JP7387267B2 - 多環芳香族骨格を有するエンドペルオキシド化合物 - Google Patents
多環芳香族骨格を有するエンドペルオキシド化合物 Download PDFInfo
- Publication number
- JP7387267B2 JP7387267B2 JP2019023018A JP2019023018A JP7387267B2 JP 7387267 B2 JP7387267 B2 JP 7387267B2 JP 2019023018 A JP2019023018 A JP 2019023018A JP 2019023018 A JP2019023018 A JP 2019023018A JP 7387267 B2 JP7387267 B2 JP 7387267B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- bis
- endoperoxide
- anthracene
- Prior art date
- 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.)
- Active
Links
- 150000001875 compounds Chemical class 0.000 title claims description 341
- 125000004432 carbon atom Chemical group C* 0.000 claims description 789
- 125000000217 alkyl group Chemical group 0.000 claims description 431
- 125000003118 aryl group Chemical group 0.000 claims description 305
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 97
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 94
- 239000000203 mixture Substances 0.000 claims description 90
- 125000005843 halogen group Chemical group 0.000 claims description 87
- 125000003545 alkoxy group Chemical group 0.000 claims description 67
- 239000001301 oxygen Substances 0.000 claims description 63
- 229910052760 oxygen Inorganic materials 0.000 claims description 63
- 238000006116 polymerization reaction Methods 0.000 claims description 62
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 61
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 54
- 125000001424 substituent group Chemical group 0.000 claims description 53
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 51
- 125000002947 alkylene group Chemical group 0.000 claims description 46
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 45
- 239000007870 radical polymerization initiator Substances 0.000 claims description 44
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 40
- 239000003505 polymerization initiator Substances 0.000 claims description 40
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 39
- 238000001723 curing Methods 0.000 claims description 38
- 238000000034 method Methods 0.000 claims description 36
- 238000004519 manufacturing process Methods 0.000 claims description 30
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 claims description 28
- 125000004104 aryloxy group Chemical group 0.000 claims description 28
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 27
- 125000005100 aryl amino carbonyl group Chemical group 0.000 claims description 27
- 125000000101 thioether group Chemical group 0.000 claims description 27
- 125000004849 alkoxymethyl group Chemical group 0.000 claims description 25
- 229910052717 sulfur Inorganic materials 0.000 claims description 23
- 238000000354 decomposition reaction Methods 0.000 claims description 20
- 229910001882 dioxygen Inorganic materials 0.000 claims description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims description 19
- 229920006395 saturated elastomer Polymers 0.000 claims description 19
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 17
- 125000004434 sulfur atom Chemical group 0.000 claims description 17
- 230000001678 irradiating effect Effects 0.000 claims description 16
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims description 15
- 125000003282 alkyl amino group Chemical group 0.000 claims description 14
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 14
- 125000001769 aryl amino group Chemical group 0.000 claims description 14
- 125000005199 aryl carbonyloxy group Chemical group 0.000 claims description 14
- 125000005200 aryloxy carbonyloxy group Chemical group 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 14
- 125000003277 amino group Chemical group 0.000 claims description 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 13
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 13
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims 4
- 238000007429 general method Methods 0.000 claims 1
- -1 oxime ester Chemical class 0.000 description 699
- SRWMCQYMZIZLAY-UHFFFAOYSA-N anthracene endoperoxide Chemical compound C12=CC=CC=C2C2OOC1C1=CC=CC=C12 SRWMCQYMZIZLAY-UHFFFAOYSA-N 0.000 description 478
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 205
- 238000006243 chemical reaction Methods 0.000 description 97
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 75
- 239000002253 acid Substances 0.000 description 55
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 49
- 239000002904 solvent Substances 0.000 description 43
- 238000005259 measurement Methods 0.000 description 39
- 238000010526 radical polymerization reaction Methods 0.000 description 37
- 230000007423 decrease Effects 0.000 description 35
- 239000000047 product Substances 0.000 description 33
- 150000003254 radicals Chemical class 0.000 description 32
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 27
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 24
- 229920001577 copolymer Polymers 0.000 description 23
- 239000003054 catalyst Substances 0.000 description 22
- 238000010438 heat treatment Methods 0.000 description 22
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 21
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 20
- 239000010408 film Substances 0.000 description 20
- 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 19
- 150000002148 esters Chemical class 0.000 description 19
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 229910052799 carbon Inorganic materials 0.000 description 16
- 239000000178 monomer Substances 0.000 description 16
- 150000002978 peroxides Chemical class 0.000 description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 15
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 150000004820 halides Chemical class 0.000 description 15
- 230000005764 inhibitory process Effects 0.000 description 15
- 239000003444 phase transfer catalyst Substances 0.000 description 15
- 239000002994 raw material Substances 0.000 description 15
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- 150000007514 bases Chemical class 0.000 description 14
- 239000000243 solution Substances 0.000 description 14
- 125000004430 oxygen atom Chemical group O* 0.000 description 13
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
- 230000003287 optical effect Effects 0.000 description 12
- 230000035484 reaction time Effects 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 11
- 230000005283 ground state Effects 0.000 description 11
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 10
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 10
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 10
- 125000000732 arylene group Chemical group 0.000 description 10
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 10
- 239000013078 crystal Substances 0.000 description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 125000001624 naphthyl group Chemical group 0.000 description 10
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 10
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- 229910052782 aluminium Inorganic materials 0.000 description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 9
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 9
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 9
- 239000003999 initiator Substances 0.000 description 9
- 230000000977 initiatory effect Effects 0.000 description 9
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 9
- 239000012299 nitrogen atmosphere Substances 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 8
- FKNQCJSGGFJEIZ-UHFFFAOYSA-N 4-methylpyridine Chemical compound CC1=CC=NC=C1 FKNQCJSGGFJEIZ-UHFFFAOYSA-N 0.000 description 8
- KSMGAOMUPSQGTB-UHFFFAOYSA-N 9,10-dibutoxyanthracene Chemical compound C1=CC=C2C(OCCCC)=C(C=CC=C3)C3=C(OCCCC)C2=C1 KSMGAOMUPSQGTB-UHFFFAOYSA-N 0.000 description 8
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 8
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 8
- 239000003638 chemical reducing agent Substances 0.000 description 8
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 8
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 8
- 238000004821 distillation Methods 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 8
- 229910052753 mercury Inorganic materials 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 230000005012 migration Effects 0.000 description 8
- 238000013508 migration Methods 0.000 description 8
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 8
- 239000011701 zinc Substances 0.000 description 8
- 239000004698 Polyethylene Substances 0.000 description 7
- 239000012535 impurity Substances 0.000 description 7
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- 229920001451 polypropylene glycol Polymers 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 6
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 6
- 239000004210 ether based solvent Substances 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 150000007529 inorganic bases Chemical class 0.000 description 6
- 239000005453 ketone based solvent Substances 0.000 description 6
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 5
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 5
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-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
- 150000001454 anthracenes Chemical class 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000003849 aromatic solvent Substances 0.000 description 5
- VZWMKHUMEIECPK-UHFFFAOYSA-M benzyl-dimethyl-octadecylazanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 VZWMKHUMEIECPK-UHFFFAOYSA-M 0.000 description 5
- 230000001588 bifunctional effect Effects 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 5
- 150000001721 carbon Chemical class 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 229910017052 cobalt Inorganic materials 0.000 description 5
- 239000010941 cobalt Substances 0.000 description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 5
- 238000004440 column chromatography Methods 0.000 description 5
- 150000001993 dienes Chemical class 0.000 description 5
- 125000005442 diisocyanate group Chemical group 0.000 description 5
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 5
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 5
- QLPMKRZYJPNIRP-UHFFFAOYSA-M methyl(trioctyl)azanium;bromide Chemical compound [Br-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC QLPMKRZYJPNIRP-UHFFFAOYSA-M 0.000 description 5
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 5
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 230000000379 polymerizing effect Effects 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- 238000007086 side reaction Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 5
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 5
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 5
- YMBCJWGVCUEGHA-UHFFFAOYSA-M tetraethylammonium chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC YMBCJWGVCUEGHA-UHFFFAOYSA-M 0.000 description 5
- DDFYFBUWEBINLX-UHFFFAOYSA-M tetramethylammonium bromide Chemical compound [Br-].C[N+](C)(C)C DDFYFBUWEBINLX-UHFFFAOYSA-M 0.000 description 5
- BGQMOFGZRJUORO-UHFFFAOYSA-M tetrapropylammonium bromide Chemical compound [Br-].CCC[N+](CCC)(CCC)CCC BGQMOFGZRJUORO-UHFFFAOYSA-M 0.000 description 5
- FBEVECUEMUUFKM-UHFFFAOYSA-M tetrapropylazanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CCC FBEVECUEMUUFKM-UHFFFAOYSA-M 0.000 description 5
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 5
- 150000003606 tin compounds Chemical class 0.000 description 5
- 229910052723 transition metal Inorganic materials 0.000 description 5
- 150000003624 transition metals Chemical class 0.000 description 5
- PIVZYJMLIVYZJA-UHFFFAOYSA-M trioctyl(propyl)azanium;bromide Chemical compound [Br-].CCCCCCCC[N+](CCC)(CCCCCCCC)CCCCCCCC PIVZYJMLIVYZJA-UHFFFAOYSA-M 0.000 description 5
- WFEXFNMTEBFLMM-UHFFFAOYSA-M trioctyl(propyl)azanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](CCC)(CCCCCCCC)CCCCCCCC WFEXFNMTEBFLMM-UHFFFAOYSA-M 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 4
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical class OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 4
- UJKPHYRXOLRVJJ-MLSVHJFASA-N CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C Chemical compound CC(O)C1=C(C)/C2=C/C3=N/C(=C\C4=C(CCC(O)=O)C(C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C)=C4C(C)O)/C(CCC(O)=O)=C3C UJKPHYRXOLRVJJ-MLSVHJFASA-N 0.000 description 4
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 4
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 4
- 229920000557 Nafion® Polymers 0.000 description 4
- 244000028419 Styrax benzoin Species 0.000 description 4
- 235000000126 Styrax benzoin Nutrition 0.000 description 4
- 235000008411 Sumatra benzointree Nutrition 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 125000005336 allyloxy group Chemical group 0.000 description 4
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 4
- 125000005577 anthracene group Chemical group 0.000 description 4
- 238000013459 approach Methods 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical class C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 4
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 4
- 239000012975 dibutyltin dilaurate Substances 0.000 description 4
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 4
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 4
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 4
- 230000005281 excited state Effects 0.000 description 4
- 235000019382 gum benzoic Nutrition 0.000 description 4
- 229960003569 hematoporphyrin Drugs 0.000 description 4
- 230000001771 impaired effect Effects 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 238000002955 isolation Methods 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 235000010755 mineral Nutrition 0.000 description 4
- DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 4
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 230000033116 oxidation-reduction process Effects 0.000 description 4
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 4
- 125000003944 tolyl group Chemical group 0.000 description 4
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 4
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 4
- QMLVEJFOUZCQQS-UHFFFAOYSA-N (10-butoxycarbonyloxy-2-ethylanthracen-9-yl) butyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCC)OC(=O)OCCCC QMLVEJFOUZCQQS-UHFFFAOYSA-N 0.000 description 3
- PMWXZQSELLEALJ-UHFFFAOYSA-N (2,3-dimethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OCCC)OC(=O)OCCC PMWXZQSELLEALJ-UHFFFAOYSA-N 0.000 description 3
- SZGADKNUNVAETK-UHFFFAOYSA-N (2-ethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCC)OC(=O)OCCC SZGADKNUNVAETK-UHFFFAOYSA-N 0.000 description 3
- ANQYUEFMBQGSKM-UHFFFAOYSA-N (4-butoxycarbonyloxy-2,3-dimethylnaphthalen-1-yl) butyl carbonate Chemical compound CCCCOC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)OCCCC)C)C ANQYUEFMBQGSKM-UHFFFAOYSA-N 0.000 description 3
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical group CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- BTJPUDCSZVCXFQ-UHFFFAOYSA-N 2,4-diethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC(CC)=C3SC2=C1 BTJPUDCSZVCXFQ-UHFFFAOYSA-N 0.000 description 3
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 3
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- CPDFPYSTXOKONN-UHFFFAOYSA-N 9,10-dipentoxy-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC)OCCCCC CPDFPYSTXOKONN-UHFFFAOYSA-N 0.000 description 3
- LBQJFQVDEJMUTF-UHFFFAOYSA-N 9,10-dipropoxyanthracene Chemical compound C1=CC=C2C(OCCC)=C(C=CC=C3)C3=C(OCCC)C2=C1 LBQJFQVDEJMUTF-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 239000002841 Lewis acid Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 239000012965 benzophenone Substances 0.000 description 3
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 3
- 229920001429 chelating resin Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- OZLBDYMWFAHSOQ-UHFFFAOYSA-N diphenyliodanium Chemical class C=1C=CC=CC=1[I+]C1=CC=CC=C1 OZLBDYMWFAHSOQ-UHFFFAOYSA-N 0.000 description 3
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000000295 emission spectrum Methods 0.000 description 3
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 3
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 3
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- 239000001530 fumaric acid Substances 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 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 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 3
- 150000007517 lewis acids Chemical class 0.000 description 3
- 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 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910001507 metal halide Inorganic materials 0.000 description 3
- 150000005309 metal halides Chemical class 0.000 description 3
- 229940098779 methanesulfonic acid Drugs 0.000 description 3
- ZEIWWVGGEOHESL-UHFFFAOYSA-N methanol;titanium Chemical compound [Ti].OC.OC.OC.OC ZEIWWVGGEOHESL-UHFFFAOYSA-N 0.000 description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 3
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 3
- 229960000907 methylthioninium chloride Drugs 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 3
- 150000003003 phosphines Chemical class 0.000 description 3
- 150000004714 phosphonium salts Chemical class 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 3
- 229910000105 potassium hydride Inorganic materials 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- RLJWTAURUFQFJP-UHFFFAOYSA-N propan-2-ol;titanium Chemical compound [Ti].CC(C)O.CC(C)O.CC(C)O.CC(C)O RLJWTAURUFQFJP-UHFFFAOYSA-N 0.000 description 3
- 229930187593 rose bengal Natural products 0.000 description 3
- 229940081623 rose bengal Drugs 0.000 description 3
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 230000001235 sensitizing effect Effects 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 239000012312 sodium hydride Substances 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 239000011973 solid acid Substances 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- WLOQLWBIJZDHET-UHFFFAOYSA-N triphenylsulfonium Chemical class C1=CC=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 WLOQLWBIJZDHET-UHFFFAOYSA-N 0.000 description 3
- 229910052724 xenon Inorganic materials 0.000 description 3
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- OBKAPNBVQRIESX-UHFFFAOYSA-N (1,5-diethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCCC)CC)OC(=O)OCCCCC OBKAPNBVQRIESX-UHFFFAOYSA-N 0.000 description 2
- DUPLYGFCVAMUBN-UHFFFAOYSA-N (1,5-diethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCC)CC)OC(=O)OCCC DUPLYGFCVAMUBN-UHFFFAOYSA-N 0.000 description 2
- AHVVTQMXJYPZEE-UHFFFAOYSA-N (1,5-dimethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound CC1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCCCCCC)C)OC(=O)OCCCCCCCC AHVVTQMXJYPZEE-UHFFFAOYSA-N 0.000 description 2
- FYPMMVCUYHHMDL-UHFFFAOYSA-N (1,5-dimethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound CC1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCCC)C)OC(=O)OCCCCC FYPMMVCUYHHMDL-UHFFFAOYSA-N 0.000 description 2
- YHYQARHERJNHGZ-UHFFFAOYSA-N (1,5-dimethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound CC1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCC)C)OC(=O)OCCC YHYQARHERJNHGZ-UHFFFAOYSA-N 0.000 description 2
- NUMNPTVZWVXURK-UHFFFAOYSA-N (1-ethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCC)OC(=O)OCCCCC NUMNPTVZWVXURK-UHFFFAOYSA-N 0.000 description 2
- SJIWVHAPKILWRL-UHFFFAOYSA-N (1-ethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCC)OC(=O)OCCC SJIWVHAPKILWRL-UHFFFAOYSA-N 0.000 description 2
- ACKUVGREPZUNCR-UHFFFAOYSA-N (1-methyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCC)OC(=O)OCCCCC ACKUVGREPZUNCR-UHFFFAOYSA-N 0.000 description 2
- CJZXSZGTPPUGBG-UHFFFAOYSA-N (10-acetyloxy-2,6-dimethylanthracen-9-yl) acetate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(C)=O)C)OC(C)=O CJZXSZGTPPUGBG-UHFFFAOYSA-N 0.000 description 2
- CTOSPCGRZKPFTA-UHFFFAOYSA-N (10-butanoyloxyanthracen-9-yl) butanoate Chemical compound C(CCC)(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OC(CCC)=O CTOSPCGRZKPFTA-UHFFFAOYSA-N 0.000 description 2
- XBQLWGMSQVDUCP-UHFFFAOYSA-N (10-butoxycarbonyloxy-1,5-diethylanthracen-9-yl) butyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCC)CC)OC(=O)OCCCC XBQLWGMSQVDUCP-UHFFFAOYSA-N 0.000 description 2
