHFFFAOYSA-M 0.000 description 1
- FBEVECUEMUUFKM-UHFFFAOYSA-M tetrapropylazanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CCC FBEVECUEMUUFKM-UHFFFAOYSA-M 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- PIVZYJMLIVYZJA-UHFFFAOYSA-M trioctyl(propyl)azanium;bromide Chemical compound [Br-].CCCCCCCC[N+](CCC)(CCCCCCCC)CCCCCCCC PIVZYJMLIVYZJA-UHFFFAOYSA-M 0.000 description 1
- WFEXFNMTEBFLMM-UHFFFAOYSA-M trioctyl(propyl)azanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](CCC)(CCCCCCCC)CCCCCCCC WFEXFNMTEBFLMM-UHFFFAOYSA-M 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229940042596 viscoat Drugs 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
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Description
まず初めに、本発明に用いる光ラジカル硬化酸素阻害低減剤について説明する。本発明に用いる光ラジカル硬化酸素阻害低減剤は、下記9,10-ビス(アルコキシカルボニルアルキレンオキシ)アントラセン化合物である。
上記9,10-ビス(アルコキシカルボニルメトキシ)アントラセン化合物は、例えば、9,10-ジヒドロキシアントラセン化合物を、塩基性化合物存在下ブロモ酢酸エステルなどのエステル化合物と反応させることにより得ることができる。
本発明の光ラジカル重合性組成物は、少なくともラジカル重合性化合物、光ラジカル重合開始剤及び下記一般式(1)で表されるエステル基を有する9,10-ビス(アルコキシカルボニルアルキレンオキシ)アントラセン化合物からなる光ラジカル硬化酸素阻害低減剤を含有する光ラジカル重合性組成物である。
本発明で用いる光ラジカル重合開始剤としては、オニウム塩系光ラジカル重合開始剤、ベンジルメチルケタール系光ラジカル重合開始剤、α-ヒドロキシアセトフェノン系光ラジカル重合開始剤、オキシムエステル系光ラジカル重合開始剤、α-アミノアルキルフェノン系光ラジカル重合開始剤、アシルホスフィンオキサイド系光ラジカル重合開始剤、ビイミダゾール系光ラジカル重合開始剤、トリアジン系光ラジカル重合開始剤等を用いることができる。
本発明の一般式(1)で表されるエステル基を有する9,10-ビス(アルコキシカルボニルアルキレンオキシ)アントラセン化合物を含有する光ラジカル硬化酸素阻害低減剤は、直接、光重合性化合物に添加することもできるが、あらかじめ光ラジカル重合開始剤と配合することにより光ラジカル重合開始剤組成物を調製した後、光重合性化合物に添加することもできる。すなわち、本発明の光ラジカル重合開始剤組成物は、少なくとも、一般式(1)で表されるエステル基を有する9,10-ビス(アルコキシカルボニルアルキレンオキシ)アントラセン化合物を含有する光ラジカル硬化酸素阻害低減剤と光ラジカル重合開始剤を含有する組成物である。
さらに該光ラジカル重合開始剤組成物と光重合性化合物を配合することにより、光重合性組成物を調製することもできる。本発明のエステル基を有する9,10-ビス(アルコキシカルボニルアルキレンオキシ)アントラセン化合物を含有する光ラジカル硬化酸素阻害低減剤と光ラジカル重合開始剤は、別々に光ラジカル重合性化合物又は光カチオン重合性化合物に添加され、光ラジカル重合性化合物又は光カチオン重合性化合物中で、結果として光ラジカル重合開始剤組成物を形成してもよい。更に、光ラジカル重合性化合物と光カチオン重合性化合物の両方を含むハイブリッド組成物としてもよい。
