CN108069932A - The colour filter and display device that compound, the colored resin composition containing compound resin, colored resin composition are formed - Google Patents
The colour filter and display device that compound, the colored resin composition containing compound resin, colored resin composition are formed Download PDFInfo
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- CN108069932A CN108069932A CN201711067616.0A CN201711067616A CN108069932A CN 108069932 A CN108069932 A CN 108069932A CN 201711067616 A CN201711067616 A CN 201711067616A CN 108069932 A CN108069932 A CN 108069932A
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- compound
- carbon number
- heterocycle
- formula
- resin composition
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 102
- 239000011342 resin composition Substances 0.000 title claims abstract description 35
- 239000011347 resin Substances 0.000 title claims abstract description 30
- 229920005989 resin Polymers 0.000 title claims abstract description 30
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 79
- 229910052799 carbon Inorganic materials 0.000 claims description 79
- 125000000623 heterocyclic group Chemical group 0.000 claims description 69
- 229910052757 nitrogen Inorganic materials 0.000 claims description 46
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 41
- 125000001424 substituent group Chemical group 0.000 claims description 33
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 68
- -1 propyl phenyl Chemical group 0.000 description 46
- 239000002585 base Substances 0.000 description 39
- 239000002904 solvent Substances 0.000 description 34
- 238000006243 chemical reaction Methods 0.000 description 20
- 239000000975 dye Substances 0.000 description 18
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 17
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 17
- 239000000049 pigment Substances 0.000 description 16
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 14
- 239000003505 polymerization initiator Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 11
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 11
- 238000006116 polymerization reaction Methods 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 125000001118 alkylidene group Chemical group 0.000 description 10
- 238000002425 crystallisation Methods 0.000 description 10
- 230000008025 crystallization Effects 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 239000003086 colorant Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 239000000470 constituent Substances 0.000 description 8
- 150000002148 esters Chemical group 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 239000012752 auxiliary agent Substances 0.000 description 7
- 238000006467 substitution reaction Methods 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- 229910006069 SO3H Inorganic materials 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000001476 alcoholic effect Effects 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000004767 nitrides Chemical class 0.000 description 3
- CBFCDTFDPHXCNY-UHFFFAOYSA-N octyldodecane Natural products CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- MKRBAPNEJMFMHU-UHFFFAOYSA-N 1-benzylpyrrole-2,5-dione Chemical class O=C1C=CC(=O)N1CC1=CC=CC=C1 MKRBAPNEJMFMHU-UHFFFAOYSA-N 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 241000534944 Thia Species 0.000 description 2
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 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
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- XUPYJHCZDLZNFP-UHFFFAOYSA-N butyl butanoate Chemical compound CCCCOC(=O)CCC XUPYJHCZDLZNFP-UHFFFAOYSA-N 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 229940116333 ethyl lactate Drugs 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- 125000006125 ethylsulfonyl group Chemical group 0.000 description 2
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 239000005453 ketone based solvent Substances 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
- 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 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000001053 orange pigment Substances 0.000 description 2
- 150000002921 oxetanes Chemical group 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 238000001259 photo etching Methods 0.000 description 2
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000001054 red pigment Substances 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 description 2
- 230000001960 triggered effect Effects 0.000 description 2
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- 0 **(*)c(c(N)c1)cc(O2)c1C(c(cccc1)c1[N+]([O-])=O)=C(C=C1*)C2=CC1=O Chemical compound **(*)c(c(N)c1)cc(O2)c1C(c(cccc1)c1[N+]([O-])=O)=C(C=C1*)C2=CC1=O 0.000 description 1
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 description 1
- 125000001376 1,2,4-triazolyl group Chemical class N1N=C(N=C1)* 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
- BTJPUDCSZVCXFQ-UHFFFAOYSA-N 2,4-diethylthioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC(CC)=CC(CC)=C3SC2=C1 BTJPUDCSZVCXFQ-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- JZIBVTUXIVIFGC-UHFFFAOYSA-N 2H-pyrrole Chemical class C1C=CC=N1 JZIBVTUXIVIFGC-UHFFFAOYSA-N 0.000 description 1
- IHXWECHPYNPJRR-UHFFFAOYSA-N 3-hydroxycyclobut-2-en-1-one Chemical compound OC1=CC(=O)C1 IHXWECHPYNPJRR-UHFFFAOYSA-N 0.000 description 1
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 1
- ZEWLHMQYEZXSBH-UHFFFAOYSA-N 4-[2-(2-methylprop-2-enoyloxy)ethoxy]-4-oxobutanoic acid Chemical compound CC(=C)C(=O)OCCOC(=O)CCC(O)=O ZEWLHMQYEZXSBH-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 description 1
- QKUKRVOSJTZJDI-UHFFFAOYSA-N C(CCC)OCCCCCCOOOCCCCC Chemical compound C(CCC)OCCCCCCOOOCCCCC QKUKRVOSJTZJDI-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- XXRCUYVCPSWGCC-UHFFFAOYSA-N Ethyl pyruvate Chemical compound CCOC(=O)C(C)=O XXRCUYVCPSWGCC-UHFFFAOYSA-N 0.000 description 1
- 241000511976 Hoya Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 1
- WRQNANDWMGAFTP-UHFFFAOYSA-N Methylacetoacetic acid Chemical compound COC(=O)CC(C)=O WRQNANDWMGAFTP-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- NPKSPKHJBVJUKB-UHFFFAOYSA-N N-phenylglycine Chemical compound OC(=O)CNC1=CC=CC=C1 NPKSPKHJBVJUKB-UHFFFAOYSA-N 0.000 description 1
- AQGDXJQRVOCUQX-UHFFFAOYSA-N N.[S] Chemical compound N.[S] AQGDXJQRVOCUQX-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 description 1
- RFFFKMOABOFIDF-UHFFFAOYSA-N Pentanenitrile Chemical compound CCCCC#N RFFFKMOABOFIDF-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 241001047482 Viola hederacea Species 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000000999 acridine dye Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000001204 arachidyl 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])[H] 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical class C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- VYHBFRJRBHMIQZ-UHFFFAOYSA-N bis[4-(diethylamino)phenyl]methanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1 VYHBFRJRBHMIQZ-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- WCZVZNOTHYJIEI-UHFFFAOYSA-N cinnoline Chemical compound N1=NC=CC2=CC=CC=C21 WCZVZNOTHYJIEI-UHFFFAOYSA-N 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical class CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 150000004816 dichlorobenzenes Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000982 direct dye Substances 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
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 229940117360 ethyl pyruvate Drugs 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000001056 green pigment Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005935 hexyloxycarbonyl group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000005342 ion exchange Methods 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
- 125000005956 isoquinolyl group Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 239000000983 mordant dye Substances 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 150000005054 naphthyridines Chemical class 0.000 description 1
- 239000001005 nitro dye Substances 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
- 125000002347 octyl 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])[H] 0.000 description 1
- 125000005447 octyloxy 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])O* 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000005304 optical glass Substances 0.000 description 1
- 125000000466 oxiranyl group Chemical group 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
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001782 photodegradation Methods 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 239000001008 quinone-imine dye Substances 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000992 solvent dye Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- FCEHBMOGCRZNNI-UHFFFAOYSA-N thianaphthalene Natural products C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000002053 thietanyl group Chemical group 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
- C07D311/82—Xanthenes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/28—Pyronines ; Xanthon, thioxanthon, selenoxanthan, telluroxanthon dyes
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
- G02F1/133509—Filters, e.g. light shielding masks
- G02F1/133514—Colour filters
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/105—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nonlinear Science (AREA)
- Optics & Photonics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mathematical Physics (AREA)
- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Structural Engineering (AREA)
- Materials For Photolithography (AREA)
- Optical Filters (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Sometimes contrast cannot fully meet needs to the colour filter formed by existing known colored resin composition.Colored resin composition the present invention relates to compound, comprising above-claimed cpd resin, the colour filter formed by above-mentioned colored resin composition and the display device for including above-mentioned colour filter.The compound of the present invention is represented by formula (1).
Description
Technical field
Colored resin composition the present invention relates to compound, comprising above-claimed cpd resin, by above-mentioned pigmentary resin group
It closes the colour filter of object formation and includes the display device of above-mentioned colour filter.