- BURWNARUFSPNIO-UHFFFAOYSA-N (10-butoxycarbonyloxy-1-ethylanthracen-9-yl) butyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCC)OC(=O)OCCCC BURWNARUFSPNIO-UHFFFAOYSA-N 0.000 description 2
- CVUDLOPTZQZAKG-UHFFFAOYSA-N (10-butoxycarbonyloxy-1-methylanthracen-9-yl) butyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCC)OC(=O)OCCCC CVUDLOPTZQZAKG-UHFFFAOYSA-N 0.000 description 2
- WGEAIXAVTXYFAI-UHFFFAOYSA-N (10-butoxycarbonyloxy-2,3-diethylanthracen-9-yl) butyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OCCCC)OC(=O)OCCCC WGEAIXAVTXYFAI-UHFFFAOYSA-N 0.000 description 2
- VGAUINDVHNFOMK-UHFFFAOYSA-N (10-butoxycarbonyloxy-2,3-dimethylanthracen-9-yl) butyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OCCCC)OC(=O)OCCCC VGAUINDVHNFOMK-UHFFFAOYSA-N 0.000 description 2
- DZIIIOIUDDUCEM-UHFFFAOYSA-N (10-butoxycarbonyloxy-2,6-diethylanthracen-9-yl) butyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCC)CC)OC(=O)OCCCC DZIIIOIUDDUCEM-UHFFFAOYSA-N 0.000 description 2
- UPKKYKXTCQXBRG-UHFFFAOYSA-N (10-butoxycarbonyloxy-2,6-dimethylanthracen-9-yl) butyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCC)C)OC(=O)OCCCC UPKKYKXTCQXBRG-UHFFFAOYSA-N 0.000 description 2
- XTSWWXVMMUDLHI-UHFFFAOYSA-N (10-butoxycarbonyloxy-2,7-diethylanthracen-9-yl) butyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCC)CC)OC(=O)OCCCC XTSWWXVMMUDLHI-UHFFFAOYSA-N 0.000 description 2
- IUZOIXWJLZRABJ-UHFFFAOYSA-N (10-butoxycarbonyloxy-2,7-dimethylanthracen-9-yl) butyl carbonate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCC)C)OC(=O)OCCCC IUZOIXWJLZRABJ-UHFFFAOYSA-N 0.000 description 2
- YLJPCNRZUKELDL-UHFFFAOYSA-N (10-butoxycarbonyloxy-2-methylanthracen-9-yl) butyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCC)OC(=O)OCCCC YLJPCNRZUKELDL-UHFFFAOYSA-N 0.000 description 2
- DFMJWQFCLBTBHC-UHFFFAOYSA-N (10-butoxycarbonyloxyanthracen-9-yl) butyl carbonate Chemical compound C(CCC)OC(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(=O)OCCCC DFMJWQFCLBTBHC-UHFFFAOYSA-N 0.000 description 2
- KJHNPUUNMOBRJK-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2,7-dimethylanthracen-9-yl) ethyl carbonate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCC)C)OC(=O)OCC KJHNPUUNMOBRJK-UHFFFAOYSA-N 0.000 description 2
- CQKSANNIOARKJR-UHFFFAOYSA-N (10-methoxycarbonyloxy-2-methylanthracen-9-yl) methyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OC)OC(=O)OC CQKSANNIOARKJR-UHFFFAOYSA-N 0.000 description 2
- QPCMKVGYDGXROK-UHFFFAOYSA-N (10-octanoyloxyanthracen-9-yl) octanoate Chemical compound C(CCCCCCC)(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(CCCCCCC)=O QPCMKVGYDGXROK-UHFFFAOYSA-N 0.000 description 2
- QXAZPMRFRYUEEP-UHFFFAOYSA-N (10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound C(CCCC)OC(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(=O)OCCCCC QXAZPMRFRYUEEP-UHFFFAOYSA-N 0.000 description 2
- LAJCSHRWLHTXHK-UHFFFAOYSA-N (10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound C(CC)OC(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(=O)OCCC LAJCSHRWLHTXHK-UHFFFAOYSA-N 0.000 description 2
- KHTNKEAKUIDVLR-UHFFFAOYSA-N (2,3-diethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OCCCCC)OC(=O)OCCCCC KHTNKEAKUIDVLR-UHFFFAOYSA-N 0.000 description 2
- NTFBYHUZHOJQNR-UHFFFAOYSA-N (2,3-diethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OCCC)OC(=O)OCCC NTFBYHUZHOJQNR-UHFFFAOYSA-N 0.000 description 2
- QVJHPTHERLPAMS-UHFFFAOYSA-N (2,3-dimethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OCCCCC)OC(=O)OCCCCC QVJHPTHERLPAMS-UHFFFAOYSA-N 0.000 description 2
- VPMHEHSPHJBQTG-UHFFFAOYSA-N (2,3-dimethyl-4-pentoxycarbonyloxynaphthalen-1-yl) pentyl carbonate Chemical compound CCCCCOC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)OCCCCC)C)C VPMHEHSPHJBQTG-UHFFFAOYSA-N 0.000 description 2
- BDOXDENDJWJYNQ-UHFFFAOYSA-N (2,3-dimethyl-4-propoxycarbonyloxynaphthalen-1-yl) propyl carbonate Chemical compound CCCOC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)OCCC)C)C BDOXDENDJWJYNQ-UHFFFAOYSA-N 0.000 description 2
- WOFXDFLJBGWMLO-UHFFFAOYSA-N (2,6-diethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCC)CC)OC(=O)OCCCCC WOFXDFLJBGWMLO-UHFFFAOYSA-N 0.000 description 2
- SFKRBGDCYYISJB-UHFFFAOYSA-N (2,6-diethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCC)CC)OC(=O)OCCC SFKRBGDCYYISJB-UHFFFAOYSA-N 0.000 description 2
- OYXPPSJBYOMLOY-UHFFFAOYSA-N (2,6-dimethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCC)C)OC(=O)OCCCCC OYXPPSJBYOMLOY-UHFFFAOYSA-N 0.000 description 2
- FGRQEYZFYCKOOQ-UHFFFAOYSA-N (2,6-dimethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCC)C)OC(=O)OCCC FGRQEYZFYCKOOQ-UHFFFAOYSA-N 0.000 description 2
- SRKYIENLLDOECI-UHFFFAOYSA-N (2,7-diethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCCC)CC)OC(=O)OCCCCC SRKYIENLLDOECI-UHFFFAOYSA-N 0.000 description 2
- KJFFYBGQHMFUMW-UHFFFAOYSA-N (2,7-diethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCC)CC)OC(=O)OCCC KJFFYBGQHMFUMW-UHFFFAOYSA-N 0.000 description 2
- KXJLRNDOHJNJII-UHFFFAOYSA-N (2,7-dimethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCCC)C)OC(=O)OCCCCC KXJLRNDOHJNJII-UHFFFAOYSA-N 0.000 description 2
- CTXGEKNCOHBURA-UHFFFAOYSA-N (2,7-dimethyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCC)C)OC(=O)OCCC CTXGEKNCOHBURA-UHFFFAOYSA-N 0.000 description 2
- JAIVSAVQGDKPEP-UHFFFAOYSA-N (2-ethyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCCC)OC(=O)OCCCCC JAIVSAVQGDKPEP-UHFFFAOYSA-N 0.000 description 2
- KVASGYWZMLLKOA-UHFFFAOYSA-N (2-methoxy-4-propoxycarbonyloxynaphthalen-1-yl) propyl carbonate Chemical compound C1=CC=C2C(OC(=O)OCCC)=CC(OC)=C(OC(=O)OCCC)C2=C1 KVASGYWZMLLKOA-UHFFFAOYSA-N 0.000 description 2
- VDTVLBAIZIZQEV-UHFFFAOYSA-N (2-methyl-10-pentoxycarbonyloxyanthracen-9-yl) pentyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCCC)OC(=O)OCCCCC VDTVLBAIZIZQEV-UHFFFAOYSA-N 0.000 description 2
- YAVOTMCURKQFIE-UHFFFAOYSA-N (2-methyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCC)OC(=O)OCCC YAVOTMCURKQFIE-UHFFFAOYSA-N 0.000 description 2
- ZGINBVSHSNEZGE-UHFFFAOYSA-N (2-methyl-4-pentoxycarbonyloxynaphthalen-1-yl) pentyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OCCCCC)OC(=O)OCCCCC ZGINBVSHSNEZGE-UHFFFAOYSA-N 0.000 description 2
- DQRWKBRCQABNKO-UHFFFAOYSA-N (2-methyl-4-propoxycarbonyloxynaphthalen-1-yl) propyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OCCC)OC(=O)OCCC DQRWKBRCQABNKO-UHFFFAOYSA-N 0.000 description 2
- WBYXBGFPUUAGNG-UHFFFAOYSA-N (2-phenoxy-4-propoxycarbonyloxynaphthalen-1-yl) propyl carbonate Chemical compound CCCOC(=O)OC=1C2=CC=CC=C2C(OC(=O)OCCC)=CC=1OC1=CC=CC=C1 WBYXBGFPUUAGNG-UHFFFAOYSA-N 0.000 description 2
- SUWOZSBZQABDLA-UHFFFAOYSA-N (3,6-dimethyl-10-octanoyloxyanthracen-9-yl) octanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(CCCCCCC)=O)C)OC(CCCCCCC)=O SUWOZSBZQABDLA-UHFFFAOYSA-N 0.000 description 2
- SFAVMNCWIUOBCX-UHFFFAOYSA-N (4-acetyloxynaphthalen-1-yl) acetate Chemical compound C1=CC=C2C(OC(=O)C)=CC=C(OC(C)=O)C2=C1 SFAVMNCWIUOBCX-UHFFFAOYSA-N 0.000 description 2
- ABIPXDIEZAOXFM-UHFFFAOYSA-N (4-butoxycarbonyloxy-2-methoxynaphthalen-1-yl) butyl carbonate Chemical compound C1=CC=C2C(OC(=O)OCCCC)=CC(OC)=C(OC(=O)OCCCC)C2=C1 ABIPXDIEZAOXFM-UHFFFAOYSA-N 0.000 description 2
- NNLOXNRIEOTUBW-UHFFFAOYSA-N (4-butoxycarbonyloxy-2-methylnaphthalen-1-yl) butyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OCCCC)OC(=O)OCCCC NNLOXNRIEOTUBW-UHFFFAOYSA-N 0.000 description 2
- DQDRCIXVHIYDLV-UHFFFAOYSA-N (4-butoxycarbonyloxy-2-phenoxynaphthalen-1-yl) butyl carbonate Chemical compound CCCCOC(=O)OC=1C2=CC=CC=C2C(OC(=O)OCCCC)=CC=1OC1=CC=CC=C1 DQDRCIXVHIYDLV-UHFFFAOYSA-N 0.000 description 2
- IFLPEERWSBAABM-UHFFFAOYSA-N (4-butoxycarbonyloxynaphthalen-1-yl) butyl carbonate Chemical compound C(CCC)OC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCCCC IFLPEERWSBAABM-UHFFFAOYSA-N 0.000 description 2
- URHNCJTUFFEWLS-UHFFFAOYSA-N (4-hexanoyloxynaphthalen-1-yl) hexanoate Chemical compound C(CCCCC)(=O)OC1=CC=C(C2=CC=CC=C12)OC(CCCCC)=O URHNCJTUFFEWLS-UHFFFAOYSA-N 0.000 description 2
- HCXHEMYLUPIHKS-UHFFFAOYSA-N (4-pentoxycarbonyloxynaphthalen-1-yl) pentyl carbonate Chemical compound C(CCCC)OC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCCCCC HCXHEMYLUPIHKS-UHFFFAOYSA-N 0.000 description 2
- LZDCGCQTFDILIX-UHFFFAOYSA-N (4-propoxycarbonyloxynaphthalen-1-yl) propyl carbonate Chemical compound C(CC)OC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCCC LZDCGCQTFDILIX-UHFFFAOYSA-N 0.000 description 2
- ZBOWSUWXPQRALP-VOTSOKGWSA-N (E)-4-hexan-3-yloxy-4-oxobut-2-enoic acid Chemical compound CCCC(CC)OC(=O)\C=C\C(O)=O ZBOWSUWXPQRALP-VOTSOKGWSA-N 0.000 description 2
- UTOVMEACOLCUCK-SNAWJCMRSA-N (e)-4-butoxy-4-oxobut-2-enoic acid Chemical compound CCCCOC(=O)\C=C\C(O)=O UTOVMEACOLCUCK-SNAWJCMRSA-N 0.000 description 2
- XLYMOEINVGRTEX-ONEGZZNKSA-N (e)-4-ethoxy-4-oxobut-2-enoic acid Chemical compound CCOC(=O)\C=C\C(O)=O XLYMOEINVGRTEX-ONEGZZNKSA-N 0.000 description 2
- WYZRFRHDHZZWIH-UHFFFAOYSA-N 1,2,4-trimethoxynaphthalene Chemical compound C1=CC=CC2=C(OC)C(OC)=CC(OC)=C21 WYZRFRHDHZZWIH-UHFFFAOYSA-N 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical class O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 2
- NEQWFYFHAJZWTN-UHFFFAOYSA-N 1,4-dibutoxy-2,3-dichloronaphthalene Chemical compound CCCCOC1=C(C(=C(C2=CC=CC=C21)OCCCC)Cl)Cl NEQWFYFHAJZWTN-UHFFFAOYSA-N 0.000 description 2
- GXMCMFFCYOVCFE-UHFFFAOYSA-N 1,4-dibutoxy-2,3-dimethylnaphthalene Chemical compound CC1=C(C2=CC=CC=C2C(=C1C)OCCCC)OCCCC GXMCMFFCYOVCFE-UHFFFAOYSA-N 0.000 description 2
- LMGXWLAVDFVNGY-UHFFFAOYSA-N 1,4-dibutoxy-2-methoxynaphthalene Chemical compound CCCCOC1=CC(OC)=C(OCCCC)C2=CC=CC=C12 LMGXWLAVDFVNGY-UHFFFAOYSA-N 0.000 description 2
- WFCCFQHLUGACLN-UHFFFAOYSA-N 1,4-dibutoxy-2-methylnaphthalene Chemical compound C1=CC=C2C(OCCCC)=CC(C)=C(OCCCC)C2=C1 WFCCFQHLUGACLN-UHFFFAOYSA-N 0.000 description 2
- UNLREXPYKSFZKK-UHFFFAOYSA-N 1,4-dibutoxy-2-phenoxynaphthalene Chemical compound CCCCOC1=CC(OC2=CC=CC=C2)=C(OCCCC)C2=CC=CC=C12 UNLREXPYKSFZKK-UHFFFAOYSA-N 0.000 description 2
- UKXGGMCMWNJILJ-UHFFFAOYSA-N 1,4-dibutoxynaphthalene Chemical compound C1=CC=C2C(OCCCC)=CC=C(OCCCC)C2=C1 UKXGGMCMWNJILJ-UHFFFAOYSA-N 0.000 description 2
- BWTYYHQMBWFSIM-UHFFFAOYSA-N 1,4-dipentoxynaphthalene Chemical compound C1=CC=C2C(OCCCCC)=CC=C(OCCCCC)C2=C1 BWTYYHQMBWFSIM-UHFFFAOYSA-N 0.000 description 2
- JJPJWPYRFJDRMH-UHFFFAOYSA-N 1,4-dipropoxynaphthalene Chemical compound C1=CC=C2C(OCCC)=CC=C(OCCC)C2=C1 JJPJWPYRFJDRMH-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 2
- KSGRJPSEWMJZIQ-UHFFFAOYSA-N 2,3-dimethyl-1,4-dipropoxynaphthalene Chemical compound CC1=C(C2=CC=CC=C2C(=C1C)OCCC)OCCC KSGRJPSEWMJZIQ-UHFFFAOYSA-N 0.000 description 2
- BRKORVYTKKLNKX-UHFFFAOYSA-N 2,4-di(propan-2-yl)thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC(C(C)C)=C3SC2=C1 BRKORVYTKKLNKX-UHFFFAOYSA-N 0.000 description 2
- LZDYZEGISBDSDP-UHFFFAOYSA-N 2-(1-ethylaziridin-1-ium-1-yl)ethanol Chemical compound OCC[N+]1(CC)CC1 LZDYZEGISBDSDP-UHFFFAOYSA-N 0.000 description 2
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- QRYJSYJDUNCUSN-UHFFFAOYSA-N 2-chloro-9,10-dihexoxyanthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCC)OCCCCCC QRYJSYJDUNCUSN-UHFFFAOYSA-N 0.000 description 2
- SQLIUQWZSOABAR-UHFFFAOYSA-N 2-chloro-9,10-dimethoxyanthracene Chemical compound ClC1=CC=C2C(OC)=C(C=CC=C3)C3=C(OC)C2=C1 SQLIUQWZSOABAR-UHFFFAOYSA-N 0.000 description 2
- UPBFJTRWIYZMQM-UHFFFAOYSA-N 2-chloro-9,10-dipentoxyanthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC)OCCCCC UPBFJTRWIYZMQM-UHFFFAOYSA-N 0.000 description 2
- XQPXFSLLKDXHKG-UHFFFAOYSA-N 2-chloro-9,10-dipropoxyanthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCC)OCCC XQPXFSLLKDXHKG-UHFFFAOYSA-N 0.000 description 2
- 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 2
- AKVUWTYSNLGBJY-UHFFFAOYSA-N 2-methyl-1-morpholin-4-ylprop-2-en-1-one Chemical compound CC(=C)C(=O)N1CCOCC1 AKVUWTYSNLGBJY-UHFFFAOYSA-N 0.000 description 2
- QXXNMRUAOIMQIV-UHFFFAOYSA-N 2-methyl-9,10-dipentoxyanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC)OCCCCC QXXNMRUAOIMQIV-UHFFFAOYSA-N 0.000 description 2
- WXUAQHNMJWJLTG-UHFFFAOYSA-N 2-methylbutanedioic acid Chemical compound OC(=O)C(C)CC(O)=O WXUAQHNMJWJLTG-UHFFFAOYSA-N 0.000 description 2
- QUSQNJIYPQNHOF-UHFFFAOYSA-N 2-pentyl-9,10-dipropoxyanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCC)OCCC QUSQNJIYPQNHOF-UHFFFAOYSA-N 0.000 description 2
- OALHHIHQOFIMEF-UHFFFAOYSA-N 3',6'-dihydroxy-2',4',5',7'-tetraiodo-3h-spiro[2-benzofuran-1,9'-xanthene]-3-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 OALHHIHQOFIMEF-UHFFFAOYSA-N 0.000 description 2
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 2
- LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 2
- MOTVYDVWODTRDF-UHFFFAOYSA-N 3-[7,12,17-tris(2-carboxyethyl)-3,8,13,18-tetrakis(carboxymethyl)-21,22-dihydroporphyrin-2-yl]propanoic acid Chemical compound N1C(C=C2C(=C(CC(O)=O)C(=CC=3C(=C(CC(O)=O)C(=C4)N=3)CCC(O)=O)N2)CCC(O)=O)=C(CC(O)=O)C(CCC(O)=O)=C1C=C1C(CC(O)=O)=C(CCC(=O)O)C4=N1 MOTVYDVWODTRDF-UHFFFAOYSA-N 0.000 description 2
- ZYLCBTRJEVHWKT-UHFFFAOYSA-N 3-phenyl-23H-porphyrin-2,18,20,21-tetracarboxylic acid zinc Chemical compound [Zn].OC(=O)C=1C(N2C(O)=O)=C(C(O)=O)C(=N3)C(C(=O)O)=CC3=CC(N3)=CC=C3C=C(N=3)C=CC=3C=C2C=1C1=CC=CC=C1 ZYLCBTRJEVHWKT-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- FUGYGGDSWSUORM-UHFFFAOYSA-N 4-hydroxystyrene Chemical compound OC1=CC=C(C=C)C=C1 FUGYGGDSWSUORM-UHFFFAOYSA-N 0.000 description 2
- SAPSSEZANLAVRT-UHFFFAOYSA-N 9,10-dibutoxy-1,2,3,4-tetrahydroanthracene Chemical compound C(CCC)OC=1C2=CC=CC=C2C(=C2CCCCC=12)OCCCC SAPSSEZANLAVRT-UHFFFAOYSA-N 0.000 description 2
- ULPWEKNQGYLSSF-UHFFFAOYSA-N 9,10-dibutoxy-1,4-dihydroanthracene Chemical compound C1=CC=C2C(OCCCC)=C(CC=CC3)C3=C(OCCCC)C2=C1 ULPWEKNQGYLSSF-UHFFFAOYSA-N 0.000 description 2
- UXUKHLWXSAOMCN-UHFFFAOYSA-N 9,10-dibutoxy-2-chloroanthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCC)OCCCC UXUKHLWXSAOMCN-UHFFFAOYSA-N 0.000 description 2
- AQZCGTBHVXIKEK-UHFFFAOYSA-N 9,10-dibutoxy-2-methylanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCC)OCCCC AQZCGTBHVXIKEK-UHFFFAOYSA-N 0.000 description 2
- OWXOYBUWHXMYEB-UHFFFAOYSA-N 9,10-dibutoxy-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCC)OCCCC OWXOYBUWHXMYEB-UHFFFAOYSA-N 0.000 description 2
- JELGMNFSBVSQRB-UHFFFAOYSA-N 9,10-dipentoxyanthracene Chemical compound C1=CC=C2C(OCCCCC)=C(C=CC=C3)C3=C(OCCCCC)C2=C1 JELGMNFSBVSQRB-UHFFFAOYSA-N 0.000 description 2
- FCNCGHJSNVOIKE-UHFFFAOYSA-N 9,10-diphenylanthracene Chemical class C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 FCNCGHJSNVOIKE-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical class C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 2
- OMXYNVMGZQSTLS-UHFFFAOYSA-N C(CC)OC=1C2=CC=CC=C2C(=C2CC=CCC=12)OCCC Chemical compound C(CC)OC=1C2=CC=CC=C2C(=C2CC=CCC=12)OCCC OMXYNVMGZQSTLS-UHFFFAOYSA-N 0.000 description 2
- ZKGLHBWAHWTTKG-UHFFFAOYSA-N C(CC)OC=1C2=CC=CC=C2C(=C2CCCCC=12)OCCC Chemical compound C(CC)OC=1C2=CC=CC=C2C(=C2CCCCC=12)OCCC ZKGLHBWAHWTTKG-UHFFFAOYSA-N 0.000 description 2
- ZMLGPFMURZZIRQ-UHFFFAOYSA-N CC1=C(C2=CC=CC=C2C(=C1)OCCCCC)OCCCCC Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OCCCCC)OCCCCC ZMLGPFMURZZIRQ-UHFFFAOYSA-N 0.000 description 2
- KITWNHAYBHUALA-AATRIKPKSA-N CCC(CC)OC(=O)\C=C\C(O)=O Chemical compound CCC(CC)OC(=O)\C=C\C(O)=O KITWNHAYBHUALA-AATRIKPKSA-N 0.000 description 2
- LJVIEWYDEFMIBG-UHFFFAOYSA-N CCCCOC1=C2CC=C(CC2=C(C3=CC=CC=C31)OCCCC)C Chemical compound CCCCOC1=C2CC=C(CC2=C(C3=CC=CC=C31)OCCCC)C LJVIEWYDEFMIBG-UHFFFAOYSA-N 0.000 description 2
- SOIJCXISINETOI-UHFFFAOYSA-N CCCOC1=C2CC=C(CC2=C(C3=CC=CC=C31)OCCC)C Chemical compound CCCOC1=C2CC=C(CC2=C(C3=CC=CC=C31)OCCC)C SOIJCXISINETOI-UHFFFAOYSA-N 0.000 description 2
- JEQSXRFKLKNYLJ-UHFFFAOYSA-N COC1=C(C2=CC=CC=C2C(=C1)OCCC)OCCC Chemical compound COC1=C(C2=CC=CC=C2C(=C1)OCCC)OCCC JEQSXRFKLKNYLJ-UHFFFAOYSA-N 0.000 description 2
- BPFHFHMBRYMBMB-UHFFFAOYSA-N COC1=C(C2=CC=CC=C2C(=C1)OCCCCC)OCCCCC Chemical compound COC1=C(C2=CC=CC=C2C(=C1)OCCCCC)OCCCCC BPFHFHMBRYMBMB-UHFFFAOYSA-N 0.000 description 2
- FSPGYVGYKIRSOL-UHFFFAOYSA-N COC1=C(C2=CC=CC=C2C(=C1)OCCCCCCC)OCCCCCCC Chemical compound COC1=C(C2=CC=CC=C2C(=C1)OCCCCCCC)OCCCCCCC FSPGYVGYKIRSOL-UHFFFAOYSA-N 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
- ROWLUXLPDQNCST-UHFFFAOYSA-N O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCC)OCCC Chemical compound O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCC)OCCC ROWLUXLPDQNCST-UHFFFAOYSA-N 0.000 description 2
- PYTGZGJYEOVLKN-UHFFFAOYSA-N O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCCCC)OCCCCC Chemical compound O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCCCC)OCCCCC PYTGZGJYEOVLKN-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- ZQNOLHGDKLEZHH-UHFFFAOYSA-N [10-(2-ethylhexanoyloxy)-2,3-dimethylanthracen-9-yl] 2-ethylhexanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(C(CCCC)CC)=O)OC(C(CCCC)CC)=O ZQNOLHGDKLEZHH-UHFFFAOYSA-N 0.000 description 2
- HJQRTIBSRGAKGQ-UHFFFAOYSA-N [2,3-dimethyl-4-(2-methylpropanoyloxy)naphthalen-1-yl] 2-methylpropanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1C)OC(=O)C(C)C)OC(=O)C(C)C HJQRTIBSRGAKGQ-UHFFFAOYSA-N 0.000 description 2
- MJWKUVCHDDHPDQ-UHFFFAOYSA-N [4-(2-ethylhexanoyloxy)-2,3-dimethylnaphthalen-1-yl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)C(CC)CCCC)C)C MJWKUVCHDDHPDQ-UHFFFAOYSA-N 0.000 description 2
- QWRDKIJEQKIFMX-UHFFFAOYSA-N [Zn].OC=1C(N2O)=C(O)C(=N3)C(O)=CC3=CC(N3)=CC=C3C=C(N=3)C=CC=3C=C2C=1C1=CC=CC=C1 Chemical compound [Zn].OC=1C(N2O)=C(O)C(=N3)C(O)=CC3=CC(N3)=CC=C3C=C(N=3)C=CC=3C=C2C=1C1=CC=CC=C1 QWRDKIJEQKIFMX-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 150000003926 acrylamides Chemical class 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 150000008366 benzophenones Chemical class 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 2
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical class C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 description 2
- 229940106691 bisphenol a Drugs 0.000 description 2
- IIUIRWHZUVIEST-UHFFFAOYSA-N butyl 10-[10-(10-butoxy-10-oxodecoxy)anthracen-9-yl]oxydecanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCC(=O)OCCCC IIUIRWHZUVIEST-UHFFFAOYSA-N 0.000 description 2
- WSUAFFYXIOWXEL-UHFFFAOYSA-N butyl 12-[10-(12-butoxy-12-oxododecoxy)anthracen-9-yl]oxydodecanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCC(=O)OCCCC WSUAFFYXIOWXEL-UHFFFAOYSA-N 0.000 description 2
- JXXICOGSJJNKGD-UHFFFAOYSA-N butyl 18-[10-(18-butoxy-18-oxooctadecoxy)anthracen-9-yl]oxyoctadecanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCC(=O)OCCCC JXXICOGSJJNKGD-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 2
- JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical compound [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- JBSLOWBPDRZSMB-BQYQJAHWSA-N dibutyl (e)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C\C(=O)OCCCC JBSLOWBPDRZSMB-BQYQJAHWSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- DSTWFRCNXMNXTR-AATRIKPKSA-N dipropyl (e)-but-2-enedioate Chemical compound CCCOC(=O)\C=C\C(=O)OCCC DSTWFRCNXMNXTR-AATRIKPKSA-N 0.000 description 2
- DYVHFPDDBMMBAX-BYYHNAKLSA-N ditetradecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCCC DYVHFPDDBMMBAX-BYYHNAKLSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 2
- 150000002460 imidazoles Chemical class 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 230000031700 light absorption Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920003240 metallophthalocyanine polymer Polymers 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000006606 n-butoxy group Chemical group 0.000 description 2
- 125000001298 n-hexoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000006608 n-octyloxy group Chemical group 0.000 description 2
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000006256 n-propyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])OC(*)=O 0.000 description 2
- 125000001038 naphthoyl group Chemical group C1(=CC=CC2=CC=CC=C12)C(=O)* 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 150000002903 organophosphorus compounds Chemical class 0.000 description 2
- 150000002926 oxygen Chemical class 0.000 description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
- 125000006678 phenoxycarbonyl group Chemical group 0.000 description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
- 239000003504 photosensitizing agent Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920005567 polycyclic polymer Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 150000004032 porphyrins Chemical class 0.000 description 2
