JPS61273544A

JPS61273544A - カラ−写真画像の形成方法

カラ−写真画像の形成方法

Info

Publication number: JPS61273544A
Authority: JP; Japan
Prior art keywords: group; general formula; substituent; groups; represented
Prior art date: 1985-05-29
Legal status : Granted

Application number

JP11558485A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0567019B2 (enrdf_load_stackoverflow

Inventor

Masao Sasaki

正男佐々木

Kaoru Onodera

薫小野寺

Current Assignee

Konica Minolta Inc

Original Assignee

Konica Minolta Inc

Priority date

1985-05-29

Filing date

1985-05-29

Publication date

1986-12-03

1985-05-29 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1985-05-29 Priority to JP11558485A priority Critical patent/JPS61273544A/ja

1986-12-03 Publication of JPS61273544A publication Critical patent/JPS61273544A/ja

1993-09-24 Publication of JPH0567019B2 publication Critical patent/JPH0567019B2/ja

Status Granted legal-status Critical Current

Links

230000015572 biosynthetic process Effects 0.000 title description 12
-1 silver halide Chemical class 0.000 claims abstract description 298
125000001424 substituent group Chemical group 0.000 claims abstract description 127
125000003118 aryl group Chemical group 0.000 claims abstract description 109
229910052709 silver Inorganic materials 0.000 claims abstract description 69
239000004332 silver Substances 0.000 claims abstract description 69
239000000839 emulsion Substances 0.000 claims abstract description 56
239000000463 material Substances 0.000 claims abstract description 53
239000003795 chemical substances by application Substances 0.000 claims abstract description 35
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 33
238000012545 processing Methods 0.000 claims abstract description 30
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 20
238000011161 development Methods 0.000 claims abstract description 12
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical group O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 claims abstract description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 71
238000000034 method Methods 0.000 claims description 50
238000005406 washing Methods 0.000 claims description 32
239000000126 substance Substances 0.000 claims description 15
229910052799 carbon Inorganic materials 0.000 claims description 13
125000004433 nitrogen atom Chemical group N* 0.000 claims description 13
238000006243 chemical reaction Methods 0.000 claims description 12
230000006641 stabilisation Effects 0.000 claims description 12
238000011105 stabilization Methods 0.000 claims description 12
125000005842 heteroatom Chemical group 0.000 abstract description 7
238000005859 coupling reaction Methods 0.000 abstract description 4
238000010186 staining Methods 0.000 abstract description 2
230000003647 oxidation Effects 0.000 abstract 1
238000007254 oxidation reaction Methods 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 description 145
150000001875 compounds Chemical class 0.000 description 91
239000010410 layer Substances 0.000 description 72
125000000623 heterocyclic group Chemical group 0.000 description 69
125000003545 alkoxy group Chemical group 0.000 description 63
125000003342 alkenyl group Chemical group 0.000 description 60
125000000753 cycloalkyl group Chemical group 0.000 description 57
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 51
125000005843 halogen group Chemical group 0.000 description 45
125000004104 aryloxy group Chemical group 0.000 description 42
125000002887 hydroxy group Chemical group [H]O* 0.000 description 40
239000000243 solution Substances 0.000 description 38
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 33
125000004453 alkoxycarbonyl group Chemical group 0.000 description 30
125000002252 acyl group Chemical group 0.000 description 29
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 28
150000003839 salts Chemical class 0.000 description 26
125000000565 sulfonamide group Chemical group 0.000 description 25
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
125000004442 acylamino group Chemical group 0.000 description 24
239000000975 dye Substances 0.000 description 24
238000009835 boiling Methods 0.000 description 23
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 22
125000004429 atom Chemical group 0.000 description 21
125000004423 acyloxy group Chemical group 0.000 description 20
150000002430 hydrocarbons Chemical group 0.000 description 20
230000000087 stabilizing effect Effects 0.000 description 20
239000003960 organic solvent Substances 0.000 description 17
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 16
238000000576 coating method Methods 0.000 description 16
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 16
NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 16
239000002253 acid Substances 0.000 description 15
239000011248 coating agent Substances 0.000 description 15
229910052757 nitrogen Inorganic materials 0.000 description 15
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 14
239000006185 dispersion Substances 0.000 description 14
108010010803 Gelatin Proteins 0.000 description 13
239000008273 gelatin Substances 0.000 description 13
229920000159 gelatin Polymers 0.000 description 13
235000019322 gelatine Nutrition 0.000 description 13
235000011852 gelatine desserts Nutrition 0.000 description 13
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
239000003381 stabilizer Substances 0.000 description 13
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 13
239000000084 colloidal system Substances 0.000 description 12