Background technology
Filter used in the display devices such as liquid crystal display device, el display device and plasma scope
Colored resin composition has been used in the manufacture of color device.As such colored resin composition, it is known that comprising by following formula table
Colored resin composition of the compound shown as colorant.
Prior art literature
Patent document
Patent document 1：Japanese Unexamined Patent Publication 2013-50693 publications
The content of the invention
The subject that the invention solves
Contrast is not sometimes for the colour filter formed by the existing known colored resin composition comprising above-mentioned compound
Needs can fully be met.
Means for solving the problems
That is, the present invention includes following invention.
[1] compound represented by formula (1).
[in formula (1), R1~R4Hydrogen atom, the saturated hydrocarbyl for the carbon number 1~20 that there can be substituent group are represented independently of each other
Or can have the aromatic hydrocarbyl of the carbon number 6~10 of substituent group, it is at least one to represent that there is carbon of the heterocycle as substituent group
The aromatic hydrocarbyl of number 6~10, contained-CH in the saturated hydrocarbyl2- it may alternatively be-O- ,-CO- or-NR5-。R1And R2
The ring of nitrogen atom, R can be formed together3And R4The ring of nitrogen atom can be formed together.R5~R7Hydrogen atom is represented independently of each other
Or the alkyl of carbon number 1~6.]
[2] compound described in [1], wherein, R1Represent that there is aromatic series of the heterocycle as the carbon number 6~10 of substituent group
Alkyl, and R2~R4Represent can there is the saturated hydrocarbyl of the carbon number 1~20 of substituent group or hydrogen atom or R independently of each other1With
R3Represent that there is aromatic hydrocarbyl of the heterocycle as the carbon number 6~10 of substituent group, and R2And R4Represent can have independently of each other
The saturated hydrocarbyl or hydrogen atom of the carbon number 1~20 of substituted base.
[3] compound described in [1] or [2], wherein, the aromatic hydrocarbyl of the above-mentioned carbon number 6~10 with heterocycle is
The group represented by formula (1x).
[in formula (1x), Q1Represent heterocycle.* the bonding end with nitrogen-atoms is represented.]
[4] any one of them compound of [1]~[3], wherein, above-mentioned heterocycle is the heterocycle of nitrogen atom.
[5] colored resin composition, it includes any one of them compounds and resin of [1]~[4].
[6] colour filter formed as the colored resin composition described in [5].
[7] display device, it includes the colour filters described in [6].
The effect of invention
Colored resin composition, being capable of the excellent filter of degree of being contrasted by being used as colorant comprising the compound of the present invention
Color device.
Specific embodiment
The compound of the present invention is represented by formula (1).The compound that will be represented sometimes by formula (1) below is known as " compound
(1)”.Also comprising its tautomer, their salt in the compound of the present invention.In addition, each ingredient illustrated below and function
Group can each be used alone or use in combination.
[in formula (1), R1~R4Hydrogen atom, the saturated hydrocarbyl for the carbon number 1~20 that there can be substituent group are represented independently of each other
Or can have the aromatic hydrocarbyl of the carbon number 6~10 of substituent group, it is at least one to represent that there is carbon of the heterocycle as substituent group
The aromatic hydrocarbyl of number 6~10, contained-CH in the saturated hydrocarbyl2- it may alternatively be-O- ,-CO- or-NR5-。R1And R2
The ring containing nitrogen-atoms, R can be formed together3And R4The ring containing nitrogen-atoms can be formed together.
R5~R7The alkyl of hydrogen atom or carbon number 1~6 is represented independently of each other.]
As R1~R4In carbon number 6~10 aromatic hydrocarbyl, such as can include phenyl, tolyl, xylyl,
Mesitylene base, propyl phenyl and butyl phenyl etc..
As the substituent group that the aromatic hydrocarbyl can have, halogen atom ,-R can be included8、-OH、-OR8、-SO3 -、-
SO3H、-SO3 -Z+、-CO2H、-CO2R8、-SR8、-SO2R8、-SO3R8、-SO2NR9R10Or heterocycle, preferably these substituent groups are by virtue
Contained hydrogen atom substitution in fragrant race's alkyl.In these, as substituent group, preferably-SO3 -、-SO3H、-SO3 -Z+With-
SO2NR9R10, more preferable-SO3 -Z+、-SO2NR9R10And heterocycle.As-SO at this time3 -Z+, preferably-SO3 -+N(R11)4。
Wherein, Z+It represents+N(R11)4、Na+Or K+, 4 R11Can it is identical also can be different.
Above-mentioned heterocycle can be saturated heterocyclyl, or unsaturated heterocycle base can be the heterocycle of monocyclic,
Or the heterocycle of condensed ring formula.The carbon number of above-mentioned heterocycle is preferably 2~10, and more preferably 3~8.
As heterocycle, the heterocycle of nitrogen atom can be included, the heterocycle of nitrogen atom and do not contained containing oxygen atom but
Heterocycle of sulphur atom but not nitrogen atom etc..
As the heterocycle of nitrogen atom, can include azete piperidinyl, pyrrolidinyl, piperidyl, piperazinyl, morpholinyl,
The saturated heterocyclyl of the nitrogen atoms such as thio-morpholinyl；Pyrrole radicals, pyrazolyl, imidazole radicals, 1,2,3- triazolyls, 1,2,4- triazoles
Base, pyridyl group, pyridazinyl, pyrimidine radicals, pyrazinyl, cyanuro 1,3,5, indolinyl, iso-dihydro-indole-group, indyl, Yin
Piperazine base, benzimidazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolyl, cinnoline base, phthalazinyl, naphthyridines Ji, oxazoles
Unsaturated heterocycle base of the nitrogen atoms such as base, benzoxazolyl, thiazolyl, benzothiazolyl etc..
As containing the oxygen atom but not heterocycle of nitrogen atom, oxetanylmethoxy, tetrahydrofuran base, oxinane can be included
Containing the oxygen atom but not saturated heterocyclyl of nitrogen atom such as base, 1,3- alkyl dioxins and 1,4- alkyl dioxins；Furyl, 2H- pyrroles
Base, 4H- pyranoses, 1- benzofuranyls, Chromanyl, different Chromanyl etc. mutter containing oxygen atom but the not unsaturated heterocycle of nitrogen atom
Base etc..
As the sulfur atom-containing but not heterocycle of nitrogen atom, can include thietanyl, thia cyclopenta, thia hexamethylene
The sulfur atom-containings such as base, 1,3- dithia cyclohexyl but the not saturated heterocyclyl of nitrogen atom；Thienyl, 4H- thiapyrans base, benzo thiophene
Unsaturated heterocycle base of the sulfur atom-containings such as fen base but not nitrogen atom etc..
Wherein, the preferred heterocycle of nitrogen atom, the saturated heterocyclyl of more preferable nitrogen atom.
R8Represent the saturated hydrocarbyl of carbon number 1~20, contained hydrogen atom can be substituted with halogen atoms in the saturated hydrocarbyl.
R9And R10Hydrogen atom is represented independently of each other or can have the saturated hydrocarbyl of the carbon number 1~20 of substituent group, the saturation
Contained-CH in aliphatic alkyl2- it may alternatively be-O- ,-CO- ,-NH- or-NR8-, R9And R10It can be combined with each other and be formed
The heterocycle of 3~10 yuan of rings of nitrogen atom.
R11Represent hydrogen atom, the saturated hydrocarbyl of carbon number 1~20 or the aralkyl of carbon number 7~10.
As R1~R4And R8~R11In carbon number 1~20 saturated hydrocarbyl, such as can include methyl, ethyl, propyl,
The straight-chain alkyls such as butyl, amyl, hexyl, heptyl, octyl group, nonyl, decyl, dodecyl, cetyl, eicosyl；It is different
Propyl, isobutyl group, isopentyl, neopentyl, 2- ethylhexyls etc. divide branched-chain alkyl；Cyclopropyl, cyclopenta, cyclohexyl, cycloheptyl
The ester ring type saturated hydrocarbyl of the carbon numbers such as base, cyclooctyl, tricyclodecyl 3~20.