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 2
- 238000004611 spectroscopical analysis Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- NQJJRFLXXVTSJI-UHFFFAOYSA-N tert-butyl 5-[10-[5-[(2-methylpropan-2-yl)oxy]-5-oxopentoxy]-3-pentylanthracen-9-yl]oxypentanoate Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC(C)(C)C)OCCCCC(=O)OC(C)(C)C NQJJRFLXXVTSJI-UHFFFAOYSA-N 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 238000002076 thermal analysis method Methods 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- ANEFWEBMQHRDLH-UHFFFAOYSA-N tris(2,3,4,5,6-pentafluorophenyl) borate Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1OB(OC=1C(=C(F)C(F)=C(F)C=1F)F)OC1=C(F)C(F)=C(F)C(F)=C1F ANEFWEBMQHRDLH-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- FUTVBRXUIKZACV-UHFFFAOYSA-J zinc;3-[18-(2-carboxylatoethyl)-8,13-bis(ethenyl)-3,7,12,17-tetramethylporphyrin-21,24-diid-2-yl]propanoate Chemical compound [Zn+2].[N-]1C2=C(C)C(CCC([O-])=O)=C1C=C([N-]1)C(CCC([O-])=O)=C(C)C1=CC(C(C)=C1C=C)=NC1=CC(C(C)=C1C=C)=NC1=C2 FUTVBRXUIKZACV-UHFFFAOYSA-J 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- AOXAPSBQNMYOSY-UHFFFAOYSA-N (1,5-diethyl-10-heptoxycarbonyloxyanthracen-9-yl) heptyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCCCCC)CC)OC(=O)OCCCCCCC AOXAPSBQNMYOSY-UHFFFAOYSA-N 0.000 description 1
- LHLAEYRGCAQNQI-UHFFFAOYSA-N (1,5-diethyl-10-hexoxycarbonyloxyanthracen-9-yl) hexyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCCCC)CC)OC(=O)OCCCCCC LHLAEYRGCAQNQI-UHFFFAOYSA-N 0.000 description 1
- FECBLMLNHMWEMW-UHFFFAOYSA-N (1-ethyl-10-heptoxycarbonyloxyanthracen-9-yl) heptyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCCCC)OC(=O)OCCCCCCC FECBLMLNHMWEMW-UHFFFAOYSA-N 0.000 description 1
- KEKRXGVMFPFKSK-UHFFFAOYSA-N (1-ethyl-10-hexoxycarbonyloxyanthracen-9-yl) hexyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCCC)OC(=O)OCCCCCC KEKRXGVMFPFKSK-UHFFFAOYSA-N 0.000 description 1
- GWOITJRJIPPAFF-UHFFFAOYSA-N (1-ethyl-10-methoxycarbonyloxyanthracen-9-yl) methyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OC)OC(=O)OC GWOITJRJIPPAFF-UHFFFAOYSA-N 0.000 description 1
- LWPKSIULCULLHI-UHFFFAOYSA-N (1-ethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCCCCC)OC(=O)OCCCCCCCC LWPKSIULCULLHI-UHFFFAOYSA-N 0.000 description 1
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- UAEXIVVJEMLSAH-UHFFFAOYSA-N (1-methyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCCCCC)OC(=O)OCCCCCCCC UAEXIVVJEMLSAH-UHFFFAOYSA-N 0.000 description 1
- NZCXMLLQAOKFQK-UHFFFAOYSA-N (1-methyl-10-propoxycarbonyloxyanthracen-9-yl) propyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCC)OC(=O)OCCC NZCXMLLQAOKFQK-UHFFFAOYSA-N 0.000 description 1
- UXUJMHIAGCGHFU-UHFFFAOYSA-N (10-acetyloxy-1,2,3,4-tetrahydroanthracen-9-yl) acetate Chemical compound C(C)(=O)OC=1C=2CCCCC=2C(=C2C=CC=CC=12)OC(C)=O UXUJMHIAGCGHFU-UHFFFAOYSA-N 0.000 description 1
- RBRAQYDQQMHRSE-UHFFFAOYSA-N (10-acetyloxy-1,4-dihydroanthracen-9-yl) acetate Chemical compound C1=CC=C2C(OC(=O)C)=C(CC=CC3)C3=C(OC(C)=O)C2=C1 RBRAQYDQQMHRSE-UHFFFAOYSA-N 0.000 description 1
- ZXMOGXGYKDWXGG-UHFFFAOYSA-N (10-acetyloxy-2,3-dimethylanthracen-9-yl) acetate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(C)=O)OC(C)=O ZXMOGXGYKDWXGG-UHFFFAOYSA-N 0.000 description 1
- JFQTZVFBVLTMLF-UHFFFAOYSA-N (10-acetyloxy-3,6-dimethylanthracen-9-yl) acetate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(C)=O)C)OC(C)=O JFQTZVFBVLTMLF-UHFFFAOYSA-N 0.000 description 1
- OKZBFYJWIQGHFQ-UHFFFAOYSA-N (10-acetyloxy-3-ethylanthracen-9-yl) acetate Chemical compound C1=CC=CC2=C(OC(C)=O)C3=CC(CC)=CC=C3C(OC(C)=O)=C21 OKZBFYJWIQGHFQ-UHFFFAOYSA-N 0.000 description 1
- GSQFDSXUVVLSIS-UHFFFAOYSA-N (10-acetyloxy-3-methylanthracen-9-yl) acetate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(C)=O)OC(C)=O GSQFDSXUVVLSIS-UHFFFAOYSA-N 0.000 description 1
- SZFUJNMVPDMJEC-UHFFFAOYSA-N (10-acetyloxy-4-ethylanthracen-9-yl) acetate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(C)=O)OC(C)=O SZFUJNMVPDMJEC-UHFFFAOYSA-N 0.000 description 1
- PNYLNFZDSUUGMV-UHFFFAOYSA-N (10-acetyloxy-4-methylanthracen-9-yl) acetate Chemical compound C1=CC=C2C(OC(=O)C)=C(C=CC=C3)C3=C(OC(C)=O)C2=C1C PNYLNFZDSUUGMV-UHFFFAOYSA-N 0.000 description 1
- WWKBBQQEPKGNGA-UHFFFAOYSA-N (10-butanoyloxy-2,3-dimethylanthracen-9-yl) butanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CCC)=O)OC(CCC)=O WWKBBQQEPKGNGA-UHFFFAOYSA-N 0.000 description 1
- ZMWNWPJBTXKCFW-UHFFFAOYSA-N (10-butanoyloxy-2,6-dimethylanthracen-9-yl) butanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CCC)=O)C)OC(CCC)=O ZMWNWPJBTXKCFW-UHFFFAOYSA-N 0.000 description 1
- XOMUEBOVHMIHFG-UHFFFAOYSA-N (10-butanoyloxy-3,6-dimethylanthracen-9-yl) butanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(CCC)=O)C)OC(CCC)=O XOMUEBOVHMIHFG-UHFFFAOYSA-N 0.000 description 1
- HFVDZHHNZKZEPO-UHFFFAOYSA-N (10-butanoyloxy-3-ethylanthracen-9-yl) butanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)CCC)OC(=O)CCC HFVDZHHNZKZEPO-UHFFFAOYSA-N 0.000 description 1
- LQTXBCQHLHSWOP-UHFFFAOYSA-N (10-butanoyloxy-3-methylanthracen-9-yl) butanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)CCC)OC(=O)CCC LQTXBCQHLHSWOP-UHFFFAOYSA-N 0.000 description 1
- GRQJABXHXUQCKB-UHFFFAOYSA-N (10-butanoyloxy-4-ethylanthracen-9-yl) butanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)CCC)OC(=O)CCC GRQJABXHXUQCKB-UHFFFAOYSA-N 0.000 description 1
- GMUROYPGSBKELF-UHFFFAOYSA-N (10-butoxycarbonyloxy-1,5-dimethylanthracen-9-yl) butyl carbonate Chemical compound CCCCOC(=O)Oc1c2cccc(C)c2c(OC(=O)OCCCC)c2cccc(C)c12 GMUROYPGSBKELF-UHFFFAOYSA-N 0.000 description 1
- CMOJYQQRELHIEJ-UHFFFAOYSA-N (10-decanoyloxy-2,3-dimethylanthracen-9-yl) decanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CCCCCCCCC)=O)OC(CCCCCCCCC)=O CMOJYQQRELHIEJ-UHFFFAOYSA-N 0.000 description 1
- KFHHEQRLMHTSRU-UHFFFAOYSA-N (10-decanoyloxy-2,6-dimethylanthracen-9-yl) decanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CCCCCCCCC)=O)C)OC(CCCCCCCCC)=O KFHHEQRLMHTSRU-UHFFFAOYSA-N 0.000 description 1
- CKLQXIHITQMAIA-UHFFFAOYSA-N (10-decanoyloxy-3-ethylanthracen-9-yl) decanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCCCCC)=O)OC(CCCCCCCCC)=O CKLQXIHITQMAIA-UHFFFAOYSA-N 0.000 description 1
- WIUVLAFFIRAJKP-UHFFFAOYSA-N (10-decanoyloxy-3-methylanthracen-9-yl) decanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCCCCC)=O)OC(CCCCCCCCC)=O WIUVLAFFIRAJKP-UHFFFAOYSA-N 0.000 description 1
- NJLBKORJUKURTK-UHFFFAOYSA-N (10-decanoyloxy-4-ethylanthracen-9-yl) decanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCCCC)=O)OC(CCCCCCCCC)=O NJLBKORJUKURTK-UHFFFAOYSA-N 0.000 description 1
- POYZSAPEDUYLHU-UHFFFAOYSA-N (10-decanoyloxy-4-methylanthracen-9-yl) decanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCCCC)=O)OC(CCCCCCCCC)=O POYZSAPEDUYLHU-UHFFFAOYSA-N 0.000 description 1
- VYLZYPDLEZLSMF-UHFFFAOYSA-N (10-decanoyloxyanthracen-9-yl) decanoate Chemical compound C(CCCCCCCCC)(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(CCCCCCCCC)=O VYLZYPDLEZLSMF-UHFFFAOYSA-N 0.000 description 1
- VGUKYGYGKBSSRQ-UHFFFAOYSA-N (10-dodecanoyloxy-2,3-dimethylanthracen-9-yl) dodecanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CCCCCCCCCCC)=O)OC(CCCCCCCCCCC)=O VGUKYGYGKBSSRQ-UHFFFAOYSA-N 0.000 description 1
- VOLOIFOIHQTSFR-UHFFFAOYSA-N (10-dodecanoyloxy-2,6-dimethylanthracen-9-yl) dodecanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CCCCCCCCCCC)=O)C)OC(CCCCCCCCCCC)=O VOLOIFOIHQTSFR-UHFFFAOYSA-N 0.000 description 1
- CONVJZUUCQFTRE-UHFFFAOYSA-N (10-dodecanoyloxy-3,6-dimethylanthracen-9-yl) dodecanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(CCCCCCCCCCC)=O)C)OC(CCCCCCCCCCC)=O CONVJZUUCQFTRE-UHFFFAOYSA-N 0.000 description 1
- MTEOXCYCLRSVJO-UHFFFAOYSA-N (10-dodecanoyloxy-3-methylanthracen-9-yl) dodecanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCCCCCCC)=O)OC(CCCCCCCCCCC)=O MTEOXCYCLRSVJO-UHFFFAOYSA-N 0.000 description 1
- STWNRZVAYNQGLA-UHFFFAOYSA-N (10-dodecanoyloxy-4-ethylanthracen-9-yl) dodecanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCCCCCC)=O)OC(CCCCCCCCCCC)=O STWNRZVAYNQGLA-UHFFFAOYSA-N 0.000 description 1
- SCUUEWSFKFWVHG-UHFFFAOYSA-N (10-dodecanoyloxy-4-methylanthracen-9-yl) dodecanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCCCCCC)=O)OC(CCCCCCCCCCC)=O SCUUEWSFKFWVHG-UHFFFAOYSA-N 0.000 description 1
- KVSCDOHSNDQLRJ-UHFFFAOYSA-N (10-ethoxycarbonyloxy-1,5-diethylanthracen-9-yl) ethyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCC)CC)OC(=O)OCC KVSCDOHSNDQLRJ-UHFFFAOYSA-N 0.000 description 1
- NHKLJPUYHNZPAP-UHFFFAOYSA-N (10-ethoxycarbonyloxy-1,5-dimethylanthracen-9-yl) ethyl carbonate Chemical compound CC1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCC)C)OC(=O)OCC NHKLJPUYHNZPAP-UHFFFAOYSA-N 0.000 description 1
- BHUQNTZOSHVWEP-UHFFFAOYSA-N (10-ethoxycarbonyloxy-1-ethylanthracen-9-yl) ethyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCC)OC(=O)OCC BHUQNTZOSHVWEP-UHFFFAOYSA-N 0.000 description 1
- AKBSDHMOPQUVOQ-UHFFFAOYSA-N (10-ethoxycarbonyloxy-1-methylanthracen-9-yl) ethyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCC)OC(=O)OCC AKBSDHMOPQUVOQ-UHFFFAOYSA-N 0.000 description 1
- ASDSCBUIRQJZOJ-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2,3-diethylanthracen-9-yl) ethyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OCC)OC(=O)OCC ASDSCBUIRQJZOJ-UHFFFAOYSA-N 0.000 description 1
- FDDUSDFCIUHEDV-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2,3-dimethylanthracen-9-yl) ethyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OCC)OC(=O)OCC FDDUSDFCIUHEDV-UHFFFAOYSA-N 0.000 description 1
- SGBCCBUDONZVKM-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2,6-diethylanthracen-9-yl) ethyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCC)CC)OC(=O)OCC SGBCCBUDONZVKM-UHFFFAOYSA-N 0.000 description 1
- GJPMVABTRVTJIC-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2,6-dimethylanthracen-9-yl) ethyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCC)C)OC(=O)OCC GJPMVABTRVTJIC-UHFFFAOYSA-N 0.000 description 1
- ALAZRCUFLUTMFN-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2,7-diethylanthracen-9-yl) ethyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCC)CC)OC(=O)OCC ALAZRCUFLUTMFN-UHFFFAOYSA-N 0.000 description 1
- OJMHBBYCIKZKPH-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2-ethylanthracen-9-yl) ethyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCC)OC(=O)OCC OJMHBBYCIKZKPH-UHFFFAOYSA-N 0.000 description 1
- WTGWDCPFSSJMQE-UHFFFAOYSA-N (10-ethoxycarbonyloxy-2-methylanthracen-9-yl) ethyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCC)OC(=O)OCC WTGWDCPFSSJMQE-UHFFFAOYSA-N 0.000 description 1
- MMQHMWYEEWVGII-UHFFFAOYSA-N (10-ethoxycarbonyloxyanthracen-9-yl) ethyl carbonate Chemical compound C(C)OC(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OC(=O)OCC MMQHMWYEEWVGII-UHFFFAOYSA-N 0.000 description 1
- IXEAUBQEBXEIQL-UHFFFAOYSA-N (10-heptanoyloxy-2,3-dimethylanthracen-9-yl) heptanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CCCCCC)=O)OC(CCCCCC)=O IXEAUBQEBXEIQL-UHFFFAOYSA-N 0.000 description 1
- BZALJSWTCBOAPJ-UHFFFAOYSA-N (10-heptanoyloxy-2,6-dimethylanthracen-9-yl) heptanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CCCCCC)=O)C)OC(CCCCCC)=O BZALJSWTCBOAPJ-UHFFFAOYSA-N 0.000 description 1
- HUWZOENVSMGQBU-UHFFFAOYSA-N (10-heptanoyloxy-3,6-dimethylanthracen-9-yl) heptanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(CCCCCC)=O)C)OC(CCCCCC)=O HUWZOENVSMGQBU-UHFFFAOYSA-N 0.000 description 1
- FWRVYDPLGKTLOJ-UHFFFAOYSA-N (10-heptanoyloxy-3-methylanthracen-9-yl) heptanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCC)=O)OC(CCCCCC)=O FWRVYDPLGKTLOJ-UHFFFAOYSA-N 0.000 description 1
- LUFPSALBGACFRG-UHFFFAOYSA-N (10-heptanoyloxy-4-methylanthracen-9-yl) heptanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCC)=O)OC(CCCCCC)=O LUFPSALBGACFRG-UHFFFAOYSA-N 0.000 description 1
- MEDLHZNRAQAHCV-UHFFFAOYSA-N (10-heptanoyloxyanthracen-9-yl) heptanoate Chemical compound C(CCCCCC)(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(CCCCCC)=O MEDLHZNRAQAHCV-UHFFFAOYSA-N 0.000 description 1
- SZURYAVETHYFCO-UHFFFAOYSA-N (10-heptoxycarbonyloxy-1,5-dimethylanthracen-9-yl) heptyl carbonate Chemical compound CC1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCCCCC)C)OC(=O)OCCCCCCC SZURYAVETHYFCO-UHFFFAOYSA-N 0.000 description 1
- IVMOOKRONKOUEO-UHFFFAOYSA-N (10-heptoxycarbonyloxy-1-methylanthracen-9-yl) heptyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCCCC)OC(=O)OCCCCCCC IVMOOKRONKOUEO-UHFFFAOYSA-N 0.000 description 1
- ZFQSWUNOIRQRGP-UHFFFAOYSA-N (10-heptoxycarbonyloxy-2,6-dimethylanthracen-9-yl) heptyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCCCC)C)OC(=O)OCCCCCCC ZFQSWUNOIRQRGP-UHFFFAOYSA-N 0.000 description 1
- NWRHSAPHVPGCBO-UHFFFAOYSA-N (10-heptoxycarbonyloxy-2,7-dimethylanthracen-9-yl) heptyl carbonate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCCCCC)C)OC(=O)OCCCCCCC NWRHSAPHVPGCBO-UHFFFAOYSA-N 0.000 description 1
- CZPBYOMDBHUCFN-UHFFFAOYSA-N (10-heptoxycarbonyloxy-2-methylanthracen-9-yl) heptyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCCCCC)OC(=O)OCCCCCCC CZPBYOMDBHUCFN-UHFFFAOYSA-N 0.000 description 1
- NPHPEIFKYFKDFM-UHFFFAOYSA-N (10-heptoxycarbonyloxyanthracen-9-yl) heptyl carbonate Chemical compound C(CCCCCC)OC(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(=O)OCCCCCCC NPHPEIFKYFKDFM-UHFFFAOYSA-N 0.000 description 1
- BWFLGGWYGJDLAI-UHFFFAOYSA-N (10-hexanoyloxy-2,3-dimethylanthracen-9-yl) hexanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CCCCC)=O)OC(CCCCC)=O BWFLGGWYGJDLAI-UHFFFAOYSA-N 0.000 description 1
- NXNYAXWBNPCAOI-UHFFFAOYSA-N (10-hexanoyloxy-2,6-dimethylanthracen-9-yl) hexanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CCCCC)=O)C)OC(CCCCC)=O NXNYAXWBNPCAOI-UHFFFAOYSA-N 0.000 description 1
- PPGXHRRVFVFWDS-UHFFFAOYSA-N (10-hexanoyloxy-3,6-dimethylanthracen-9-yl) hexanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(CCCCC)=O)C)OC(CCCCC)=O PPGXHRRVFVFWDS-UHFFFAOYSA-N 0.000 description 1
- WQPHEZOZQLUCLP-UHFFFAOYSA-N (10-hexanoyloxy-3-methylanthracen-9-yl) hexanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCC)=O)OC(CCCCC)=O WQPHEZOZQLUCLP-UHFFFAOYSA-N 0.000 description 1
- LNJOCYPJKWYISL-UHFFFAOYSA-N (10-hexanoyloxy-4-methylanthracen-9-yl) hexanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCC)=O)OC(CCCCC)=O LNJOCYPJKWYISL-UHFFFAOYSA-N 0.000 description 1
- HDXJWZHGDQGINF-UHFFFAOYSA-N (10-hexanoyloxyanthracen-9-yl) hexanoate Chemical compound C(CCCCC)(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(CCCCC)=O HDXJWZHGDQGINF-UHFFFAOYSA-N 0.000 description 1
- OJYZEVCQONVRNU-UHFFFAOYSA-N (10-hexoxycarbonyloxy-1,5-dimethylanthracen-9-yl) hexyl carbonate Chemical compound CC1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCCCCCC)C)OC(=O)OCCCCCC OJYZEVCQONVRNU-UHFFFAOYSA-N 0.000 description 1
- FUFRRSNVDXWIKY-UHFFFAOYSA-N (10-hexoxycarbonyloxy-1-methylanthracen-9-yl) hexyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCCCCCC)OC(=O)OCCCCCC FUFRRSNVDXWIKY-UHFFFAOYSA-N 0.000 description 1
- UWYHDIWNQCCECU-UHFFFAOYSA-N (10-hexoxycarbonyloxy-2,3-dimethylanthracen-9-yl) hexyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OCCCCCC)OC(=O)OCCCCCC UWYHDIWNQCCECU-UHFFFAOYSA-N 0.000 description 1
- HQMQWNXEWADIFY-UHFFFAOYSA-N (10-hexoxycarbonyloxy-2,6-dimethylanthracen-9-yl) hexyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCCC)C)OC(=O)OCCCCCC HQMQWNXEWADIFY-UHFFFAOYSA-N 0.000 description 1
- RIBFPROPSJPBLC-UHFFFAOYSA-N (10-hexoxycarbonyloxyanthracen-9-yl) hexyl carbonate Chemical compound C(CCCCC)OC(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(=O)OCCCCCC RIBFPROPSJPBLC-UHFFFAOYSA-N 0.000 description 1
- LYHPWXDXYCATPU-UHFFFAOYSA-N (10-methoxycarbonyloxy-1-methylanthracen-9-yl) methyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OC)OC(=O)OC LYHPWXDXYCATPU-UHFFFAOYSA-N 0.000 description 1
- SOFYMNUCCVFQJT-UHFFFAOYSA-N (10-methoxycarbonyloxy-2,3-dimethylanthracen-9-yl) methyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OC)OC(=O)OC SOFYMNUCCVFQJT-UHFFFAOYSA-N 0.000 description 1
- CONHLWHTNQIHAX-UHFFFAOYSA-N (10-methoxycarbonyloxy-2,6-dimethylanthracen-9-yl) methyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OC)C)OC(=O)OC CONHLWHTNQIHAX-UHFFFAOYSA-N 0.000 description 1
- KMSYEORPZWYIER-UHFFFAOYSA-N (10-methoxycarbonyloxy-2,7-dimethylanthracen-9-yl) methyl carbonate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OC)C)OC(=O)OC KMSYEORPZWYIER-UHFFFAOYSA-N 0.000 description 1
- GDFQRDTZOFMSSM-UHFFFAOYSA-N (10-methoxycarbonyloxyanthracen-9-yl) methyl carbonate Chemical compound C1=CC=C2C(OC(=O)OC)=C(C=CC=C3)C3=C(OC(=O)OC)C2=C1 GDFQRDTZOFMSSM-UHFFFAOYSA-N 0.000 description 1
- YPESPOJYFDMJPO-UHFFFAOYSA-N (10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound C(CCCCCCCC)(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(CCCCCCCC)=O YPESPOJYFDMJPO-UHFFFAOYSA-N 0.000 description 1
- ICDVRRFJYKMRAK-UHFFFAOYSA-N (10-propanoyloxyanthracen-9-yl) propanoate Chemical compound C(CC)(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OC(CC)=O ICDVRRFJYKMRAK-UHFFFAOYSA-N 0.000 description 1
- GVRDJBJMGPOXOG-UHFFFAOYSA-N (2,3-diethyl-10-hexoxycarbonyloxyanthracen-9-yl) hexyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OCCCCCC)OC(=O)OCCCCCC GVRDJBJMGPOXOG-UHFFFAOYSA-N 0.000 description 1
- YIUYUPJUHPGWLM-UHFFFAOYSA-N (2,3-diethyl-10-methoxycarbonyloxyanthracen-9-yl) methyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OC)OC(=O)OC YIUYUPJUHPGWLM-UHFFFAOYSA-N 0.000 description 1
- DCTYMSGKXOUIDU-UHFFFAOYSA-N (2,3-diethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OCCCCCCCC)OC(=O)OCCCCCCCC DCTYMSGKXOUIDU-UHFFFAOYSA-N 0.000 description 1
- WBEBZYCLWZUALJ-UHFFFAOYSA-N (2,3-dimethyl-10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CCCCCCCC)=O)OC(CCCCCCCC)=O WBEBZYCLWZUALJ-UHFFFAOYSA-N 0.000 description 1
- YIFPGOHPSWQHTP-UHFFFAOYSA-N (2,3-dimethyl-10-octanoyloxyanthracen-9-yl) octanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CCCCCCC)=O)OC(CCCCCCC)=O YIFPGOHPSWQHTP-UHFFFAOYSA-N 0.000 description 1
- OVPSYELAWLHTAM-UHFFFAOYSA-N (2,3-dimethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OCCCCCCCC)OC(=O)OCCCCCCCC OVPSYELAWLHTAM-UHFFFAOYSA-N 0.000 description 1
- VPNOWAFTQQMPGC-UHFFFAOYSA-N (2,3-dimethyl-10-propanoyloxyanthracen-9-yl) propanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(CC)=O)OC(CC)=O VPNOWAFTQQMPGC-UHFFFAOYSA-N 0.000 description 1
- AJCCNFTVBQOSAK-UHFFFAOYSA-N (2,3-dimethyl-4-nonanoyloxynaphthalen-1-yl) nonanoate Chemical compound CCCCCCCCC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)CCCCCCCC)C)C AJCCNFTVBQOSAK-UHFFFAOYSA-N 0.000 description 1
- QDSSPYDCMXZPAV-UHFFFAOYSA-N (2,3-dimethyl-4-octoxycarbonyloxynaphthalen-1-yl) octyl carbonate Chemical compound CCCCCCCCOC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)OCCCCCCCC)C)C QDSSPYDCMXZPAV-UHFFFAOYSA-N 0.000 description 1
- PEEHRIVIKLSNDW-UHFFFAOYSA-N (2,3-dimethyl-4-propanoyloxynaphthalen-1-yl) propanoate Chemical compound CCC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)CC)C)C PEEHRIVIKLSNDW-UHFFFAOYSA-N 0.000 description 1
- BDCRHPLCIBOSNR-UHFFFAOYSA-N (2,6-diethyl-10-heptoxycarbonyloxyanthracen-9-yl) heptyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCCCC)CC)OC(=O)OCCCCCCC BDCRHPLCIBOSNR-UHFFFAOYSA-N 0.000 description 1
- LSXRRSDDRLLVEV-UHFFFAOYSA-N (2,6-diethyl-10-hexoxycarbonyloxyanthracen-9-yl) hexyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCCC)CC)OC(=O)OCCCCCC LSXRRSDDRLLVEV-UHFFFAOYSA-N 0.000 description 1
- MWFAUVUHMCSOTB-UHFFFAOYSA-N (2,6-diethyl-10-methoxycarbonyloxyanthracen-9-yl) methyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OC)CC)OC(=O)OC MWFAUVUHMCSOTB-UHFFFAOYSA-N 0.000 description 1
- QSTZDCFBGDNEFS-UHFFFAOYSA-N (2,6-diethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCCCCC)CC)OC(=O)OCCCCCCCC QSTZDCFBGDNEFS-UHFFFAOYSA-N 0.000 description 1
- ROTUPJFYPTWCIR-UHFFFAOYSA-N (2,6-dimethyl-10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CCCCCCCC)=O)C)OC(CCCCCCCC)=O ROTUPJFYPTWCIR-UHFFFAOYSA-N 0.000 description 1
- MHZCSQAUMFEJGZ-UHFFFAOYSA-N (2,6-dimethyl-10-octanoyloxyanthracen-9-yl) octanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CCCCCCC)=O)C)OC(CCCCCCC)=O MHZCSQAUMFEJGZ-UHFFFAOYSA-N 0.000 description 1
- TYPURIGDJAPYAK-UHFFFAOYSA-N (2,6-dimethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCCCCCCCC)C)OC(=O)OCCCCCCCC TYPURIGDJAPYAK-UHFFFAOYSA-N 0.000 description 1
- MTHLBHDSIJYAKA-UHFFFAOYSA-N (2,6-dimethyl-10-propanoyloxyanthracen-9-yl) propanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(CC)=O)C)OC(CC)=O MTHLBHDSIJYAKA-UHFFFAOYSA-N 0.000 description 1