本発明の光ラジカル重合性塗膜は、少なくともラジカル重合性化合物と光ラジカル重合開始剤と光ラジカル硬化酸素阻害低減剤を含有する。光ラジカル重合性塗膜における光ラジカル重合開始剤の含有量は、光ラジカル重合性組成物の総質量に対して2.0質量%以上、10質量%以下であり、9,10-ビス(アルコキシカルボニルアルキレンオキシ)アントラセン化合物の含有量が、光ラジカル重合性組成物の総質量に対して0.20質量%以上、5.0質量%以下である。光ラジカル重合開始剤の含有量が2.0質量%未満の場合は塗膜の重合が十分に進行せず、10質量%を超える量を添加しても溶解性が悪く十分な効果を発揮できない。
本発明の光ラジカル重合性塗膜の膜厚は特に制限されないが、通常は1000μm以下であることが好ましい。更に、塗膜表面での酸素阻害の影響が塗膜全体の硬化状態に影響を及ぼすこととなる薄膜状態、すなわち10μm未満であることが好ましい。10μm以上であっても、該組成物の硬化時の酸素阻害低減効果が観測されるが、本発明の効果が際立って顕著となるという意味で10μm未満であることが好ましい。更には、4μm以下であることが更に好ましい。
れらの複合材料も挙げることが出来る。上質紙、コート紙、アート紙、模造紙、薄紙、厚紙等の紙、各種合成紙等に各種フィルムをラミネートしたものでも有用である。特に、PEやPPなどのプラスチックフィルムが好ましい。
当該光ラジカル重合性塗膜は、大気と接触している面から波長が360nmから410nmの波長範囲の光を含むエネルギー線を照射して重合、硬化させる。当該波長範囲の光により光ラジカル重合開始剤は励起され、開始ラジカル種を発生することができる。
用いる照射源としては405nmの光を中心波長とする紫外LED、395nmの光を中心波長とする紫外LED、385nm光を中心波長とする紫外LED、365nm光を中心波長とする紫外LED及び405nmの光を中心波長とする半導体レーザが好ましいが、波長が360nmから410nmの間に発光スペクトルを持つランプであれば使用可能であり、フュージョン社製のD-バルブ、V-バルブ等の無電極ランプや、キセノンランプ、ブラックライト、超高圧水銀ランプ、メタルハライドランプ及びガリウムドープドランプ等も使用可能である。特に、405nmの光を中心波長とする紫外LED、395nmの光を中心波長とする紫外LED、385nm光を中心波長とする紫外LED、365nm光を中心波長とする紫外LED、405nmの光を中心波長とする半導体レーザが好ましい。
光硬化の判定方法としては、FT-IR(光硬化性I)、Photo-DSC(光硬化性II)、Photo-Rheometer(光硬化性III)を用いた。
FT-IR測定では、透過反射法で測定を行った。810cm-1、1409cm-1または1635cm-1付近における(メタ)アクリル酸エステルC=C結合の振動のピークの吸収強度をもとに硬化率を算出した。ラジカル重合性化合物である(メタ)アクリル酸エステルは重合反応とともに、C=C結合が消費されていくために、当該C=C結合の振動のピークの光を照射する前の吸収強度を硬化率0%として、当該吸収強度が0となるときを硬化率100%として算出した。なお、FT-IR測定条件は下記のとおりである。
測定雰囲気:
窒素下:試料チャンバー内を窒素置換
大気下:窒素置換なし
試料厚み:4μm
UV照射器:浜松ホトニクス社製LIGHTNINGCURE(高圧水銀-キセノンランプ)365nmバンドパスフィルター
照射強度:100mW/cm2
照射時間:96秒間
積算光量:9600mJ/cm2
UV照射器:浜松ホトニクス社製LIGHTNINGCURE LC-LIB3 L11921(385nm)
照射強度:200mW/cm2
照射時間:48秒間
積算光量:9600mJ/cm2
UV照射器:Altec社395nm LEDライティングボックス(LLBK1)
照射強度:160mW/cm2
照射時間:60秒間
積算光量:9600mJ/cm2
UV照射器:Altec社405nm LEDライティングボックス(LLBK1)
照射強度:30mW/cm2
照射時間:300秒間
積算光量:9000mJ/cm2
UV照射器:Altec社405nm LEDライティングボックス(LLBK1)
照射強度:30mW/cm2
照射時間:300秒間
