JPH0581029B2 - - Google Patents

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Publication number

JPH0581029B2

JPH0581029B2 JP1756886A JP1756886A JPH0581029B2 JP H0581029 B2 JPH0581029 B2 JP H0581029B2 JP 1756886 A JP1756886 A JP 1756886A JP 1756886 A JP1756886 A JP 1756886A JP H0581029 B2 JPH0581029 B2 JP H0581029B2

Authority

JP

Japan

Prior art keywords

group

groups

examples

formula

represented

Prior art date

1986-01-29

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired - Lifetime

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• -1 silver halide Chemical class 0.000 claims description 339
• 125000000217 alkyl group Chemical group 0.000 claims description 119
• 125000001424 substituent group Chemical group 0.000 claims description 108
• 125000003118 aryl group Chemical group 0.000 claims description 86
• 229910052709 silver Inorganic materials 0.000 claims description 76
• 239000004332 silver Substances 0.000 claims description 76
• 238000000034 method Methods 0.000 claims description 56
• 239000000463 material Substances 0.000 claims description 40
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 34
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 33
• 239000003795 chemical substances by application Substances 0.000 claims description 32
• 150000004696 coordination complex Chemical class 0.000 claims description 28
• 125000004429 atom Chemical group 0.000 claims description 17
• 238000006243 chemical reaction Methods 0.000 claims description 17
• 229910052751 metal Inorganic materials 0.000 claims description 17
• 239000002184 metal Substances 0.000 claims description 17
• 239000003960 organic solvent Substances 0.000 claims description 16
• 238000009835 boiling Methods 0.000 claims description 13
• 239000010410 layer Substances 0.000 description 82
• 239000000839 emulsion Substances 0.000 description 64
• 239000000975 dye Substances 0.000 description 58
• 150000001875 compounds Chemical class 0.000 description 43
• 125000000623 heterocyclic group Chemical group 0.000 description 39
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 38
• 125000003545 alkoxy group Chemical group 0.000 description 32
• 125000004432 carbon atom Chemical group C* 0.000 description 29
• 125000005843 halogen group Chemical group 0.000 description 29
• 125000004104 aryloxy group Chemical group 0.000 description 22
• 125000003342 alkenyl group Chemical group 0.000 description 20
• 125000004453 alkoxycarbonyl group Chemical group 0.000 description 18
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 18
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 17
• 125000002252 acyl group Chemical group 0.000 description 16
• 239000000126 substance Substances 0.000 description 16
• 238000000576 coating method Methods 0.000 description 15
• 125000004093 cyano group Chemical group *C#N 0.000 description 15
• 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 14
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 14
• 239000011248 coating agent Substances 0.000 description 14
• 238000012545 processing Methods 0.000 description 14
• 108010010803 Gelatin Proteins 0.000 description 13
• 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 13
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 13
• 229910052801 chlorine Inorganic materials 0.000 description 13
• 238000005562 fading Methods 0.000 description 13
• 229920000159 gelatin Polymers 0.000 description 13
• 239000008273 gelatin Substances 0.000 description 13
• 235000019322 gelatine Nutrition 0.000 description 13
• 235000011852 gelatine desserts Nutrition 0.000 description 13
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 13
• 239000003381 stabilizer Substances 0.000 description 13
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 13
• 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 12
• 125000004442 acylamino group Chemical group 0.000 description 12
• 125000004414 alkyl thio group Chemical group 0.000 description 12
• 125000005110 aryl thio group Chemical group 0.000 description 12
• 239000000084 colloidal system Substances 0.000 description 12
• 230000000694 effects Effects 0.000 description 12
• 125000001624 naphthyl group Chemical group 0.000 description 12
• 229910052731 fluorine Inorganic materials 0.000 description 11
• NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 11
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 11
• 239000002245 particle Substances 0.000 description 11
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 11
• 125000004422 alkyl sulphonamide group Chemical group 0.000 description 10
• 125000000565 sulfonamide group Chemical group 0.000 description 10
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 9
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 9
• 125000005153 alkyl sulfamoyl group Chemical group 0.000 description 9
• 125000004421 aryl sulphonamide group Chemical group 0.000 description 9
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 9
• 239000000460 chlorine Substances 0.000 description 9
• 238000004040 coloring Methods 0.000 description 9
• 239000006185 dispersion Substances 0.000 description 9
• 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 9
• 239000011737 fluorine Substances 0.000 description 9
• XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 9
• 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 9
• 150000003839 salts Chemical class 0.000 description 9
• 125000004423 acyloxy group Chemical group 0.000 description 8
• 238000011161 development Methods 0.000 description 8
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 8
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
• 230000008569 process Effects 0.000 description 8
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 8
• KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical group NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 7
• 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 7
• SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 7
• 239000006096 absorbing agent Substances 0.000 description 7
• 239000002253 acid Substances 0.000 description 7
• 125000003277 amino group Chemical group 0.000 description 7
• 125000004391 aryl sulfonyl group Chemical group 0.000 description 7
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
• 229910052794 bromium Inorganic materials 0.000 description 7
• 229910052799 carbon Inorganic materials 0.000 description 7
• 230000000052 comparative effect Effects 0.000 description 7
• 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 7
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 7
• 150000002430 hydrocarbons Chemical group 0.000 description 7
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 7
• 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 7
• 230000001235 sensitizing effect Effects 0.000 description 7
• 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 7
• MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 6
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
• BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
• 125000004448 alkyl carbonyl group Chemical group 0.000 description 6
• 125000004390 alkyl sulfonyl group Chemical group 0.000 description 6
• 125000002947 alkylene group Chemical group 0.000 description 6
• BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 6
• 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 6
• 125000000392 cycloalkenyl group Chemical group 0.000 description 6
• 230000006866 deterioration Effects 0.000 description 6
• 150000002148 esters Chemical class 0.000 description 6
• 150000007524 organic acids Chemical class 0.000 description 6
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 6
• 125000004149 thio group Chemical group *S* 0.000 description 6
• CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 5
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 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
• 125000005129 aryl carbonyl group Chemical group 0.000 description 5
• 125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 5
• 150000001721 carbon Chemical group 0.000 description 5
• 239000013078 crystal Substances 0.000 description 5
• 230000008313 sensitization Effects 0.000 description 5
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
• FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 4
• 150000007513 acids Chemical class 0.000 description 4
• 229910052783 alkali metal Inorganic materials 0.000 description 4
• 238000004061 bleaching Methods 0.000 description 4
• DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical group CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 4
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
• 125000001309 chloro group Chemical group Cl* 0.000 description 4
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
• 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 4
• 230000002209 hydrophobic effect Effects 0.000 description 4
• 125000005462 imide group Chemical group 0.000 description 4
• 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 4
• HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical group CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 4
• 239000000203 mixture Substances 0.000 description 4
• MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 4
• QWOKKHXWFDAJCZ-UHFFFAOYSA-N octane-1-sulfonamide Chemical group CCCCCCCCS(N)(=O)=O QWOKKHXWFDAJCZ-UHFFFAOYSA-N 0.000 description 4
• 125000000962 organic group Chemical group 0.000 description 4
• 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
• 125000005499 phosphonyl group Chemical group 0.000 description 4
• 229910000027 potassium carbonate Inorganic materials 0.000 description 4
• 235000011181 potassium carbonates Nutrition 0.000 description 4
• 238000010791 quenching Methods 0.000 description 4
• 230000000171 quenching effect Effects 0.000 description 4
• 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 4
• JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 4
• 239000002904 solvent Substances 0.000 description 4
• 150000003413 spiro compounds Chemical group 0.000 description 4
• NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical group NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 4
• 229910052717 sulfur Inorganic materials 0.000 description 4
• 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-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
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
• MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
• 229910019142 PO4 Inorganic materials 0.000 description 3
• 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 3
• 125000005115 alkyl carbamoyl group Chemical group 0.000 description 3
• 125000003368 amide group Chemical group 0.000 description 3
• 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 3
• 125000005116 aryl carbamoyl group Chemical group 0.000 description 3
• 239000012964 benzotriazole Substances 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
• KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
• 238000005859 coupling reaction Methods 0.000 description 3
• 150000001925 cycloalkenes Chemical class 0.000 description 3
• 229940093915 gynecological organic acid Drugs 0.000 description 3
• 125000000400 lauroyl group Chemical group O=C([*])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
• 239000007788 liquid Substances 0.000 description 3
• 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 3
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
• 229910052757 nitrogen Inorganic materials 0.000 description 3
• 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 3
• 235000005985 organic acids Nutrition 0.000 description 3
• 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 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
• 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
• 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 3
• 235000021317 phosphate Nutrition 0.000 description 3
• 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
• 239000011241 protective layer Substances 0.000 description 3
• 125000004076 pyridyl group Chemical group 0.000 description 3
• 230000009467 reduction Effects 0.000 description 3
• 230000003595 spectral effect Effects 0.000 description 3
• 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 3
• 229910052724 xenon Inorganic materials 0.000 description 3
• FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
• 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
• CLDZVCMRASJQFO-UHFFFAOYSA-N 2,5-bis(2,4,4-trimethylpentan-2-yl)benzene-1,4-diol Chemical compound CC(C)(C)CC(C)(C)C1=CC(O)=C(C(C)(C)CC(C)(C)C)C=C1O CLDZVCMRASJQFO-UHFFFAOYSA-N 0.000 description 2
• 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 2
• 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 2
• PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
• LVRCEUVOXCJYSV-UHFFFAOYSA-N CN(C)S(=O)=O Chemical group CN(C)S(=O)=O LVRCEUVOXCJYSV-UHFFFAOYSA-N 0.000 description 2
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
• PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 2
• MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
• URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical compound CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
• 239000004698 Polyethylene Substances 0.000 description 2
• DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 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
• 229960000583 acetic acid Drugs 0.000 description 2
• 239000000654 additive Substances 0.000 description 2
• 230000002411 adverse Effects 0.000 description 2
• 125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 2
• 125000003282 alkyl amino group Chemical group 0.000 description 2
• 125000005196 alkyl carbonyloxy group Chemical group 0.000 description 2
• 239000002216 antistatic agent Substances 0.000 description 2
• 125000001769 aryl amino group Chemical group 0.000 description 2
• 125000005199 aryl carbonyloxy group Chemical group 0.000 description 2
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
• 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 2
• 125000004744 butyloxycarbonyl group Chemical group 0.000 description 2
• 230000008859 change Effects 0.000 description 2
• 229910052802 copper Inorganic materials 0.000 description 2
• 239000010949 copper Substances 0.000 description 2
• 230000008878 coupling Effects 0.000 description 2
• 238000010168 coupling process Methods 0.000 description 2
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