- ZXBQCYXXDBDSSW-UHFFFAOYSA-N (2,7-diethyl-10-heptoxycarbonyloxyanthracen-9-yl) heptyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCCCCC)CC)OC(=O)OCCCCCCC ZXBQCYXXDBDSSW-UHFFFAOYSA-N 0.000 description 1
- RICPHWPUFBHOPM-UHFFFAOYSA-N (2,7-diethyl-10-methoxycarbonyloxyanthracen-9-yl) methyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OC)CC)OC(=O)OC RICPHWPUFBHOPM-UHFFFAOYSA-N 0.000 description 1
- MOXSDWWAWHGHKY-UHFFFAOYSA-N (2,7-diethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCCCCCC)CC)OC(=O)OCCCCCCCC MOXSDWWAWHGHKY-UHFFFAOYSA-N 0.000 description 1
- GCOXELOKDLUGST-UHFFFAOYSA-N (2,7-dimethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCCCCCCCC)C)OC(=O)OCCCCCCCC GCOXELOKDLUGST-UHFFFAOYSA-N 0.000 description 1
- NYQCJKFKJUMGCM-UHFFFAOYSA-N (2-ethyl-10-heptoxycarbonyloxyanthracen-9-yl) heptyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCCCCC)OC(=O)OCCCCCCC NYQCJKFKJUMGCM-UHFFFAOYSA-N 0.000 description 1
- FFJLAOOEKBLXRQ-UHFFFAOYSA-N (2-ethyl-10-hexoxycarbonyloxyanthracen-9-yl) hexyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCCCC)OC(=O)OCCCCCC FFJLAOOEKBLXRQ-UHFFFAOYSA-N 0.000 description 1
- ZZMPPWTUNDJXHM-UHFFFAOYSA-N (2-ethyl-10-methoxycarbonyloxyanthracen-9-yl) methyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OC)OC(=O)OC ZZMPPWTUNDJXHM-UHFFFAOYSA-N 0.000 description 1
- TUAIFUXPYNTSAF-UHFFFAOYSA-N (2-ethyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCCCCCC)OC(=O)OCCCCCCCC TUAIFUXPYNTSAF-UHFFFAOYSA-N 0.000 description 1
- RICMDJUGGAKHMN-UHFFFAOYSA-N (2-methoxy-4-methoxycarbonyloxynaphthalen-1-yl) methyl carbonate Chemical compound C1=CC=C2C(OC(=O)OC)=CC(OC)=C(OC(=O)OC)C2=C1 RICMDJUGGAKHMN-UHFFFAOYSA-N 0.000 description 1
- BODAWUCPTNUJCE-UHFFFAOYSA-N (2-methyl-10-octoxycarbonyloxyanthracen-9-yl) octyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCCCCCCCC)OC(=O)OCCCCCCCC BODAWUCPTNUJCE-UHFFFAOYSA-N 0.000 description 1
- MSUSHXZWMYSDCU-UHFFFAOYSA-N (2-methyl-4-octoxycarbonyloxynaphthalen-1-yl) octyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OCCCCCCCC)OC(=O)OCCCCCCCC MSUSHXZWMYSDCU-UHFFFAOYSA-N 0.000 description 1
- ZFUMZNKZQRZHCN-UHFFFAOYSA-N (3,6-dimethyl-10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(CCCCCCCC)=O)C)OC(CCCCCCCC)=O ZFUMZNKZQRZHCN-UHFFFAOYSA-N 0.000 description 1
- VYNQOBCFFMZVLA-UHFFFAOYSA-N (3,6-dimethyl-10-propanoyloxyanthracen-9-yl) propanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(CC)=O)C)OC(CC)=O VYNQOBCFFMZVLA-UHFFFAOYSA-N 0.000 description 1
- XAEKRSRKNTXACJ-UHFFFAOYSA-N (3-ethyl-10-heptanoyloxyanthracen-9-yl) heptanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCC)=O)OC(CCCCCC)=O XAEKRSRKNTXACJ-UHFFFAOYSA-N 0.000 description 1
- XOOSAUCRBMLRSX-UHFFFAOYSA-N (3-ethyl-10-hexanoyloxyanthracen-9-yl) hexanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCC)=O)OC(CCCCC)=O XOOSAUCRBMLRSX-UHFFFAOYSA-N 0.000 description 1
- LOWXQHUAHQRFDF-UHFFFAOYSA-N (3-ethyl-10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCCCC)=O)OC(CCCCCCCC)=O LOWXQHUAHQRFDF-UHFFFAOYSA-N 0.000 description 1
- HFRWTSQXTIGXAR-UHFFFAOYSA-N (3-ethyl-10-octanoyloxyanthracen-9-yl) octanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCCC)=O)OC(CCCCCCC)=O HFRWTSQXTIGXAR-UHFFFAOYSA-N 0.000 description 1
- HQUHMERMBCGWOI-UHFFFAOYSA-N (3-ethyl-10-propanoyloxyanthracen-9-yl) propanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC)=O)OC(CC)=O HQUHMERMBCGWOI-UHFFFAOYSA-N 0.000 description 1
- UEMZSICGMKYBMK-UHFFFAOYSA-N (3-methyl-10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCCCC)=O)OC(CCCCCCCC)=O UEMZSICGMKYBMK-UHFFFAOYSA-N 0.000 description 1
- SRWVIVALKRRZCH-UHFFFAOYSA-N (3-methyl-10-octanoyloxyanthracen-9-yl) octanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CCCCCCC)=O)OC(CCCCCCC)=O SRWVIVALKRRZCH-UHFFFAOYSA-N 0.000 description 1
- XZDSTAGSSDDBQV-UHFFFAOYSA-N (3-methyl-10-propanoyloxyanthracen-9-yl) propanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC)=O)OC(CC)=O XZDSTAGSSDDBQV-UHFFFAOYSA-N 0.000 description 1
- FVBIJRRMVLYNEJ-UHFFFAOYSA-N (3-methyl-4-nonanoyloxynaphthalen-1-yl) nonanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(CCCCCCCC)=O)OC(CCCCCCCC)=O FVBIJRRMVLYNEJ-UHFFFAOYSA-N 0.000 description 1
- GDVWJEZXRXFWKO-UHFFFAOYSA-N (3-methyl-4-octanoyloxynaphthalen-1-yl) octanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(CCCCCCC)=O)OC(CCCCCCC)=O GDVWJEZXRXFWKO-UHFFFAOYSA-N 0.000 description 1
- CFVWAZUILCCFKU-UHFFFAOYSA-N (3-methyl-4-propanoyloxynaphthalen-1-yl) propanoate Chemical compound C1=CC=C2C(OC(=O)CC)=CC(C)=C(OC(=O)CC)C2=C1 CFVWAZUILCCFKU-UHFFFAOYSA-N 0.000 description 1
- SJOCCIVQSKINSZ-UHFFFAOYSA-N (4-acetyloxy-2,3-dichloronaphthalen-1-yl) acetate Chemical compound C1=CC=C2C(OC(=O)C)=C(Cl)C(Cl)=C(OC(C)=O)C2=C1 SJOCCIVQSKINSZ-UHFFFAOYSA-N 0.000 description 1
- VSRIGQPGMBVZBS-UHFFFAOYSA-N (4-acetyloxy-2,3-dimethylnaphthalen-1-yl) acetate Chemical compound C1=CC=C2C(OC(=O)C)=C(C)C(C)=C(OC(C)=O)C2=C1 VSRIGQPGMBVZBS-UHFFFAOYSA-N 0.000 description 1
- ABUWWKFXLGAHEP-UHFFFAOYSA-N (4-acetyloxy-3-methoxynaphthalen-1-yl) acetate Chemical compound C1=CC=CC2=C(OC(C)=O)C(OC)=CC(OC(C)=O)=C21 ABUWWKFXLGAHEP-UHFFFAOYSA-N 0.000 description 1
- MMNXTLHEYRPKCF-UHFFFAOYSA-N (4-acetyloxy-3-phenoxynaphthalen-1-yl) acetate Chemical compound CC(=O)OC=1C2=CC=CC=C2C(OC(=O)C)=CC=1OC1=CC=CC=C1 MMNXTLHEYRPKCF-UHFFFAOYSA-N 0.000 description 1
- MJNCHXPSNDYAIH-UHFFFAOYSA-N (4-benzoyloxy-3-methoxynaphthalen-1-yl) benzoate Chemical compound C=12C=CC=CC2=C(OC(=O)C=2C=CC=CC=2)C(OC)=CC=1OC(=O)C1=CC=CC=C1 MJNCHXPSNDYAIH-UHFFFAOYSA-N 0.000 description 1
- BVVDINJVWBJRHY-UHFFFAOYSA-N (4-benzoyloxy-3-methylnaphthalen-1-yl) benzoate Chemical compound C=12C=CC=CC2=C(OC(=O)C=2C=CC=CC=2)C(C)=CC=1OC(=O)C1=CC=CC=C1 BVVDINJVWBJRHY-UHFFFAOYSA-N 0.000 description 1
- ZFZQDZJXXXTHLA-UHFFFAOYSA-N (4-benzoyloxy-3-phenoxynaphthalen-1-yl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C1=CC=CC=C1C=1OC(=O)C=2C=CC=CC=2)=CC=1OC1=CC=CC=C1 ZFZQDZJXXXTHLA-UHFFFAOYSA-N 0.000 description 1
- ZUFFXNUGFYKMGW-UHFFFAOYSA-N (4-benzoyloxynaphthalen-1-yl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C1=CC=CC=C11)=CC=C1OC(=O)C1=CC=CC=C1 ZUFFXNUGFYKMGW-UHFFFAOYSA-N 0.000 description 1
- LDLBCMXGZZXKSJ-UHFFFAOYSA-N (4-butanoyloxy-2,3-dimethylnaphthalen-1-yl) butanoate Chemical compound CCCC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)CCC)C)C LDLBCMXGZZXKSJ-UHFFFAOYSA-N 0.000 description 1
- QXCRROHGXXEBJV-UHFFFAOYSA-N (4-butanoyloxy-3-methoxynaphthalen-1-yl) butanoate Chemical compound C1=CC=C2C(OC(=O)CCC)=CC(OC)=C(OC(=O)CCC)C2=C1 QXCRROHGXXEBJV-UHFFFAOYSA-N 0.000 description 1
- MYPHKHXZQVKLIM-UHFFFAOYSA-N (4-butanoyloxy-3-phenoxynaphthalen-1-yl) butanoate Chemical compound CCCC(=O)OC=1C2=CC=CC=C2C(OC(=O)CCC)=CC=1OC1=CC=CC=C1 MYPHKHXZQVKLIM-UHFFFAOYSA-N 0.000 description 1
- YMPUTTSDWQSRCI-UHFFFAOYSA-N (4-butanoyloxynaphthalen-1-yl) butanoate Chemical compound C(CCC)(=O)OC1=CC=C(C2=CC=CC=C12)OC(CCC)=O YMPUTTSDWQSRCI-UHFFFAOYSA-N 0.000 description 1
- RPNYJAJQZFRVDG-UHFFFAOYSA-N (4-decanoyloxy-3-methylnaphthalen-1-yl) decanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(CCCCCCCCC)=O)OC(CCCCCCCCC)=O RPNYJAJQZFRVDG-UHFFFAOYSA-N 0.000 description 1
- WGZGWWDVFDEDHG-UHFFFAOYSA-N (4-dodecanoyloxy-3-methylnaphthalen-1-yl) dodecanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(CCCCCCCCCCC)=O)OC(CCCCCCCCCCC)=O WGZGWWDVFDEDHG-UHFFFAOYSA-N 0.000 description 1
- OIKCVRVIJVIWEJ-UHFFFAOYSA-N (4-dodecanoyloxynaphthalen-1-yl) dodecanoate Chemical compound C(CCCCCCCCCCC)(=O)OC1=CC=C(C2=CC=CC=C12)OC(CCCCCCCCCCC)=O OIKCVRVIJVIWEJ-UHFFFAOYSA-N 0.000 description 1
- YDSGBACWHOSLKT-UHFFFAOYSA-N (4-ethoxycarbonyloxy-2-methylnaphthalen-1-yl) ethyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OCC)OC(=O)OCC YDSGBACWHOSLKT-UHFFFAOYSA-N 0.000 description 1
- ZBCJDMZKPKLAQL-UHFFFAOYSA-N (4-ethoxycarbonyloxynaphthalen-1-yl) ethyl carbonate Chemical compound C(C)OC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCC ZBCJDMZKPKLAQL-UHFFFAOYSA-N 0.000 description 1
- FXWDFIHHBTYNLG-UHFFFAOYSA-N (4-ethyl-10-heptanoyloxyanthracen-9-yl) heptanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCC)=O)OC(CCCCCC)=O FXWDFIHHBTYNLG-UHFFFAOYSA-N 0.000 description 1
- WVCAHYOSKXNPGB-UHFFFAOYSA-N (4-ethyl-10-hexanoyloxyanthracen-9-yl) hexanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCC)=O)OC(CCCCC)=O WVCAHYOSKXNPGB-UHFFFAOYSA-N 0.000 description 1
- GLCHEWLEOKVRTN-UHFFFAOYSA-N (4-ethyl-10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCCC)=O)OC(CCCCCCCC)=O GLCHEWLEOKVRTN-UHFFFAOYSA-N 0.000 description 1
- ABQGBHVVJHJYJZ-UHFFFAOYSA-N (4-ethyl-10-octanoyloxyanthracen-9-yl) octanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCC)=O)OC(CCCCCCC)=O ABQGBHVVJHJYJZ-UHFFFAOYSA-N 0.000 description 1
- UQGLIMXWVSMFRZ-UHFFFAOYSA-N (4-ethyl-10-propanoyloxyanthracen-9-yl) propanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CC)=O)OC(CC)=O UQGLIMXWVSMFRZ-UHFFFAOYSA-N 0.000 description 1
- FDWFLANUEWZJKY-UHFFFAOYSA-N (4-heptanoyloxy-3-methylnaphthalen-1-yl) heptanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(CCCCCC)=O)OC(CCCCCC)=O FDWFLANUEWZJKY-UHFFFAOYSA-N 0.000 description 1
- GKARUOOERNCAGK-UHFFFAOYSA-N (4-heptoxycarbonyloxy-2,3-dimethylnaphthalen-1-yl) heptyl carbonate Chemical compound CCCCCCCOC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)OCCCCCCC)C)C GKARUOOERNCAGK-UHFFFAOYSA-N 0.000 description 1
- QJTSZRBTYXJWLK-UHFFFAOYSA-N (4-heptoxycarbonyloxynaphthalen-1-yl) heptyl carbonate Chemical compound C(CCCCCC)OC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCCCCCCC QJTSZRBTYXJWLK-UHFFFAOYSA-N 0.000 description 1
- FRCWMEHJZYCFLY-UHFFFAOYSA-N (4-hexanoyloxy-2,3-dimethylnaphthalen-1-yl) hexanoate Chemical compound CCCCCC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)CCCCC)C)C FRCWMEHJZYCFLY-UHFFFAOYSA-N 0.000 description 1
- WPUUZNHUXYGYIB-UHFFFAOYSA-N (4-hexanoyloxy-3-methoxynaphthalen-1-yl) hexanoate Chemical compound C1=CC=C2C(OC(=O)CCCCC)=CC(OC)=C(OC(=O)CCCCC)C2=C1 WPUUZNHUXYGYIB-UHFFFAOYSA-N 0.000 description 1
- ZVPBTDVYHRGSSA-UHFFFAOYSA-N (4-hexoxycarbonyloxy-2-methoxynaphthalen-1-yl) hexyl carbonate Chemical compound C1=CC=C2C(OC(=O)OCCCCCC)=CC(OC)=C(OC(=O)OCCCCCC)C2=C1 ZVPBTDVYHRGSSA-UHFFFAOYSA-N 0.000 description 1
- ATRLZQDUQHWTDN-UHFFFAOYSA-N (4-hexoxycarbonyloxy-2-methylnaphthalen-1-yl) hexyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OCCCCCC)OC(=O)OCCCCCC ATRLZQDUQHWTDN-UHFFFAOYSA-N 0.000 description 1
- IWRKAIJYNMLBQM-UHFFFAOYSA-N (4-hexoxycarbonyloxy-2-phenoxynaphthalen-1-yl) hexyl carbonate Chemical compound CCCCCCOC(=O)OC=1C2=CC=CC=C2C(OC(=O)OCCCCCC)=CC=1OC1=CC=CC=C1 IWRKAIJYNMLBQM-UHFFFAOYSA-N 0.000 description 1
- QGMSXRHTFMAISD-UHFFFAOYSA-N (4-hexoxycarbonyloxynaphthalen-1-yl) hexyl carbonate Chemical compound C(CCCCC)OC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCCCCCC QGMSXRHTFMAISD-UHFFFAOYSA-N 0.000 description 1
- BQBKHHBYOKJGRB-UHFFFAOYSA-N (4-methoxycarbonyloxy-2,3-dimethylnaphthalen-1-yl) methyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1C)OC(=O)OC)OC(=O)OC BQBKHHBYOKJGRB-UHFFFAOYSA-N 0.000 description 1
- AHKJBUCJBFVEAU-UHFFFAOYSA-N (4-methoxycarbonyloxy-2-methylnaphthalen-1-yl) methyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OC)OC(=O)OC AHKJBUCJBFVEAU-UHFFFAOYSA-N 0.000 description 1
- BMVUFKRIJNFMPY-UHFFFAOYSA-N (4-methoxycarbonyloxynaphthalen-1-yl) methyl carbonate Chemical compound C1=CC=C2C(OC(=O)OC)=CC=C(OC(=O)OC)C2=C1 BMVUFKRIJNFMPY-UHFFFAOYSA-N 0.000 description 1
- HZMZQRNFQBCTHY-UHFFFAOYSA-N (4-methyl-10-nonanoyloxyanthracen-9-yl) nonanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCCC)=O)OC(CCCCCCCC)=O HZMZQRNFQBCTHY-UHFFFAOYSA-N 0.000 description 1
- GFMMOTFZHQWKPE-UHFFFAOYSA-N (4-methyl-10-octanoyloxyanthracen-9-yl) octanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CCCCCCC)=O)OC(CCCCCCC)=O GFMMOTFZHQWKPE-UHFFFAOYSA-N 0.000 description 1
- GRZFSYCHQMXSMH-UHFFFAOYSA-N (4-methyl-10-propanoyloxyanthracen-9-yl) propanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(CC)=O)OC(CC)=O GRZFSYCHQMXSMH-UHFFFAOYSA-N 0.000 description 1
- WMNNJTNVRPKPSR-UHFFFAOYSA-N (4-nonanoyloxynaphthalen-1-yl) nonanoate Chemical compound C(CCCCCCCC)(=O)OC1=CC=C(C2=CC=CC=C12)OC(CCCCCCCC)=O WMNNJTNVRPKPSR-UHFFFAOYSA-N 0.000 description 1
- LYSJWHLJCMCEQK-UHFFFAOYSA-N (4-octanoyloxynaphthalen-1-yl) octanoate Chemical compound C(CCCCCCC)(=O)OC1=CC=C(C2=CC=CC=C12)OC(CCCCCCC)=O LYSJWHLJCMCEQK-UHFFFAOYSA-N 0.000 description 1
- NISITOMOCKDHQZ-UHFFFAOYSA-N (4-octoxycarbonyloxynaphthalen-1-yl) octyl carbonate Chemical compound C(CCCCCCC)OC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCCCCCCCC NISITOMOCKDHQZ-UHFFFAOYSA-N 0.000 description 1
- DPLOKUQRNXVAGL-UHFFFAOYSA-N (4-pentanoyloxynaphthalen-1-yl) pentanoate Chemical compound C(CCCC)(=O)OC1=CC=C(C2=CC=CC=C12)OC(CCCC)=O DPLOKUQRNXVAGL-UHFFFAOYSA-N 0.000 description 1
- MFJKSWMNKDWLOL-UHFFFAOYSA-N (4-propanoyloxynaphthalen-1-yl) propanoate Chemical compound C(CC)(=O)OC1=CC=C(C2=CC=CC=C12)OC(CC)=O MFJKSWMNKDWLOL-UHFFFAOYSA-N 0.000 description 1
- MNJOCVGPWJDKGX-QZQOTICOSA-N (E)-4-icosoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCOC(=O)\C=C\C(O)=O MNJOCVGPWJDKGX-QZQOTICOSA-N 0.000 description 1
- ZMQWRASVUXJXGM-VOTSOKGWSA-N (e)-4-cyclohexyloxy-4-oxobut-2-enoic acid Chemical compound OC(=O)\C=C\C(=O)OC1CCCCC1 ZMQWRASVUXJXGM-VOTSOKGWSA-N 0.000 description 1
- VPTNWGPGDXUKCY-ZHACJKMWSA-N (e)-4-decoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCOC(=O)\C=C\C(O)=O VPTNWGPGDXUKCY-ZHACJKMWSA-N 0.000 description 1
- IIPCXIGUIPAGQB-OUKQBFOZSA-N (e)-4-dodecoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCOC(=O)\C=C\C(O)=O IIPCXIGUIPAGQB-OUKQBFOZSA-N 0.000 description 1
- CUOOOYOREBCEAQ-ISLYRVAYSA-N (e)-4-heptadecoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCCCCCCOC(=O)\C=C\C(O)=O CUOOOYOREBCEAQ-ISLYRVAYSA-N 0.000 description 1
- IMHNCCFPIDJWFF-BQYQJAHWSA-N (e)-4-heptoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCOC(=O)\C=C\C(O)=O IMHNCCFPIDJWFF-BQYQJAHWSA-N 0.000 description 1
- YXIQOXQGELPIFQ-WUKNDPDISA-N (e)-4-hexadecoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCCCCCOC(=O)\C=C\C(O)=O YXIQOXQGELPIFQ-WUKNDPDISA-N 0.000 description 1
- RNERBJNDXXEXTK-VOTSOKGWSA-N (e)-4-hexoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCOC(=O)\C=C\C(O)=O RNERBJNDXXEXTK-VOTSOKGWSA-N 0.000 description 1
- ZUWTZMUABDXFJW-MDZDMXLPSA-N (e)-4-nonoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCOC(=O)\C=C\C(O)=O ZUWTZMUABDXFJW-MDZDMXLPSA-N 0.000 description 1
- MHQJUHSHQGQVTM-VHEBQXMUSA-N (e)-4-octadecoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)\C=C\C(O)=O MHQJUHSHQGQVTM-VHEBQXMUSA-N 0.000 description 1
- VTWGIDKXXZRLGH-CMDGGOBGSA-N (e)-4-octoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCOC(=O)\C=C\C(O)=O VTWGIDKXXZRLGH-CMDGGOBGSA-N 0.000 description 1
- AXKKHKOJPYVIKN-FOCLMDBBSA-N (e)-4-oxo-4-pentadecoxybut-2-enoic acid Chemical compound CCCCCCCCCCCCCCCOC(=O)\C=C\C(O)=O AXKKHKOJPYVIKN-FOCLMDBBSA-N 0.000 description 1
- BOFGUJVLYGISIU-AATRIKPKSA-N (e)-4-oxo-4-pentoxybut-2-enoic acid Chemical compound CCCCCOC(=O)\C=C\C(O)=O BOFGUJVLYGISIU-AATRIKPKSA-N 0.000 description 1
- AYAUWVRAUCDBFR-ONEGZZNKSA-N (e)-4-oxo-4-propoxybut-2-enoic acid Chemical compound CCCOC(=O)\C=C\C(O)=O AYAUWVRAUCDBFR-ONEGZZNKSA-N 0.000 description 1
- FGACNJFGXDUISO-BUHFOSPRSA-N (e)-4-oxo-4-tridecoxybut-2-enoic acid Chemical compound CCCCCCCCCCCCCOC(=O)\C=C\C(O)=O FGACNJFGXDUISO-BUHFOSPRSA-N 0.000 description 1
- HLSDOKOCNQHWHV-VAWYXSNFSA-N (e)-4-oxo-4-undecoxybut-2-enoic acid Chemical compound CCCCCCCCCCCOC(=O)\C=C\C(O)=O HLSDOKOCNQHWHV-VAWYXSNFSA-N 0.000 description 1
- OBDUMNZXAIUUTH-HWKANZROSA-N (e)-tetradec-2-ene Chemical group CCCCCCCCCCC\C=C\C OBDUMNZXAIUUTH-HWKANZROSA-N 0.000 description 1
- HFVIYAZBVIGNAN-UHFFFAOYSA-N 1,1-dibromodecane Chemical compound CCCCCCCCCC(Br)Br HFVIYAZBVIGNAN-UHFFFAOYSA-N 0.000 description 1
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 1
- SAWCWRKKWROPRB-UHFFFAOYSA-N 1,1-dibromohexane Chemical compound CCCCCC(Br)Br SAWCWRKKWROPRB-UHFFFAOYSA-N 0.000 description 1
- FSTKSTMFMLANPA-UHFFFAOYSA-N 1,1-dibromononane Chemical compound CCCCCCCCC(Br)Br FSTKSTMFMLANPA-UHFFFAOYSA-N 0.000 description 1
- STBMZSJLFYGOJU-UHFFFAOYSA-N 1,1-dibromooctane Chemical compound CCCCCCCC(Br)Br STBMZSJLFYGOJU-UHFFFAOYSA-N 0.000 description 1
- ATWLRNODAYAMQS-UHFFFAOYSA-N 1,1-dibromopropane Chemical compound CCC(Br)Br ATWLRNODAYAMQS-UHFFFAOYSA-N 0.000 description 1
- XKSUVRWJZCEYQQ-UHFFFAOYSA-N 1,1-dimethoxyethylbenzene Chemical compound COC(C)(OC)C1=CC=CC=C1 XKSUVRWJZCEYQQ-UHFFFAOYSA-N 0.000 description 1
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- NNOZGCICXAYKLW-UHFFFAOYSA-N 1,2-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC=C1C(C)(C)N=C=O NNOZGCICXAYKLW-UHFFFAOYSA-N 0.000 description 1
- QWQFVUQPHUKAMY-UHFFFAOYSA-N 1,2-diphenyl-2-propoxyethanone Chemical compound C=1C=CC=CC=1C(OCCC)C(=O)C1=CC=CC=C1 QWQFVUQPHUKAMY-UHFFFAOYSA-N 0.000 description 1
- IHVBAGIRJQOVGF-UHFFFAOYSA-N 1,2-dipropoxynaphthalene Chemical compound C1=CC=CC2=C(OCCC)C(OCCC)=CC=C21 IHVBAGIRJQOVGF-UHFFFAOYSA-N 0.000 description 1
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- BYOXZKJEOMUPRR-UHFFFAOYSA-N 1,4-bis(2-ethylhexoxy)-2,3-dimethylnaphthalene Chemical compound CC1=C(C2=CC=CC=C2C(=C1C)OCC(CCCC)CC)OCC(CCCC)CC BYOXZKJEOMUPRR-UHFFFAOYSA-N 0.000 description 1
- VVUWHPVSGPXRNP-UHFFFAOYSA-N 1,4-bis(2-ethylhexoxy)-2-methoxynaphthalene Chemical compound CCCCC(CC)COC1=CC(OC)=C(OCC(CC)CCCC)C2=CC=CC=C12 VVUWHPVSGPXRNP-UHFFFAOYSA-N 0.000 description 1
- PAMDCHJUDVZLRB-UHFFFAOYSA-N 1,4-bis(2-ethylhexoxy)-2-methylnaphthalene Chemical compound CCCCC(CC)COC1=CC(C)=C(OCC(CC)CCCC)C2=CC=CC=C12 PAMDCHJUDVZLRB-UHFFFAOYSA-N 0.000 description 1
- MKRBXTCYGQCXMJ-UHFFFAOYSA-N 1,4-bis(2-ethylhexoxy)-2-phenoxynaphthalene Chemical compound CCCCC(CC)COC1=CC(OC2=CC=CC=C2)=C(OCC(CC)CCCC)C2=CC=CC=C12 MKRBXTCYGQCXMJ-UHFFFAOYSA-N 0.000 description 1
- YETWMJKJLSWJNL-UHFFFAOYSA-N 1,4-bis(methoxymethoxy)naphthalene Chemical compound COCOC1=CC=C(C2=CC=CC=C21)OCOC YETWMJKJLSWJNL-UHFFFAOYSA-N 0.000 description 1
- WSUBCIDEIKWNOV-UHFFFAOYSA-N 1,4-diethoxy-2,3-dimethylnaphthalene Chemical compound CC1=C(C2=CC=CC=C2C(=C1C)OCC)OCC WSUBCIDEIKWNOV-UHFFFAOYSA-N 0.000 description 1
- WGIRROCGBDJGQS-UHFFFAOYSA-N 1,4-diethoxy-2-methoxynaphthalene Chemical compound CCOC1=CC(OC)=C(OCC)C2=CC=CC=C12 WGIRROCGBDJGQS-UHFFFAOYSA-N 0.000 description 1
- KWBXHASEDLXPHA-UHFFFAOYSA-N 1,4-diethoxy-2-methylnaphthalene Chemical compound C1=CC=C2C(OCC)=CC(C)=C(OCC)C2=C1 KWBXHASEDLXPHA-UHFFFAOYSA-N 0.000 description 1
- KFWZVAPTWLMLBM-UHFFFAOYSA-N 1,4-diethoxy-2-phenoxynaphthalene Chemical compound CCOC1=CC(OC2=CC=CC=C2)=C(OCC)C2=CC=CC=C12 KFWZVAPTWLMLBM-UHFFFAOYSA-N 0.000 description 1
- LJSLYKNKVQMIJY-UHFFFAOYSA-N 1,4-diethoxynaphthalene Chemical compound C1=CC=C2C(OCC)=CC=C(OCC)C2=C1 LJSLYKNKVQMIJY-UHFFFAOYSA-N 0.000 description 1
- MLLSZSJZDOQCSQ-UHFFFAOYSA-N 1,4-diheptoxynaphthalene Chemical compound C(CCCCCC)OC1=CC=C(C2=CC=CC=C12)OCCCCCCC MLLSZSJZDOQCSQ-UHFFFAOYSA-N 0.000 description 1
- AGANRYIVLGOPFT-UHFFFAOYSA-N 1,4-dihexoxy-2,3-dimethylnaphthalene Chemical compound CC1=C(C2=CC=CC=C2C(=C1C)OCCCCCC)OCCCCCC AGANRYIVLGOPFT-UHFFFAOYSA-N 0.000 description 1
- GLOFORNNCSOOBE-UHFFFAOYSA-N 1,4-dihexoxynaphthalene Chemical compound C1=CC=C2C(OCCCCCC)=CC=C(OCCCCCC)C2=C1 GLOFORNNCSOOBE-UHFFFAOYSA-N 0.000 description 1
- FPHPDLRTHCTWFI-UHFFFAOYSA-N 1,4-dimethoxy-2,3-dimethylnaphthalene Chemical compound C1=CC=C2C(OC)=C(C)C(C)=C(OC)C2=C1 FPHPDLRTHCTWFI-UHFFFAOYSA-N 0.000 description 1
- HWLZAXLHFSPJDM-UHFFFAOYSA-N 1,4-dimethoxy-2-methylnaphthalene Chemical compound C1=CC=C2C(OC)=CC(C)=C(OC)C2=C1 HWLZAXLHFSPJDM-UHFFFAOYSA-N 0.000 description 1
- JJJSYOYFBPYNBA-UHFFFAOYSA-N 1,4-dimethoxy-2-phenoxynaphthalene Chemical compound COC1=CC(OC2=CC=CC=C2)=C(OC)C2=CC=CC=C12 JJJSYOYFBPYNBA-UHFFFAOYSA-N 0.000 description 1
- HUPXYLXDKXHZKU-UHFFFAOYSA-N 1,4-dimethoxynaphthalen-2-ol Chemical compound C1=CC=C2C(OC)=CC(O)=C(OC)C2=C1 HUPXYLXDKXHZKU-UHFFFAOYSA-N 0.000 description 1
- FWWRTYBQQDXLDD-UHFFFAOYSA-N 1,4-dimethoxynaphthalene Chemical compound C1=CC=C2C(OC)=CC=C(OC)C2=C1 FWWRTYBQQDXLDD-UHFFFAOYSA-N 0.000 description 1
- APQSQLNWAIULLK-UHFFFAOYSA-N 1,4-dimethoxynaphthalene Natural products C1=CC=C2C(C)=CC=C(C)C2=C1 APQSQLNWAIULLK-UHFFFAOYSA-N 0.000 description 1
- LKAHMPSBGROAPY-UHFFFAOYSA-N 1,4-dioctoxy-2-phenoxynaphthalene Chemical compound CCCCCCCCOC1=CC(OC2=CC=CC=C2)=C(OCCCCCCCC)C2=CC=CC=C12 LKAHMPSBGROAPY-UHFFFAOYSA-N 0.000 description 1
- YAWGUJQFNTWCCA-UHFFFAOYSA-N 1,4-dioctoxynaphthalene Chemical compound C1=CC=C2C(OCCCCCCCC)=CC=C(OCCCCCCCC)C2=C1 YAWGUJQFNTWCCA-UHFFFAOYSA-N 0.000 description 1