積算光量:9000mJ/cm2
UV照射器:松尾産業社製UV-LED(405nm)ベルトコンベア式照射機
照射強度:1.67W/cm2
コンベア速度:0.581m/min
積算光量:4.57J/cm2
Photo-DSC測定では、試料1.00mg当たりの光照射開始から5分間の総発熱量を求めた。なお、Photo-DSCの測定条件は下記の通りである。
Photo-DSC装置:HITACHI製示差熱分析装置 X-DSC700
UV照射器:HAYASHI LA-410UV 405nmバンドパスフィルター
照射強度:50mW/cm2
照射時間:300秒間
測定雰囲気:空気気流中100ml/分又は窒素気流中100ml/分
サンプル量:1mg
試料厚み:300μm程度
Photo-Rheometer測定では、光照射後140秒時点における貯蔵弾性率を求めた。なお、Photo-Rheometerの測定条件は下記の通りである。
Photo-Rheometer装置:Anton Paar社製Modular Compact Rheometer MCR102
UV照射器:浜松ホトニクス社製LIGHTNINGCURE(高圧水銀-キセノンランプ)405nmバンドパスフィルター
照射強度:50mW/cm2
照射時間:300秒間
測定雰囲気:空気気流中100ml/分
試料厚み:10μm
赤外線(IR)分光光度計:Thermo社製、型式is50 FT-IR
核磁気共鳴装置(NMR):日本電子社製、型式ECS-400
数平均分子量(GPC):日本分光社製、2000シリーズ
攪拌機、温度計付きの100mlの四つ口フラスコに、窒素雰囲気下で、溶媒のメチルイソブチルケトンを15g、触媒のテトラブチルアンモニウムブロマイドの50%水溶液を0.8g(1.2ミリモル)、ブロモ酢酸エチルを10.4g(62.5ミリモル)加えた。反応系の温度を20~25℃に保ちながら9,10-ジヒドロキシアントラセンのジナトリウム塩の17wt%水溶液29.1g(アントラキノンとして24ミリモル)を1時間以上かけて、滴下した。滴下終了後、さらに1時間撹拌した。その後、吸引濾過により、収量5.0g(粗収率55mol%)の薄黄色の結晶を得た。
(2)IR(cm-1):1754,1742,1382,1367,1241,1212,1168,1087,1034,1004,936,809,768,720,691,669,585.
(3)1H-NMR(400MHz,CDCl3):δ=1.370(t,J=14Hz,6H),4.376(k,J=21.6Hz,4H),4.777(s,4H),7.261-7.540(m,4H).
攪拌機、温度計付きの300mlの四つ口フラスコに、窒素雰囲気下で、ブロモ酢酸32.5g(234ミリモル)、n-ペンタノール41.1g(466ミリモル)、溶媒のо-キシレン75.7g、触媒の硫酸1.5g(16ミリモル)を加えた。反応系の温度を140~150℃に保ち、共沸する水を除去しながら2時間攪拌した。室温まで冷却後、炭酸水素ナトリウム水溶液で中和し、水層を除いた。そこに触媒のテトラブチルアンモニウムブロマイドの50%水溶液を2.8g(4.3ミリモル)を加え、反応系の温度を20~30℃に保ちながら9,10-ジヒドロキシアントラセンのジナトリウム塩の18.7wt%水溶液100g(アントラキノンとして90ミリモル)を1時間かけて滴下した。滴下終了後、さらに1時間撹拌し、55~60℃まで昇温して1時間攪拌した。室温まで冷却後、分液し水洗を2回実施し、吸引濾過によりアントラキノンを取り除き、濃縮を行った。濃縮液にメタノールを加えて晶析を行い、析出結晶を吸引濾過、乾燥することにより、収量26.6g(粗収率57mol%)の薄黄色の結晶を得た。
(2)IR(cm-1):2693,2922,2855,1750,1470,1436,1381,1368,1356,1274,1200,1164,1052,1006,976,951,780,711,677,608,581,400.
(3)1H-NMR(400MHz,CDCl3):δ=0.921(t,J=12.8Hz,6H),1.363-1.396(m,8H),1.696-1.747(m,4H),4.306(t,J=13.2Hz,4H),4.780(s,4H),7.505-7.536(m,4H),8.356-8.387(m,4H).