R1~R4In the saturated hydrocarbyl in contained hydrogen atom for example can be by the virtue of the carbon number 6~10 as substituent group
Fragrant race's alkyl or halogen atom substitution.As can be by R1~R4Saturated hydrocarbyl hydrogen atom substitution carbon number 6~10 aromatic series
Alkyl can be included with being used as R1~R4In carbon number 6~10 aromatic hydrocarbyl illustrate the same group of group.
R9And R10In the saturated hydrocarbyl in contained hydrogen atom for example can be former by the hydroxyl as substituent group or halogen
Son substitution.
As R1And R2The ring and R formed together3And R4The ring formed together, such as following ring can be included.Formula
In, * represents bonding end.
As-OR8, such as methoxyl group, ethyoxyl, propoxyl group, butoxy, amoxy, hexyloxy, oxygen in heptan can be included
Alkoxies such as base, octyloxy, 2- ethyl hexyl oxies and eicosane epoxide etc..
As-CO2R8, such as can include methoxycarbonyl, ethoxy carbonyl, propoxycarbonyl, tert-butoxycarbonyl,
Alkoxy carbonyls such as hexyloxy carbonyl and eicosane epoxide carbonyl etc..
As-SR8, such as methylsulfanyl, Ethylsulfanyl, butyl sulfanyl, hexyl sulfanyl, decyl can be included
Alkyl alkylthio bases such as sulfanyl and eicosyl sulfanyl etc..
As-SO2R8, such as methyl sulphonyl, ethylsulfonyl, butyl sulfonyl, hexyl sulfonyl, the last of the ten Heavenly stems can be included
Alkyl sulphonyls such as base sulfonyl and eicosyl sulfonyl etc..
As-SO3R8, such as methoxysulfonyl, ethoxysulfonyl, propoxysulfonyl, tert-butoxy can be included
Alkyloxysulfonyls such as sulfonyl, hexyloxy sulfonyl and eicosane epoxide sulfonyl etc..
As-SO2NR9R10, such as sulfamoyl can be included；
N- Methylsulfamoyls, N- ethylsulfamovls, N- propylsulfamovs, N- isopropylsulfamoyls base, N- butyl
Sulfamoyl, N- isobutyl groups sulfamoyl, N- sec-butyls sulfamoyl, N- tertiary butyls sulfamoyl, N- amyls sulfamoyl, N-
(1- ethyl propyls) sulfamoyl, N- (1,1- dimethyl propyls) sulfamoyl, N- (1,2- dimethyl propyls) sulfamoyl, N-
(2,2- dimethyl propyls) sulfamoyl, N- (1- methyl butyls) sulfamoyl, N- (2- methyl butyls) sulfamoyl, N- (3-
Methyl butyl) sulfamoyl, N- Cyclopentylsulfamoyls base, N- hexyls sulfamoyl, N- (1,3- dimethylbutyls) sulfamoyl,
N- (3,3- dimethylbutyls) sulfamoyl, N- heptyl sulfamoyl, N- (1- methylhexyls) sulfamoyl, N- (1,4- diformazans
Base amyl) sulfamoyl, N- octyl groups sulfamoyl, N- (2- ethylhexyls) sulfamoyl, N- (1,5- dimethylhexanyls) ammonia sulphur
The N-1 such as acyl group, N- (1,1,2,2- tetramethyl butyls) sulfamoyl substitute sulfamoyl；
N, N- DimethylsuIfamoyl, N, N- ethyl-methyls sulfamoyl, N, N- diethyl aminos sulfonyl, N, N- propyl first
Base sulfamoyl, N, N- isopropyl methyls sulfamoyl, N, N- tertbutyl methyls sulfamoyl, N, N- butyl ethyl sulfonamides
Base, N, double (1- methyl-propyls) sulfamoyls of N-, N, N-2 the substitution sulfamoyl such as N, N- hept-ylmethyl sulfamoyls etc..
As R5, preferably-CO2H、-CO2 -Z+、-CO2R8、-SO3 -、-SO3 -Z+、-SO3H or-SO2NHR9, more preferable-SO3 -、-
SO3 -Z+、-SO3H or-SO2NHR9。
As R5~R7In carbon number 1~6 alkyl, the alkyl of carbon number 1~6 in the above-mentioned alkyl enumerated can be included.Make
For R6、R7, preferred hydrogen atom.
As R11In carbon number 7~10 aralkyl, benzyl, phenylethyl, phenyl butyl etc. can be included.
Z+For+N(R11)4、Na+Or K+, it is preferably+N(R11)4。
As above-mentioned+N(R11)4, preferably 4 R11Middle at least two is the saturated hydrocarbyl of carbon number 5~20.In addition, 4 R11's
Total carbon number preferably 20~80, more preferable 20~60.
In compound (1), preferably R1Represent that there is aromatic hydrocarbyl of the heterocycle as the carbon number 6~10 of substituent group, and
And R2~R4Represent can there is the saturated hydrocarbyl of the carbon number 1~20 of substituent group or hydrogen atom or R independently of each other1And R3It represents
Aromatic hydrocarbyl with heterocycle as the carbon number 6~10 of substituent group, and R2And R4Represent there can be substitution independently of each other
The saturated hydrocarbyl or hydrogen atom of the carbon number 1~20 of base.
As the aromatic hydrocarbyl of the above-mentioned carbon number 6~10 with heterocycle, the group preferably represented by formula (1x).
[in formula (1x), Q1Represent heterocycle.* the bonding end with nitrogen-atoms is represented.]
As by Q1The heterocycle of expression can be included with being used as by R1What the substituent group of the aromatic hydrocarbyl of expression illustrated
The same group of heterocycle, the preferably heterocycle of nitrogen atom, the saturated heterocyclyl of more preferable nitrogen atom.
The group represented by formula (1x) is more preferably the group represented by formula (1x-1).
[in formula (1x-1), L1Represent the alkylidene of carbon number 3~10, contained-CH in the alkylidene2- may alternatively be-
O- ,-S- or-NH-.]
As by L1The alkylidene of expression, can include ethylidene, propane -1,3- diyl, butane-Isosorbide-5-Nitrae-diyl, pentane -
The alkylidene of the straight-chains such as 1,5- diyls.By L1The carbon number of the alkylidene of expression is preferably 3~8, and more preferably 4~6.As this
Contained-CH in alkylidene2- group of-O- ,-S- or-NH- is replaced by, *-CH can be included2CH2-O-
CH2CH2- *, *-CH2CH2-S-CH2CH2- * or *-CH2CH2-NH-CH2CH2- * etc..Wherein, * is represented and nitrogen-atoms
Bonding end.
Wherein ,-CH contained preferably in alkylidene2- it is replaced by the group of-O-.
As compound (1), the compound (hereinafter sometimes referred to " compound (2) " preferably represented by formula (2).).Chemical combination
Object (2) can be its tautomer.
[in formula (2), R21~R24Hydrogen atom ,-R are represented independently of each other26Or there can be the virtue of the carbon number 6~10 of substituent group
Fragrant race's alkyl, it is at least one to represent that there is aromatic hydrocarbyl of the heterocycle as the carbon number 6~10 of substituent group.R21And R22It can one
Act the ring for forming nitrogen atom, R23And R24The ring of nitrogen atom can be formed together.
R26Represent the saturated hydrocarbyl of carbon number 1~20.]
As R21~R24In carbon number 6~10 aromatic hydrocarbyl, can include with as above-mentioned R1~R4Aromatic series
The same group of group that alkyl includes.Contained hydrogen atom can be by-SO in the aromatic hydrocarbyl3 -、-SO3H、-SO3 -Z1+、-SO3R26、-SO2NHR26Or heterocycle substitution.
As above-mentioned heterocycle, can include with being used as by R1The heterocycle that the substituent group of the aromatic heterocycle of expression illustrates
The same group of base, the preferably heterocycle of nitrogen atom, the saturated heterocyclyl of more preferable nitrogen atom.
Z1+It represents+N(R27)4、Na+Or K+, 4 R27Can it is identical also can be different.
R27Represent the saturated hydrocarbyl or benzyl of carbon number 1~20.
As R21And R22The ring and R of the nitrogen atom formed together23And R24The ring of the nitrogen atom formed together, can
It includes and R1And R2The ring of the same nitrogen atom of ring formed together.Wherein preferred aliphat heterocycle.It is miscellaneous as the aliphatic
Ring, such as following aliphatic heterocycles can be included.In formula, * represents bonding end.
As R26And R27In carbon number 1~20 saturated hydrocarbyl, can include and R8~R11It is middle to be enumerated as saturated hydrocarbyl
The same group of group gone out.
R21~R24For-R26In the case of, preferably-R26Each stand alone as methyl or ethyl.In addition, conduct-SO3R26With-
SO2NHR26In R26, the preferred branch's chain state alkyl of carbon number 3~20, the branch's chain state alkyl of more preferable carbon number 6~12, into one
Walk preferred 2- ethylhexyls.
Z1+For+N(R27)4、Na+Or K+, it is preferably+N(R27)4。
As above-mentioned+N(R27)4, preferably 4 R27Middle at least two is the saturated hydrocarbyl of carbon number 5~20.In addition, 4 R27's
Total carbon number preferably 20~80, more preferable 20~60.
In compound (2), preferably R21Represent that there is aromatic hydrocarbyl of the heterocycle as the carbon number 6~10 of substituent group, and
And R22~R24Hydrogen atom or-R are represented independently of each other26Or R21And R23Represent that there is carbon number 6 of the heterocycle as substituent group
~10 aromatic hydrocarbyl, and R22And R24Hydrogen atom or-R are represented independently of each other26。
As the aromatic hydrocarbyl of the above-mentioned carbon number 6~10 with heterocycle, the group preferably represented by formula (1x) is more excellent
The group that choosing is represented by formula (1x-1).
In addition, as compound (1), it is also preferred that the compound (hereinafter sometimes referred to " compound represented by formula (3)
(3)”.).Compound (3) can be its tautomer.
[in formula (3), R31And R32The saturated hydrocarbyl of carbon number 1~10, the R are represented independently of each other31、R32Saturated hydrocarbyl in
Contained hydrogen atom can be substituted by the aromatic hydrocarbyl of carbon number 6~10 or halogen atom, contained hydrogen in the aromatic hydrocarbyl
Atom can be substituted by the alkoxy of carbon number 1~3, above-mentioned R31、R32Saturated hydrocarbyl in contained-CH2- may alternatively be-
O- ,-CO- or-NR11-。
R33And R34The alkyl of carbon number 1~4, the alkyl alkylthio base of carbon number 1~4, the alkane of carbon number 1~4 are represented independently of each other
Base sulfonyl or heterocycle, at least one expression heterocycle.
R31And R33The ring of nitrogen atom, R can be formed together32And R34The ring of nitrogen atom can be formed together.
P and q represents 0~5 integer independently of each other.When p is more than 2, multiple R33Can it is identical also can be different, q for 2 with
When upper, multiple R34Can it is identical also can be different.But, p and q adds up to more than 1.
R11Represent meaning same as described above.]
As R31And R32In carbon number 1~10 saturated hydrocarbyl, R can be included8In saturated hydrocarbyl in carbon number 1~10
Group.
As the aromatic hydrocarbyl that can be used as carbon number 6~10 that substituent group has, can include and R1In group it is identical
Group.
As the alkoxy of carbon number 1~3, such as methoxyl group, ethyoxyl, propoxyl group etc. can be included.
R31And R32It is preferred that it is independently of one another the saturated hydrocarbyl of carbon number 1~3.
As R33And R34In carbon number 1~4 alkyl, methyl, ethyl, propyl, butyl, isopropyl, isobutyl can be included
Base, sec-butyl, tertiary butyl etc..
As R33And R34In carbon number 1~4 alkyl alkylthio base, methylsulfanyl, Ethylsulfanyl, third can be included
Base sulfanyl, butyl sulfanyl and isopropyl sulfanyl etc..
As R33And R34In carbon number 1~4 alkyl sulphonyl, methyl sulphonyl, ethylsulfonyl, third can be included
Base sulfonyl, butyl sulfonyl and isopropelsulfonyl etc..
As R33And R34In heterocycle, can include with as by R1The aromatic hydrocarbyl of the carbon number 6~10 of expression
The same group of heterocycle that substituent group illustrates, the preferably heterocycle of nitrogen atom, the saturated heterocyclyl of more preferable nitrogen atom.
As R33And R34, the preferred alkyl or heterocycle of carbon number 1~4, more preferable methyl or heterocycle.
The integer of p and q preferably 0~2, preferably 0 or 1.
In compound (3), R33And R34At least one for heterocycle, preferably R33And R34For heterocycle.
Compound (3) is preferably the compound represented by formula (3-1).
[in formula (3-1), R31And R32With it is above-mentioned synonymous.Q31And Q32Heterocycle is represented independently of each other.]
As by Q31And Q32The heterocycle of expression can be included with being used as by R1The substituent group example of the aromatic hydrocarbyl of expression
The same group of heterocycle shown, the preferably heterocycle of nitrogen atom, the saturated heterocyclyl of more preferable nitrogen atom.
Compound (3) is more preferably the compound represented by formula (3-2).
[in formula (3-2), R31And R32With it is above-mentioned synonymous.L31And L32The alkylidene of carbon number 3~10 is represented independently of each other, it should
Contained-CH in alkylidene2- it may alternatively be-O- ,-S- or-NH-.]
As by L31And L32Contained-CH in the alkylidene and alkylidene of expression2- it is replaced by-O- ,-S- or-NH-
Group can be included respectively with being used as by L1Contained-CH in the alkylidene and alkylidene of expression2- be replaced by-O- ,-S- or-
The same group of group that the group of NH- illustrates, contained-CH preferably in alkylidene2- it is replaced by the group of-O-.By L31With
L32The carbon number of the alkylidene of expression is preferably 3~8, and more preferably 4~6.
As compound (1), such as compound (I-1)~(I-252) represented by formula (I) can be included.
【Table 1】
| R1a | R2a | R3a | R4a | |
| (I-1) | (p1) | H | (p1) | H |
| (I-2) | (p1) | Me | (p1) | Me |
| (I-3) | (p1) | Et | (p1) | Et |
| (I-4) | (p1) | Pr | (p1) | Pr |
| (I-5) | (p1) | iPr | (p1) | iPr |
| (I-6) | (p1) | Bu | (p1) | Bu |
| (I-7) | (p1) | 2EH | (p1) | 2EH |
| (I-8) | (p2) | H | (p2) | H |
| (I-9) | (p2) | Me | (p2) | Me |
| (I-10) | (p2) | Et | (p2) | Et |
| (I-11) | (p2) | Pr | (p2) | Pr |
| (I-12) | (p2) | iPr | (p2) | iPr |
| (I-13) | (p2) | Bu | (p2) | Bu |
| (I-14) | (p2) | 2EH | (p2) | 2EH |
| (I-15) | (p3) | H | (p3) | H |
| (I-16) | (p3) | Me | (p3) | Me |
| (I-17) | (p3) | Et | (p3) | Et |
| (I-18) | (p3) | Pr | (p3) | Pr |
| (I-19) | (p3) | iPr | (p3) | iPr |
| (I-20) | (p3) | Bu | (p3) | Bu |
| (I-21) | (p3) | 2EH | (p3) | 2EH |
| (I-22) | (p4) | H | (p4) | H |
| (I-23) | (p4) | Me | (p4) | Me |
| (I-24) | (p4) | Et | (p4) | Et |
| (I-25) | (p4) | Pr | (p4) | Pr |
| (I-26) | (p4) | iPr | (p4) | iPr |
| (I-27) | (p4) | Bu | (p4) | Bu |
| (I-28) | (p4) | 2EH | (p4) | 2EH |
【Table 2】
【Table 3】
【Table 4】
【Table 5】
Wherein, H represents hydrogen atom, and Me represents methyl, and Et represents ethyl, and Pr represents n-propyl, and iPr represents 2- propyl, Bu
Represent normal-butyl, 2EH represents 2- ethylhexyls, and (p1)~(p4) represents following group respectively.In formula, * represents bonding end.
