JPS61240240A

JPS61240240A - ハロゲン化銀カラ−写真感光材料

ハロゲン化銀カラ−写真感光材料

Info

Publication number: JPS61240240A
Authority: JP; Japan
Prior art keywords: group; coupler; groups; silver; color
Prior art date: 1985-04-08
Legal status : Granted

Application number

JP7504085A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0549091B2 (enrdf_load_stackoverflow

Inventor

Yasushi Ichijima

市嶋　靖司

Keiji Obayashi

慶司御林

Current Assignee

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

Priority date

1985-04-08

Filing date

1985-04-08

Publication date

1986-10-25

1985-04-08 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1985-04-08 Priority to JP7504085A priority Critical patent/JPS61240240A/ja

1986-10-25 Publication of JPS61240240A publication Critical patent/JPS61240240A/ja

1993-07-23 Publication of JPH0549091B2 publication Critical patent/JPH0549091B2/ja

Status Granted legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 114
239000000463 material Substances 0.000 title claims abstract description 34
229910052709 silver Inorganic materials 0.000 title claims description 53
239000004332 silver Substances 0.000 title claims description 53
239000003795 chemical substances by application Substances 0.000 claims abstract description 33
238000005859 coupling reaction Methods 0.000 claims abstract description 14
239000002243 precursor Substances 0.000 claims abstract description 7
150000001875 compounds Chemical group 0.000 claims description 43
238000011161 development Methods 0.000 abstract description 29
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 12
239000003112 inhibitor Substances 0.000 abstract description 12
238000006243 chemical reaction Methods 0.000 abstract description 10
230000003647 oxidation Effects 0.000 abstract description 7
238000007254 oxidation reaction Methods 0.000 abstract description 7
125000004430 oxygen atom Chemical group O* 0.000 abstract description 6
230000035945 sensitivity Effects 0.000 abstract description 6
238000004040 coloring Methods 0.000 abstract description 5
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 abstract description 4
230000002860 competitive effect Effects 0.000 abstract description 3
238000006479 redox reaction Methods 0.000 abstract description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 abstract description 2
QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical compound C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 abstract description 2
239000010410 layer Substances 0.000 description 71
239000000975 dye Substances 0.000 description 53
239000000839 emulsion Substances 0.000 description 41
125000003118 aryl group Chemical group 0.000 description 37
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 34
125000001424 substituent group Chemical group 0.000 description 29
238000000034 method Methods 0.000 description 26
125000000623 heterocyclic group Chemical group 0.000 description 25
125000000217 alkyl group Chemical group 0.000 description 23
125000004432 carbon atom Chemical group C* 0.000 description 22
125000001931 aliphatic group Chemical group 0.000 description 19
125000004435 hydrogen atom Chemical group [H]* 0.000 description 19
125000004442 acylamino group Chemical group 0.000 description 18
125000003342 alkenyl group Chemical group 0.000 description 17
125000004453 alkoxycarbonyl group Chemical group 0.000 description 15
230000001235 sensitizing effect Effects 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
108010010803 Gelatin Proteins 0.000 description 14
239000008273 gelatin Substances 0.000 description 14
229920000159 gelatin Polymers 0.000 description 14
235000019322 gelatine Nutrition 0.000 description 14
235000011852 gelatine desserts Nutrition 0.000 description 14
125000003545 alkoxy group Chemical group 0.000 description 13
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 12
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 12
235000013339 cereals Nutrition 0.000 description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 11
125000005843 halogen group Chemical group 0.000 description 11
125000000565 sulfonamide group Chemical group 0.000 description 11
JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 10
229910021612 Silver iodide Inorganic materials 0.000 description 10
125000002252 acyl group Chemical group 0.000 description 10
239000011248 coating agent Substances 0.000 description 10
238000000576 coating method Methods 0.000 description 10
239000000084 colloidal system Substances 0.000 description 10
125000004122 cyclic group Chemical group 0.000 description 10
239000000203 mixture Substances 0.000 description 10
229940045105 silver iodide Drugs 0.000 description 10
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 9
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
239000002253 acid Substances 0.000 description 9
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 9
239000002245 particle Substances 0.000 description 9
229920000642 polymer Polymers 0.000 description 9
150000003839 salts Chemical class 0.000 description 9
125000003277 amino group Chemical group 0.000 description 8
125000004104 aryloxy group Chemical group 0.000 description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 8
238000012545 processing Methods 0.000 description 8
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 8
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 8
238000005406 washing Methods 0.000 description 8
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 7
125000005110 aryl thio group Chemical group 0.000 description 7
230000008878 coupling Effects 0.000 description 7
238000010168 coupling process Methods 0.000 description 7
239000007788 liquid Substances 0.000 description 7
239000000243 solution Substances 0.000 description 7
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 7
125000003710 aryl alkyl group Chemical group 0.000 description 6
125000004093 cyano group Chemical group *C#N 0.000 description 6
125000006165 cyclic alkyl group Chemical group 0.000 description 6
239000006185 dispersion Substances 0.000 description 6
239000000178 monomer Substances 0.000 description 6
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
125000004433 nitrogen atom Chemical group N* 0.000 description 6
230000008569 process Effects 0.000 description 6
239000000047 product Substances 0.000 description 6
230000000087 stabilizing effect Effects 0.000 description 6
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 6
JVXHQHGWBAHSSF-UHFFFAOYSA-L 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;hydron;iron(2+) Chemical compound [H+].[H+].[Fe+2].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O JVXHQHGWBAHSSF-UHFFFAOYSA-L 0.000 description 5
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 5
125000004390 alkyl sulfonyl group Chemical group 0.000 description 5
125000004414 alkyl thio group Chemical group 0.000 description 5
150000001412 amines Chemical class 0.000 description 5
125000005116 aryl carbamoyl group Chemical group 0.000 description 5
125000004391 aryl sulfonyl group Chemical group 0.000 description 5
229910052799 carbon Inorganic materials 0.000 description 5
238000003776 cleavage reaction Methods 0.000 description 5
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 5
238000011160 research Methods 0.000 description 5
229910052717 sulfur Inorganic materials 0.000 description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
206010070834 Sensitisation Diseases 0.000 description 4
125000004423 acyloxy group Chemical group 0.000 description 4
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
125000001769 aryl amino group Chemical group 0.000 description 4
239000007844 bleaching agent Substances 0.000 description 4
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 4
230000006872 improvement Effects 0.000 description 4
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
230000008313 sensitization Effects 0.000 description 4
230000006641 stabilisation Effects 0.000 description 4
238000011105 stabilization Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
125000004466 alkoxycarbonylamino group Chemical group 0.000 description 3
125000003282 alkyl amino group Chemical group 0.000 description 3
125000004422 alkyl sulphonamide group Chemical group 0.000 description 3
125000002947 alkylene group Chemical group 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000009835 boiling Methods 0.000 description 3
239000002738 chelating agent Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
229910052802 copper Inorganic materials 0.000 description 3
239000010949 copper Substances 0.000 description 3
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 3
125000004663 dialkyl amino group Chemical group 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
238000009792 diffusion process Methods 0.000 description 3
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 3
150000002148 esters Chemical class 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
125000002883 imidazolyl group Chemical group 0.000 description 3
239000004848 polyfunctional curative Substances 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
125000004076 pyridyl group Chemical group 0.000 description 3
125000005493 quinolyl group Chemical group 0.000 description 3
230000001603 reducing effect Effects 0.000 description 3
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulphite Substances [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 3
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 3
125000004434 sulfur atom Chemical group 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 2
FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
230000009471 action Effects 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
125000005153 alkyl sulfamoyl group Chemical group 0.000 description 2
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
125000005129 aryl carbonyl group Chemical group 0.000 description 2
125000004421 aryl sulphonamide group Chemical group 0.000 description 2
125000000732 arylene group Chemical group 0.000 description 2
239000003899 bactericide agent Substances 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
150000001565 benzotriazoles Chemical class 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
150000001661 cadmium Chemical class 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 2
239000002131 composite material Substances 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
239000013078 crystal Substances 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
230000006870 function Effects 0.000 description 2
125000002541 furyl group Chemical group 0.000 description 2
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical class OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
150000002460 imidazoles Chemical class 0.000 description 2
150000002475 indoles Chemical class 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
229910052742 iron Inorganic materials 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
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
150000002739 metals Chemical class 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
229910000510 noble metal Inorganic materials 0.000 description 2
239000012038 nucleophile Substances 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
230000036961 partial effect Effects 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
150000004986 phenylenediamines Chemical class 0.000 description 2
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000011241 protective layer Substances 0.000 description 2
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical class N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 2
125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000005504 styryl group Chemical group 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
125000003441 thioacyl group Chemical group 0.000 description 2
150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 2
239000006097 ultraviolet radiation absorber Substances 0.000 description 2
229920001567 vinyl ester resin Polymers 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
AIGNCQCMONAWOL-UHFFFAOYSA-N 1,3-benzoselenazole Chemical class C1=CC=C2[se]C=NC2=C1 AIGNCQCMONAWOL-UHFFFAOYSA-N 0.000 description 1
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
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