攪拌機、温度計付きの300mlの四つ口フラスコに、窒素雰囲気下で、ブロモ酢酸32.4g(234ミリモル)、シクロヘキサノール46.8g(467ミリモル)、溶媒のо-キシレン75.0g、触媒の硫酸1.5g(15ミリモル)を加えた。反応系の温度を140~150℃に保ち、共沸する水を除去しながら2時間攪拌した。室温まで冷却後、炭酸水素ナトリウム水溶液で中和し、水層を除いた。そこに触媒のテトラブチルアンモニウムブロマイドの50%水溶液を2.8g(4.4ミリモル)を加え、反応系の温度を35~40℃に保ちながら9,10-ジヒドロキシアントラセンのジナトリウム塩の18.7wt%水溶液100g(アントラキノンとして90ミリモル)を1時間かけて滴下した。滴下終了後、さらに1時間撹拌し、55~60℃まで昇温して1時間攪拌した。室温まで冷却後、吸引濾過によりアントラキノンを取り除き、分液し水洗を2回実施し、濃縮を行った。濃縮液にメタノールを加えて晶析を行い、析出結晶を吸引濾過、乾燥することにより、収量25.5g(粗収率54mol%)の薄黄色の結晶を得た。
(2)IR(cm-1):2930,2857,1745,1677,1621,1453,1438,1399,1369,1360,1206,1168,1086,1035,1006,954,922,891,813,715,693,672,659,608,585,455.
(3)1H-NMR(400MHz,CDCl3):δ=1.239-1.596(m,12H),1.754-1.786(m,4H),1.939-1.961(m,4H),4.760(s,4H),4.985-5.050(m,2H),7.501-7.526(m,4H),8.372-8.398(m,4H).
攪拌機、温度計付きの100mlの四つ口フラスコに、窒素雰囲気下で、触媒のテトラブチルアンモニウムブロマイドの50%水溶液を0.77g(1.19ミリモル)、5-ブロモ吉草酸エチルを12.9g(61.8ミリモル)、9,10-ジヒドロキシアントラセンを5.0g(23.8ミリモル)、炭酸カリウムを9.9g(71.4ミリモル)、溶媒のN,N-ジメチルホルムアミドを40g加えた。反応系の温度を20~30℃に保ちながら1時間撹拌した。その後、吸引濾過によりアントラキノンを取り除き、得られた濾液をトルエンに溶かし、分液操作により、2度水で洗浄した。エバポレーターで溶液を濃縮した。一晩放置し、メタノールを加え、溶解しなかったアントラキノンを吸引濾過により取り除いた。濾液を冷凍庫で冷却し結晶を析出させた。析出した結晶をさらに吸引濾過することにより、収量6.2g(粗収率55mol%)の橙色の結晶を得た。
(2)IR(cm-1):1722,1403,1337,1284,1269,1229,1178,1167,1068,1021,934,763,675.
(3)1H-NMR(400MHz,CDCl3):δ=1.286(t,J=14.4Hz,6H),2.018-2.103(m,8H),2.496(t,J=13.6Hz,4H),4.151-4.205(m,8H),7.463-7.487(m,4H),8.243-8.268(m,4H).