- ANVMPSZGRYDRBR-UHFFFAOYSA-N 1,4-diphenoxynaphthalene Chemical compound C=1C=C(OC=2C=CC=CC=2)C2=CC=CC=C2C=1OC1=CC=CC=C1 ANVMPSZGRYDRBR-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- YDPZWUMQKMLLHC-UHFFFAOYSA-N 1,5-dibromo-3-methylpentane Chemical compound BrCCC(C)CCBr YDPZWUMQKMLLHC-UHFFFAOYSA-N 0.000 description 1
- QGLRLXLDMZCFBP-UHFFFAOYSA-N 1,6-diisocyanato-2,4,4-trimethylhexane Chemical compound O=C=NCC(C)CC(C)(C)CCN=C=O QGLRLXLDMZCFBP-UHFFFAOYSA-N 0.000 description 1
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- WUZKBGUWVJJFLO-UHFFFAOYSA-N 1,8-dibutoxy-15,16-dioxatetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaene Chemical compound C(CCC)OC12C3=CC=CC=C3C(C=3C=CC=CC13)(OO2)OCCCC WUZKBGUWVJJFLO-UHFFFAOYSA-N 0.000 description 1
- WGYZMNBUZFHYRX-UHFFFAOYSA-N 1-(1-methoxypropan-2-yloxy)propan-2-ol Chemical compound COCC(C)OCC(C)O WGYZMNBUZFHYRX-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- VQHKICGSBBPFFJ-UHFFFAOYSA-N 1-(2-methylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=CC=C1C VQHKICGSBBPFFJ-UHFFFAOYSA-N 0.000 description 1
- QLCFJROVGLBZQE-UHFFFAOYSA-N 1-butoxyanthracene Chemical compound C1=CC=C2C=C3C(OCCCC)=CC=CC3=CC2=C1 QLCFJROVGLBZQE-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- 125000005978 1-naphthyloxy group Chemical group 0.000 description 1
- WCJHIZQTNJPMPL-MDZDMXLPSA-N 1-o-ethyl 4-o-heptyl (e)-but-2-enedioate Chemical compound CCCCCCCOC(=O)\C=C\C(=O)OCC WCJHIZQTNJPMPL-MDZDMXLPSA-N 0.000 description 1
- YGWLMFNSGMKGIB-CMDGGOBGSA-N 1-o-ethyl 4-o-hexyl (e)-but-2-enedioate Chemical compound CCCCCCOC(=O)\C=C\C(=O)OCC YGWLMFNSGMKGIB-CMDGGOBGSA-N 0.000 description 1
- UVLWRTIHOMYLHX-ZHACJKMWSA-N 1-o-ethyl 4-o-octyl (e)-but-2-enedioate Chemical compound CCCCCCCCOC(=O)\C=C\C(=O)OCC UVLWRTIHOMYLHX-ZHACJKMWSA-N 0.000 description 1
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- CERJZAHSUZVMCH-UHFFFAOYSA-N 2,2-dichloro-1-phenylethanone Chemical compound ClC(Cl)C(=O)C1=CC=CC=C1 CERJZAHSUZVMCH-UHFFFAOYSA-N 0.000 description 1
- GIMQKKFOOYOQGB-UHFFFAOYSA-N 2,2-diethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)(OCC)C(=O)C1=CC=CC=C1 GIMQKKFOOYOQGB-UHFFFAOYSA-N 0.000 description 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- BXXWFOGWXLJPPA-UHFFFAOYSA-N 2,3-dibromobutane Chemical compound CC(Br)C(C)Br BXXWFOGWXLJPPA-UHFFFAOYSA-N 0.000 description 1
- MTGKEIQJKJCFFN-UHFFFAOYSA-N 2,3-dichloro-1,4-dimethoxynaphthalene Chemical compound C1=CC=C2C(OC)=C(Cl)C(Cl)=C(OC)C2=C1 MTGKEIQJKJCFFN-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- KMHSUNDEGHRBNV-UHFFFAOYSA-N 2,4-dichloropyrimidine-5-carbonitrile Chemical class ClC1=NC=C(C#N)C(Cl)=N1 KMHSUNDEGHRBNV-UHFFFAOYSA-N 0.000 description 1
- YMZIFDLWYUSZCC-UHFFFAOYSA-N 2,6-dibromo-4-nitroaniline Chemical compound NC1=C(Br)C=C([N+]([O-])=O)C=C1Br YMZIFDLWYUSZCC-UHFFFAOYSA-N 0.000 description 1
- SEFYJVFBMNOLBK-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxymethyl]oxirane Chemical compound C1OC1COCCOCCOCC1CO1 SEFYJVFBMNOLBK-UHFFFAOYSA-N 0.000 description 1
- NREFJJBCYMZUEK-UHFFFAOYSA-N 2-[2-[4-[2-[4-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]phenyl]propan-2-yl]phenoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound C1=CC(OCCOCCOC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OCCOCCOC(=O)C(C)=C)C=C1 NREFJJBCYMZUEK-UHFFFAOYSA-N 0.000 description 1
- SHKUUQIDMUMQQK-UHFFFAOYSA-N 2-[4-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical compound C1OC1COCCCCOCC1CO1 SHKUUQIDMUMQQK-UHFFFAOYSA-N 0.000 description 1
- WTYYGFLRBWMFRY-UHFFFAOYSA-N 2-[6-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COCCCCCCOCC1CO1 WTYYGFLRBWMFRY-UHFFFAOYSA-N 0.000 description 1
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 description 1
- FSYPIGPPWAJCJG-UHFFFAOYSA-N 2-[[4-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane Chemical compound C1OC1COC(C=C1)=CC=C1OCC1CO1 FSYPIGPPWAJCJG-UHFFFAOYSA-N 0.000 description 1
- RXNOYRCWKRFNIM-UHFFFAOYSA-N 2-carbonochloridoylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(Cl)=O RXNOYRCWKRFNIM-UHFFFAOYSA-N 0.000 description 1
- MAFUGWKJEFXAAD-UHFFFAOYSA-N 2-chloro-9,10-bis(2-ethylhexoxy)anthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCC(CCCC)CC)OCC(CCCC)CC MAFUGWKJEFXAAD-UHFFFAOYSA-N 0.000 description 1
- UVJDKLCHLIUHLT-UHFFFAOYSA-N 2-chloro-9,10-bis(2-methylphenoxy)anthracene Chemical compound CC1=CC=CC=C1OC2=C3C=CC(=CC3=C(C4=CC=CC=C42)OC5=CC=CC=C5C)Cl UVJDKLCHLIUHLT-UHFFFAOYSA-N 0.000 description 1
- WFHLECZNQPYPCE-UHFFFAOYSA-N 2-chloro-9,10-bis(ethoxymethoxy)anthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOCC)OCOCC WFHLECZNQPYPCE-UHFFFAOYSA-N 0.000 description 1
- RSZMBANPECWXFH-UHFFFAOYSA-N 2-chloro-9,10-bis(methoxymethoxy)anthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOC)OCOC RSZMBANPECWXFH-UHFFFAOYSA-N 0.000 description 1
- PRDTZBZARVYDNG-UHFFFAOYSA-N 2-chloro-9,10-diethoxyanthracene Chemical compound ClC1=CC=C2C(OCC)=C(C=CC=C3)C3=C(OCC)C2=C1 PRDTZBZARVYDNG-UHFFFAOYSA-N 0.000 description 1
- RCVGTWSISFIPTO-UHFFFAOYSA-N 2-chloro-9,10-diheptoxyanthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCC)OCCCCCCC RCVGTWSISFIPTO-UHFFFAOYSA-N 0.000 description 1
- PNKJIOYWIWMJPC-UHFFFAOYSA-N 2-chloro-9,10-dioctoxyanthracene Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCC)OCCCCCCCC PNKJIOYWIWMJPC-UHFFFAOYSA-N 0.000 description 1
- FPKCTSIVDAWGFA-UHFFFAOYSA-N 2-chloroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3C(=O)C2=C1 FPKCTSIVDAWGFA-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 1
- ZWVHTXAYIKBMEE-UHFFFAOYSA-N 2-hydroxyacetophenone Chemical class OCC(=O)C1=CC=CC=C1 ZWVHTXAYIKBMEE-UHFFFAOYSA-N 0.000 description 1
- NJRHMGPRPPEGQL-UHFFFAOYSA-N 2-hydroxybutyl prop-2-enoate Chemical compound CCC(O)COC(=O)C=C NJRHMGPRPPEGQL-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- KAANWDFVHVHHME-UHFFFAOYSA-N 2-methoxy-1,4-dioctoxynaphthalene Chemical compound CCCCCCCCOC1=CC(OC)=C(OCCCCCCCC)C2=CC=CC=C12 KAANWDFVHVHHME-UHFFFAOYSA-N 0.000 description 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- NFCBWWYWKSOWNK-UHFFFAOYSA-N 2-methyl-1,4-dioctoxynaphthalene Chemical compound CCCCCCCCOC1=CC(C)=C(OCCCCCCCC)C2=CC=CC=C12 NFCBWWYWKSOWNK-UHFFFAOYSA-N 0.000 description 1
- QTJAHIGJLSGOHF-UHFFFAOYSA-N 2-methyl-1,4-diphenoxynaphthalene Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC3=CC=CC=C3)OC4=CC=CC=C4 QTJAHIGJLSGOHF-UHFFFAOYSA-N 0.000 description 1
- LAGRACHHBNQZAL-UHFFFAOYSA-N 2-methyl-1,4-dipropoxynaphthalene Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OCCC)OCCC LAGRACHHBNQZAL-UHFFFAOYSA-N 0.000 description 1
- RICQMHDEJGXKNB-UHFFFAOYSA-N 2-methyl-9,10-bis(2-methylphenoxy)anthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC4=CC=CC=C4C)OC5=CC=CC=C5C RICQMHDEJGXKNB-UHFFFAOYSA-N 0.000 description 1
- AZEKKIMZIMDYCA-UHFFFAOYSA-N 2-methyl-9,10-bis(propoxymethoxy)anthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOCCC)OCOCCC AZEKKIMZIMDYCA-UHFFFAOYSA-N 0.000 description 1
- YSDIXNNAIJQFOC-UHFFFAOYSA-N 2-methyl-9,10-dioctoxyanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCC)OCCCCCCCC YSDIXNNAIJQFOC-UHFFFAOYSA-N 0.000 description 1
- KCYSEXMGPHIRHT-UHFFFAOYSA-N 2-methyl-9,10-dipropoxyanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCC)OCCC KCYSEXMGPHIRHT-UHFFFAOYSA-N 0.000 description 1
- 125000005979 2-naphthyloxy group Chemical group 0.000 description 1
- ZSZQGXICXSZWNN-UHFFFAOYSA-N 2-pentyl-9,10-bis(propoxymethoxy)anthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOCCC)OCOCCC ZSZQGXICXSZWNN-UHFFFAOYSA-N 0.000 description 1
- FMDOSBWXLJMBKL-UHFFFAOYSA-N 2-pentyl-9,10-diphenoxyanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC1=CC=CC=C1)OC1=CC=CC=C1 FMDOSBWXLJMBKL-UHFFFAOYSA-N 0.000 description 1
- UMWZLYTVXQBTTE-UHFFFAOYSA-N 2-pentylanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(CCCCC)=CC=C3C(=O)C2=C1 UMWZLYTVXQBTTE-UHFFFAOYSA-N 0.000 description 1
- KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- YTPSFXZMJKMUJE-UHFFFAOYSA-N 2-tert-butylanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(C(C)(C)C)=CC=C3C(=O)C2=C1 YTPSFXZMJKMUJE-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- TZFKFDQPHRPMKH-UHFFFAOYSA-N 4,4-dibromoheptane Chemical compound CCCC(Br)(Br)CCC TZFKFDQPHRPMKH-UHFFFAOYSA-N 0.000 description 1
- CLPFFLWZZBQMAO-UHFFFAOYSA-N 4-(5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-5-yl)benzonitrile Chemical compound C1=CC(C#N)=CC=C1C1N2C=NC=C2CCC1 CLPFFLWZZBQMAO-UHFFFAOYSA-N 0.000 description 1
- KRHMGQFGGUBDJI-UHFFFAOYSA-N 4-ethyl-1-(2-hydroxyethoxy)octan-2-ol Chemical compound CCCCC(CC)CC(O)COCCO KRHMGQFGGUBDJI-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- QJNLUNBGDFUULX-UHFFFAOYSA-N 4-n,4-n'-dimethyl-3h-pyridine-4,4-diamine Chemical compound CNC1(NC)CC=NC=C1 QJNLUNBGDFUULX-UHFFFAOYSA-N 0.000 description 1
- SAFXRWJUFXUQOY-CMDGGOBGSA-N 4-o-cyclohexyl 1-o-ethyl (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OC1CCCCC1 SAFXRWJUFXUQOY-CMDGGOBGSA-N 0.000 description 1
- JDOZUYVDIAKODH-SNAWJCMRSA-N 4-o-ethyl 1-o-methyl (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OC JDOZUYVDIAKODH-SNAWJCMRSA-N 0.000 description 1
- CZFQVAZEWFKUTC-VOTSOKGWSA-N 4-o-tert-butyl 1-o-ethyl (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OC(C)(C)C CZFQVAZEWFKUTC-VOTSOKGWSA-N 0.000 description 1
- HTYRTGGIOAMLRR-UHFFFAOYSA-N 5-amino-4-hydroxybenzene-1,3-disulfonic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC(S(O)(=O)=O)=C1O HTYRTGGIOAMLRR-UHFFFAOYSA-N 0.000 description 1
- PCFMUWBCZZUMRX-UHFFFAOYSA-N 9,10-Dihydroxyanthracene Chemical compound C1=CC=C2C(O)=C(C=CC=C3)C3=C(O)C2=C1 PCFMUWBCZZUMRX-UHFFFAOYSA-N 0.000 description 1
- VQEOOYKSPDFVRH-UHFFFAOYSA-N 9,10-bis(2-ethylhexoxy)-2-methylanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCC(CCCC)CC)OCC(CCCC)CC VQEOOYKSPDFVRH-UHFFFAOYSA-N 0.000 description 1
- UJEMIUDZEXNRNT-UHFFFAOYSA-N 9,10-bis(2-ethylhexoxy)-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCC(CCCC)CC)OCC(CCCC)CC UJEMIUDZEXNRNT-UHFFFAOYSA-N 0.000 description 1
- ZXRULULEMFAFAS-UHFFFAOYSA-N 9,10-bis(2-ethylhexoxy)anthracene Chemical compound C1=CC=C2C(OCC(CC)CCCC)=C(C=CC=C3)C3=C(OCC(CC)CCCC)C2=C1 ZXRULULEMFAFAS-UHFFFAOYSA-N 0.000 description 1
- VUJBYVDFUMYRMB-UHFFFAOYSA-N 9,10-bis(2-methylphenoxy)-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC1=C(C=CC=C1)C)OC1=C(C=CC=C1)C VUJBYVDFUMYRMB-UHFFFAOYSA-N 0.000 description 1
- BEZMIQYRCVRKRS-UHFFFAOYSA-N 9,10-bis(2-methylphenoxy)anthracene Chemical compound CC1=CC=CC=C1OC2=C3C=CC=CC3=C(C4=CC=CC=C42)OC5=CC=CC=C5C BEZMIQYRCVRKRS-UHFFFAOYSA-N 0.000 description 1
- KNYIINVKUJGKFW-UHFFFAOYSA-N 9,10-bis(butoxymethoxy)-2-chloroanthracene Chemical compound CCCCOCOC1=C2C=CC(=CC2=C(C3=CC=CC=C31)OCOCCCC)Cl KNYIINVKUJGKFW-UHFFFAOYSA-N 0.000 description 1
- NTUVQILMDIFJHU-UHFFFAOYSA-N 9,10-bis(butoxymethoxy)-2-methylanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOCCCC)OCOCCCC NTUVQILMDIFJHU-UHFFFAOYSA-N 0.000 description 1
- XTBAIEOPDAWOKS-UHFFFAOYSA-N 9,10-bis(butoxymethoxy)-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOCCCC)OCOCCCC XTBAIEOPDAWOKS-UHFFFAOYSA-N 0.000 description 1
- OCHMYEIGTFJMHN-UHFFFAOYSA-N 9,10-bis(butoxymethoxy)anthracene Chemical compound CCCCOCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCOCCCC OCHMYEIGTFJMHN-UHFFFAOYSA-N 0.000 description 1
- WWGRSTJEGYHVTM-UHFFFAOYSA-N 9,10-bis(ethoxymethoxy)-2-methylanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOCC)OCOCC WWGRSTJEGYHVTM-UHFFFAOYSA-N 0.000 description 1
- BGDORFHOWAYEKT-UHFFFAOYSA-N 9,10-bis(ethoxymethoxy)-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOCC)OCOCC BGDORFHOWAYEKT-UHFFFAOYSA-N 0.000 description 1
- FNPWCSHIBIBGLQ-UHFFFAOYSA-N 9,10-bis(ethoxymethoxy)anthracene Chemical compound C(C)OCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCOCC FNPWCSHIBIBGLQ-UHFFFAOYSA-N 0.000 description 1
- IYJWNROMMAPRRT-UHFFFAOYSA-N 9,10-bis(methoxymethoxy)-2-methylanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOC)OCOC IYJWNROMMAPRRT-UHFFFAOYSA-N 0.000 description 1
- YDYGXEGTCGPHMZ-UHFFFAOYSA-N 9,10-bis(methoxymethoxy)-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCOC)OCOC YDYGXEGTCGPHMZ-UHFFFAOYSA-N 0.000 description 1
- JMZCWCQJGJBXPE-UHFFFAOYSA-N 9,10-bis(methoxymethoxy)anthracene Chemical compound COCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCOC JMZCWCQJGJBXPE-UHFFFAOYSA-N 0.000 description 1
- PFMLCJDCXBSLRP-UHFFFAOYSA-N 9,10-bis(propoxymethoxy)anthracene Chemical compound CCCOCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCOCCC PFMLCJDCXBSLRP-UHFFFAOYSA-N 0.000 description 1
- IDYMRUYZUOLRHT-UHFFFAOYSA-N 9,10-di(nonoxy)-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC)OCCCCCCCCC IDYMRUYZUOLRHT-UHFFFAOYSA-N 0.000 description 1
- GSMYTXQTSBPOET-UHFFFAOYSA-N 9,10-diethoxy-2-methylanthracene Chemical compound CC1=CC=C2C(OCC)=C(C=CC=C3)C3=C(OCC)C2=C1 GSMYTXQTSBPOET-UHFFFAOYSA-N 0.000 description 1
- QHFSSPHFYFDTAS-UHFFFAOYSA-N 9,10-diethoxy-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCC)OCC QHFSSPHFYFDTAS-UHFFFAOYSA-N 0.000 description 1
- GJNKQJAJXSUJBO-UHFFFAOYSA-N 9,10-diethoxyanthracene Chemical compound C1=CC=C2C(OCC)=C(C=CC=C3)C3=C(OCC)C2=C1 GJNKQJAJXSUJBO-UHFFFAOYSA-N 0.000 description 1
- OJPDDUBIZICTHP-UHFFFAOYSA-N 9,10-diheptoxy-2-methylanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCC)OCCCCCCC OJPDDUBIZICTHP-UHFFFAOYSA-N 0.000 description 1
- HEOHVYAOMULBEZ-UHFFFAOYSA-N 9,10-diheptoxy-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCC)OCCCCCCC HEOHVYAOMULBEZ-UHFFFAOYSA-N 0.000 description 1
- NZNCSLHAZCRBSB-UHFFFAOYSA-N 9,10-diheptoxyanthracene Chemical compound C(CCCCCC)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCC NZNCSLHAZCRBSB-UHFFFAOYSA-N 0.000 description 1
- KCFSPEVZEXNBFZ-UHFFFAOYSA-N 9,10-dihexoxy-2-methylanthracene Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCC)OCCCCCC KCFSPEVZEXNBFZ-UHFFFAOYSA-N 0.000 description 1
- ZDTMMQHVAGNFSA-UHFFFAOYSA-N 9,10-dihexoxy-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCC)OCCCCCC ZDTMMQHVAGNFSA-UHFFFAOYSA-N 0.000 description 1
- LWRCGYDAUMSFSM-UHFFFAOYSA-N 9,10-dihexoxyanthracene Chemical compound C1=CC=C2C(OCCCCCC)=C(C=CC=C3)C3=C(OCCCCCC)C2=C1 LWRCGYDAUMSFSM-UHFFFAOYSA-N 0.000 description 1
- NNVIATIFPQFFFA-UHFFFAOYSA-N 9,10-dimethoxy-1,2,3,4-tetrahydroanthracene Chemical compound COC=1C2=CC=CC=C2C(=C2CCCCC=12)OC NNVIATIFPQFFFA-UHFFFAOYSA-N 0.000 description 1
- GKGQODVOHMVVQJ-UHFFFAOYSA-N 9,10-dimethoxy-1,4-dihydroanthracene Chemical compound C1=CC=C2C(OC)=C(CC=CC3)C3=C(OC)C2=C1 GKGQODVOHMVVQJ-UHFFFAOYSA-N 0.000 description 1
- AORITAKWERAXQO-UHFFFAOYSA-N 9,10-dimethoxy-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC)OC AORITAKWERAXQO-UHFFFAOYSA-N 0.000 description 1
- NIPGMUMAGATLBV-UHFFFAOYSA-N 9,10-dioctoxy-2-pentylanthracene Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCC)OCCCCCCCC NIPGMUMAGATLBV-UHFFFAOYSA-N 0.000 description 1
- SHBQKXHLNLKYPT-UHFFFAOYSA-N 9,10-dioctoxyanthracene Chemical compound C1=CC=C2C(OCCCCCCCC)=C(C=CC=C3)C3=C(OCCCCCCCC)C2=C1 SHBQKXHLNLKYPT-UHFFFAOYSA-N 0.000 description 1
- RYWSYCQQUDFMAU-UHFFFAOYSA-N Acetomenaphthone Chemical compound C1=CC=C2C(OC(=O)C)=CC(C)=C(OC(C)=O)C2=C1 RYWSYCQQUDFMAU-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- KHAJQRXTAQSRHN-UHFFFAOYSA-N C(C)C(COC=1C2=CC=CC=C2C(=C2CC=CCC12)OCC(CCCC)CC)CCCC Chemical compound C(C)C(COC=1C2=CC=CC=C2C(=C2CC=CCC12)OCC(CCCC)CC)CCCC KHAJQRXTAQSRHN-UHFFFAOYSA-N 0.000 description 1
- WEHXTTLRUKETPB-UHFFFAOYSA-N C(C)OC=1C2=CC=CC=C2C(=C2CC=CCC12)OCC Chemical compound C(C)OC=1C2=CC=CC=C2C(=C2CC=CCC12)OCC WEHXTTLRUKETPB-UHFFFAOYSA-N 0.000 description 1
- VBYHNIGFQFFVFW-UHFFFAOYSA-N C(C)OC=1C2=CC=CC=C2C(=C2CCCCC=12)OCC Chemical compound C(C)OC=1C2=CC=CC=C2C(=C2CCCCC=12)OCC VBYHNIGFQFFVFW-UHFFFAOYSA-N 0.000 description 1
- AZHDNPNOKUMXEI-UHFFFAOYSA-N C(CCCCCCCC)OC1=CC=C(C2=CC=CC=C12)OCCCCCCCCC Chemical compound C(CCCCCCCC)OC1=CC=C(C2=CC=CC=C12)OCCCCCCCCC AZHDNPNOKUMXEI-UHFFFAOYSA-N 0.000 description 1
- JXGRISHUJQKZKV-UHFFFAOYSA-N C1=CC=C(C=C1)OC2=C3C=CC(=CC3=C(C4=CC=CC=C42)OC5=CC=CC=C5)Cl Chemical compound C1=CC=C(C=C1)OC2=C3C=CC(=CC3=C(C4=CC=CC=C42)OC5=CC=CC=C5)Cl JXGRISHUJQKZKV-UHFFFAOYSA-N 0.000 description 1
- JYSDROPYFMOQPO-UHFFFAOYSA-N CC1=C(C(=O)C=2C(=C(C=CC=2)P(C2=CC=CC=C2)=O)C(C2=C(C=C(C=C2C)C)C)=O)C(=CC(=C1)C)C Chemical compound CC1=C(C(=O)C=2C(=C(C=CC=2)P(C2=CC=CC=C2)=O)C(C2=C(C=C(C=C2C)C)C)=O)C(=CC(=C1)C)C JYSDROPYFMOQPO-UHFFFAOYSA-N 0.000 description 1
- HCTYOFJCAACHMC-UHFFFAOYSA-N CC1=C(C2=CC=CC=C2C(=C1)OCCCCCC)OCCCCCC Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OCCCCCC)OCCCCCC HCTYOFJCAACHMC-UHFFFAOYSA-N 0.000 description 1
- OHQOBJNEMAUPIC-UHFFFAOYSA-N CC1=C(C2=CC=CC=C2C(=C1)OCCCCCCC)OCCCCCCC Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OCCCCCCC)OCCCCCCC OHQOBJNEMAUPIC-UHFFFAOYSA-N 0.000 description 1
- HIFJZCWWNMVSLI-UHFFFAOYSA-N CC1=C(C2=CC=CC=C2C(=C1)OCCCCCCCCC)OCCCCCCCCC Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OCCCCCCCCC)OCCCCCCCCC HIFJZCWWNMVSLI-UHFFFAOYSA-N 0.000 description 1
- BUNHUUKBRRJAEI-UHFFFAOYSA-N CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC1=CC=CC=C1)OC1=CC=CC=C1 Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC1=CC=CC=C1)OC1=CC=CC=C1 BUNHUUKBRRJAEI-UHFFFAOYSA-N 0.000 description 1
- JXTOQGWEZMSRQX-UHFFFAOYSA-N CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC)OCCCCCCCCC Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC)OCCCCCCCCC JXTOQGWEZMSRQX-UHFFFAOYSA-N 0.000 description 1
- IFUJHFYHSSRTIJ-UHFFFAOYSA-N CC1=CCC2=C(C3=CC=CC=C3C(=C2C1)OC)OC Chemical compound CC1=CCC2=C(C3=CC=CC=C3C(=C2C1)OC)OC IFUJHFYHSSRTIJ-UHFFFAOYSA-N 0.000 description 1
- LNDMXIHIVZAICZ-UHFFFAOYSA-N CC1CC2=C(C3=CC=CC=C3C(=C2CC1)OCC)OCC Chemical compound CC1CC2=C(C3=CC=CC=C3C(=C2CC1)OCC)OCC LNDMXIHIVZAICZ-UHFFFAOYSA-N 0.000 description 1
- XDCIVSYBFGBKBO-UHFFFAOYSA-N CC=1CC2=C(C3=CC=CC=C3C(=C2CC1)OCC)OCC Chemical compound CC=1CC2=C(C3=CC=CC=C3C(=C2CC1)OCC)OCC XDCIVSYBFGBKBO-UHFFFAOYSA-N 0.000 description 1
- SUOQCNKFNVQCMO-CCEZHUSRSA-N CCCCCCCCCCCC(CC)OC(=O)\C=C\C(O)=O Chemical compound CCCCCCCCCCCC(CC)OC(=O)\C=C\C(O)=O SUOQCNKFNVQCMO-CCEZHUSRSA-N 0.000 description 1
- QVYVNSKIIQQVCZ-VHEBQXMUSA-N CCCCCCCCCCCCCCCC(CC)OC(=O)\C=C\C(O)=O Chemical compound CCCCCCCCCCCCCCCC(CC)OC(=O)\C=C\C(O)=O QVYVNSKIIQQVCZ-VHEBQXMUSA-N 0.000 description 1
- IWCHOIKCEFZOHP-UHFFFAOYSA-N CCCCCCOC1=C2CC=CCC2=C(C3=CC=CC=C31)OCCCCCC Chemical compound CCCCCCOC1=C2CC=CCC2=C(C3=CC=CC=C31)OCCCCCC IWCHOIKCEFZOHP-UHFFFAOYSA-N 0.000 description 1
- DKDAMMLYIPBOGF-UHFFFAOYSA-N COC1=C(C2=CC=CC=C2C(=C1)OCCCCCC)OCCCCCC Chemical compound COC1=C(C2=CC=CC=C2C(=C1)OCCCCCC)OCCCCCC DKDAMMLYIPBOGF-UHFFFAOYSA-N 0.000 description 1
- JDXMGCFXWVBWCK-UHFFFAOYSA-N COC1=C(C2=CC=CC=C2C(=C1)OCCCCCCCCC)OCCCCCCCCC Chemical compound COC1=C(C2=CC=CC=C2C(=C1)OCCCCCCCCC)OCCCCCCCCC JDXMGCFXWVBWCK-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- XVZXOLOFWKSDSR-UHFFFAOYSA-N Cc1cc(C)c([C]=O)c(C)c1 Chemical group Cc1cc(C)c([C]=O)c(C)c1 XVZXOLOFWKSDSR-UHFFFAOYSA-N 0.000 description 1
- UQFGWDNBXFTMFK-UHFFFAOYSA-N ClC1=C(C2=CC=CC=C2C(=C1Cl)OCC)OCC Chemical compound ClC1=C(C2=CC=CC=C2C(=C1Cl)OCC)OCC UQFGWDNBXFTMFK-UHFFFAOYSA-N 0.000 description 1
- GOGVAWQKINWJSN-UHFFFAOYSA-N ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC)OCCCCCCCCC Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC)OCCCCCCCCC GOGVAWQKINWJSN-UHFFFAOYSA-N 0.000 description 1
- RWIBPIQLZCGSLV-UHFFFAOYSA-N ClC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OCCC)OCCC Chemical compound ClC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OCCC)OCCC RWIBPIQLZCGSLV-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 1
- 238000005698 Diels-Alder reaction Methods 0.000 description 1
- VIZORQUEIQEFRT-UHFFFAOYSA-N Diethyl adipate Chemical compound CCOC(=O)CCCCC(=O)OCC VIZORQUEIQEFRT-UHFFFAOYSA-N 0.000 description 1
- DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical compound CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 description 1
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
- MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- LOMVENUNSWAXEN-UHFFFAOYSA-N Methyl oxalate Chemical compound COC(=O)C(=O)OC LOMVENUNSWAXEN-UHFFFAOYSA-N 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- OXKOSESJFSACRA-UHFFFAOYSA-N O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCCCCC)OCCCCCC Chemical compound O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCCCCC)OCCCCCC OXKOSESJFSACRA-UHFFFAOYSA-N 0.000 description 1
- IPNPVUMIZBRSPG-UHFFFAOYSA-N O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCCCCCCCC)OCCCCCCCCC Chemical compound O(C1=CC=CC=C1)C1=C(C2=CC=CC=C2C(=C1)OCCCCCCCCC)OCCCCCCCCC IPNPVUMIZBRSPG-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 1