(h1)~(h4) represents R respectively3aWith R4aTogether form following ring.In formula, * represents bonding end.
As compound (1), preferred compound (I-1)~(I-7), compound (I-29)~(I-83).
As the manufacturing method of compound (1), it can enumerate and send as an envoy to by the compound of formula (1x) expression and by formula (1z-1) table
The compound shown and the compound represented by formula (1z-2) are in presence of organic solvent or the method for solvent-free lower reaction.Reaction
Temperature is preferably 30 DEG C~180 DEG C, more preferably 50 DEG C~110 DEG C.When reaction time is preferably 1~12 small, more preferably 3~
8 it is small when.
[in formula (1x), formula (1z-1), formula (1z-2) and formula (1), R1~R7Respectively with it is above-mentioned synonymous.]
As above-mentioned organic solvent, the hydrocarbon solvents such as toluene, dimethylbenzene can be included；The halogenated hydrocarbons such as chlorobenzene, dichloro-benzenes, chloroform
Solvent；The alcoholic solvents such as methanol, ethyl alcohol, butanol；The nitros hydrocarbon solvent such as nitrobenzene；The ketone solvents such as methyl iso-butyl ketone (MIBK)；1- methyl -2-
Amide solvents such as pyrrolidones etc..
The compound and the usage amount of the compound represented by formula (1z-2) represented by formula (1z-1), compared with by formula (1x)
1 mole of the compound of expression, respectively preferably more than 1 mole and less than 8 moles, be more preferably 1 mole or more and 5 moles with
Under.Make its reaction stages respectively, can also make its reaction simultaneously.
Compound (1) is R1~R4Any one be hydrogen atom compound (hereinafter sometimes referred to " compound (1a) ".)
In the case of, compound (1a) can be made with the compound that is represented by formula (1z-3) into one in presence of organic solvent or under solvent-free
Step reaction.Reaction temperature is preferably 30 DEG C~180 DEG C, more preferably 50 DEG C~110 DEG C.When reaction time is preferably 1~12 small,
More preferably 3~8 it is small when.
R12-Br (1z-3)
[in formula (1z-3), R12Represent there can be the saturated hydrocarbyl of the carbon number 1~20 of substituent group.]
As above-mentioned organic solvent, can include makes compound (1x) be reacted with compound (1z-1) and (1z-2) with being used as
When organic solvent illustrate the same solvent of solvent.
When making compound (1a) with being reacted by the compound of formula (1z-3) expression, the basic species such as sodium carbonate, potassium carbonate can be made
Matter coexists.
The method that the compound (1) as target compound is obtained by reaction mixture is not particularly limited, can be adopted
With well known various gimmicks.For example, reaction mixture can be mixed with water, the crystallization that leaching is precipitated.By reaction mixture with
Temperature when water mixes is preferably 10 DEG C or more and less than 50 DEG C.In addition, hereafter, preferably stirring 0.5~2 is small at the same temperature
When or so.The crystallization of leaching is preferably cleaned with water etc., followed by drying.In addition, as needed, the public affairs such as recrystallization can be used
The gimmick known further refines.
The colored resin composition of the present invention includes compound (1) and resin.
It is preferably 0.1~100 mass parts, more preferably compared with 100 mass parts of resin for the content of compound (1)
For 1~50 mass parts, further preferably 1~20 mass parts.
＜ resins (B) ＞
Resin (B) is not particularly limited, is preferably alkali soluble resin, more preferably have come from from unsaturated carboxylic acid and
The resin of the structural unit of at least one kind of (a) (hereinafter sometimes referred to " (a) ") that is selected in unsaturated carboxylic acid anhydrides.Resin (B) is preferred
Also with from from the annular ether structure with carbon number 2~4 and the monomer (b) of ethylenic unsaturated bond (hereinafter sometimes referred to
" (b) ") structural unit, from can with (a) be copolymerized monomer (c) it is (but, different from (a) and (b).) (hereinafter sometimes referred to
" (c) ") structural unit and side chain there is at least one structural unit for selecting in the structural unit of ethylenic unsaturated bond.
As (a), specifically, such as acrylic acid, methacrylic acid, maleic anhydride, itaconic anhydride, 3 can be included, 4,5,
6- tetrabydrophthalic anhydrides, mono succinate [2- (methyl) acryloyl-oxyethyl] ester etc., can preferably include acrylic acid,
Methacrylic acid, maleic anhydride.
(b) the annular ether structure of carbon number 2~4 is preferably had (such as selected from oxirane ring, oxetanes ring and tetrahydrochysene
It is at least one kind of in furan nucleus) and (methyl) acryloxy monomer.
It should be illustrated that in this specification, " (methyl) acrylic acid " represents at least 1 in acrylic acid and methacrylic acid
Kind.The token of " (methyl) acryloyl group " and " (methyl) acrylate " etc. also has same meaning.
As (b), such as (methyl) glycidyl acrylate, vinylbenzyl glycidyl base ether, (first can be included
Base) acrylic acid 3,4- epoxy tricyclics [5.2.1.02,6] last of the ten Heavenly stems ester, 3- ethyls -3- (methyl) acryloyloxymethyls oxetanes,
(methyl) tetrahydrofurfuryl acrylate etc., preferably (methyl) glycidyl acrylate, (methyl) acrylic acid 3,4- epoxy tricyclics
[5.2.1.02,6] last of the ten Heavenly stems ester, 3- ethyls -3- (methyl) acryloyloxymethyl oxetanes.
As (c), such as (methyl) methyl acrylate, (methyl) butyl acrylate, (methyl) acrylic acid ring can be included
Own ester, (methyl) acrylic acid 2- methyl cyclohexyls, (methyl) acrylic acid tricyclic [5.2.1.02,6] decane -8- base esters, (methyl) third
Olefin(e) acid benzyl ester, (methyl) acrylic acid 2- hydroxy methacrylates, N-phenylmaleimide, N- N-cyclohexylmaleimides, N- benzyl horses
Come acid imide, styrene, vinyltoluene etc., can preferably include styrene, vinyltoluene, N- benzyl maleimides
Amine, N- N-cyclohexylmaleimides, N- benzyl maleimides etc..
It can be by making (b) addition in (a) and (c) with the resin in structural unit of the side chain with ethylenic unsaturated bond
Copolymer or (a) addition is made to be manufactured in the copolymer of (b) and (c).The resin can be make (a) addition in (b) with
(c) copolymer and then the resin for forming carboxylic acid anhydride reactant.
The weight average molecular weight of the polystyrene conversion of resin (B) is preferably 3000~100000, more preferably 5000~
50000, further preferably 5000~30000.
The dispersion degree [weight average molecular weight (Mw)/number-average molecular weight (Mn)] of resin (B) is preferably 1.1~6, more preferably
1.2~4.
The acid value of resin (B) is preferably 50~170mg-KOH/g in terms of solid constituent conversion, more preferably 60~
150mg-KOH/g, further preferably 70~135mg-KOH/g.Wherein acid value be as in order to will resin (B) 1g neutralize needed for
Potassium hydroxide the value that measures of amount (mg), such as can be titrated and be obtained by using potassium hydroxide aqueous solution.
It is preferably 7~65 mass %, more preferably compared with the total amount of solid constituent for the containing ratio of resin (B)
13~60 mass %, further preferably 17~55 mass %.
＜ colorants (A) ＞
The colored resin composition of the present invention can include dyestuff (A1) and pigment (A2) conduct in addition to compound (1)
Colorant (A).
Dyestuff (A1) is not particularly limited, well known dyestuff can be used, such as solvent dye, acid dye can be included
Material, direct dyes, mordant dye etc..As dyestuff, such as colour index (The Society of Dyers and can be included
Colourists publish) in be categorized as beyond pigment the substance with form and aspect compound, dyeing notes (Se Ran societies) in note
The well known dyestuff carried.In addition, according to chemical constitution, azo dyes, cyanine dyes, triphenhlmethane dye, xanthene can be included
Dyestuff, phthalocyanine dye, anthraquinone dye, naphthoquinone dyestuff, quinoneimine dye, methine dyes, azomethine dyes, squaraine dye,
Acridine dye, styryl dye, coumarine dye, quinoline dye and nitro dye etc..Preferable organic solvent is solvable in these
Property dyestuff.In addition, as dyestuff, it is also preferred that Japanese Unexamined Patent Publication 2015-28121 publications, Japanese Unexamined Patent Publication 2013-7032 publications,
Dyestuff described in Japanese Unexamined Patent Publication 2013-144724 publications, Japanese Unexamined Patent Publication 2013-53292 publications.
It as pigment (A2), is not particularly limited, well known pigment can be used, such as can be included in colour index (The
Society of Dyers and Colourists are published) in be categorized as the pigment of pigment.
As pigment, for example, can include C.I. pigment yellows 1,3,12,13,14,15,16,17,20,24,31,53,83,
86、93、94、109、110、117、125、128、137、138、139、147、148、150、153、154、166、173、194、214
Wait yellow uitramarines；
C.I. the orange pigments such as pigment orange 13,31,36,38,40,42,43,51,55,59,61,64,65,71,73；
C.I. Pigment Red 9,97,105,122,123,144,149,166,168,176,177,180,192,209,215,
216th, the red pigments such as 224,242,254,255,264,265；
C.I. pigment blue 15,15：3、15：4、15：6th, the green pigments such as 60；
C.I. violet pigments such as pigment violet 1,19,23,29,32,36,38 etc..
In the case that the colored resin composition of the present invention is cyan colored resin composition, pigment is preferably selected from cyan face
At least one of material and violet pigment.In the case that the colored resin composition of the present invention is red colored resin combination,
Pigment is preferably selected from least one of yellow uitramarine, orange pigment and red pigment.
It is preferably 0.1~60 mass % compared with the total amount of solid constituent for the containing ratio of colorant (A), it is more excellent
Elect 0.5~55 mass % as, further preferably 1~50 mass %.
It is preferably more than 50 mass %, more preferably in the total amount of colorant (A) for the containing ratio of compound (1)
For more than 80 mass %, further preferably more than 90 mass %.
Wherein, " total amount of solid constituent " in this specification refers to eliminate from the total amount of colored resin composition molten
Amount after the content of agent.The total amount of solid constituent and it can for example use liquid chromatogram or gas compared with the content of its each ingredient
Analysis means well known to phase chromatography etc. measure.
The colored resin composition of the present invention can include polymerizable compound (C) and/or polymerization initiator (D).Have below
When by the colored resin composition comprising polymerizable compound and polymerization initiator be known as " colored curable resin composition ".
＜ polymerizable compounds (C) ＞
Polymerizable compound (C) is polymerize using the living radical and/or acid that are generated by polymerization initiator (D)
Compound, such as the compound of the ethylenic unsaturated bond with polymerism can be included etc., be preferably (methyl) acrylate
Compound.
Wherein, polymerizable compound (C) is preferably the polymerizable compound with 3 or more ethylenic unsaturated bonds.As
Such polymerizable compound, such as trimethylolpropane tris (methyl) acrylate, pentaerythrite three (methyl) can be included
Acrylate, pentaerythrite four (methyl) acrylate, dipentaerythritol five (methyl) acrylate, six (first of dipentaerythritol
Base) acrylate etc..
The weight average molecular weight of polymerizable compound (C) is preferably more than 150 and less than 2900, more preferably more than 250 and
Less than 1500.
In the case of comprising polymerizable compound (C), for the containing ratio of polymerizable compound (C), compared with solid
The total amount of ingredient is preferably 7~65 mass %, more preferably 13~60 mass %, further preferably 17~55 mass %.
＜ polymerization initiators (D) ＞
Polymerization initiator (D) as long as living radical, acid etc. are generated under the action of light, heat and polymerization can be triggered
Compound is then not particularly limited, and can use well known polymerization initiator.Trigger as the polymerization for generating living radical
Agent, such as N- benzoyloxys -1- (4- Phenylsulfanyls phenyl) butane -1- ketone -2- imines, N- benzoxies can be included
Base -1- (4- Phenylsulfanyls phenyl) octane -1- ketone -2- imines, N- benzoyloxys -1- (4- Phenylsulfanyls phenyl) -3-
Cyclopenta propane -1- ketone -2- imines, 2- methyl -2- morpholinoes -1- (4- methylsulfanyls phenyl) propane -1- ketone, 2- dimethyl
Double (the trichloromethyl) -6- of amino -1- (4- morphlinophenyls) -2- benzyl butane -1- ketone, 1- hydroxycyclohexylphenylketones, 2,4-
Piperonyl -1,3,5- triazines, 2,4,6- trimethyl benzoyl diphenyl bases phosphine oxide, 2,2 '-bis- (2- chlorphenyls) -4,4 ', 5,
5 '-tetraphenyl bisglyoxaline etc..
In the case of comprising polymerization initiator (D), for the content of polymerization initiator (D), compared with resin (B) and
100 mass parts of total amount of polymerizable compound (C) are preferably 0.1~30 mass parts, more preferably 1~20 mass parts.If
The content of polymerization initiator (D) then with high sensitivity, the tendency for shortening the time for exposure, therefore is filtered in above-mentioned scope
The productivity of color device improves.
The colored resin composition of the present invention can include polymerization and trigger auxiliary agent.
＜ polymerizations trigger auxiliary agent (D1) ＞
It is for promoting the polymerization for the polymerizable compound for having triggered polymerization by polymerization initiator that polymerization, which triggers auxiliary agent (D1),
Compound or sensitizer.In the case of triggering auxiliary agent (D1) comprising polymerization, usually it is applied in combination with polymerization initiator (D).
Trigger auxiliary agent (D1) as polymerization, it can include 4,4 '-bis- (dimethylamino) benzophenone (common name Michler's keton),
4,4 '-bis- (diethylamino) benzophenone, 9,10- dimethoxys anthracene, 2,4- diethyl thioxanthones, N-phenylglycine etc..
It uses in the case that these polymerizations trigger auxiliary agents (D1), compared with adding up to for resin (B) and polymerizable compound (C)
100 mass parts are measured, content is preferably 0.1~30 mass parts, more preferably 1~20 mass parts.If polymerization triggers auxiliary agent
(D1) amount in the range, then further can form colored pattern, the productivity of colour filter is tended to improve with high sensitivity.
The colored resin composition of the present invention preferably comprises solvent (E).
＜ solvents (E) ＞
Solvent (E) is not particularly limited, solvent usually used in the field can be used.Such as can to enumerate ester output molten
Agent (molecule includes-COO- and the solvent without-O-), ether solvents (molecule includes-O- and the solvent without-COO-), ether-ether are molten
Agent (molecule includes the solvent of-COO- and-O-), ketone solvent (molecule includes-CO- and the solvent without-COO-), alcoholic solvent (divide
Son includes OH and the solvent without-O- ,-CO- and-COO-), aromatic hydrocarbon solvents, amide solvent, dimethyl sulfoxide (DMSO) etc..
As solvent (E), ethyl lactate, butyl lactate, 2- hydroxy-methyl isobutyl acids, n-butyl acetate, fourth can be included
Ester solvents (the molecule such as acetoacetic ester, butyl butyrate, ethyl pyruvate, methyl acetoacetate, adnoral acetate and gamma-butyrolacton
Include-COO- and the solvent without-O-)；
Ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, propylene glycol monomethyl ether, 3- methoxyl groups-n-butyl alcohol, diethylene glycol (DEG) two
The ether solvents such as methyl ether, diethylene glycol (DEG) methyl ethyl ether (molecule includes-O- and the solvent without-COO-)；
3- methoxy methyl propionates, 3- ethoxyl ethyl propionates, acetic acid 3- methoxybutyls, propylene glycol monomethyl ether
(molecule includes the molten of-COO- and-O- to the ether-ethers such as ester, ethylene glycol monomethyl ether acetate, diethylene glycol monoethyl ether acetate solvent
Agent)；
The ketone solvents such as 4- hydroxy-4-methyl-2-pentanones, heptanone, 4-methyl-2 pentanone, cyclohexanone (molecule include-CO- and
Solvent without-COO-)；
The alcoholic solvents such as butanol, cyclohexanol, propylene glycol (molecule includes OH and the solvent without-O- ,-CO- and-COO-)；
Amide solvents such as N,N-dimethylformamide, DMAC N,N' dimethyl acetamide and N-Methyl pyrrolidone etc..
As solvent (E), more preferable propylene glycol monomethyl ether, propylene glycol monomethyl ether, ethyl lactate, N- methyl
Pyrrolidones and 3- ethoxyl ethyl propionates.
In the case of comprising solvent (E), for the containing ratio of solvent (E), combined compared with the pigmentary resin of the present invention
The total amount of object is preferably 70~95 mass %, more preferably 75~92 mass %.In other words, the solid of colored resin composition
The total amount of ingredient is preferably 5~30 mass %, more preferably 8~25 mass %.If the content of solvent (E) is in above-mentioned scope
Interior, then flatness when being coated with becomes good, the in addition no deficiency of colour saturation when foring colour filter, therefore special with display
Property becomes good tendency.
＜ other compositions ＞
The coloring oil/fat composition of the present invention can include levelling agent, filler, other high-molecular compounds, closely sealed as needed
Well known additive in the technical field such as accelerating agent, antioxidant, light stabilizer, chain-transferring agent.
The manufacturing method ＞ of ＜ colored resin compositions
The colored resin composition of the present invention can be by by colorant (A), resin (B) and used as needed poly-
Conjunction property compound (C), polymerization initiator (D), solvent (E) and other compositions are mixed and prepared.
The manufacturing method ＞ of ＜ colour filters
As by the present invention colored resin composition manufacture colored pattern method, can include photoetching process, ink-jet method,
Print process etc..Wherein, preferred photoetching process.
It is especially excellent can to make contrast by being used as colorant comprising the compound of the present invention for colored resin composition
Colour filter.The colour filter can be used as in display device (such as liquid crystal display device, organic el device, Electronic Paper etc.) and solid
The colour filter used in photographing element.
Embodiment
Embodiment is exemplified below more specifically to illustrate the present invention, it is not limited by the following examples certainly by the present invention,
It is suitably deformed to implement also to be possible certainly in the range of aftermentioned purport before it can be suitble to, they are included in
In the technical scope of the present invention.
It should be illustrated that below as long as no special instructions, " part " means " mass parts ", " % " means " quality % ".
Embodiment 1
It will be by 4.9 parts of 5.1 parts of compound and 4- morpholinoes aniline (Tokyo chemical conversion industry (strain) system of formula (1x-1) expression
Make) add in 30 parts of n-methyl-2-pyrrolidone in, stirred at 70 DEG C 5 it is small when.Above-mentioned reaction solution is cooled to room temperature
Afterwards, add in 100 parts of water, stirred 1 it is small when.Suction strainer is carried out to the crystallization of precipitation, is cleaned 3 times for 100 parts with water, crystallization decompression is dry
It is dry, obtain 6.0 parts of the compound represented by formula (I-1).
Next, by by formula (I-1) represent 4.1 parts of compound, 4.4 parts of 1- N-Propyl Bromides (Tokyo chemical conversion industry (strain) make
Make) and 5.0 parts of potassium carbonate add in 30 parts of n-methyl-2-pyrrolidone, stirred at 80 DEG C 4 it is small when.By above-mentioned reaction
After liquid is cooled to room temperature, 100 parts of water is added in, when stirring 1 is small.Suction strainer is carried out to the crystallization of precipitation, is cleaned 3 times for 100 parts with water, it is right
Crystallization is dried under reduced pressure, and has obtained 4.5 parts of the compound represented by formula (I-4).
Embodiment 2
50.0 parts of the compound represented by formula (1x-1), 350 parts of isopropanol are mixed at room temperature, no more than 20 DEG C
At a temperature of 18.1 parts of diethylamine (Tokyo chemical conversion industry (strain) manufacture) is instilled in mixtures, stirred at 20 DEG C 3 it is small when.It will
In reaction solution 2100 parts of 10% hydrochloric acid of input.The precipitate that residue as suction strainer obtains, with 373 parts of ion exchange water
It is cleaned and dried, has obtained 23.6 parts of the compound represented by formula (1y-1).
Next, 5.0 parts of 6.6 parts of compound, 4- morpholinoes aniline (Tokyo chemical conversion industries will being represented by formula (1y-1)
(strain) manufactures) and 10.4 parts of potassium carbonate, 30 parts of n-methyl-2-pyrrolidone of addition in, stirred at 80 DEG C 5 it is small when.It will be above-mentioned
Reaction solution be cooled to room temperature after, add in 100 parts of water, stirred 1 it is small when.Suction strainer is carried out to the crystallization of precipitation, it is clear with 100 parts of water
It washes 3 times, crystallization is dried under reduced pressure, obtained 6.0 parts of the compound represented by formula (I-30).
And then by by formula (I-30) represent 4.1 parts of compound, 2.6 parts of 1- N-Propyl Bromides (Tokyo chemical conversion industry (strain) make
Make) and 2.9 parts of potassium carbonate add in 30 parts of n-methyl-2-pyrrolidone, stirred at 80 DEG C 1 it is small when.By above-mentioned reaction
After liquid is cooled to room temperature, add in 100 parts of water, stirred 1 it is small when.Suction strainer is carried out to the crystallization of precipitation, is cleaned 3 times for 100 parts with water,
Crystallization is dried under reduced pressure, has obtained 4.0 parts of the compound represented by formula (I-54).
Synthesis example 1
In the flask with mixer, thermometer, reflux cooler and dropping funel, with 0.02L/ point make nitrogen flow into and
As blanket of nitrogen, 305 parts of propylene glycol monomethyl ether is put into, is heated to 70 DEG C while stirring.Next, by acrylic acid 60
Part, acrylic acid 3,4- epoxy tricyclics [5.2.1.02,6] last of the ten Heavenly stems ester (and will by formula (I-1) represent compound and by formula (II-1) represent
Compound with molar ratio 50：50 mixing.) 440 parts be dissolved in 140 parts of propylene glycol monomethyl ether, prepare solution, use
Dropping funel, last 4 it is small when by the lysate instill heat preservation in 70 DEG C of flask.
On the other hand, using other dropping funel last 4 it is small when by polymerization initiator 2, (2, the 4- diformazans of 2 '-azo two
Base valeronitrile) 30 parts be dissolved in the solution that 225 parts of propylene glycol monomethyl ether forms and instill in flask.In polymerization initiator
After the instillation of solution, be held in 70 DEG C last 4 it is small when, be then cooled to room temperature, obtained weight average molecular weight (Mw) as 9.1
×103, dispersion degree 2.16, solid constituent 34.8%, solid constituent conversion acid value be 81mg-KOH/g resin B 1 it is molten
Liquid.Resin B 1 has following shown structural units.
The weight average molecular weight (Mw) of the resin obtained in synthesis example and the measure of number-average molecular weight (Mn) using GPC method,
It is carried out under conditions of below.
Device：K2479 (manufacture of (strain) Shimadzu Seisakusho Ltd.)
Column：SHIMADZU Shim-pack GPC-80M
Column temperature：40℃
Solvent：THF (tetrahydrofuran)
Flow velocity：1.0mL/min
Detector：RI correction standard substances；TSK STANDARD POLYSTYRENE F-40、F-4、F-288、A-
2500th, A-500 (Tosoh (strain) manufacture)
The ratio between weight average molecular weight and number-average molecular weight that polystyrene obtained above is converted (Mw/Mn) are as scattered
Degree.
Embodiment 3,4 and comparative example 1
(preparation of colored resin composition)
Each ingredient is mixed according to following composition, has obtained colored resin composition.
【Table 6】
In table 1, each ingredient represents following compound.