ラジカル重合性化合物としてシリコーンジアクリレートEbecryl350(ダイセル・オルネクス社製)100部に対し、光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)5部、ラジカル硬化酸素阻害低減剤として原料合成実施例1と同様にして合成した9,10-ビス(エトキシカルボニルメトキシ)アントラセン3部、界面活性剤・表面改質剤としてメガファックF-556(DIC社製)を数滴加え、撹拌し溶解させ、光ラジカル重合性組成物の液状物が得られた。当該光ラジカル重合性組成物を、アルミ板上にローラーバー(松尾産業社製Select-Roller L60 OSP-04)を用い、厚みが4μmになるように塗布し、窒素置換していない試料チャンバー内に設置した。該光ラジカル重合性組成物の塗膜に対し、光硬化性I/光硬化条件(1)の方法で光硬化判定を行った。評価波数として1409cm-1を用いた。硬化率は41%であった。結果を表1に記載した。
光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)の代わりに2,2-ジメトキシ-1,2-ジフェニルエタン-1-オン(商品名「イルガキュア651」ビー・エー・エス・エフ社製)を5部、ラジカル硬化酸素阻害低減剤として原料合成実施例1と同様にして合成した9,10-ビス(エトキシカルボニルメトキシ)アントラセンを4部添加し、光硬化判定I/光硬化条件(2)の方法にした以外は実施例1と同様な方法で光硬化判定を行った。評価波数として1409cm-1を用いた。硬化率は24%であった。結果を表1に記載した。
光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)の代わりに2-メチル-1-[4-メチルチオフェニル]-2-モルホリノプロパン-1-オン(商品名「イルガキュア907」ビー・エー・エス・エフ社製)を6部添加し、光硬化判定I/光硬化条件(3)の方法にした以外は実施例1と同様の方法で光硬化判定を行った。評価波数として1409cm-1を用いた。硬化率は35%であった。結果を表1に記載した。
光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)の代わりに2,4,6-トリメチルベンゾイルジフェニルフォスフィンオキシド(商品名「イルガキュアTPO」ビー・エー・エス・エフ社製)を4部添加し、光硬化判定I/光硬化条件(4)の方法にした以外は実施例1と同様の方法で光硬化判定を行った。評価波数として1409cm-1を用いた。硬化率は46%であった。結果を表1に記載した。
ラジカル重合性化合物としてトリメチロールプロパントリアクリレート(東京化成工業社製)100部に対し、光ラジカル重合開始剤として2,4,6-トリメチルベンゾイルジフェニルフォスフィンオキシド(商品名「イルガキュアTPO」ビー・エー・エス・エフ社製)4部、ラジカル硬化酸素阻害低減剤として原料合成実施例1と同様にして合成した9,10-ビス(エトキシカルボニルメトキシ)アントラセン3部、界面活性剤・表面改質剤としてメガファックF-556(DIC社製)を数滴加え、撹拌し溶解させ、光ラジカル重合性組成物の液状物が得られた。当該光ラジカル重合性組成物を、アルミ板上にローラーバー(松尾産業社製Select-Roller L60 OSP-04)を用い、厚みが4μmになるように塗布し、窒素置換していない試料チャンバー内に設置した。該光ラジカル重合性組成物の塗膜に対し、光硬化性I/光硬化条件(4)の方法で光硬化判定を行った。評価波数として1635cm-1を用いた。硬化率は53%であった。結果を表1に記載した。
光ラジカル重合開始剤として2,4,6-トリメチルベンゾイルジフェニルフォスフィンオキシド(商品名「イルガキュアTPO」ビー・エー・エス・エフ社製)8部、ラジカル硬化酸素阻害低減剤として原料合成実施例1と同様にして合成した9,10-ビス(エトキシカルボニルメトキシ)アントラセン2部、光硬化性I/光硬化条件(5)の方法にした以外は実施例5と同様な方法で光硬化判定を行った。評価波数として1635cm-1を用いた。硬化率は35%であった。結果を表1に記載した。
光ラジカル重合開始剤として2,4,6-トリメチルベンゾイルジフェニルフォスフィンオキシド(商品名「イルガキュアTPO」ビー・エー・エス・エフ社製)2部、1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)4部にした以外は実施例5と同様な方法で光硬化判定を行った。評価波数として1635cm-1を用いた。硬化率は43%であった。結果を表1に記載した。