- DVOGCYZOJDSYGQ-UHFFFAOYSA-N [1,5-diethyl-10-(2-ethylhexoxycarbonyloxy)anthracen-9-yl] 2-ethylhexyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCC(CCCC)CC)CC)OC(=O)OCC(CCCC)CC DVOGCYZOJDSYGQ-UHFFFAOYSA-N 0.000 description 1
- SWIRGKBXVUOPCB-UHFFFAOYSA-N [1-ethyl-10-(2-ethylhexoxycarbonyloxy)anthracen-9-yl] 2-ethylhexyl carbonate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCC(CCCC)CC)OC(=O)OCC(CCCC)CC SWIRGKBXVUOPCB-UHFFFAOYSA-N 0.000 description 1
- DJWCKLCRAYBZOB-UHFFFAOYSA-N [10-(2-ethylhexanoyloxy)-2,6-dimethylanthracen-9-yl] 2-ethylhexanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(C(CCCC)CC)=O)C)OC(C(CCCC)CC)=O DJWCKLCRAYBZOB-UHFFFAOYSA-N 0.000 description 1
- UBLADIAZOICSMA-UHFFFAOYSA-N [10-(2-ethylhexanoyloxy)-3-methylanthracen-9-yl] 2-ethylhexanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(C(CCCC)CC)=O)OC(C(CCCC)CC)=O UBLADIAZOICSMA-UHFFFAOYSA-N 0.000 description 1
- XEXYJUATHCAPBF-UHFFFAOYSA-N [10-(2-ethylhexanoyloxy)-4-methylanthracen-9-yl] 2-ethylhexanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(C(CCCC)CC)=O)OC(C(CCCC)CC)=O XEXYJUATHCAPBF-UHFFFAOYSA-N 0.000 description 1
- KHEDNBRORNZTNH-UHFFFAOYSA-N [10-(2-ethylhexanoyloxy)anthracen-9-yl] 2-ethylhexanoate Chemical compound C(C)C(C(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(C(CCCC)CC)=O)CCCC KHEDNBRORNZTNH-UHFFFAOYSA-N 0.000 description 1
- JSGDBELVQLWMDO-UHFFFAOYSA-N [10-(2-ethylhexoxycarbonyloxy)-1,5-dimethylanthracen-9-yl] 2-ethylhexyl carbonate Chemical compound CC1=CC=CC2=C(C3=C(C=CC=C3C(=C12)OC(=O)OCC(CCCC)CC)C)OC(=O)OCC(CCCC)CC JSGDBELVQLWMDO-UHFFFAOYSA-N 0.000 description 1
- IHRNHWDZCDFETA-UHFFFAOYSA-N [10-(2-ethylhexoxycarbonyloxy)-1-methylanthracen-9-yl] 2-ethylhexyl carbonate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)OCC(CCCC)CC)OC(=O)OCC(CCCC)CC IHRNHWDZCDFETA-UHFFFAOYSA-N 0.000 description 1
- CQVAVBBGVHDQBU-UHFFFAOYSA-N [10-(2-ethylhexoxycarbonyloxy)-2,3-dimethylanthracen-9-yl] 2-ethylhexyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(=O)OCC(CCCC)CC)OC(=O)OCC(CCCC)CC CQVAVBBGVHDQBU-UHFFFAOYSA-N 0.000 description 1
- AVHVWTUXFCFGPM-UHFFFAOYSA-N [10-(2-ethylhexoxycarbonyloxy)-2,6-dimethylanthracen-9-yl] 2-ethylhexyl carbonate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(=O)OCC(CCCC)CC)C)OC(=O)OCC(CCCC)CC AVHVWTUXFCFGPM-UHFFFAOYSA-N 0.000 description 1
- UWQHRWZWBBTDGG-UHFFFAOYSA-N [10-(2-ethylhexoxycarbonyloxy)-2-methylanthracen-9-yl] 2-ethylhexyl carbonate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCC(CCCC)CC)OC(=O)OCC(CCCC)CC UWQHRWZWBBTDGG-UHFFFAOYSA-N 0.000 description 1
- GROQZUISBOBUSK-UHFFFAOYSA-N [10-(2-ethylhexoxycarbonyloxy)anthracen-9-yl] 2-ethylhexyl carbonate Chemical compound C(C)C(COC(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(=O)OCC(CCCC)CC)CCCC GROQZUISBOBUSK-UHFFFAOYSA-N 0.000 description 1
- BPRSJRDASARHQE-UHFFFAOYSA-N [10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound C(C)(C)C(=O)OC=1C2=CC=CC=C2C(=C2C=CC=CC=12)OC(=O)C(C)C BPRSJRDASARHQE-UHFFFAOYSA-N 0.000 description 1
- FURBIHKPDRPOLD-UHFFFAOYSA-N [2,3-diethyl-10-(2-ethylhexoxycarbonyloxy)anthracen-9-yl] 2-ethylhexyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1CC)OC(=O)OCC(CCCC)CC)OC(=O)OCC(CCCC)CC FURBIHKPDRPOLD-UHFFFAOYSA-N 0.000 description 1
- SIWXKTOPAFIDJJ-UHFFFAOYSA-N [2,3-dimethyl-10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1C)OC(C(C)C)=O)OC(C(C)C)=O SIWXKTOPAFIDJJ-UHFFFAOYSA-N 0.000 description 1
- UDSBLBDNPJMVAP-UHFFFAOYSA-N [2,6-dimethyl-10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound CC1=CC2=C(C3=CC=C(C=C3C(=C2C=C1)OC(C(C)C)=O)C)OC(C(C)C)=O UDSBLBDNPJMVAP-UHFFFAOYSA-N 0.000 description 1
- OMZDOZHLIWWMKA-UHFFFAOYSA-N [2,7-diethyl-10-(2-ethylhexoxycarbonyloxy)anthracen-9-yl] 2-ethylhexyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(=O)OCC(CCCC)CC)CC)OC(=O)OCC(CCCC)CC OMZDOZHLIWWMKA-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- NAWYTRXMSQFFRK-UHFFFAOYSA-N [2-ethyl-10-(2-ethylhexoxycarbonyloxy)anthracen-9-yl] 2-ethylhexyl carbonate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)OCC(CCCC)CC)OC(=O)OCC(CCCC)CC NAWYTRXMSQFFRK-UHFFFAOYSA-N 0.000 description 1
- JWQXKWJQEFJKEF-UHFFFAOYSA-N [3,6-dimethyl-10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound CC1=CC2=C(C3=CC(=CC=C3C(=C2C=C1)OC(C(C)C)=O)C)OC(C(C)C)=O JWQXKWJQEFJKEF-UHFFFAOYSA-N 0.000 description 1
- ZNJQNHPBIMQJMA-UHFFFAOYSA-N [3-ethyl-10-(2-ethylhexanoyloxy)anthracen-9-yl] 2-ethylhexanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(C(CCCC)CC)=O)OC(C(CCCC)CC)=O ZNJQNHPBIMQJMA-UHFFFAOYSA-N 0.000 description 1
- MKHAHFMGHLJRDD-UHFFFAOYSA-N [3-ethyl-10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(C(C)C)=O)OC(C(C)C)=O MKHAHFMGHLJRDD-UHFFFAOYSA-N 0.000 description 1
- MTFLJQLLOLTWGA-UHFFFAOYSA-N [3-methyl-10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound CC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(=O)C(C)C)OC(=O)C(C)C MTFLJQLLOLTWGA-UHFFFAOYSA-N 0.000 description 1
- UDHGPFTVFBYAPA-UHFFFAOYSA-N [3-methyl-4-(2-methylpropanoyloxy)naphthalen-1-yl] 2-methylpropanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(C(C)C)=O)OC(C(C)C)=O UDHGPFTVFBYAPA-UHFFFAOYSA-N 0.000 description 1
- QVTLESJAVARTIV-UHFFFAOYSA-N [4-(2-ethylhexanoyloxy)-3-methylnaphthalen-1-yl] 2-ethylhexanoate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(C(CCCC)CC)=O)OC(C(CCCC)CC)=O QVTLESJAVARTIV-UHFFFAOYSA-N 0.000 description 1
- XVHBXHNJFKHYFM-UHFFFAOYSA-N [4-(2-ethylhexanoyloxy)naphthalen-1-yl] 2-ethylhexanoate Chemical compound C(C)C(C(=O)OC1=CC=C(C2=CC=CC=C12)OC(C(CCCC)CC)=O)CCCC XVHBXHNJFKHYFM-UHFFFAOYSA-N 0.000 description 1
- VAVRMEMRVDHTPC-UHFFFAOYSA-N [4-(2-ethylhexoxycarbonyloxy)-2,3-dimethylnaphthalen-1-yl] 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OC1=C(C(=C(C2=CC=CC=C21)OC(=O)OCC(CC)CCCC)C)C VAVRMEMRVDHTPC-UHFFFAOYSA-N 0.000 description 1
- WTLFSMSFQCLYLM-UHFFFAOYSA-N [4-(2-ethylhexoxycarbonyloxy)-2-methylnaphthalen-1-yl] 2-ethylhexyl carbonate Chemical compound CC1=C(C2=CC=CC=C2C(=C1)OC(=O)OCC(CCCC)CC)OC(=O)OCC(CCCC)CC WTLFSMSFQCLYLM-UHFFFAOYSA-N 0.000 description 1
- XXIVJMFMLWKKNM-UHFFFAOYSA-N [4-(2-ethylhexoxycarbonyloxy)naphthalen-1-yl] 2-ethylhexyl carbonate Chemical compound C(C)C(COC(=O)OC1=CC=C(C2=CC=CC=C12)OC(=O)OCC(CCCC)CC)CCCC XXIVJMFMLWKKNM-UHFFFAOYSA-N 0.000 description 1
- PYBJBOQKVSFYSR-UHFFFAOYSA-N [4-(2-methylpropanoyloxy)-3-phenoxynaphthalen-1-yl] 2-methylpropanoate Chemical compound CC(C)C(=O)OC=1C2=CC=CC=C2C(OC(=O)C(C)C)=CC=1OC1=CC=CC=C1 PYBJBOQKVSFYSR-UHFFFAOYSA-N 0.000 description 1
- OOARHPULTUFBQK-UHFFFAOYSA-N [4-(2-methylpropanoyloxy)naphthalen-1-yl] 2-methylpropanoate Chemical compound C1=CC=C2C(OC(=O)C(C)C)=CC=C(OC(=O)C(C)C)C2=C1 OOARHPULTUFBQK-UHFFFAOYSA-N 0.000 description 1
- DBHQYYNDKZDVTN-UHFFFAOYSA-N [4-(4-methylphenyl)sulfanylphenyl]-phenylmethanone Chemical compound C1=CC(C)=CC=C1SC1=CC=C(C(=O)C=2C=CC=CC=2)C=C1 DBHQYYNDKZDVTN-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- QUVWUXWRQOLLND-UHFFFAOYSA-N [4-ethyl-10-(2-ethylhexanoyloxy)anthracen-9-yl] 2-ethylhexanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(C(CCCC)CC)=O)OC(C(CCCC)CC)=O QUVWUXWRQOLLND-UHFFFAOYSA-N 0.000 description 1
- LPUIKPMAYSZIAI-UHFFFAOYSA-N [4-ethyl-10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound C(C)C1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)C(C)C)OC(=O)C(C)C LPUIKPMAYSZIAI-UHFFFAOYSA-N 0.000 description 1
- RHXHUJFGJBXVGZ-UHFFFAOYSA-N [4-methyl-10-(2-methylpropanoyloxy)anthracen-9-yl] 2-methylpropanoate Chemical compound CC1=CC=CC2=C(C3=CC=CC=C3C(=C12)OC(=O)C(C)C)OC(=O)C(C)C RHXHUJFGJBXVGZ-UHFFFAOYSA-N 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 239000000999 acridine dye Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- PWAXUOGZOSVGBO-UHFFFAOYSA-N adipoyl chloride Chemical compound ClC(=O)CCCCC(Cl)=O PWAXUOGZOSVGBO-UHFFFAOYSA-N 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- OUOWYULOORWTPH-UHFFFAOYSA-N anthracen-1-yl propyl carbonate Chemical compound C(CC)OC(=O)OC1=CC=CC2=CC3=CC=CC=C3C=C12 OUOWYULOORWTPH-UHFFFAOYSA-N 0.000 description 1
- RURGWVZQAKAYDM-UHFFFAOYSA-N anthracene-9,10-diol diacetate Chemical compound C1=CC=C2C(OC(=O)C)=C(C=CC=C3)C3=C(OC(C)=O)C2=C1 RURGWVZQAKAYDM-UHFFFAOYSA-N 0.000 description 1
- 125000005427 anthranyl group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000007869 azo polymerization initiator Substances 0.000 description 1
- 125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 1
- ROPXFXOUUANXRR-BUHFOSPRSA-N bis(2-ethylhexyl) (e)-but-2-enedioate Chemical compound CCCCC(CC)COC(=O)\C=C\C(=O)OCC(CC)CCCC ROPXFXOUUANXRR-BUHFOSPRSA-N 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- WXZOXVVKILCOPG-UHFFFAOYSA-N bis(2-ethylhexyl) benzene-1,3-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC(C(=O)OCC(CC)CCCC)=C1 WXZOXVVKILCOPG-UHFFFAOYSA-N 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- HXTBYXIZCDULQI-UHFFFAOYSA-N bis[4-(methylamino)phenyl]methanone Chemical compound C1=CC(NC)=CC=C1C(=O)C1=CC=C(NC)C=C1 HXTBYXIZCDULQI-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- IRXBNHGNHKNOJI-UHFFFAOYSA-N butanedioyl dichloride Chemical compound ClC(=O)CCC(Cl)=O IRXBNHGNHKNOJI-UHFFFAOYSA-N 0.000 description 1
- KDVXVMQILCJWCD-UHFFFAOYSA-N butyl 14-[10-(14-butoxy-14-oxotetradecoxy)anthracen-9-yl]oxytetradecanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCC(=O)OCCCC KDVXVMQILCJWCD-UHFFFAOYSA-N 0.000 description 1
- ZWEBAWYQTWEPNV-UHFFFAOYSA-N butyl 15-[10-(15-butoxy-15-oxopentadecoxy)anthracen-9-yl]oxypentadecanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCC(=O)OCCCC ZWEBAWYQTWEPNV-UHFFFAOYSA-N 0.000 description 1
- BZYJNJRSRZZWIW-UHFFFAOYSA-N butyl 16-[10-(16-butoxy-16-oxohexadecoxy)anthracen-9-yl]oxyhexadecanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCC(=O)OCCCC BZYJNJRSRZZWIW-UHFFFAOYSA-N 0.000 description 1
- IWGZKXDEJKLBCT-UHFFFAOYSA-N butyl 17-[10-(17-butoxy-17-oxoheptadecoxy)-3-chloroanthracen-9-yl]oxyheptadecanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCC(=O)OCCCC)OCCCCCCCCCCCCCCCCC(=O)OCCCC IWGZKXDEJKLBCT-UHFFFAOYSA-N 0.000 description 1
- MZYVWYDOLXSUCC-UHFFFAOYSA-N butyl 17-[10-(17-butoxy-17-oxoheptadecoxy)-3-ethylanthracen-9-yl]oxyheptadecanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCC(=O)OCCCC)OCCCCCCCCCCCCCCCCC(=O)OCCCC MZYVWYDOLXSUCC-UHFFFAOYSA-N 0.000 description 1
- QPOMJKKNQPLHGI-UHFFFAOYSA-N butyl 19-[10-(19-butoxy-19-oxononadecoxy)anthracen-9-yl]oxynonadecanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCC(=O)OCCCC QPOMJKKNQPLHGI-UHFFFAOYSA-N 0.000 description 1
- NMEGSGKCIWQRDB-UHFFFAOYSA-N butyl 2-bromoacetate Chemical compound CCCCOC(=O)CBr NMEGSGKCIWQRDB-UHFFFAOYSA-N 0.000 description 1
- YJRGMUWRPCPLNH-UHFFFAOYSA-N butyl 2-chloroacetate Chemical compound CCCCOC(=O)CCl YJRGMUWRPCPLNH-UHFFFAOYSA-N 0.000 description 1
- WNAJUVKEROMCIW-UHFFFAOYSA-N butyl 20-[10-(20-butoxy-20-oxoicosoxy)anthracen-9-yl]oxyicosanoate Chemical compound CCCCOC(=O)CCCCCCCCCCCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCCCCC(=O)OCCCC WNAJUVKEROMCIW-UHFFFAOYSA-N 0.000 description 1
- YESNNYPJOCXTSE-UHFFFAOYSA-N butyl 21-[10-(21-butoxy-21-oxohenicosoxy)-3-chloroanthracen-9-yl]oxyhenicosanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OCCCC)OCCCCCCCCCCCCCCCCCCCCC(=O)OCCCC YESNNYPJOCXTSE-UHFFFAOYSA-N 0.000 description 1
- MSMLORAMPYZEMK-UHFFFAOYSA-N butyl 21-[10-(21-butoxy-21-oxohenicosoxy)-3-ethylanthracen-9-yl]oxyhenicosanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OCCCC)OCCCCCCCCCCCCCCCCCCCCC(=O)OCCCC MSMLORAMPYZEMK-UHFFFAOYSA-N 0.000 description 1
- SXEURQSFNRXNDB-UHFFFAOYSA-N butyl 21-[10-(21-butoxy-21-oxohenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound C(CCC)OC(=O)CCCCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCCCC(=O)OCCCC SXEURQSFNRXNDB-UHFFFAOYSA-N 0.000 description 1
- XVPMHDCFOSZEEM-UHFFFAOYSA-N butyl 3-[10-(4-butoxy-4-oxobutan-2-yl)oxy-3-chloroanthracen-9-yl]oxybutanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OCCCC)C)OC(CC(=O)OCCCC)C XVPMHDCFOSZEEM-UHFFFAOYSA-N 0.000 description 1
- IVTNFDVPYXPYHU-UHFFFAOYSA-N butyl 3-[10-(4-butoxy-4-oxobutan-2-yl)oxy-3-ethylanthracen-9-yl]oxybutanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OCCCC)C)OC(CC(=O)OCCCC)C IVTNFDVPYXPYHU-UHFFFAOYSA-N 0.000 description 1
- VUNYJBYNAFUCQT-UHFFFAOYSA-N butyl 3-[10-(4-butoxy-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)OCCCC)C)OC(CC(=O)OCCCC)C VUNYJBYNAFUCQT-UHFFFAOYSA-N 0.000 description 1
- FHSAZEBODSHNOS-UHFFFAOYSA-N butyl 3-[10-(4-butoxy-4-oxobutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound C(CCC)OC(=O)CC(C)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OC(CC(=O)OCCCC)C FHSAZEBODSHNOS-UHFFFAOYSA-N 0.000 description 1
- CGPFPSPTQBYDHR-UHFFFAOYSA-N butyl 5-[10-(5-butoxy-5-oxopentoxy)-3-chloroanthracen-9-yl]oxypentanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OCCCC)OCCCCC(=O)OCCCC CGPFPSPTQBYDHR-UHFFFAOYSA-N 0.000 description 1
- LDKBGZITYMLLGP-UHFFFAOYSA-N butyl 5-[10-(5-butoxy-5-oxopentoxy)-3-ethylanthracen-9-yl]oxypentanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OCCCC)OCCCCC(=O)OCCCC LDKBGZITYMLLGP-UHFFFAOYSA-N 0.000 description 1
- RPTYNMDKOIVGRU-UHFFFAOYSA-N butyl 5-[10-(5-butoxy-5-oxopentoxy)-3-pentylanthracen-9-yl]oxypentanoate Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OCCCC)OCCCCC(=O)OCCCC RPTYNMDKOIVGRU-UHFFFAOYSA-N 0.000 description 1
- HCXLWOQKOIKMGC-UHFFFAOYSA-N butyl 6-[10-(6-butoxy-6-oxohexoxy)anthracen-9-yl]oxyhexanoate Chemical compound C(CCC)OC(=O)CCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCC(=O)OCCCC HCXLWOQKOIKMGC-UHFFFAOYSA-N 0.000 description 1
- WUENXMGWNFAYDL-UHFFFAOYSA-N butyl 8-[10-(8-butoxy-8-oxooctoxy)anthracen-9-yl]oxyoctanoate Chemical compound C(CCC)OC(=O)CCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCC(=O)OCCCC WUENXMGWNFAYDL-UHFFFAOYSA-N 0.000 description 1
- PQXXMBMDAKMNNT-UHFFFAOYSA-N butyl 9-[10-(9-butoxy-9-oxononoxy)-3-chloroanthracen-9-yl]oxynonanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCC(=O)OCCCC)OCCCCCCCCC(=O)OCCCC PQXXMBMDAKMNNT-UHFFFAOYSA-N 0.000 description 1
- 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
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 229940089960 chloroacetate Drugs 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- PESYEWKSBIWTAK-UHFFFAOYSA-N cyclopenta-1,3-diene;titanium(2+) Chemical class [Ti+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 PESYEWKSBIWTAK-UHFFFAOYSA-N 0.000 description 1
- WMPOZLHMGVKUEJ-UHFFFAOYSA-N decanedioyl dichloride Chemical compound ClC(=O)CCCCCCCCC(Cl)=O WMPOZLHMGVKUEJ-UHFFFAOYSA-N 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- FJBFPHVGVWTDIP-UHFFFAOYSA-N dibromomethane Chemical compound BrCBr FJBFPHVGVWTDIP-UHFFFAOYSA-N 0.000 description 1
- BLKQQTCUGZJWLN-VAWYXSNFSA-N dicyclohexyl (e)-but-2-enedioate Chemical compound C1CCCCC1OC(=O)/C=C/C(=O)OC1CCCCC1 BLKQQTCUGZJWLN-VAWYXSNFSA-N 0.000 description 1
- BVVRPLNLVUMGSL-FMQUCBEESA-N didecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCC BVVRPLNLVUMGSL-FMQUCBEESA-N 0.000 description 1
- HEJZJSIRBLOWPD-WCWDXBQESA-N didodecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCC HEJZJSIRBLOWPD-WCWDXBQESA-N 0.000 description 1
- JLVWYWVLMFVCDI-UHFFFAOYSA-N diethyl benzene-1,3-dicarboxylate Chemical compound CCOC(=O)C1=CC=CC(C(=O)OCC)=C1 JLVWYWVLMFVCDI-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
- WYACBZDAHNBPPB-UHFFFAOYSA-N diethyl oxalate Chemical compound CCOC(=O)C(=O)OCC WYACBZDAHNBPPB-UHFFFAOYSA-N 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- ZUWLIWZVBOETHU-JEIPZWNWSA-N diheptadecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCCCCCC ZUWLIWZVBOETHU-JEIPZWNWSA-N 0.000 description 1
- KUUZQLFCCOGXKQ-BUHFOSPRSA-N diheptyl (e)-but-2-enedioate Chemical compound CCCCCCCOC(=O)\C=C\C(=O)OCCCCCCC KUUZQLFCCOGXKQ-BUHFOSPRSA-N 0.000 description 1
- NXQIBFMKDQPBGW-QNEJGDQOSA-N dihexadecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCCCCC NXQIBFMKDQPBGW-QNEJGDQOSA-N 0.000 description 1
- KJSFAWHPSSOGNK-XQQUEIPISA-N diicosyl (E)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCCCCCCCCC KJSFAWHPSSOGNK-XQQUEIPISA-N 0.000 description 1
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
- LDCRTTXIJACKKU-ONEGZZNKSA-N dimethyl fumarate Chemical compound COC(=O)\C=C\C(=O)OC LDCRTTXIJACKKU-ONEGZZNKSA-N 0.000 description 1
- 229960004419 dimethyl fumarate Drugs 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- BEPAFCGSDWSTEL-UHFFFAOYSA-N dimethyl malonate Chemical compound COC(=O)CC(=O)OC BEPAFCGSDWSTEL-UHFFFAOYSA-N 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- PSXSMZCCYBNWAT-HEFFKOSUSA-N dinonadecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCCCCCCCC PSXSMZCCYBNWAT-HEFFKOSUSA-N 0.000 description 1
- PQJYOOFQDXGDDS-ISLYRVAYSA-N dinonyl (e)-but-2-enedioate Chemical compound CCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCC PQJYOOFQDXGDDS-ISLYRVAYSA-N 0.000 description 1
- XHSDDKAGJYJAQM-ULDVOPSXSA-N dioctadecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCCCCCCC XHSDDKAGJYJAQM-ULDVOPSXSA-N 0.000 description 1
- TVWTZAGVNBPXHU-FOCLMDBBSA-N dioctyl (e)-but-2-enedioate Chemical compound CCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCC TVWTZAGVNBPXHU-FOCLMDBBSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- NFCMRHDORQSGIS-MDZDMXLPSA-N dipentyl (e)-but-2-enedioate Chemical compound CCCCCOC(=O)\C=C\C(=O)OCCCCC NFCMRHDORQSGIS-MDZDMXLPSA-N 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical class C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- OWZDULOODZHVCQ-UHFFFAOYSA-N diphenyl-(4-phenylsulfanylphenyl)sulfanium Chemical compound C=1C=C([S+](C=2C=CC=CC=2)C=2C=CC=CC=2)C=CC=1SC1=CC=CC=C1 OWZDULOODZHVCQ-UHFFFAOYSA-N 0.000 description 1
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- MSVGHYYKWDQHFV-BQYQJAHWSA-N ditert-butyl (e)-but-2-enedioate Chemical compound CC(C)(C)OC(=O)\C=C\C(=O)OC(C)(C)C MSVGHYYKWDQHFV-BQYQJAHWSA-N 0.000 description 1
- DFKBFBPHOGVNGQ-OCEACIFDSA-N ditridecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCCCC DFKBFBPHOGVNGQ-OCEACIFDSA-N 0.000 description 1
- FBVIPHHSIBKNAH-QURGRASLSA-N diundecyl (e)-but-2-enedioate Chemical compound CCCCCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCCCCC FBVIPHHSIBKNAH-QURGRASLSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 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
- 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
- XIMFCGSNSKXPBO-UHFFFAOYSA-N ethyl 2-bromobutanoate Chemical compound CCOC(=O)C(Br)CC XIMFCGSNSKXPBO-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
- XEJJPVOVIDZYKS-UHFFFAOYSA-N ethyl 3-[10-(4-ethoxy-4-oxobutan-2-yl)oxy-3-ethylanthracen-9-yl]oxybutanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OCC)C)OC(CC(=O)OCC)C XEJJPVOVIDZYKS-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
- 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
- SEGNXGUVVWDNOM-UHFFFAOYSA-N ethyl 5-[10-(5-ethoxy-5-oxopentoxy)anthracen-9-yl]oxypentanoate Chemical compound C(C)OC(=O)CCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCC(=O)OCC SEGNXGUVVWDNOM-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
- 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
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-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
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-M hydroperoxide group Chemical class [O-]O MHAJPDPJQMAIIY-UHFFFAOYSA-M 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229940119545 isobornyl methacrylate Drugs 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- OTRIMLCPYJAPPD-UHFFFAOYSA-N methanol prop-2-enoic acid Chemical compound OC.OC.OC(=O)C=C.OC(=O)C=C OTRIMLCPYJAPPD-UHFFFAOYSA-N 0.000 description 1
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 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
- 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
- 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
- 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
- HWPYAGFFBABTDN-UHFFFAOYSA-N methyl 21-[3-chloro-10-(21-methoxy-21-oxohenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound COC(=O)CCCCCCCCCCCCCCCCCCCCOC1=C2C=CC(=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCCCCCC(=O)OC)Cl HWPYAGFFBABTDN-UHFFFAOYSA-N 0.000 description 1
- OUOGUTARKIZZDH-UHFFFAOYSA-N methyl 21-[3-ethyl-10-(21-methoxy-21-oxohenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound CCC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OC)OCCCCCCCCCCCCCCCCCCCCC(=O)OC OUOGUTARKIZZDH-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