125000001624 naphthyl group Chemical group 0.000 description 12
238000010521 absorption reaction Methods 0.000 description 11
125000004414 alkyl thio group Chemical group 0.000 description 11
239000013078 crystal Substances 0.000 description 11
238000003786 synthesis reaction Methods 0.000 description 11
125000003302 alkenyloxy group Chemical group 0.000 description 10
125000005110 aryl thio group Chemical group 0.000 description 10
239000002738 chelating agent Substances 0.000 description 10
229910052801 chlorine Inorganic materials 0.000 description 10
239000000203 mixture Substances 0.000 description 10
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
HBEDSQVIWPRPAY-UHFFFAOYSA-N 2,3-dihydrobenzofuran Chemical compound C1=CC=C2OCCC2=C1 HBEDSQVIWPRPAY-UHFFFAOYSA-N 0.000 description 9
125000001931 aliphatic group Chemical group 0.000 description 9
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 9
VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 description 9
230000000694 effects Effects 0.000 description 9
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 9
239000002245 particle Substances 0.000 description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
239000000460 chlorine Substances 0.000 description 8
229910052739 hydrogen Inorganic materials 0.000 description 8
239000007788 liquid Substances 0.000 description 8
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 8
230000008569 process Effects 0.000 description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 7
150000001721 carbon Chemical group 0.000 description 7
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 7
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
238000012360 testing method Methods 0.000 description 7
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 6
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 6
125000004390 alkyl sulfonyl group Chemical group 0.000 description 6
125000004391 aryl sulfonyl group Chemical group 0.000 description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 6
229910052794 bromium Inorganic materials 0.000 description 6
125000004093 cyano group Chemical group *C#N 0.000 description 6
125000000392 cycloalkenyl group Chemical group 0.000 description 6
150000002148 esters Chemical class 0.000 description 6
125000005462 imide group Chemical group 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
230000001235 sensitizing effect Effects 0.000 description 6
125000003003 spiro group Chemical group 0.000 description 6
229910052717 sulfur Inorganic materials 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 5
206010070834 Sensitisation Diseases 0.000 description 5
125000004466 alkoxycarbonylamino group Chemical group 0.000 description 5
125000000304 alkynyl group Chemical group 0.000 description 5
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 5
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 5
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 5
GLUUGHFHXGJENI-UHFFFAOYSA-N diethylenediamine Natural products C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 5
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 5
229910052731 fluorine Inorganic materials 0.000 description 5
239000011737 fluorine Substances 0.000 description 5
125000006038 hexenyl group Chemical group 0.000 description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 5
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 5
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 5
229910000027 potassium carbonate Inorganic materials 0.000 description 5
235000011181 potassium carbonates Nutrition 0.000 description 5
230000008313 sensitization Effects 0.000 description 5
239000002904 solvent Substances 0.000 description 5
230000003595 spectral effect Effects 0.000 description 5
150000003413 spiro compounds Chemical group 0.000 description 5
238000003860 storage Methods 0.000 description 5
125000004149 thio group Chemical group *S* 0.000 description 5
125000004417 unsaturated alkyl group Chemical group 0.000 description 5
PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 4
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 4
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 4
229910019142 PO4 Inorganic materials 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
239000000654 additive Substances 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
125000002947 alkylene group Chemical group 0.000 description 4
239000003429 antifungal agent Substances 0.000 description 4
229940121375 antifungal agent Drugs 0.000 description 4
239000012964 benzotriazole Substances 0.000 description 4
238000004061 bleaching Methods 0.000 description 4
239000013522 chelant Substances 0.000 description 4
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 4
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 4
229910052742 iron Inorganic materials 0.000 description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
150000007524 organic acids Chemical class 0.000 description 4
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
235000021317 phosphate Nutrition 0.000 description 4
125000005499 phosphonyl group Chemical group 0.000 description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
239000011241 protective layer Substances 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 4
229940124530 sulfonamide Drugs 0.000 description 4
125000004434 sulfur atom Chemical group 0.000 description 4
OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 3