光ラジカル開始剤として2,4,6-トリメチルベンゾイルジフェニルフォスフィンオキシド(商品名「イルガキュアTPO」ビー・エー・エス・エフ社製)を6部添加し、光硬化性I/光硬化条件(6)の方法にした以外は実施例7と同様な方法で光硬化判定を行った。評価波数として810cm-1を用いた。硬化率は39%であった。結果を表1に記載した。
ラジカル硬化酸素阻害低減剤を添加しない以外は実施例1~8と同様の方法で光硬化判定を行った。結果を表1に記載した。
測定雰囲気を窒素下にすること以外は比較例1と同様な方法で光硬化判定を行った。評価波数として1409cm-1を用いた。硬化率は58%であった。結果を表1に記載した。
測定雰囲気を窒素下にすること以外は比較例4と同様な方法で光硬化判定を行った。評価波数として1409cm-1を用いた。硬化率は62%であった。結果を表1に記載した。
ラジカル重合性化合物としてトリメチロールプロパントリアクリレート(東京化成工業社製)100部に対し、光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)5部、光ラジカル硬化酸素阻害低減剤として原料合成実施例1と同様にして合成した9,10-ビス(エトキシカルボニルメトキシ)アントラセン0.2部を加え撹拌し溶解させ、光ラジカル重合性組成物の液状物が得られた。当該光ラジカル重合性組成物について空気気流中でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は161mJ/mgであった。結果を表2に記載した。
光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)の代わりに2,2-ジメトキシ-1,2-ジフェニルエタン-1-オン(商品名「イルガキュア651」ビー・エー・エス・エフ社製)を5部添加した以外は実施例9と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は360mJ/mgであった。結果を表2に記載した。
光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)の代わりに2-ジメチルアミノ-1-(4-モルホリノフェニル)-2-ベンジル-1-ブタオン(商品名「イルガキュア369」ビー・エー・エス・エフ社製)を5部添加した以外は実施例9と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は497mJ/mgであった。結果を表2に記載した。
光ラジカル重合開始剤として1-ヒドロキシシクロヘキシルフェニルケトン(商品名「イルガキュア184」ビー・エー・エス・エフ社製)の代わりに4-イソブチルフェニル-4’-メチルフェニルヨードニウムヘキサフルオロフォスフェート(商品名「イルガキュア250」ビー・エー・エス・エフ社製)を4部、光ラジカル硬化酸素阻害低減剤として9,10-ビス(エトキシカルボニルメトキシ)アントラセン0.5部添加した以外は実施例9と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は364mJ/mgであった。結果を表2に記載した。
光ラジカル硬化酸素阻害低減剤として9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに原料合成実施例3と同様にして合成した9,10-ビス(シクロヘキシルオキシカルボニルメトキシ)アントラセン(cHCM-A)を0.2部添加した以外は実施例10と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は364mJ/mgであった。結果を表2に記載した。
光ラジカル硬化酸素阻害低減剤として9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに原料合成実施例2と同様にして合成した9,10-ビス(n-ペンチルオキシカルボニルメトキシ)アントラセン(ACM-A)を0.2部添加した以外は実施例10と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は334mJ/mgであった。結果を表2に記載した。
光ラジカル硬化酸素阻害低減剤として9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに原料合成実施例4と同様にして合成した9,10-ビス(エトキシカルボニルブチレンオキシ)アントラセン(ECB-A)を0.2部添加した以外は実施例10と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は328mJ/mgであった。結果を表2に記載した。