(A-1)：The compound represented by formula (I-4)
(A-2)：The compound represented by formula (I-54)
(A-3)：The compound represented by formula (1-x)
(B-1)：Resin B 1 (solid constituent conversion)
(C-1)：Dipentaerythritol hexaacrylate (カ ヤ ラ ッ De (registered trademark) DPHA；Japanese chemical drug (strain) manufacture)
(D-1)：(IRGACURE (the registrations of N- benzoyloxys -1- (4- Phenylsulfanyls phenyl) octane -1- ketone -2- imines
Trade mark) OXE 01；BASF AG manufactures)
(E-1)：N-Methyl pyrrolidone
(E-2)：Propylene glycol monomethyl ether
The making ＞ of ＜ colored patterns
In the glass substrate (EAGLE 2000 of 5cm square；Corning Incorporated manufacture) on using spin-coating method be coated with pigmentary resin
After composition, prebake 3 minutes at 100 DEG C have obtained coloring compositions nitride layer.After letting cool, make to form coloring compositions nitride layer
The interval of substrate and quartz glass photomask become 100 μm, use exposure machine (TME-150RSK；ト プ Us Application (strain) is made
Make), under air atmosphere, use 150mJ/cm2Light exposure (365nm benchmark) carried out light irradiation.As photomask, use
Form the photomask of 100 μm of lines and space pattern.Coloring compositions nitride layer after light is irradiated is lived comprising nonionic system surface
Property agent 0.12% and potassium hydroxide 0.04% water system imaging liquid at 24 DEG C dipping imaging 60 seconds, after washing, in an oven,
It is baked after twenty minutes at 230 DEG C, has obtained colored pattern.
＜ Investigation on Photodegradation ＞
Ultraviolet cutoff optical filter (COLORED is configured on the colored pattern obtained in embodiment 3,4 and comparative example 1
OPTICAL GLASS L38；HOYA companies manufacture；End the light of below 380nm.), use light fastness test machine (SUNTEST
CPS+：Toyo Seiki Co., Ltd. manufacture) irradiated 24 it is small when xenon lamp.
The colourity of the colored pattern after irradiation is measured, the aberration after pre-irradiation has been obtained.It shows the result in table 7.
＜ contrasts evaluate ＞
For the colored pattern obtained in embodiment 3,4 and comparative example 1, contrast meter (CT-1 is used；Pot slope motor (strain)
Manufacture, color evaluating BM-5A；The manufacture of ト プ コン companies, light source；F-10, light polarizing film；Pot slope motor (strain) manufactures), by sky
White value is set to 30000, determines contrast.It shows the result in table 7.
【Table 7】
Industrial availability
By being used as colorant comprising the compound of the present invention, the especially excellent colour filter of contrast can be made.The filter
Color device can be used as making in display device (such as liquid crystal display device, organic el device, Electronic Paper etc.) and solid-state imager
Colour filter.
Claims (7)
1. the compound represented by formula (1)：
In formula (1), R1~R4Independently of each other represent hydrogen atom, can have substituent group carbon number 1~20 saturated hydrocarbyl or can
The aromatic hydrocarbyl of carbon number 6~10 with substituent group, it is at least one to represent that there is carbon number 6~10 of the heterocycle as substituent group
Aromatic hydrocarbyl, contained-CH in the saturated hydrocarbyl2- it can be replaced by-O- ,-CO- or-NR5-, R1And R2It can be formed together
The ring of nitrogen atom, R3And R4The ring of nitrogen atom, R can be formed together5~R7Hydrogen atom or carbon number 1~6 are represented independently of each other
Alkyl.
2. compound according to claim 1, wherein, R1Represent that there is virtue of the heterocycle as the carbon number 6~10 of substituent group
Fragrant race's alkyl, and R2~R4Independently of each other represent can have substituent group carbon number 1~20 saturated hydrocarbyl or hydrogen atom or
Person R1And R3Represent that there is aromatic hydrocarbyl of the heterocycle as the carbon number 6~10 of substituent group, and R2And R4Mutual indepedent earth's surface
Show the saturated hydrocarbyl or hydrogen atom for the carbon number 1~20 that there can be substituent group.
3. compound according to claim 1 or 2, wherein, the aromatic hydrocarbyl of the carbon number 6~10 with heterocycle
For the group represented by formula (1x)：
In formula (1x), Q1Represent heterocycle, * represents the bonding end with nitrogen-atoms.
4. compound according to claim 1 or 2, wherein, the heterocycle is the heterocycle of nitrogen atom.
5. colored resin composition, it includes compound according to claim 1 or 2 and resins.
6. the colour filter formed by colored resin composition according to claim 5.
7. display device, it includes colour filters according to claim 6.
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| JP2016217468A JP6937110B2 (en) | 2016-11-07 | 2016-11-07 | Compound |
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| JP (1) | JP6937110B2 (en) |
| KR (1) | KR102328826B1 (en) |
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| CN113045529A (en) * | 2019-12-27 | 2021-06-29 | 东友精细化工有限公司 | Compound, colored resin composition, color filter and display device |
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| JP7527929B2 (en) | 2020-01-28 | 2024-08-05 | 保土谷化学工業株式会社 | Xanthene dye, coloring composition containing the dye, colorant for color filter, and color filter |
| JP2022056354A (en) | 2020-09-29 | 2022-04-08 | 保土谷化学工業株式会社 | Xanthene dye, coloring composition containing the dye, colorant for color filters, and color filter |
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| GB1503380A (en) * | 1974-12-20 | 1978-03-08 | Hoechst Ag | Process for the manufacture of xanthene dyestuffs |
| CN1331266A (en) * | 2000-07-05 | 2002-01-16 | 科莱恩有限公司 | Coloring agent mixture |
| CN1516872A (en) * | 2001-03-28 | 2004-07-28 | 拜尔公司 | Optical data carrier that contains triazacyanine dye as light-absorbing compound in information layer |
| JP2015163665A (en) * | 2014-01-29 | 2015-09-10 | 東洋インキＳｃホールディングス株式会社 | Color-filter rhodamine dye and use thereof |
| JP2015193801A (en) * | 2014-03-27 | 2015-11-05 | 富士フイルム株式会社 | Compound, coloring composition, ink for inkjet recording, inkjet recording method, inkjet printer cartridge, and inkjet recorded matter |
| CN105408427A (en) * | 2013-05-31 | 2016-03-16 | 东友精细化工有限公司 | Compound and colored curable resin composition |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6028326B2 (en) | 2011-08-04 | 2016-11-16 | 住友化学株式会社 | Colored curable resin composition |
-
2016
- 2016-11-07 JP JP2016217468A patent/JP6937110B2/en active Active
-
2017
- 2017-11-03 KR KR1020170146154A patent/KR102328826B1/en active IP Right Grant
- 2017-11-03 CN CN201711067616.0A patent/CN108069932B/en active Active
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Patent Citations (6)
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|---|---|---|---|---|
| GB1503380A (en) * | 1974-12-20 | 1978-03-08 | Hoechst Ag | Process for the manufacture of xanthene dyestuffs |
| CN1331266A (en) * | 2000-07-05 | 2002-01-16 | 科莱恩有限公司 | Coloring agent mixture |
| CN1516872A (en) * | 2001-03-28 | 2004-07-28 | 拜尔公司 | Optical data carrier that contains triazacyanine dye as light-absorbing compound in information layer |
| CN105408427A (en) * | 2013-05-31 | 2016-03-16 | 东友精细化工有限公司 | Compound and colored curable resin composition |
| JP2015163665A (en) * | 2014-01-29 | 2015-09-10 | 東洋インキＳｃホールディングス株式会社 | Color-filter rhodamine dye and use thereof |
| JP2015193801A (en) * | 2014-03-27 | 2015-11-05 | 富士フイルム株式会社 | Compound, coloring composition, ink for inkjet recording, inkjet recording method, inkjet printer cartridge, and inkjet recorded matter |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113045529A (en) * | 2019-12-27 | 2021-06-29 | 东友精细化工有限公司 | Compound, colored resin composition, color filter and display device |
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| JP6937110B2 (en) | 2021-09-22 |
| KR20180051396A (en) | 2018-05-16 |
| CN108069932B (en) | 2023-11-21 |
| JP2018076403A (en) | 2018-05-17 |
| TWI745474B (en) | 2021-11-11 |
| TW201821422A (en) | 2018-06-16 |
| KR102328826B1 (en) | 2021-11-19 |
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