- JZHUYAKKDZZYJJ-UHFFFAOYSA-N methyl 3-[10-(4-methoxy-4-oxobutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound COC(=O)CC(C)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OC(CC(=O)OC)C JZHUYAKKDZZYJJ-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
- BOIXHMQUMXEZFV-UHFFFAOYSA-N methyl 3-[3-ethyl-10-(4-methoxy-4-oxobutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OC)C)OC(CC(=O)OC)C BOIXHMQUMXEZFV-UHFFFAOYSA-N 0.000 description 1
- GFNVEJJRPHZLCH-UHFFFAOYSA-N methyl 5-[10-(5-methoxy-5-oxopentoxy)-3-pentylanthracen-9-yl]oxypentanoate Chemical compound CCCCCC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC)OCCCCC(=O)OC GFNVEJJRPHZLCH-UHFFFAOYSA-N 0.000 description 1
- GSTXMDTYBTUQHJ-UHFFFAOYSA-N methyl 5-[10-(5-methoxy-5-oxopentoxy)anthracen-9-yl]oxypentanoate Chemical compound COC(=O)CCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCC(=O)OC GSTXMDTYBTUQHJ-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
- 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
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 229940074369 monoethyl fumarate Drugs 0.000 description 1
- NKHAVTQWNUWKEO-NSCUHMNNSA-N monomethyl fumarate Chemical compound COC(=O)\C=C\C(O)=O NKHAVTQWNUWKEO-NSCUHMNNSA-N 0.000 description 1
- 229940005650 monomethyl fumarate Drugs 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- BHZDUUIJMMLTMB-UHFFFAOYSA-N naphthalen-1-yl decanoate Chemical compound C1=CC=C2C(OC(=O)CCCCCCCCC)=CC=CC2=C1 BHZDUUIJMMLTMB-UHFFFAOYSA-N 0.000 description 1
- JDOSNGUCZXVIFA-UHFFFAOYSA-N naphthalen-1-yl(phenyl)iodanium Chemical class C=1C=CC2=CC=CC=C2C=1[I+]C1=CC=CC=C1 JDOSNGUCZXVIFA-UHFFFAOYSA-N 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical compound C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000005184 naphthylamino group Chemical group C1(=CC=CC2=CC=CC=C12)N* 0.000 description 1
- 125000005029 naphthylthio group Chemical group C1(=CC=CC2=CC=CC=C12)S* 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000005815 pentoxymethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical class OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- MIHJJLGYORHMAQ-UHFFFAOYSA-N propan-2-yl 10-[10-(10-oxo-10-propan-2-yloxydecoxy)anthracen-9-yl]oxydecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCC(=O)OC(C)C MIHJJLGYORHMAQ-UHFFFAOYSA-N 0.000 description 1
- KGPLGHWWXMJMKG-UHFFFAOYSA-N propan-2-yl 11-[10-(11-oxo-11-propan-2-yloxyundecoxy)anthracen-9-yl]oxyundecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCC(=O)OC(C)C KGPLGHWWXMJMKG-UHFFFAOYSA-N 0.000 description 1
- VAWZEMFIGRPKBB-UHFFFAOYSA-N propan-2-yl 12-[10-(12-oxo-12-propan-2-yloxydodecoxy)anthracen-9-yl]oxydodecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCC(=O)OC(C)C VAWZEMFIGRPKBB-UHFFFAOYSA-N 0.000 description 1
- HDSMMHHBWZGKNP-UHFFFAOYSA-N propan-2-yl 13-[10-(13-oxo-13-propan-2-yloxytridecoxy)anthracen-9-yl]oxytridecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCC(=O)OC(C)C HDSMMHHBWZGKNP-UHFFFAOYSA-N 0.000 description 1
- PYZRUKPAINRCFG-UHFFFAOYSA-N propan-2-yl 14-[10-(14-oxo-14-propan-2-yloxytetradecoxy)anthracen-9-yl]oxytetradecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCC(=O)OC(C)C PYZRUKPAINRCFG-UHFFFAOYSA-N 0.000 description 1
- LMZKTDAFOANSQZ-UHFFFAOYSA-N propan-2-yl 15-[10-(15-oxo-15-propan-2-yloxypentadecoxy)anthracen-9-yl]oxypentadecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCC(=O)OC(C)C LMZKTDAFOANSQZ-UHFFFAOYSA-N 0.000 description 1
- GNTZRRBBUWIMQL-UHFFFAOYSA-N propan-2-yl 16-[10-(16-oxo-16-propan-2-yloxyhexadecoxy)anthracen-9-yl]oxyhexadecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCC(=O)OC(C)C GNTZRRBBUWIMQL-UHFFFAOYSA-N 0.000 description 1
- IQPOOCUOKNFZIZ-UHFFFAOYSA-N propan-2-yl 17-[10-(17-oxo-17-propan-2-yloxyheptadecoxy)anthracen-9-yl]oxyheptadecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCC(=O)OC(C)C IQPOOCUOKNFZIZ-UHFFFAOYSA-N 0.000 description 1
- MYIJDNTVFCWKAP-UHFFFAOYSA-N propan-2-yl 18-[10-(18-oxo-18-propan-2-yloxyoctadecoxy)anthracen-9-yl]oxyoctadecanoate Chemical compound CC(C)OC(=O)CCCCCCCCCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCCC(=O)OC(C)C MYIJDNTVFCWKAP-UHFFFAOYSA-N 0.000 description 1
- GDFJHWQKQHYOLF-UHFFFAOYSA-N propan-2-yl 19-[10-(19-oxo-19-propan-2-yloxynonadecoxy)anthracen-9-yl]oxynonadecanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCC(=O)OC(C)C GDFJHWQKQHYOLF-UHFFFAOYSA-N 0.000 description 1
- VODRWDBLLGYRJT-UHFFFAOYSA-N propan-2-yl 2-chloroacetate Chemical compound CC(C)OC(=O)CCl VODRWDBLLGYRJT-UHFFFAOYSA-N 0.000 description 1
- SQADXTBKSJAWFP-UHFFFAOYSA-N propan-2-yl 20-[10-(20-oxo-20-propan-2-yloxyicosoxy)anthracen-9-yl]oxyicosanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCCC(=O)OC(C)C SQADXTBKSJAWFP-UHFFFAOYSA-N 0.000 description 1
- GOEPNZIBSPEGDQ-UHFFFAOYSA-N propan-2-yl 21-[3-chloro-10-(21-oxo-21-propan-2-yloxyhenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)C)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)C GOEPNZIBSPEGDQ-UHFFFAOYSA-N 0.000 description 1
- ZSVUZVGJCLANHQ-UHFFFAOYSA-N propan-2-yl 21-[3-ethyl-10-(21-oxo-21-propan-2-yloxyhenicosoxy)anthracen-9-yl]oxyhenicosanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)C)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)C ZSVUZVGJCLANHQ-UHFFFAOYSA-N 0.000 description 1
- ZWAQHMMOVRGLJB-UHFFFAOYSA-N propan-2-yl 3-[10-(4-oxo-4-propan-2-yloxybutan-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)C)C)OC(CC(=O)OC(C)C)C ZWAQHMMOVRGLJB-UHFFFAOYSA-N 0.000 description 1
- BAOFEEPMOWUCAO-UHFFFAOYSA-N propan-2-yl 3-[10-(4-oxo-4-propan-2-yloxybutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound C(C)(C)OC(=O)CC(C)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OC(CC(=O)OC(C)C)C BAOFEEPMOWUCAO-UHFFFAOYSA-N 0.000 description 1
- QHCWZPPXZQKLBG-UHFFFAOYSA-N propan-2-yl 3-[3-chloro-10-(4-oxo-4-propan-2-yloxybutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OC(C)C)C)OC(CC(=O)OC(C)C)C QHCWZPPXZQKLBG-UHFFFAOYSA-N 0.000 description 1
- XWWZEWRVPRSKTR-UHFFFAOYSA-N propan-2-yl 3-[3-ethyl-10-(4-oxo-4-propan-2-yloxybutan-2-yl)oxyanthracen-9-yl]oxybutanoate Chemical compound CCC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(C)CC(=O)OC(C)C)OC(C)CC(=O)OC(C)C XWWZEWRVPRSKTR-UHFFFAOYSA-N 0.000 description 1
- GLKQVHGXSOUQKU-UHFFFAOYSA-N propan-2-yl 5-[10-(5-oxo-5-propan-2-yloxypentoxy)-3-pentylanthracen-9-yl]oxypentanoate Chemical compound C(CCCC)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC(C)C)OCCCCC(=O)OC(C)C GLKQVHGXSOUQKU-UHFFFAOYSA-N 0.000 description 1
- DXAWFGUHBGHSCE-UHFFFAOYSA-N propan-2-yl 5-[10-(5-oxo-5-propan-2-yloxypentoxy)anthracen-9-yl]oxypentanoate Chemical compound C(C)(C)OC(=O)CCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCC(=O)OC(C)C DXAWFGUHBGHSCE-UHFFFAOYSA-N 0.000 description 1
- FGEVLECHCFEPSE-UHFFFAOYSA-N propan-2-yl 5-[3-chloro-10-(5-oxo-5-propan-2-yloxypentoxy)anthracen-9-yl]oxypentanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC(C)C)OCCCCC(=O)OC(C)C FGEVLECHCFEPSE-UHFFFAOYSA-N 0.000 description 1
- MHLMVIUIYRIOIV-UHFFFAOYSA-N propan-2-yl 5-[3-ethyl-10-(5-oxo-5-propan-2-yloxypentoxy)anthracen-9-yl]oxypentanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC(C)C)OCCCCC(=O)OC(C)C MHLMVIUIYRIOIV-UHFFFAOYSA-N 0.000 description 1
- KSANGBRGYNNARK-UHFFFAOYSA-N propan-2-yl 6-[10-(6-oxo-6-propan-2-yloxyhexoxy)anthracen-9-yl]oxyhexanoate Chemical compound C(C)(C)OC(=O)CCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCC(=O)OC(C)C KSANGBRGYNNARK-UHFFFAOYSA-N 0.000 description 1
- SWDJELKZEXPGOV-UHFFFAOYSA-N propan-2-yl 7-[10-(7-oxo-7-propan-2-yloxyheptoxy)anthracen-9-yl]oxyheptanoate Chemical compound C(C)(C)OC(=O)CCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCC(=O)OC(C)C SWDJELKZEXPGOV-UHFFFAOYSA-N 0.000 description 1
- PIMOEZSICZQPAV-UHFFFAOYSA-N propan-2-yl 8-[10-(8-oxo-8-propan-2-yloxyoctoxy)anthracen-9-yl]oxyoctanoate Chemical compound C(C)(C)OC(=O)CCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCC(=O)OC(C)C PIMOEZSICZQPAV-UHFFFAOYSA-N 0.000 description 1
- GJLFVJHXWPMGPM-UHFFFAOYSA-N propan-2-yl 9-[10-(9-oxo-9-propan-2-yloxynonoxy)anthracen-9-yl]oxynonanoate Chemical compound C(C)(C)OC(=O)CCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCC(=O)OC(C)C GJLFVJHXWPMGPM-UHFFFAOYSA-N 0.000 description 1
- 125000005767 propoxymethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])[#8]C([H])([H])* 0.000 description 1
- ISYUCUGTDNJIHV-UHFFFAOYSA-N propyl 2-bromoacetate Chemical compound CCCOC(=O)CBr ISYUCUGTDNJIHV-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
- ZFDDOXQDQRAABC-UHFFFAOYSA-N tert-butyl 10-[10-[10-[(2-methylpropan-2-yl)oxy]-10-oxodecoxy]anthracen-9-yl]oxydecanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCC(=O)OC(C)(C)C ZFDDOXQDQRAABC-UHFFFAOYSA-N 0.000 description 1
- PBNRDBNLYGQYDI-UHFFFAOYSA-N tert-butyl 11-[10-[11-[(2-methylpropan-2-yl)oxy]-11-oxoundecoxy]anthracen-9-yl]oxyundecanoate Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCC(=O)OC(C)(C)C PBNRDBNLYGQYDI-UHFFFAOYSA-N 0.000 description 1
- RANYLCPMXBURIE-UHFFFAOYSA-N tert-butyl 12-[10-[12-[(2-methylpropan-2-yl)oxy]-12-oxododecoxy]anthracen-9-yl]oxydodecanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCC(=O)OC(C)(C)C RANYLCPMXBURIE-UHFFFAOYSA-N 0.000 description 1
- FOGZAJWQTLXNMO-UHFFFAOYSA-N tert-butyl 13-[10-[13-[(2-methylpropan-2-yl)oxy]-13-oxotridecoxy]anthracen-9-yl]oxytridecanoate Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCCCOC1=C2C=CC=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCC(=O)OC(C)(C)C FOGZAJWQTLXNMO-UHFFFAOYSA-N 0.000 description 1
- INDFNHSZFAKNLU-UHFFFAOYSA-N tert-butyl 14-[10-[14-[(2-methylpropan-2-yl)oxy]-14-oxotetradecoxy]anthracen-9-yl]oxytetradecanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCC(=O)OC(C)(C)C INDFNHSZFAKNLU-UHFFFAOYSA-N 0.000 description 1
- DNYQGVBNWDXQLR-UHFFFAOYSA-N tert-butyl 15-[10-[15-[(2-methylpropan-2-yl)oxy]-15-oxopentadecoxy]anthracen-9-yl]oxypentadecanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCC(=O)OC(C)(C)C DNYQGVBNWDXQLR-UHFFFAOYSA-N 0.000 description 1
- RDXSHPQJLXQRMC-UHFFFAOYSA-N tert-butyl 16-[10-[16-[(2-methylpropan-2-yl)oxy]-16-oxohexadecoxy]anthracen-9-yl]oxyhexadecanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCC(=O)OC(C)(C)C RDXSHPQJLXQRMC-UHFFFAOYSA-N 0.000 description 1
- NSIMEHVVXIOWJN-UHFFFAOYSA-N tert-butyl 17-[3-chloro-10-[17-[(2-methylpropan-2-yl)oxy]-17-oxoheptadecoxy]anthracen-9-yl]oxyheptadecanoate Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCCCCCCCOC1=C2C=CC(=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C)Cl NSIMEHVVXIOWJN-UHFFFAOYSA-N 0.000 description 1
- HLZNPPNNZMVTLE-UHFFFAOYSA-N tert-butyl 17-[3-ethyl-10-[17-[(2-methylpropan-2-yl)oxy]-17-oxoheptadecoxy]anthracen-9-yl]oxyheptadecanoate Chemical compound CCC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C)OCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C HLZNPPNNZMVTLE-UHFFFAOYSA-N 0.000 description 1
- IOZGXWAXRPGEFU-UHFFFAOYSA-N tert-butyl 18-[10-[18-[(2-methylpropan-2-yl)oxy]-18-oxooctadecoxy]anthracen-9-yl]oxyoctadecanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C IOZGXWAXRPGEFU-UHFFFAOYSA-N 0.000 description 1
- VTSKOHHSPUHYTH-UHFFFAOYSA-N tert-butyl 19-[10-[19-[(2-methylpropan-2-yl)oxy]-19-oxononadecoxy]anthracen-9-yl]oxynonadecanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C VTSKOHHSPUHYTH-UHFFFAOYSA-N 0.000 description 1
- BNWCETAHAJSBFG-UHFFFAOYSA-N tert-butyl 2-bromoacetate Chemical compound CC(C)(C)OC(=O)CBr BNWCETAHAJSBFG-UHFFFAOYSA-N 0.000 description 1
- DQYDCJMUBCEDRP-UHFFFAOYSA-N tert-butyl 20-[10-[20-[(2-methylpropan-2-yl)oxy]-20-oxoicosoxy]anthracen-9-yl]oxyicosanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C DQYDCJMUBCEDRP-UHFFFAOYSA-N 0.000 description 1
- MRBQNDLGCZDWLM-UHFFFAOYSA-N tert-butyl 21-[10-[21-[(2-methylpropan-2-yl)oxy]-21-oxohenicosoxy]anthracen-9-yl]oxyhenicosanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCCCCCCCCCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C MRBQNDLGCZDWLM-UHFFFAOYSA-N 0.000 description 1
- YVNYFQSMPNBHAY-UHFFFAOYSA-N tert-butyl 21-[3-chloro-10-[21-[(2-methylpropan-2-yl)oxy]-21-oxohenicosoxy]anthracen-9-yl]oxyhenicosanoate Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCCCCCCCCCCCOC1=C2C=CC(=CC2=C(C3=CC=CC=C31)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C)Cl YVNYFQSMPNBHAY-UHFFFAOYSA-N 0.000 description 1
- AACVYXLAWVSYLR-UHFFFAOYSA-N tert-butyl 21-[3-ethyl-10-[21-[(2-methylpropan-2-yl)oxy]-21-oxohenicosoxy]anthracen-9-yl]oxyhenicosanoate Chemical compound CCC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C)OCCCCCCCCCCCCCCCCCCCCC(=O)OC(C)(C)C AACVYXLAWVSYLR-UHFFFAOYSA-N 0.000 description 1
- ICUJNCSTEAQMAI-UHFFFAOYSA-N tert-butyl 3-[10-[4-[(2-methylpropan-2-yl)oxy]-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)(C)C)C)OC(CC(=O)OC(C)(C)C)C ICUJNCSTEAQMAI-UHFFFAOYSA-N 0.000 description 1
- VXEKOFGJOHHQCN-UHFFFAOYSA-N tert-butyl 3-[10-[4-[(2-methylpropan-2-yl)oxy]-4-oxobutan-2-yl]oxyanthracen-9-yl]oxybutanoate Chemical compound C(C)(C)(C)OC(=O)CC(C)OC=1C2=CC=CC=C2C(=C2C=CC=CC12)OC(CC(=O)OC(C)(C)C)C VXEKOFGJOHHQCN-UHFFFAOYSA-N 0.000 description 1
- GALSQXVWHDDUJD-UHFFFAOYSA-N tert-butyl 3-[3-chloro-10-[4-[(2-methylpropan-2-yl)oxy]-4-oxobutan-2-yl]oxyanthracen-9-yl]oxybutanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OC(C)(C)C)C)OC(CC(=O)OC(C)(C)C)C GALSQXVWHDDUJD-UHFFFAOYSA-N 0.000 description 1
- YQCNBYMRFPHHFS-UHFFFAOYSA-N tert-butyl 3-[3-ethyl-10-[4-[(2-methylpropan-2-yl)oxy]-4-oxobutan-2-yl]oxyanthracen-9-yl]oxybutanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OC(CC(=O)OC(C)(C)C)C)OC(CC(=O)OC(C)(C)C)C YQCNBYMRFPHHFS-UHFFFAOYSA-N 0.000 description 1
- QSACMJQITJKWEX-UHFFFAOYSA-N tert-butyl 5-[10-[5-[(2-methylpropan-2-yl)oxy]-5-oxopentoxy]anthracen-9-yl]oxypentanoate Chemical compound C(C)(C)(C)OC(=O)CCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCC(=O)OC(C)(C)C QSACMJQITJKWEX-UHFFFAOYSA-N 0.000 description 1
- YTUYLXBSGYATHN-UHFFFAOYSA-N tert-butyl 5-[3-chloro-10-[5-[(2-methylpropan-2-yl)oxy]-5-oxopentoxy]anthracen-9-yl]oxypentanoate Chemical compound ClC1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC(C)(C)C)OCCCCC(=O)OC(C)(C)C YTUYLXBSGYATHN-UHFFFAOYSA-N 0.000 description 1
- CAIQVNDDOPHGCL-UHFFFAOYSA-N tert-butyl 5-[3-ethyl-10-[5-[(2-methylpropan-2-yl)oxy]-5-oxopentoxy]anthracen-9-yl]oxypentanoate Chemical compound C(C)C1=CC2=C(C3=CC=CC=C3C(=C2C=C1)OCCCCC(=O)OC(C)(C)C)OCCCCC(=O)OC(C)(C)C CAIQVNDDOPHGCL-UHFFFAOYSA-N 0.000 description 1
- OGQKUCCYRLKEFM-UHFFFAOYSA-N tert-butyl 6-[10-[6-[(2-methylpropan-2-yl)oxy]-6-oxohexoxy]anthracen-9-yl]oxyhexanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCC(=O)OC(C)(C)C OGQKUCCYRLKEFM-UHFFFAOYSA-N 0.000 description 1
- QQPZNEHKVUYQEI-UHFFFAOYSA-N tert-butyl 7-[10-[7-[(2-methylpropan-2-yl)oxy]-7-oxoheptoxy]anthracen-9-yl]oxyheptanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCC(=O)OC(C)(C)C QQPZNEHKVUYQEI-UHFFFAOYSA-N 0.000 description 1
- BTNLKCLRHIHXEU-UHFFFAOYSA-N tert-butyl 8-[10-[8-[(2-methylpropan-2-yl)oxy]-8-oxooctoxy]anthracen-9-yl]oxyoctanoate Chemical compound C(C)(C)(C)OC(=O)CCCCCCCOC=1C2=CC=CC=C2C(=C2C=CC=CC12)OCCCCCCCC(=O)OC(C)(C)C BTNLKCLRHIHXEU-UHFFFAOYSA-N 0.000 description 1
- 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
- LZPBKINTWROMEA-UHFFFAOYSA-N tetracene-5,12-dione Chemical class C1=CC=C2C=C3C(=O)C4=CC=CC=C4C(=O)C3=CC2=C1 LZPBKINTWROMEA-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000001016 thiazine dye Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940042596 viscoat Drugs 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/02—1,2-Dioxanes; Hydrogenated 1,2-dioxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
- C08F4/34—Per-compounds with one peroxy-radical
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides
Description
本発明の多環芳香族骨格を有するエンドペルオキシド化合物は、上記一般式(1)、一般式(3)、一般式(5)、一般式(7)、一般式(9)の構造を有する。
次に、本発明の多環芳香族骨格を有するエンドペルオキシド化合物の製造方法について説明する。本発明の多環芳香族骨格を有するエンドペルオキシド化合物は、対応する多環芳香族骨格を有する化合物と一重項酸素との反応より製造される。
本発明において原料として用いられる多環芳香族骨格を有する化合物は、一般式(2)、一般式(4)、一般式(6)、一般式(8)又は一般式(10)の構造を有する化合物である。まず、下記一般式(2)で表される多環芳香族骨格を有する化合物について説明する。
上記一般式(2)、(4)で表される多環芳香族骨格を有する化合物は、例えば、アントラセン化合物の場合で、Rが炭素数1から10のアルキル基、炭素数1から5のアルコキシ基を持つアルコキシメチル基、炭素数6から10のアリール基である9,10-ジアルコキシアントラセン化合物は、例えば特開2003-104925号公報に記載の方法で製造することができる。すなわち、一般式(2)によって表される9,10-ジアルコキシアントラセン化合物に対応する9,10-ジヒドロキシアントラセン化合物にエーテル化剤を作用させることにより得ることができる。また、上記一般式(2)で表される多環芳香族骨格を有する化合物のうち、Rが炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から20のアリール基を有するアリールカルボニル基である9,10-ビス(置換アシルオキシ)アントラセン化合物は、例えば特開2014-101442号公報に記載の方法で製造することができる。すなわち、一般式(2)によって表される9,10-ビス(置換アシルオキシ)アントラセン化合物に対応する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、アシル化剤を作用させることにより得ることができる。そして、Rが炭素数1から10のアルキル基を有するアルキルオキシカルボニル基、炭素数6から20のアリール基を有するアリールオキシカルボニル基である9,10-ビス(置換カルボニルオキシ)アントラセン化合物は、例えば特開2011-42743号公報、特開2014-70203号公報に記載のように、9,10-ビス(置換カルボニルオキシ)アントラセン化合物に対応する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、炭酸エステル化剤を作用させることにより得ることができる。ナフタレン化合物についても同様の反応で得ることができる。
上記一般式(6)で表される多環芳香族骨格を有する化合物は、対応する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、例えば、クロロ酢酸メチル、クロロ酢酸エチル、クロロ酢酸n―プロピル、クロロ酢酸イソプロピル、クロロ酢酸n―ブチル、ブロモ酢酸メチル、ブロモ酢酸エチル、ブロモ酢酸n―プロピル、ブロモ酢酸イソプロピル、ブロモ酢酸n―ブチル、ブロモ酢酸tert-ブチル、2-ブロモプロピオン酸メチル、4-ブロモ酪酸エチルなどハロゲン化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。
上記一般式(8)で表される多環芳香族骨格を有する化合物は、対応する9,10-ジヒドロキシアントラセン化合物を触媒存在下あるいは無触媒で対応する二官能性化合物と反応させることにより得ることができる。
上記一般式(10)で表される多環芳香族骨格を有する化合物は、対応する9,10-ビス(2-ヒドロキシアルコキシ)アントラセン化合物を触媒存在下あるいは無触媒で対応する二官能性化合物と反応させることにより得ることができる。
本発明の一般式(1)、(3)、(5)、(7)、(9)で表される多環芳香族骨格を有するエンドペルオキシド化合物は、それぞれ対応する一般式(2)、(4)、(6)、(8)、(10)で表される多環芳香族骨格を有する化合物を300nmから410nmの波長範囲内にピーク波長を有する光の照射下で分子状酸素と反応させることにより製造することができる。
共存させることができる多環芳香族骨格を有する化合物以外の一重項酸素ジェネレーターとしては、ローズベンガル、メチレンブルー、アズールA、様々なポリフィリン類及びメタロポルフィリン類(たとえば亜鉛テトラヒドロキシフェニルポルフィリン、亜鉛テトラカルボキシフェニルポリフィリン、亜鉛ウロポルフィリン、亜鉛プロトポルフィリン、テトラスルホナトフェニルポルフィリン、Znテトラスルホナトフェニルポルフィリン類、テトラメチルピリジニウムポルフィリン、Znテトラメチルピリジニウムポルフィリン類、ヘマトポルフィリン、Znヘマトポルフィリンなど)、様々なフタロシアニン類及びメタロフタロシアニン類、チオキサントン類、エオシンYなどのフルオレセイン類などが挙げられる。
ラジカル重合性化合物にラジカル重合開始剤として本発明の多環芳香族骨格を有するエンドペルオキシド化合物を添加することにより、ラジカル重合性組成物を調製することができる。
本発明の多環芳香族骨格を有するエンドペルオキシド化合物は、特定の波長範囲を含む光を照射することにより励起され、該励起種がラジカル重合性化合物のラジカル重合を開始する能力を有するラジカル種に変化し、ラジカル重合性化合物のラジカル重合を開始する光ラジカル重合開始剤として作用する。
また、本発明の多環芳香族骨格を有するエンドペルオキシド化合物は、熱により分解しラジカル種を発生し、ラジカル重合性化合物のラジカル重合を開始する熱ラジカル重合開始剤として作用する。
本発明に用いることができるラジカル重合性化合物としては、例えば、スチレン、メチルスチレン、ジビニルベンゼン、p-ヒドロキシスチレン、酢酸ビニル、(メタ)アクリル酸、アクリロニトリル、メタクリロニトリル、アクリルアミド、(メタ)アクリル酸エステル、フマル酸エステル等、又はこれらのオリゴマーが挙げられる。
本発明のラジカル重合性組成物をラジカル重合する方法について説明する。
まず、ラジカル重合の開始エネルギーが光である場合について説明する。本発明のラジカル重合性組成物は特定の波長範囲を含む光を照射することにより重合硬化させることができる。
フィルム状に重合させる場合に用いられる基材としてはフィルム、紙、アルミ箔、金属等が主に用いられるが特に限定されない。基材としてのフィルムに用いられる素材としてはポリエステル、トリアセチルセルロース(TAC)、ポリビニルアルコール(PVA)等が用いられる。該基材フィルムの膜厚は通常100μm未満の膜厚のものを使用する。ラジカル重合性組成物を塗布して得られる塗膜の膜厚を調整するために使用するバーコーターは特に指定しないが、膜厚が1μm以上100μm未満に調整できるバーコーターを使用する。一方、スピンコーティング法やスクリーン印刷法により、さらに薄い膜厚あるいは厚い膜厚にして塗布することもできる。
このようにして調製したラジカル重合性組成物からなる塗膜に、波長が230nmから330nmまでの波長範囲を含む光を含むエネルギー線を1から2000mW/cm2程度の強さで光照射することにより、光硬化物を得ることができる。用いられる照射源としては、230nmから330nmまでの波長範囲を含む光を照射できるものであれば、どのようなものでも用いることができる。例えば、高圧水銀ランプ、低圧水銀灯、エキシマーランプ、DeepUVランプ等が用いられる。
次に、ラジカル重合の開始エネルギーが熱である場合について説明する。本発明のラジカル重合性組成物は、所定の温度に加熱することにより重合硬化させることができる。
本発明のラジカル重合性組成物の硬化方法その1は、上記のように本発明の多環芳香族骨格を有するエンドペルオキシド化合物をラジカル重合開始剤としてラジカル重合性化合物に添加する方法であるが、ラジカル重合性組成物中で多環芳香族骨格を有するエンドペルオキシド化合物を生成させながら、ラジカル重合性化合物を重合硬化させることも可能である。
また、硬化方法その2では、一重項酸素を生成するため酸素存在下で行う。酸素存在下とは、積極的に酸素を除去しないということを意味し、窒素ガス、ヘリウムガス等で雰囲気を置換することなく行う等のことを意味する。逆に、積極的に、空気や酸素を吹き込んでもよい。
共存させることができる多環芳香族骨格を有する化合物以外の一重項酸素ジェネレーターとしては、ローズベンガル、メチレンブルー、アズールA、様々なポリフィリン類及びメタロポルフィリン類(たとえば亜鉛テトラヒドロキシフェニルポルフィリン、亜鉛テトラカルボキシフェニルポリフィリン、亜鉛ウロポルフィリン、亜鉛プロトポルフィリン、テトラスルホナトフェニルポルフィリン、Znテトラスルホナトフェニルポルフィリン類、テトラメチルピリジニウムポルフィリン、Znテトラメチルピリジニウムポルフィリン類、ヘマトポルフィリン、Znヘマトポルフィリンなど)、様々なフタロシアニン類及びメタロフタロシアニン類、チオキサントン類、エオシンYなどのフルオレセイン類などが挙げられる。
赤外線(IR)分光光度計:Thermo社製、型式is50 FT-IR
核磁気共鳴装置(1H―NMR):日本電子社製、型式ECS-400
本実施例において、光DSC測定は下記のようにして行った。DSC測定装置は日立ハイテク社製XDSC-7000を用い、それに光DSC測定用ユニットを装着し光を照射しながらDSC測定ができるよう設えた。
重合反応が進行したか否かは粘度上昇の有無でも観測することが可能である。これは、レオメーターで複素粘度の経時変化を測定することによって重合反応の進行を確認する手法である。ここでは、レオメーターはアントンパール社製のMCR102に温度・雰囲気制御する為のH-PTD200というオプションのついたものを使用した。測定は10mmφのパラレルプレートを用いて、ひずみ:100%、周波数:1Hz、温度:25℃一定、測定間隔:0.33分、ギャップ:0.5mmの条件で行った。また、モノマーにトリメチロールプロパントリアクリラート(TMPTA)を用いて複素粘度の測定を行った場合、複素粘度が10,000Pa・sに達した時点で重合したものと判断した。なお、モノマーのトリメチロールプロパントリアクリラート(TMPTA)の複素粘度は通常0.1~0.6Pa・s程度である。
50ml三角フラスコ中、空気下、9,10-ジブトキシアントラセン226mg(0.701ミリモル)を酢酸エチル(和光純薬工業株式会社製,分光分析用)7.5mlに溶かした。385nm、122mW/cm2のLEDランプ(オプトコード株式会社製,LED385/L-STND)を2時間照射し、減圧乾燥の後、薄層クロマトグラフィー(シリカゲル、酢酸エチル:ヘキサン=1:20、Rf値0.31)で単離し、無色透明液体の9,10-ジブトキシアントラセン-9,10-エンドペルオキシド144mg(0.406ミリモル)を得た。原料9,10-ジブトキシアントラセンに対する収率は58.0モル%であった。
(2)IR(液膜法,cm-1):2957,2872,1461,1298,1073,759.