光ラジカル硬化酸素阻害低減剤を添加しないこと以外は実施例8、9、10、11と同様な方法でPhoto-DSC測定を行い、光照射から5分間の総発熱量を求めた。結果を表2に記載した。
光ラジカル硬化酸素阻害低減剤として添加した9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに、類似の化学構造を有し光重合増感剤として一般に添加されている公知の9,10-ジブトキシアントラセン(DBA)を0.2部添加した以外は実施例10と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は258mJ/mgであった。結果を表2に記載した。
窒素気流中で測定を行うこと以外は比較例12と同様の方法でPhoto-DSC測定を行い、総発熱量を求めた。光照射開始から5分間の総発熱量は339mJ/mgであった。結果を表2に記載した。
ラジカル重合性化合物として1,6-ヘキサンジオールジアクリレート(商品名「ビスコート#230」大阪有機化学工業社製)100部に対し、光ラジカル重合開始剤として2-(4-メトキシフェニル)-4,6-ビス(トリクロロメチル)-1,3,5-トリアジン(富士フィルム和光純薬社製)5部、ラジカル硬化酸素阻害低減剤として原料合成実施例1と同様にして合成した9,10-ビス(エトキシカルボニルメトキシ)アントラセン0.2部を加え撹拌し溶解させ、光ラジカル重合性組成物の液状物が得られた。当該光ラジカル重合性組成物についてPhoto-Rheometer測定を行い、貯蔵弾性率を求めた。光照射後140秒時点における貯蔵弾性率は2.45×106Paであった。結果を表3に記載した。
ラジカル硬化酸素阻害低減剤を添加しないこと以外は実施例16と同様な方法でPhoto-Rheometer測定を行い、貯蔵弾性率を求めた。結果を表3に記載した。
(組成物の耐マイグレーション性の判定)
本発明の光重合性組成物に含まれるラジカル硬化酸素阻害低減剤がフィルム等に移行(マイグレーション)するかどうかを判定する方法としては、ラジカル硬化酸素阻害低減剤を含む光重合性組成物を薄いフィルム状物に塗布したものを作成し、その上にポリエチレンフィルムを被せて一定温度(26℃)で一定期間保管し、その後ポリエチレンフィルムを剥がし、ラジカル硬化酸素阻害低減剤がポリエチレンフィルムに移行しているかを調べ、耐マイグレーション性を判定した。剥がしたポリエチレンフィルムは、アセトンで表面の組成物を洗った後乾燥し、当該ポリエチレンフィルムのUVスペクトルを測定し、ラジカル硬化酸素阻害低減剤に起因する吸収強度の増大を調べることにより耐マイグレーション性を測定した。なお、当該測定には、紫外・可視分光光度計(島津製作所製、型式:UV2600)を用いた。比較例の化合物である9,10-ジブトキシアントラセンと量的な比較するために、得られた吸光度を9,10-ジブトキシアントラセンの吸光度の値に換算した。換算に当たっては、紫外・可視分光光度計により本発明の化合物及び9,10-ジブトキシアントラセンの260nmにおける吸光度を測定し、その吸光度の値とモル濃度からそれぞれのモル吸光係数を計算し、その比をもちいて換算した。
(耐マイグレーション性評価実施例1)
光ラジカル重合性化合物として、トリメチロールプロパントリアクリレート100部、光ラジカル重合増感剤として、原料合成実施例1と同様の方法で合成した9,10-ビス(エトキシカルボニルメトキシ)アントラセン1部を混合し、調製した組成物をポリエステルフィルム上で膜厚が12ミクロンになるようにバーコーターを用いて塗布した。次いで、得られた塗布物上に低密度ポリエチレンフィルム(膜厚30ミクロン)を被せて、暗所で一日間保管したものと七日間保管したものを調製し、それぞれ保管後、被せたポリエチレンフィルムを剥がし、ポリエチレンフィルムをアセトンで洗い、乾燥した後、当該ポリエチレンフィルムのUVスペクトルを測定し、260nmの吸光度を測定したが、9,10-ビス(エトキシカルボニルメトキシ)アントラセンに起因する吸収は、一日保管後0.014、七日保管後0.015であった。
9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに原料合成実施例4と同様の方法で合成した9,10-ビス(エトキシカルボニルブチレンオキシ)アントラセンを使用すること以外は耐マイグレーション性評価実施例1と同様に調製して試験した。アセトン洗いしたポリエチレンフィルムの260nmの吸光度を測定したが、9,10-ビス(エトキシカルボニルブチレンオキシ)アントラセンに起因する吸収は、一日保管後0.022、七日保管後0.021であった。
9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに原料合成実施例2と同様の方法で合成した9,10-ビス(n-ペンチルオキシカルボニルメチレンオキシ)アントラセンを使用すること以外は耐マイグレーション性評価実施例1と同様に調製して試験した。アセトン洗いしたポリエチレンフィルムの260nmの吸光度を測定したが、9,10-ビス(n-ペンチルオキシカルボニルメチレンオキシ)アントラセンに起因する吸収は、一日保管後0.051、七日保管後0.032であった。
9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに原料合成実施例3と同様の方法で合成した9,10-ビス(シクロヘキシルオキシカルボニルメチレンオキシ)アントラセンを使用すること以外は耐マイグレーション性評価実施例1と同様に調製して試験した。アセトン洗いしたポリエチレンフィルムの260nmの吸光度を測定したが、9,10-ビス(シクロヘキシルオキシカルボニルメチレンオキシ)アントラセンに起因する吸収は、一日保管後0.051、七日保管後0.035であった。
9,10-ビス(エトキシカルボニルメトキシ)アントラセンの代わりに公知の光ラジカル増感剤である9,10-ジブトキシアントラセンを使用すること以外は耐マイグレーション性評価実施例1と同様にして試験した。アセトン洗いしたポリエチレンフィルムの260nmの吸光度を測定した結果、得られた9,10-ジブトキシアントラセンの吸光度は、一日保管後1.661、七日後1.741であった。
Claims (11)
- 下記一般式(1)で表されるエステル基を有する9,10-ビス(アルコキシカルボニルアルキレンオキシ)アントラセン化合物からなる、酸素によるラジカル重合阻害を低減できる光ラジカル硬化酸素阻害低減剤。
(一般式(1)において、Aは炭素数1から20のアルキレン基を表し、該アルキレン基はアルキル基によって分岐していてもよい。Rは炭素数1から20のアルキル基を表し、該アルキル基は、アルキル基によって分岐していてもよく、シクロアルキル基でもよく、ヒドロキシ基で置換されていてもよく、炭素原子の一部が酸素原子によって置き換わっていてもよい(但し、過酸化物を形成する場合は除く)。X、Yは同一であっても異なってもよく、水素原子、炭素数1から8のアルキル基又はハロゲン原子を表す。) - 少なくともラジカル重合性化合物、光ラジカル重合開始剤及び請求項1に記載の光ラジカル硬化酸素阻害低減剤を含有することを特徴とする、光ラジカル重合性組成物。
- 光ラジカル重合開始剤がα-ヒドロキシアセトフェノン系光ラジカル重合開始剤、ベンジルメチルケタール系光ラジカル重合開始剤、α-アミノアルキルフェノン系光ラジカル重合開始剤、アシルホスフィンオキサイド系光ラジカル重合開始剤、オニウム塩系光ラジカル重合開始剤又はトリアジン系光ラジカル重合開始剤であることを特徴とする、請求項2に記載の光ラジカル重合性組成物。
- 光ラジカル重合開始剤の含有量が、光ラジカル重合性組成物の総質量に対して2.0質量%以上10質量%以下であり、光ラジカル硬化酸素阻害低減剤の含有量が、光ラジカル重合性組成物の総質量に対して0.20質量%以上5.0質量%以下であることを特徴とする、請求項2又は3に記載の光ラジカル重合性組成物。
- 請求項2乃至4のいずれか一項に記載の光ラジカル重合性組成物よりなる塗膜であって、塗膜の一方の表面は大気に接触していることを特徴とする、光ラジカル重合性塗膜。
- 請求項2乃至4のいずれか一項に記載の光ラジカル重合性組成物を基材フィルム上に塗布してなる塗膜であって、塗膜の一方の表面は大気に接触していることを特徴とする、光ラジカル重合性塗膜。
- 請求項5又は6に記載の光ラジカル重合性塗膜の表面が大気に接触した状態で該塗膜にエネルギー線を照射することを特徴とする、光ラジカル重合性塗膜の硬化方法。
- 照射するエネルギー線が、360nm~410nmの波長範囲の光を含むエネルギー線であることを特徴とする、請求項7に記載の光ラジカル重合性塗膜の硬化方法。
- 360nm~410nmの波長範囲の光が、365nm、385nm、395nm若しくは405nmのいずれかひとつを中心波長とするLED光又は405nmの光を中心波長とする半導体レーザ光であることを特徴とする、請求項8に記載の光ラジカル重合性塗膜の硬化方法。
- LED光又は半導体レーザ光の照射強度が10mW/cm2以上2000mW/cm2未満であることを特徴とする、請求項9に記載の光ラジカル重合性塗膜の硬化方法。
- LED光又は半導体レーザ光の照射エネルギーが、50mJ/cm2以上10000mJ/cm2未満であることを特徴とする、請求項9又は10に記載の光ラジカル重合性塗膜の硬化方法。
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