JKRNNIGZNCVVHA-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;trimethylazanium Chemical compound C[NH+](C)C.C[NH+](C)C.C[NH+](C)C.C[NH+](C)C.[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O JKRNNIGZNCVVHA-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 3
125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 3
125000003277 amino group Chemical group 0.000 description 3
150000003868 ammonium compounds Chemical class 0.000 description 3
239000000908 ammonium hydroxide Substances 0.000 description 3
229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 3
125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
239000007844 bleaching agent Substances 0.000 description 3
DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
150000001925 cycloalkenes Chemical class 0.000 description 3
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
229910021645 metal ion Inorganic materials 0.000 description 3
125000002958 pentadecyl 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])[H] 0.000 description 3
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 3
230000001681 protective effect Effects 0.000 description 3
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 3
125000000714 pyrimidinyl group Chemical group 0.000 description 3
150000003856 quaternary ammonium compounds Chemical class 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 3
125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 3
239000011593 sulfur Substances 0.000 description 3
239000004094 surface-active agent Substances 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
239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 3
229910052724 xenon Inorganic materials 0.000 description 3
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
KOFZTCSTGIWCQG-UHFFFAOYSA-N 1-bromotetradecane Chemical compound CCCCCCCCCCCCCCBr KOFZTCSTGIWCQG-UHFFFAOYSA-N 0.000 description 2
HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 description 2
HRBLHUVHOWWBEN-UHFFFAOYSA-N 1-n,4-n-diethylbenzene-1,4-diamine;hydrochloride Chemical compound Cl.CCNC1=CC=C(NCC)C=C1 HRBLHUVHOWWBEN-UHFFFAOYSA-N 0.000 description 2
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
BWZVCCNYKMEVEX-UHFFFAOYSA-N 2,4,6-Trimethylpyridine Chemical compound CC1=CC(C)=NC(C)=C1 BWZVCCNYKMEVEX-UHFFFAOYSA-N 0.000 description 2
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 2
229940100555 2-methyl-4-isothiazolin-3-one Drugs 0.000 description 2
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 2
125000003341 7 membered heterocyclic group Chemical group 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
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YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 2
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125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
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KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
239000003086 colorant Substances 0.000 description 2
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230000006866 deterioration Effects 0.000 description 2
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230000005611 electricity Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
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150000004050 homopiperazines Chemical class 0.000 description 2
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PTFYQSWHBLOXRZ-UHFFFAOYSA-N imidazo[4,5-e]indazole Chemical compound C1=CC2=NC=NC2=C2C=NN=C21 PTFYQSWHBLOXRZ-UHFFFAOYSA-N 0.000 description 2
PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
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235000019341 magnesium sulphate Nutrition 0.000 description 2
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125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 2
150000002780 morpholines Chemical class 0.000 description 2
CLJDCQWROXMJAZ-UHFFFAOYSA-N n-[2-(4-amino-n-ethyl-3-methylanilino)ethyl]methanesulfonamide;sulfuric acid Chemical compound OS(O)(=O)=O.CS(=O)(=O)NCCN(CC)C1=CC=C(N)C(C)=C1 CLJDCQWROXMJAZ-UHFFFAOYSA-N 0.000 description 2
229910000510 noble metal Inorganic materials 0.000 description 2
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125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 2
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
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IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
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235000019982 sodium hexametaphosphate Nutrition 0.000 description 2
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230000003068 static effect Effects 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
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LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 1
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AZPVYDDUIKAUGT-UHFFFAOYSA-N 3-octadec-1-enylpyrrolidine-2,5-dione Chemical group CCCCCCCCCCCCCCCCC=CC1CC(=O)NC1=O AZPVYDDUIKAUGT-UHFFFAOYSA-N 0.000 description 1
FWBHETKCLVMNFS-UHFFFAOYSA-N 4',6-Diamino-2-phenylindol Chemical compound C1=CC(C(=N)N)=CC=C1C1=CC2=CC=C(C(N)=N)C=C2N1 FWBHETKCLVMNFS-UHFFFAOYSA-N 0.000 description 1
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WTIUUMRTSWJRFF-UHFFFAOYSA-N 4-(aminomethyl)benzenesulfonamide;dihydrate;trihydrochloride Chemical compound O.O.Cl.Cl.Cl.NCC1=CC=C(S(N)(=O)=O)C=C1.NCC1=CC=C(S(N)(=O)=O)C=C1.NCC1=CC=C(S(N)(=O)=O)C=C1 WTIUUMRTSWJRFF-UHFFFAOYSA-N 0.000 description 1
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