(3)1H-NMR(300MHz、CDCl3):δ=1.01(t,J=7.3Hz,6H),1.48-1.64(m,4H),1.78-1.90(m,4H),4.27(t,J=6.6Hz,4H),7.28(dd,J=5.3Hz,3.0Hz,4H),7.52(dd,J=5.7Hz,3.4Hz,4H).
50ml三角フラスコに、空気下、合成実施例2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チレンオキシ)アントラセン97.3mg(0.254ミリモル)及び一重項酸素ジェネレーターとしてエオシンY4.9mg(7.6ミリモル)を加え、N,N-ジメチルホルムアミド(和光純薬工業株式会社製,分光分析用)10mlに溶かした。この溶液に三角フラスコ上部から530nm集光型LEDライト(オプトコード株式会社製,LED530/L-STND)を3.5時間照射した。その後、酢酸エチルと洗浄水で2回、酢酸エチルと純水で1回洗浄して酢酸エチル層を抽出し、硫酸ナトリウムを加えて、水を除いた。その後、酢酸エチル層を濃縮し、減圧乾燥の後、薄層クロマトグラフィー(酢酸エチル:ヘキサン=1:2、Rf値=0.7)で単離し、無色透明液体の9,10-ビス(エトキシカルボニルメチレンオキシ)アントラセン-9,10-エンドペルオキシド48.5mg(0.117ミリモル)を得た。原料9,10-ビス(エトキシカルボニルメチレンオキシ)アントラセンに対する収率は46.1モル%であった。
(2)IR(液膜法,cm-1):2988,2950,1763、1753、1200、1139、1086、1054、902、753.
(3)1H-NMR(500MHz、CDCl3):δ=1.30-1.33(t,J=7.3Hz,6H),4.28-4.32(q,J=7.0Hz,4H),4.78(s,4H),7.28-7.32(dd,J=5.5Hz,3.0Hz,4H),7.55-7.58(dd,J=5.5Hz,3.5Hz,4H).
(4)13C-NMR(125MHz、CDCl3):δ=14.3,61.5,64.0,102.9,120.6,127.9,137.9,169.2.
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ラート(TMPTA)(東京化成社製)100重量部に対し、光ラジカル重合開始剤として実施例1と同様の方法で得た9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を1.5重量部添加して、ラジカル重合性組成物を調製した。該ラジカル重合性組成物1mgを測定用アルミパンの中に精秤し、DSC測定部に収めた後、光DSCユニットを装着した。該サンプルを、窒素雰囲気下で高圧水銀ランプ全波長を30秒間照射した。その時の発熱量は470mJ/mgであり、転化率は83.9%であった(結果を表1に記載)。
光ラジカル重合開始剤として9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を添加しなかった他は実施例3と同様に測定を実施した。その時の発熱量は26.3mJ/mgであり、転化率は7.4%であった(結果を表1に記載)。
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ラート(TMPTA)(東京化成社製)100重量部に対し、熱ラジカル重合開始剤として実施例1と同様の方法で得た9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を1.5重量部添加して、ラジカル重合性組成物を調製した。該ラジカル重合性組成物1mgを測定用アルミ製密閉パンの中に窒素雰囲気下で精秤し、DSC測定部に収めた後、30℃から170℃まで5℃/minの昇温速度で測定を実施した。その時の発熱量は503mJ/mgであり、転化率は88.2%であった(結果を表1に記載)。
熱ラジカル重合開始剤として9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を添加しなかった他は実施例4と同様に測定を実施した。その時の発熱量は0mJ/mgであり、転化率は0.0%であった(結果を表1に記載)。
実施例3の9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を1.5部の代わりに実施例2と同様に合成した9,10-ビス(エトキシカルボニルメチレンオキシ)アントラセン-9,10-エンドペルオキシド(ECMAEPO)を1.5部添加した他は実施例3と同様に測定した。その時の発熱量は284mJ/mgであり、転化率は49.8%であった(結果を表1に記載)。
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ラート(TMPTA)(東京化成社製)100重量部に対し、エンドペルオキシドの分解を促進させる還元剤としてナフテン酸コバルト・ミネラルスピリット溶液(Co:6%)(和光純薬)を5重量部添加した。この溶液をギャップ:0.5mmで10mmφのパラレルプレートで挟み込める量をレオメーターの25℃に保持したヒートプレートに載せた。この溶液に熱ラジカル重合開始剤として、実施例1と同様の方法で得た9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を微量(50mg程度)の載せ、直ちにパラレルプレートで溶液を挟み込み、レオメーターで複素粘度の測定を開始した。この結果、測定から約20分程度で複素粘度の上昇が見られ、測定から61分後には10,080Pa・sに達し、90分後では44,260Pa・sであった。このことからこの溶液では重合反応が進行したことが確認できた(結果を表2に記載)。
熱ラジカル重合開始剤として、9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を添加しなかった他は実施例6と同様に測定を実施した。その結果測定から90分経過しても複素粘度の上昇はほとんど見られず、90分後の粘度は0.3Pa・sであった。このことからこの溶液では重合反応は進行しなかったことが確認できた(結果を表2に記載)。
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ラート(TMPTA)(東京化成社製)100重量部に対し、光ラジカル重合開始剤として実施例1と同様の方法で得た9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を1.5重量部添加して、更に、光ラジカル重合増感剤としてDBA(9,10-ジブトキシアントラセン)を0.01重量部添加し、ラジカル重合性組成物を調製した。該ラジカル重合性組成物1mgを測定用アルミパンの中に精秤し、DSC測定部に収めた後、光DSCユニットを装着した。該サンプルを、窒素雰囲気下で405nmの光を2分間照射した。その時の発熱量は266mJ/mgであり、転化率は53.2%であった(結果を表3に記載)。
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ラート(TMPTA)(東京化成社製)100重量部に対し、光ラジカル重合開始剤として実施例1と同様の方法で得た9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を1.5重量部添加して、更に、光ラジカル重合増感剤としてOcA(9,10-ビス(オクタノイルオキシ)アントラセン)を0.5重量部添加し、ラジカル重合性組成物を調製した。該ラジカル重合性組成物1mgを測定用アルミパンの中に精秤し、DSC測定部に収めた後、光DSCユニットを装着した。該サンプルを、窒素雰囲気下で405nmの光を5分間照射した。その時の発熱量は359mJ/mgであり、転化率は71.8%であった(結果を表3に記載)。
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ラート(TMPTA)(東京化成社製)100重量部に対し、光ラジカル重合開始剤として実施例1と同様の方法で得た9,10-ジブトキシアントラセン-9,10-エンドペルオキシド(DBAEPO)を1.5重量部添加して、更に、光ラジカル重合増感剤として合成実施例2と同様にして合成したECMA(9,10-ビス(エトキシカルボニルメチレンオキシ)アントラセン)を0.5重量部添加し、ラジカル重合性組成物を調製した。該ラジカル重合性組成物1mgを測定用アルミパンの中に精秤し、DSC測定部に収めた後、光DSCユニットを装着した。該サンプルを、窒素雰囲気下で405nmの光を2分間照射した。その時の発熱量は400mJ/mgであり、転化率は70.1%であった(結果を表3に記載)。
Claims (20)
- 下記一般式(1)で表される多環芳香族骨格を有するエンドペルオキシド化合物を含有することを特徴とする、光ラジカル重合開始剤。
(一般式(1)において、Rは炭素数1から20のアルキル基、炭素数6から10のアリール基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から10のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基、炭素数6から10のアリール基を有するアリールオキシカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニル基、炭素数6から10のアリール基を有するアリールアミノカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニルオキシ基、炭素数6から10のアリール基を有するアリールアミノカルボニルオキシ基のいずれかを表す。Rが炭素数1から20のアルキル基を表す場合の当該アルキル基は、ヒドロキシ基、炭素数1から10のアルコキシ基、炭素数6から10のアリールオキシ基、炭素数6から10のアリール基、炭素数6から10のアリール基を持つアリールアルキル基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から10のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基、炭素数6から10のアリール基を有するアリールオキシカルボニル基、炭素数1から10のアルキル基を有するアルキルカルボニルオキシ基、炭素数6から10のアリール基を有するアリールカルボニルオキシ基、炭素数1から10のアルキル基を有するアルキルオキシカルボニルオキシ基、炭素数6から10のアリール基を有するアリールオキシカルボニルオキシ基、カルボキシル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニル基、炭素数6から10のアリール基を有するアリールアミノカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニルオキシ基、炭素数6から10のアリール基を有するアリールアミノカルボニルオキシ基、ヒドロキシアルコキシ基で置換されていてもよい。また、X1、X2は同一であっても異なっていてもよく、水素原子、炭素数1から8のアルキル基、炭素数6~10のアリール基、炭素数1~5のアルコキシ基、炭素数6~10のアリールオキシ基、ヒドロキシ基、アミノ基、炭素数1~5のアルキルアミノ基、炭素数6から10のアリールアミノ基、メルカプト基、炭素数1から5のアルキルスルフィド基、炭素数6から10のアリールスルフィド基、ハロゲン原子、又は、X1とX2は互いに結合して飽和又は不飽和の環を形成してもよく、酸素原子、窒素原子、硫黄原子を挟んで環を形成しても良く、形成した環は更に置換基を有していてもよい。Y1は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 下記一般式(1)で表される多環芳香族骨格を有するエンドペルオキシド化合物を含有することを特徴とする、熱ラジカル重合開始剤。
- 下記一般式(3)で表される多環芳香族骨格を有するエンドペルオキシド化合物を含有することを特徴とする、光ラジカル重合開始剤。
(一般式(3)において、Rは炭素数1から10のアルキル基、炭素数1から5のアルコキシ基を持つアルコキシメチル基、炭素数6から10のアリール基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から20のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基又は炭素数6から10のアリール基を有するアリールオキシカルボニル基のいずれかを表し、Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 下記一般式(3)で表される多環芳香族骨格を有するエンドペルオキシド化合物を含有することを特徴とする、熱ラジカル重合開始剤。
(一般式(3)において、Rは炭素数1から10のアルキル基、炭素数1から5のアルコキシ基を持つアルコキシメチル基、炭素数6から10のアリール基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から20のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基又は炭素数6から10のアリール基を有するアリールオキシカルボニル基のいずれかを表し、Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 下記一般式(5)で表される多環芳香族骨格を有するエンドペルオキシド化合物。
(一般式(5)において、T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。R3、R4は、同一であって異なっていてもよく、炭素数1から20のアルキル基を表す。Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 下記一般式(6)で表される多環芳香族骨格を有する化合物を300nmから410nmの波長範囲内にピーク波長を有する光の照射下で分子状酸素と反応させることを特徴とする、下記一般式(5)で表される多環芳香族骨格を有するエンドペルオキシド化合物の製造方法。
(一般式(5)において、T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。R3、R4は、同一であって異なっていてもよく、炭素数1から20のアルキル基を表す。Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 下記一般式(6)で表される多環芳香族骨格を有する化合物を、一般式(6)で表される多環芳香族骨格を有する化合物以外の一重項酸素ジェネレーター共存下に該一重項酸素ジェネレーターと分子状酸素により発生させた一重項酸素と、反応させることを特徴とする、下記一般式(5)で表される多環芳香族骨格を有するエンドペルオキシド化合物の製造方法。
(一般式(5)において、T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。R3、R4は、同一であって異なっていてもよく、炭素数1から20のアルキル基を表す。Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 請求項5に記載の多環芳香族骨格を有するエンドペルオキシド化合物を含有することを特徴とする、光ラジカル重合開始剤。
- 請求項5に記載の多環芳香族骨格を有するエンドペルオキシド化合物を含有することを特徴とする、熱ラジカル重合開始剤。
- 請求項1、請求項3又は請求項8のいずれか一項に記載の光ラジカル重合開始剤と、ラジカル重合性化合物とを含有することを特徴とする、ラジカル重合性組成物。
- 請求項2、請求項4又は請求項9のいずれか一項に記載の熱ラジカル重合開始剤と、ラジカル重合性化合物とを含有することを特徴とする、ラジカル重合性組成物。
- 請求項10に記載のラジカル重合性組成物に更に光ラジカル重合増感剤を含有することを特徴とする、ラジカル重合性組成物。
- 請求項11に記載のラジカル重合性組成物に更に熱ラジカル重合開始剤の分解促進剤を含有することを特徴とする、ラジカル重合性組成物。
- 請求項10又は12に記載のラジカル重合性組成物に、230nmから330nmの波長範囲内にピーク波長を有する光を含むエネルギー線を照射することにより重合反応を行うことを特徴とするラジカル重合性組成物の硬化方法。
- 請求項10又は12に記載のラジカル重合性組成物に、300nmから410nmの波長範囲内にピーク波長を有する光を含むエネルギー線を照射することにより重合反応を行うことを特徴とするラジカル重合性組成物の硬化方法。
- 請求項11又は13に記載のラジカル重合性組成物を加熱処理することにより重合反応を行うことを特徴とするラジカル重合性組成物の硬化方法。
- 下記一般式(2)で表される多環芳香族骨格を有する化合物及びラジカル重合性化合物を含有するラジカル重合性組成物において、酸素存在下で紫外線を照射することにより下記一般式(1)で表される多環芳香族骨格を有するエンドペルオキシド化合物を製造し、該多環芳香族骨格を有するエンドペルオキシド化合物を光ラジカル重合開始剤及び/又は熱ラジカル重合開始剤として重合反応を行うことを特徴とする、ラジカル重合性組成物の硬化方法。
(一般式(2)において、Rは炭素数1から20のアルキル基、炭素数6から10のアリール基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から10のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基、炭素数6から10のアリール基を有するアリールオキシカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニル基、炭素数6から10のアリール基を有するアリールアミノカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニルオキシ基、炭素数6から10のアリール基を有するアリールアミノカルボニルオキシ基のいずれかを表す。Rが炭素数1から20のアルキル基を表す場合の当該アルキル基は、ヒドロキシ基、炭素数1から10のアルコキシ基、炭素数6から10のアリールオキシ基、炭素数6から10のアリール基、炭素数6から10のアリール基を持つアリールアルキル基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から10のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基、炭素数6から10のアリール基を有するアリールオキシカルボニル基、炭素数1から10のアルキル基を有するアルキルカルボニルオキシ基、炭素数6から10のアリール基を有するアリールカルボニルオキシ基、炭素数1から10のアルキル基を有するアルキルオキシカルボニルオキシ基、炭素数6から10のアリール基を有するアリールオキシカルボニルオキシ基、カルボキシル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニル基、炭素数6から10のアリール基を有するアリールアミノカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニルオキシ基、炭素数6から10のアリール基を有するアリールアミノカルボニルオキシ基、ヒドロキシアルコキシ基で置換されていてもよい。また、X1、X2は同一であっても異なっていてもよく、水素原子、炭素数1から8のアルキル基、炭素数6~10のアリール基、炭素数1~5のアルコキシ基、炭素数6~10のアリールオキシ基、ヒドロキシ基、アミノ基、炭素数1~5のアルキルアミノ基、炭素数6から10のアリールアミノ基、メルカプト基、炭素数1から5のアルキルスルフィド基、炭素数6から10のアリールスルフィド基、ハロゲン原子、又は、X1とX2は互いに結合して飽和又は不飽和の環を形成してもよく、酸素原子、窒素原子、硫黄原子を挟んで環を形成しても良く、形成した環は更に置換基を有していてもよい。Y1は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。)
(一般式(1)において、Rは炭素数1から20のアルキル基、炭素数6から10のアリール基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から10のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基、炭素数6から10のアリール基を有するアリールオキシカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニル基、炭素数6から10のアリール基を有するアリールアミノカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニルオキシ基、炭素数6から10のアリール基を有するアリールアミノカルボニルオキシ基のいずれかを表す。Rが炭素数1から20のアルキル基を表す場合の当該アルキル基は、ヒドロキシ基、炭素数1から10のアルコキシ基、炭素数6から10のアリールオキシ基、炭素数6から10のアリール基、炭素数6から10のアリール基を持つアリールアルキル基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から10のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基、炭素数6から10のアリール基を有するアリールオキシカルボニル基、炭素数1から10のアルキル基を有するアルキルカルボニルオキシ基、炭素数6から10のアリール基を有するアリールカルボニルオキシ基、炭素数1から10のアルキル基を有するアルキルオキシカルボニルオキシ基、炭素数6から10のアリール基を有するアリールオキシカルボニルオキシ基、カルボキシル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニル基、炭素数6から10のアリール基を有するアリールアミノカルボニル基、炭素数1から10のアルキル基を有するアルキルアミノカルボニルオキシ基、炭素数6から10のアリール基を有するアリールアミノカルボニルオキシ基、ヒドロキシアルコキシ基で置換されていてもよい。また、X1、X2は同一であっても異なっていてもよく、水素原子、炭素数1から8のアルキル基、炭素数6~10のアリール基、炭素数1~5のアルコキシ基、炭素数6~10のアリールオキシ基、ヒドロキシ基、アミノ基、炭素数1~5のアルキルアミノ基、炭素数6から10のアリールアミノ基、メルカプト基、炭素数1から5のアルキルスルフィド基、炭素数6から10のアリールスルフィド基、ハロゲン原子、又は、X1とX2は互いに結合して飽和又は不飽和の環を形成してもよく、酸素原子、窒素原子、硫黄原子を挟んで環を形成しても良く、形成した環は更に置換基を有していてもよい。Y1は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 下記一般式(4)で表される多環芳香族骨格を有する化合物及びラジカル重合性化合物を含有するラジカル重合性組成物において、酸素存在下で紫外線を照射することにより下記一般式(3)で表される多環芳香族骨格を有するエンドペルオキシド化合物を製造し、該多環芳香族骨格を有するエンドペルオキシド化合物を光ラジカル重合開始剤及び/又は熱ラジカル重合開始剤として重合反応を行うことを特徴とする、ラジカル重合性組成物の硬化方法。
(一般式(4)において、Rは炭素数1から10のアルキル基、炭素数1から5のアルコキシ基を持つアルコキシメチル基、炭素数6から10のアリール基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から20のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基又は炭素数6から10のアリール基を有するアリールオキシカルボニル基のいずれかを表し、Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。)
(一般式(3)において、Rは炭素数1から10のアルキル基、炭素数1から5のアルコキシ基を持つアルコキシメチル基、炭素数6から10のアリール基、炭素数1から10のアルキル基を有するアルキルカルボニル基、炭素数6から20のアリール基を有するアリールカルボニル基、炭素数1から10のアルキル基を有するアルキルオキシカルボニル基又は炭素数6から10のアリール基を有するアリールオキシカルボニル基のいずれかを表し、Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 下記一般式(6)で表される多環芳香族骨格を有する化合物及びラジカル重合性化合物を含有するラジカル重合性組成物において、酸素存在下で紫外線を照射することにより下記一般式(5)で表される多環芳香族骨格を有するエンドペルオキシド化合物を製造し、該多環芳香族骨格を有するエンドペルオキシド化合物を光ラジカル重合開始剤及び/又は熱ラジカル重合開始剤として重合反応を行うことを特徴とする、ラジカル重合性組成物の硬化方法。
(一般式(5)において、T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。R3、R4は、同一であって異なっていてもよく、炭素数1から20のアルキル基を表す。Y1、Y2は水素原子、炭素数1から8のアルキル基又はハロゲン原子のいずれかを表す。) - 照射する紫外線が300nmから410nmの波長範囲内にピーク波長を有する光であることを特徴とする、請求項17、請求項18又は請求項19のいずれか一項に記載のラジカル重合性組成物の硬化方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018023575 | 2018-02-13 | ||
JP2018023575 | 2018-02-13 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2019137682A JP2019137682A (ja) | 2019-08-22 |
JP2019137682A5 JP2019137682A5 (ja) | 2022-03-10 |
JP7387267B2 true JP7387267B2 (ja) | 2023-11-28 |
Family
ID=67619920
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2019023018A Active JP7387267B2 (ja) | 2018-02-13 | 2019-02-12 | 多環芳香族骨格を有するエンドペルオキシド化合物 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20220127385A1 (ja) |
JP (1) | JP7387267B2 (ja) |
KR (1) | KR20210116497A (ja) |
CN (1) | CN113454090A (ja) |
WO (1) | WO2019159908A1 (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020054874A1 (ja) * | 2018-09-15 | 2020-03-19 | 川崎化成工業株式会社 | 光重合増感剤 |
WO2020121384A1 (ja) * | 2018-12-10 | 2020-06-18 | 川崎化成工業株式会社 | 耐マイグレーション性を有する光重合増感剤 |
JP7276652B2 (ja) * | 2019-04-11 | 2023-05-18 | エア・ウォーター・パフォーマンスケミカル株式会社 | 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 |
CN113929699B (zh) * | 2021-07-22 | 2023-01-10 | 大连理工大学 | 一类psma靶向的内过氧化物体系及应用 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015183139A (ja) | 2014-03-25 | 2015-10-22 | 川崎化成工業株式会社 | エネルギー線重合性組成物 |
JP2017057249A (ja) | 2015-09-14 | 2017-03-23 | 川崎化成工業株式会社 | 光重合性組成物 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4563413A (en) * | 1984-04-23 | 1986-01-07 | Hercules Incorporated | Photopolymer process and composition employing a photooxidizable component capable of forming endoperoxides |
JP3888163B2 (ja) | 2002-01-16 | 2007-02-28 | 昭和電工株式会社 | 変性(メタ)アクリレート化合物 |
JP4252755B2 (ja) | 2002-03-08 | 2009-04-08 | 独立行政法人科学技術振興機構 | アントラセン酸素錯体及びその製造方法 |
JP2004277660A (ja) | 2003-03-18 | 2004-10-07 | Toagosei Co Ltd | 熱硬化型組成物 |
JP2007118396A (ja) | 2005-10-28 | 2007-05-17 | Toyo Ink Mfg Co Ltd | 積層体およびその製造方法 |
JP4841471B2 (ja) | 2007-03-14 | 2011-12-21 | 三洋電機株式会社 | 機器のドレン水浄化装置 |
US20100168334A1 (en) | 2008-12-29 | 2010-07-01 | Fina Technology, Inc. | Polymeric Compositions and Polymerization Initiators Using Photo-Peroxidation Process |
JP5594510B2 (ja) | 2009-08-21 | 2014-09-24 | 川崎化成工業株式会社 | 9,10−ビス(置換カルボニルオキシ)アントラセン化合物及びそれを含有する光ラジカル重合開始剤。 |
JP5603130B2 (ja) | 2010-05-07 | 2014-10-08 | 株式会社ブリヂストン | 硬化物の製造方法、並びに硬化物、電子部品用シール材及び電子部品用ガスケット材 |
JP5556375B2 (ja) | 2010-05-27 | 2014-07-23 | 川崎化成工業株式会社 | 光硬化性組成物 |
JP6277692B2 (ja) | 2013-11-28 | 2018-02-14 | 川崎化成工業株式会社 | 光カチオン重合性組成物及びその重合方法 |
JP6459394B2 (ja) | 2014-10-29 | 2019-01-30 | 川崎化成工業株式会社 | 光重合増感剤組成物とそれを含む光重合性組成物 |
CN105037587B (zh) * | 2015-06-24 | 2017-03-22 | 常州强力先端电子材料有限公司 | 一种适用于uv‑led光固化体系的增感剂 |
JP6088105B1 (ja) * | 2015-08-27 | 2017-03-01 | 東京応化工業株式会社 | 感光性組成物、パターン形成方法、硬化物、及び表示装置 |
CN107300833B (zh) * | 2016-04-15 | 2019-12-13 | 常州强力先端电子材料有限公司 | 一种自由基光固化体系及其组合物的应用 |
CN107325237B (zh) * | 2016-04-15 | 2020-04-21 | 常州强力电子新材料股份有限公司 | 一种自由基-阳离子混杂型光固化体系及其应用 |
JP2017197675A (ja) * | 2016-04-28 | 2017-11-02 | 川崎化成工業株式会社 | 光重合増感剤組成物とそれを含む光重合性組成物 |
WO2020121384A1 (ja) * | 2018-12-10 | 2020-06-18 | 川崎化成工業株式会社 | 耐マイグレーション性を有する光重合増感剤 |
-
2019
- 2019-02-12 JP JP2019023018A patent/JP7387267B2/ja active Active
- 2019-02-12 US US17/427,850 patent/US20220127385A1/en active Pending
- 2019-02-12 WO PCT/JP2019/004912 patent/WO2019159908A1/ja active Application Filing
- 2019-02-12 KR KR1020217023596A patent/KR20210116497A/ko not_active Application Discontinuation
- 2019-02-12 CN CN201980091720.4A patent/CN113454090A/zh active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015183139A (ja) | 2014-03-25 | 2015-10-22 | 川崎化成工業株式会社 | エネルギー線重合性組成物 |
JP2017057249A (ja) | 2015-09-14 | 2017-03-23 | 川崎化成工業株式会社 | 光重合性組成物 |
Also Published As
Publication number | Publication date |
---|---|
KR20210116497A (ko) | 2021-09-27 |
WO2019159908A1 (ja) | 2019-08-22 |
CN113454090A (zh) | 2021-09-28 |
US20220127385A1 (en) | 2022-04-28 |
JP2019137682A (ja) | 2019-08-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP7387267B2 (ja) | 多環芳香族骨格を有するエンドペルオキシド化合物 | |
CN110662738B (zh) | 三嗪过氧化物衍生物、含有该化合物的聚合性组合物 | |
WO2018049976A1 (zh) | 芴类光引发剂、其制备方法、具有其的光固化组合物及其在光固化领域的应用 | |
JP2019043864A (ja) | ペルオキシエステル基を有するベンゾフェノン誘導体、該化合物を含有する重合性組成物およびその硬化物、当該硬化物の製造方法 | |
KR102566078B1 (ko) | 광 중합성 조성물 | |
WO2018110179A1 (ja) | ペルオキシシンナメート誘導体、該化合物を含有する重合性組成物 | |
JP6997942B2 (ja) | 光硬化性樹脂組成物、インキ及び塗料 | |
JP6260851B2 (ja) | ラジカル重合増感剤 | |
JP5136956B2 (ja) | 重合性組成物及びその重合物 | |
CN111448280A (zh) | 光敏化剂和活性能量射线固化性组合物 | |
JP6064300B2 (ja) | ラジカル重合増感剤 | |
JP2014070203A (ja) | ラジカル重合増感剤 | |
JP5354353B2 (ja) | 自己光重合性化合物を含有する光硬化性組成物及びその硬化方法 | |
JP6660547B2 (ja) | 光重合増感剤 | |
JP6040772B2 (ja) | 9’−アシルオキシ−10’−[1,4−ビス(アシルオキシ)−2−ナフチル]アントラセン化合物、その製造法及びその用途 | |
JP5387939B2 (ja) | 重合性組成物及びその重合物 | |
US20230086413A1 (en) | Photoradical polymerizable composition | |
JPH09235321A (ja) | 新規なエステルおよびその利用 | |
JP5182511B2 (ja) | 樹脂用添加剤及び当該添加剤を含有する重合性組成物 | |
JPH1072404A (ja) | ソルビトールの(メタ)アクリル酸エステル及びその製法 | |
JP2021017417A (ja) | 多環芳香族骨格を有するハイドロパーオキサイド化合物 | |
JP7356644B2 (ja) | 高分子光重合増感剤 | |
JP2014129309A (ja) | ラジカル重合増感剤 | |
JP7290150B2 (ja) | 感光性樹脂組成物、硬化物、絶縁材料、ソルダーレジスト用樹脂材料及びレジスト部材 | |
JP2022007950A (ja) | 光ラジカル重合性組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20190213 |
|
AA64 | Notification of invalidation of claim of internal priority (with term) |
Free format text: JAPANESE INTERMEDIATE CODE: A241764 Effective date: 20190308 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20190331 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20220210 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20220210 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20220216 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20230405 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20230530 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20230814 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20230817 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20230830 |
|
R155 | Notification before disposition of declining of application |
Free format text: JAPANESE INTERMEDIATE CODE: R155 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20231115 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 7387267 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |