TW473512B - Cationic thiadiazolediphenylamine dyes and their anhydro bases - Google Patents
Cationic thiadiazolediphenylamine dyes and their anhydro bases Download PDFInfo
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- TW473512B TW473512B TW087107921A TW87107921A TW473512B TW 473512 B TW473512 B TW 473512B TW 087107921 A TW087107921 A TW 087107921A TW 87107921 A TW87107921 A TW 87107921A TW 473512 B TW473512 B TW 473512B
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- Prior art keywords
- formula
- represent
- dye
- hydrogen
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- 239000000975 dye Substances 0.000 title claims abstract description 83
- 125000002091 cationic group Chemical group 0.000 title claims abstract description 22
- 238000012546 transfer Methods 0.000 claims abstract description 9
- 238000013500 data storage Methods 0.000 claims abstract description 7
- -1 butanedioxy Chemical group 0.000 claims description 79
- 239000001257 hydrogen Substances 0.000 claims description 43
- 229910052739 hydrogen Inorganic materials 0.000 claims description 43
- 150000002431 hydrogen Chemical group 0.000 claims description 27
- 238000011049 filling Methods 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 21
- 239000000976 ink Substances 0.000 claims description 21
- 150000001450 anions Chemical class 0.000 claims description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 16
- 239000003513 alkali Substances 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 13
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 13
- 229910052736 halogen Inorganic materials 0.000 claims description 12
- 150000002367 halogens Chemical group 0.000 claims description 12
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 12
- 230000018044 dehydration Effects 0.000 claims description 11
- 238000006297 dehydration reaction Methods 0.000 claims description 11
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 11
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
- 239000007789 gas Chemical group 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
- 238000012360 testing method Methods 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 8
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- 238000009792 diffusion process Methods 0.000 claims description 6
- 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 claims description 6
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical group COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 claims description 6
- 230000002079 cooperative effect Effects 0.000 claims description 5
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical group COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 claims description 4
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
- NCBZRJODKRCREW-UHFFFAOYSA-N m-anisidine Chemical group COC1=CC=CC(N)=C1 NCBZRJODKRCREW-UHFFFAOYSA-N 0.000 claims description 3
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 3
- LGDHZCLREKIGKJ-UHFFFAOYSA-N 3,4-dimethoxyaniline Chemical compound COC1=CC=C(N)C=C1OC LGDHZCLREKIGKJ-UHFFFAOYSA-N 0.000 claims description 2
- 238000012856 packing Methods 0.000 claims description 2
- NBNMILRUCCOAFH-UHFFFAOYSA-N n-phenylaniline;thiadiazole Chemical compound C1=CSN=N1.C=1C=CC=CC=1NC1=CC=CC=C1 NBNMILRUCCOAFH-UHFFFAOYSA-N 0.000 claims 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 4
- ALNKTVLUDWIWIH-UHFFFAOYSA-N 3a-(5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl)-2,4-dihydro-1h-furo[2,3-b]indol-8b-ol Chemical group C1C(C(C2)C=C)CCN2C1C12OCCC1(O)C1=CC=CC=C1N2 ALNKTVLUDWIWIH-UHFFFAOYSA-N 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- ALNKTVLUDWIWIH-HLQCWHFUSA-N Quinamine Chemical group C([C@H]([C@H](C1)C=C)C2)CN1[C@@H]2[C@]12OCC[C@@]1(O)C1=CC=CC=C1N2 ALNKTVLUDWIWIH-HLQCWHFUSA-N 0.000 claims 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims 1
- SLXWCHVGTKNYQY-UHFFFAOYSA-N n-phenylaniline;stilbene Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1.C=1C=CC=CC=1C=CC1=CC=CC=C1 SLXWCHVGTKNYQY-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical compound OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 claims 1
- 238000012549 training Methods 0.000 claims 1
- 238000007641 inkjet printing Methods 0.000 abstract description 6
- 125000001424 substituent group Chemical group 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- 239000000203 mixture Substances 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
- 239000000463 material Substances 0.000 description 20
- 239000002253 acid Substances 0.000 description 18
- 238000007639 printing Methods 0.000 description 18
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 17
- 239000002904 solvent Substances 0.000 description 17
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 238000000576 coating method Methods 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 239000002585 base Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 11
- 230000002378 acidificating effect Effects 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 125000004093 cyano group Chemical group *C#N 0.000 description 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 8
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- 238000004043 dyeing Methods 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229960000583 acetic acid Drugs 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 235000011054 acetic acid Nutrition 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000012265 solid product Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical group [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 125000004104 aryloxy group Chemical group 0.000 description 4
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 4
- 230000008878 coupling Effects 0.000 description 4
- 238000010168 coupling process Methods 0.000 description 4
- 238000005859 coupling reaction Methods 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 125000002757 morpholinyl group Chemical group 0.000 description 4
- 150000002825 nitriles Chemical class 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
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- 229920006255 plastic film Polymers 0.000 description 4
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- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
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- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical group C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 3
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- 238000005516 engineering process Methods 0.000 description 3
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- 238000009835 boiling Methods 0.000 description 2
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- 239000010985 leather Substances 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- JJYPMNFTHPTTDI-UHFFFAOYSA-N meta-toluidine Natural products CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940095102 methyl benzoate Drugs 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- UCFFGYASXIPWPD-UHFFFAOYSA-N methyl hypochlorite Chemical group COCl UCFFGYASXIPWPD-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- FSUMZUVANZAHBW-UHFFFAOYSA-N n,n-dimethoxyaniline Chemical compound CON(OC)C1=CC=CC=C1 FSUMZUVANZAHBW-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical class CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 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
- 239000006259 organic additive Substances 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N pentadecanoic acid Chemical class CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- WEAYWASEBDOLRG-UHFFFAOYSA-N pentane-1,2,5-triol Chemical compound OCCCC(O)CO WEAYWASEBDOLRG-UHFFFAOYSA-N 0.000 description 1
- 125000006187 phenyl benzyl group Chemical group 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- DZMOLBFHXFZZBF-UHFFFAOYSA-N prop-2-enyl dihydrogen phosphate Chemical compound OP(O)(=O)OCC=C DZMOLBFHXFZZBF-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- XJMOSONTPMZWPB-UHFFFAOYSA-M propidium iodide Chemical compound [I-].[I-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CCC[N+](C)(CC)CC)=C1C1=CC=CC=C1 XJMOSONTPMZWPB-UHFFFAOYSA-M 0.000 description 1
- JTTWNTXHFYNETH-UHFFFAOYSA-N propyl 4-methylbenzenesulfonate Chemical compound CCCOS(=O)(=O)C1=CC=C(C)C=C1 JTTWNTXHFYNETH-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- TYNUXRBLGSXPAQ-UHFFFAOYSA-N sodium nitrate hydrochloride Chemical compound [Na+].Cl.[O-][N+]([O-])=O TYNUXRBLGSXPAQ-UHFFFAOYSA-N 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 238000007651 thermal printing Methods 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0074—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms
- C09B29/0092—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms containing a five-membered heterocyclic ring with two nitrogen and one sulfur as heteroatoms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/385—Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
- B41M5/388—Azo dyes
-
- 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
- C09B44/00—Azo dyes containing onium groups
- C09B44/10—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system
- C09B44/107—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system characterised by a cyclammonium five-membered specific ring not mentioned hereafter: thiadiazolium, (benz)oxazolium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/328—Inkjet printing inks characterised by colouring agents characterised by dyes
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/253—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates
- G11B7/2533—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
473512 IT Μ A7 B7 五、發明説明( 本發明係有關新穎之陽離子性聯笨胺染料、彼等之脫水 鹼、製備方法和用於噴墨印刷法及於光寫入數據儲存介質 及染料轉移膜方面之用途。 ΕΡ-Α-0 579 011揭示陽離子性嘐二唑聯苯胺染料及彼等 之脫水鹼。此染料實質上被用於染色各種紡織品及非紡織 材料。他們亦堆合用於喷墨油墨。此外彼等之脫水鹼亦 適用於昇華轉移印刷法。 然而,經發現利用習知的染料是不可能製備在三色印刷 t有令人滿意藍綠色之噴墨油墨的。對此種顏色而言,除 了長波吸收性(>630nm )外尚必須為鮮亮的且染料應 為可溶的°於昇華轉移印刷中,脫水鹼通常提供有限耐光 性之紅色色澤。 因此,需要-種染料,能提供噴墨油墨鮮亮、強烈的綠 藍色色澤’且在油墨所使用之溶劑中為易溶的。亦需要脫 水驗,能用於昇華或擴散轉移印刷法令,且能提供鮮亮、 耐光的印刷。 本發明係有關式(I) <陽離子性„塞二唾聯苯胺染料: (讀先閱讀背面之注意事項再填寫本頁) *·1Τ 經免部中央榀率而只-x消费合作私印製 其中 R2
(Ο χ· R1及R2,互相獨立地代表氫、燒基、缔基、環烧基、芳 本紙張尺度適用肀國國^標準(CNS ) Μ規格(一21〇><297公釐 473512 A7 B7 五、發明説明(2 ) 烷基或代表選擇地經由一亞甲基或伸乙基架橋 鍵接的雜環, R1及R2,與其所鍵接之氮原子一起代表一雜環, R3 代表烷基、烯基、環烷基或芳烷基, R4及R9 互相獨立地代表氫、烷基、烷氧基或鹵素, R4a 代表氫, 或 R4 及 R4a,一 起代表-CH=CH-CH^CH-架橋, R5 代表氩、烷基、烷氧基、芳氧基、芳胺基、鹵 素、氰基、烷氧羰基或硝基, R及R, 互相獨立地代表烧基、炫氧基或邊素,且r8 另外可代表氫, R7 代表烷氧基、芳氧基或nr^r11, 或 R6 及 R7, 一 起形成-〇CH20-、-OCH2CH20-、-CH2CH2-iji-、
Rio _CH2-CH2-CH2-1|J-或-0-CH2-CH2-i|i-架橋, 經¾‘部中央榀丰而妇工消f合作il印t! 、(讀先閲讀背面之注意事項再填寫本頁)
Ri〇 Rio R1〇及R11互相獨立地代表烷基、烯基、環烷基、芳烷基、 芳基或雜環基團,且R10另外可代表氫, R10及R11與其所鍵接之氮原子一起代表一雜環, 且其中 右R?代表NR^Rii,則R6及R8互相獨立地具有上述定義 且另外可代表氫,而R5具有上述所給定義且另外可代表 本紙張尺錢^(ϋχ29_ 473512 %浐部中央樣4,-^只工消費合作妇卬裳 A7 B7 酸鹽、硫酸氫鹽、硫酸鹽、磷酸二氫鹽、磷酸氫鹽、甲基 硫酸鹽、乙基硫酸鹽、四氣鋅酸鹽、四氣鐵酸鹽及飽和與 不飽和之具1至22碳原子的脂族、芳族或雜環羧酸及磺 酸之陰離子,諸如甲酸鹽 '乙酸鹽、四氟乙酸鹽、幾基乙 酸鹽、氰基乙酸鹽、丙酸鹽、羥基丙睃鹽、草酸鹽、檸檬 酸鹽、乳酸鹽、酒石酸鹽、氣己烷羧酸之陰離子、苯基乙 酸鹽、苯甲酸鹽、菸鹼酸之陰離子、甲烷磺酸鹽、三氟甲 烷磺酸鹽、乙烷磺酸鹽、丁烷磺酸鹽、壬氟丁烷磺酸鹽、 己烧績酸鹽、辛炫續酸鹽、十四烧續酸鹽、十五烧續酸鹽、 苯磺酸鹽、氣苯磺酸鹽、甲苯磺酸鹽、丁基苯磺酸鹽、 第四丁基苯續酸鹽或十二燒基苯續酸鹽。 若有關之陰離子為多價的,如硫酸鹽或草酸鹽,則式⑴ 中之X·代表此種多價陰離子之均等物。 以下為陽離子性嘍二唑聯苯胺染料之較佳例,其特徵在 於式(I)中: R1及R2 互相獨立地代表於各情況中選擇地經羥基_、 鹵素-、氰基-、CrC4-烷氧基-、胺基羰基-及 /或cvcv烷氧羰基-取代之Ci_C8_烷基、烯 丙基、環戍基、壤己基,或代奉於各情況中 選擇地經鹵素-、氰基-、crc4•烷基-及/或 CrCV烷氧基取代之苄基·或苯乙基基團、伸 丁基墙醯基基團、四氫呋喃基甲基、呲啶申 基或毗啶乙基基團; 或 —6- 私紙張尺度適扣中國國家禕準(CNS)A4規格(210x297公釐) t讀先閱讀背面之注意事項再镇寫本頁} 訂 473512 經浐部中央標準而只工消拎合作妇印絮 A7 B7 五、發明説明(s) R2 代表氫; 或 R1及R2與其所鍵接之氮原子一起代表吡咯啶基、六氫 毗啶基或嗎福啉基基團,其各自選擇地可被至 多4個甲基取代,或代表六氫吡啩基團其選 擇地於氮上可被甲基、乙基、經乙基或胺乙基 取代; R3 代表Ci-c^0-貌基,其選擇地可被經基、鹵素、 氰基、CrC4-貌氧基、胺基羰基及/或Ci-C4-烧氧羰基取代,或代表烯丙基或分別可選擇地 經鹵素、CrC4_烷基及/或q-Cr烷氧基取代 之苄基或苯6基基團; R4及R9 互相獨立地代表氫、CrC4-烧基' crc4-烷氧 基或鹵素, R4a 代表氫, 或 R4 及 R4a,一 起代表-CH=CH-CH=CH-架橋, •r R5 代表氫、cvcv烧基、C「c4-燒氧基、c6-c10- 芳氧基、C6-C1()-芳胺基、自素、氰基、crC4- 烷氧羰基或硝基; R6及R8,互相獨立地代表CrC4-烷基、Cl-c4·烷氧基或 鹵素,且R8另外可代表氫, R7 代表Ci-Cg-炫氧基、選擇地可被鹵素、氰基、 烧基及/或C^-C^-院氧基所取代之c6- —7— 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (誚先閱讀背面之注意事項再填寫本茛) 一装· 訂 A7 B7 五 、發 説明(6 ) C10-芳氧基,或代表NR1GRU; 或 R6 及 R7,一起形成-〇ch2o-、-CH2-CH2-y-、-ch2-ch2-ch2-n, R1。 1 丨。 或-0-CH2-CH2-ijl·架橋; R10 R10及R"互相獨立地代表crc8-烷基,其環擇地可被羥 基、鹵素、氰基或crc4-烷氧基取代,或代表 稀丙基、環戊基或環己基,或代表分別選擇地 經羥基、鹵素、氰基、crc8-燒基、q-cv烧 氧基或NRlGR"所取代之c6-ci()_芳基或吡啶 基; 或 R1° 代表氮; 或 R及R11與其所鍵接之氮原子一起代表一毗咯啶基、六 氫吡啶基或嗎福啉基,其各自選擇地可被丨至 4個甲基取代,或代表六氫毗啩基團其選擇 地於氮上可被甲基、乙基、羥乙基或胺乙基 取代; 且其中 若R7代表NR!❶R'則^及…互相獨立地具有上述定義, 或代表氳,而R5具有上述定義,或代表]^^1€〇1112或 NHS02R13, - -8— 本紙張尺度適用中國國家標準(CNS ) 格(210X297公釐j -- (讀先閲讀背面之注意事項再填寫本頁) >裝. 1T- 473512 A7 經浐部中央榀率而及工消费合作妇印製 ----_ B7丄、發明説明(7 ) Rl2及R13互相獨立地代表(Vc12-烷基或crc8-烷氧基, 其各自選擇地可被羥基、鹵素、氰基或crc4-烷氧基取代,或代表c6-c10-芳基、苄基或„比 啶基,其各自選擇地可被羥基、鹵素、氰基、 Cj-C4-烧基或(^-04-烧氧基取代,或代表稀丙 基、環戊基、環己基或NR1GRU;或 & 代表氫.,及 X" 代表陰離子。 以下為陽離子性噻二唑聯苯胺染料之特佳例,其特徵在 於式(I)中: R及R 互相獨立地代表曱基、乙基、丙基、異丙基、 丁基、甲丙基、戊基、甲丁基、二甲基丙基、 己基、羥乙基、羥丙基、氣乙基、氰甲基、氰 乙基、氰丙基、甲氧乙基、乙氧乙基、申氧丙 基、胺基羰基甲基、胺基羰基乙基、甲氧羰基 甲基、甲氧幾基乙基、浠丙基、環己基'苄棊、 苯乙基、甲基苄基、氣苄基、甲氧苄基、伸丁 基磺-3-基、呋喃甲基、2“或4-毗啶甲基或2_ 或4·毗啶乙基; 或 R2 代表氫;或 R及R 與其所鍵接之氮原子一起代表毗咯啶基、六氫 —-9— 本紙張尺度適;國家標準(CNS ) A4規格(21〇χ297公釐)------- ·(諳先閱讀背面之注意事項再填寫本頁} -裝 •訂 Φ 473512 A7 --------------------------^B7_ 五、發明説明(8 ) ~ 毗啶基或嗎福啉基,或代表六氫毗啩基團,其 _(請先閲讀背面之注意事項再填寫本頁) 選擇地於氮上可被甲基、乙基、羥乙基或胺乙 基取代; R 代表甲基、乙基、丙基、丁基'己基'辛基、 十二烷基、羥乙基、羥丙基、氣乙基、氰乙基、 甲氧乙基、乙氧乙基、甲氧丙基、甲氧羰基乙 基、烯丙基或苄基; R4 代表甲基、乙基、甲氧基、乙氧基或氣; R4a 代表氫, 或 R4 及 R4a _ 起代表-CH=CH-CH=CH-架橋, R5 代表氫、甲基、甲氧基、氯或氰基; R 'R8及R9互相獨立地代表甲基、乙基、甲氧基或乙氧基; 或 R8及R9 互相獨立地代表氫; R7 代表甲氧基、乙氧基、丙氧基、丁氧基、苯氧 基或 NR1QR1]; 或 R6及R7, 一起形成-0-CH2-0-架橋; R10及R11互相獨立地代表甲基、乙基、丙基、丁基、甲 丙基、戊基、甲丁基、二甲基丙基、己基、羥 乙基、羥丙基、氯乙基、氰甲基、氰乙基、氰 丙基、甲氧乙基、乙氧乙基、甲氧丙基、烯丙 基、環己基、苄基、苯基、甲苯基、甲氧苯基 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公嫠) A7 B7 五、 發明説明(9) 或R10 或 R10 及 Rii 乙氧笨基、苯氧苯基、氣笨基、二甲氧苯基、 二甲氧苯基、二甲基胺基苯基、二乙基胺基苯 基、二丁基胺基苯基、吡略啶苯基、六氫毗啶 基苯基、苯胺苯基、仏甲基苯胺基苯基、Ν,Ν· 二苯胺基苯基; 代表氫; 鯉M-部中央榀芈而只工消贽合作私印架 與其所鍵接之氮原子一起代表毗咯啶基、六 氫毗啶基或嗎福4基,或代表六氫毗听基團, 其選擇地於氮上可被曱基、乙基、羥乙基或胺 乙基取代; 且其中 若R7代表NRiGRH,則R6及R8具有上述定義,或互相獨 立地代表氫,而R5具有上述定義,或代表乙醯胺基、丙 醯胺基、三氟乙醯胺基、甲氧羰胺基、甲基磺醯胺基或全 氟丁基磺醯胺基; Χ' 代表陰離子。 以下為陽離子性噻二唑聯苯胺染料之極佳例,其特徵在 於式(I)中: R1及R2 互相獨立地代表甲基、乙基、丙基、異丙基、 丁基、羥乙基、羥丙基、氰甲基、氰乙基或甲 氧乙基或R1及R2與介於其間冬氮原子一起代 表毗咯啶基、六氫吡咬基或嗎福4基, -ll· 本紙張尺度適用中國國家標率(CNS ) A4規格(210X297公釐) (諳先閱讀背面之注意事項再填寫本頁) *11 —0, 473512 A7 B7___ 五 '發明説明(10 ) R3 代表甲基、乙基、丙基、丁基、己基或苄基; R4 代表甲氧基; (讀先閱讀背面之注意事項再填寫本頁) R4a 代表氫, R5 代表氫、甲基或甲氧基; R6 代表曱基或甲氧基; R7 代表甲氧基、乙氧基、苯氧基、甲基胺基、乙 基胺基、二甲基胺基、二乙基胺基、二丁基胺 基、苯胺基、2- ' 3-或4-甲基苯胺基、2-、3_ 或4-曱氧基苯胺基、2,4-或3,4-二甲氧基苯胺 基、4-二甲基胺基苯胺基、N-甲基苯胺基或4-苯胺苯胺基; 或 R6及R7 —起形成-0-CH2-0-架橋; R8及R9 代表氫,及 χ- 代表陰離子。 以下同樣為陽離子性噻二唑聯苯胺染料之極佳例,其特 徵在於式(I)中: R1及R2 互相獨立地代表甲基、乙基、丙基、異丙基、 丁基、羥乙基i羥丙基、氰乙基或甲氧乙基, 或 R1及R2 與其所鍵接之氮原子一起代表毗咯啶基、六氫 吡啶基或嗎福啉基, R3 代表甲基、乙基、丙基、丁基、己基或苄基; R4 代表甲氧基; t _______________~~^12— 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 473512 A7 B7 五、發明説明(υ) R4a R5 R6 R7 或 R6 及 R7 R8 及 R9 X- 代表氫, 代表氩、甲基、甲氧基或乙醯胺基; 代表氫、甲基或甲氧基; 代表甲胺基、乙胺基、二甲基胺基、二乙基胺 基、二丁基胺基、苯胺基、2-、3-或4-甲基苯 胺基、2-、3-或4-甲氧基苯胺基' 2,4-或3,4· 二甲氧基苯胺基、4-二甲基胺基苯胺基、N_甲 基苯胺基或‘苯胺苯胺基; 一起形成-0-CH2-0-架橋; 代表氫,及 代表陰離子。 本發明另外係有關式(II)之脫水鹼: (讀先閱讀背面之注意事項再填寫本頁) .裝· ·訂 R3
經浐部中央榀準^只工消贽合作私印來 (II), 其中 R1至R9具有上述之定義。 於較佳、特佳和極佳之脫水鹼中,基圏R1| Μ具有上 述為較佳、特佳和極佳之定義。 式(II)之脫水驗可在_之存在τ,藉切)之染料斑驗 之反應而得。 η 一 13- 本紙張尺度適用中國國家標準(CNS ) Α4規格 473512 A7 五、發明说明(12) 適合此目的之鹼之實例為氫氧仆 MUfUb物,Μ氡化鈉、钟和 鈣;氧化物’如氧化鎂;醇鹽如 X Τ%鈉、乙醇鈉和第三 丁醇納;胺類,如三乙胺、鮮削弟一 妝—或二乙醇胺;六氫吡啶 或毗咬,或如以苯乙婦/二乙嫌芏氣並 締本為基質的鹼性離子交換 劑。 適合溶劑之實例為水,醇類,如甲醇、乙醇、異丙醇或 二醇類;酮類,如丙鲷或丁酮;醯胺類,如二甲基甲醯胺、 二甲基乙醯胺、Ν·甲基麵咬_或队甲基己内酿胺腈 類,如乙腈和3-羥基丙腈;亞砥類如_ 糊,如一甲亞砜;硪類, 如環丁减(sulpholane )及二甲硪或Α $人仏 式(π)之脫水驗為製備式(1)之具有陰離;^之染料的適 宜中間體,其不能,或不易藉由以下所述式⑴染料之任一 製法所導入。 因此,式(I)之染料可藉改變陰離子X-來製備,以獲得 特殊性質,#更好的溶解度及/或更適合製備液體配方。 為此目的,可將式(II)之脫水鹼與式Ηχ之酸(其陰離子 將被導入)反應。反應可選擇地在溶劑之存在下進行,且 隨之在室溫或在高至基質沸點的溫度下冷卻。 然而,亦可藉將式(I)之染料與所需要之新陰離子,如 NaX或((^ΗΑΝ+Χ-,於適當溶劑下反應,以直接交換式⑴ 染料之陰離子。 可用於兩種方法中的溶劑為,例如一過量之酸Ηχ、水.、 醇類(如甲醇、乙醇、丁醇或二丙_醇)、二醇類(如乙 二醇、丙二醇或1,6-己二醇)、酮類(如丁鋼或環己綱)、 本紙張尺廋適用中國國家標準(CNS ) A4規格(210X297公釐) (讀先閱讀背面之注意事項蒋填寫本筲) >装_ 訂 473512 A7 --—________________B7_ 五、發明説明(彳3 ) 酿胺類(如ε-己内醯胺或N_甲基毗咯啶酮)、腈類(如乙 腈或羥丙腈),上述與脫水鹼之製備有關的溶劑或彼等之 混合物。 依此製得之式(I)之染料可由反應混合物中沉激出來或 於其中提供一種安定的溶液。 式(I)之染料可藉本身已知且描述於例如Ep_a_〇 579 011 中的方法來製備。 方法之一的特徵在於重氮化式(III)之2_胺基_ι,3,4_嚷二 R1\ (HI). »------0^-- (讀先閱讀背面之注意事項再填寫本頁) 其中 1 D 2 R和R具有關於式(I)所述之一般、較佳及特佳的定義 將重氮化之產物偶合至式(IV)之聯笨胺衍生物上,
,1T
R7 (IV), ^"•部中央#碑而妇工消於合作社印" 其中 Μ至R9具有關於式⑴所述之一般、較佳及特佳的定義 及隨後將產物以式(V)化合物或其先質予以四級化, R3X (V) 其中
473512 A7 B7
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z X'
H-N
五、發明説明(U R3和X具有關於式⑴所述之一般、較佳及特佳的定義。 式(III)之2-胺基-1,3,4-嚷二》坐,例如可由DE-A-2 811 258 中獲知或可由其中以類似方式獲得。式(IV)之聯苯胺衍生 物可由例如 Houben-Weyl, Methoden der Organischen Chemie, 第XI/1卷中獲知,或以類似方式獲得。 本發明亦有關製備式(I)之陽離子性塞二唾聯苯胺染料 之另一種方法,其特徵在於將式(VI)之染料 (VI). 其中 R1至R5及X'具有關於式(I)所述之一般、較佳及特佳的定 義,及 Z代表齒素、羥基、烷氧基、環烷氧基、芳氧基、胺基、 二炫胺基、醢氧基或醯胺基, 與式(VII)之胺反應, (VII), 其中 R6至R9具有關於式(I)所述之一般、較佳及特佳的定義。 於式(vi)中,z較佳代表氟、氯、溴、羥基、烧 16- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公楚) -^ϋ·#. fl^n Al^^ff· V ^—>^1 ml tnn —HI— n n^i ,. ^ n^i a nn nn m·— •(誚先閱讀背面之注意事項再填寫本頁) 473512 A7 B7 五、發明説明(15 ) 氧基、C5-C7-環烷氧基、C6-C10•芳氧基、NR R’,其中R’ 及R”互相獨立地代表氫或q-Cr烷基,或代表CrC6-烷酿 氧基、Q-c!。-芳醯氧基、cvcv烷磺醯氧基、cvq。-芳磺 醯氧基、crc6-烷醯胺基、cvcv烷磺醯胺基或c6-c1(r芳 基磺醯胺基。 式(VI)之化合物可藉例如重氮化式(III)之2-胺基-1,3,4-嗔二唑及將重氮化產物偶合至式(VIII)之苯何生物,
---J---^---裝-- (讀先閱讀背面之注意事項再填寫本頁) Z (VIII). R3 1 if 其中 R4、1143及R5具有關於式(I)所述之一般、較佳及特佳的定 義,且 z具有關於式(VI)所逑之一般及較佳的定義,且選擇地 若Z代表經基或胺基,則以crC6_脂族或c6-ci(r芳族缓 酸酐或羧酸氣化物或磺酸氣化物將產物酿化, 然後以式(IV)之化合物四級化該產物而得。 ’ 上述之重氮化反應可以本身習知的方式與例如含於80 至90%重量強度磷酸中或含於此種磷酸與乙酸、丙釀及 /或硫酸之混合物中之亞硝酸硫酸,或與在水性礦酸(如 氫氯酸)中之亞硝酸鈉一起進行。 上述之偶合同樣可以本Μ知方式進行,如在可為水性 或水性-有機性之酸性基質中進行。
經Μ‘部中央樣率沿匁工消贽合作相印 473512 A7 ---—__________________ 五、發明説明(16) ~- 重I化及偶合亦可藉其他本身習知的方法同時進行例 如藉式(III)化合物及式(IV)化合物與亞硝酸鈉,於例如一 酸性基質中共同反應。適宜之酸性基質的實例為水性礦酸 或有機酸或其混合物,適當之礦酸例如為氫氣酸、硫酸或 碟酸,而適當之有機酸例如為甲酸、乙酸或丙酸。加壓液 化之二氧化碳亦可充作酸性基質。 適當之四級化試劑為如式(V)者,彼等在反應條件下, 一般會提供式(V)之化合物。實例為鹵化烷類、南化乙醯 胺類、卜處化丙腈、函代醇、環氧烷烴、硫酸之烷基酯、 有機磺酸之烷基酯、腈類、醢胺類及α,β_不飽和羧酸、鹵 代烷氧烷類及乙烯吡啶。實例為氯甲烷、溴甲烷、碘曱烷、 氣甲苯、溴甲苯、氣乙醯胺、卜氯丙腈、伸乙基氯醇、硫 酸二甲酯 '硫酸二乙酯、苯續酸曱酯、苯績酸乙酯、甲苯 磺酸曱酯、甲苯磺酸乙酯、甲苯磺酸丙酯、氣丙烯、溴丙 稀、氧化乙烯、氧化丙稀、丙婦腈、丙烯酸、丙稀酿胺、 丙烯酸甲酯、2-及4-乙烯毗啶、環丁烯颯(=1ϊ1_二氧_2,5_ 二氫噻吩)、表氯醇、氧化苯乙烯、甲基磷酸二甲酯及烯 丙基磷酸酯。 上述之四級化反應可在例如惰性溶劑中、於水中或於彼 等t混合物中實施,選擇地可添加酸結合劑,如氧化鎂、 碳酸鈉、碳酸氫鈉、碳酸鈣或乙酸鈉。適當有機溶劑之實 例為烴類、氯化烴類、硝基烴類、腈類、醯胺類、羧酸類、 羧酸酐類、酮類及二烷亞硪類,諸如苯、甲苯、四氣乙烷、 早··及二氯笨、補基苯、乙腈、丙腈、二甲基曱酿胺、N- 1 " -——— —18— 本紙張尺度適财國國家標準(CNS) M規格(2丨οχ2· ‘(諳先閱讀背面之注意事項再填寫本頁) 擎裝· 訂 A7 s----------------:__ 五、發明説明(π) — 甲基吡咯啶酮、乙酸、丙酸、乳酸、乙酸酐、丙嗣、丁_ 及二甲亞硪。式(VI)之染料與式(VII)之胺類的反應選擇地 可在有機溶劑'水或其混合物中實施。適當之溶劑為如上 所述者。反應選擇地可在介於例如〇和100〇C之間,較佳 在10和50°C之間的溫度下,以過量式(VII)之胺來進行。 不論是可直接由溶劑中形成沉澱且可藉過濾分離之式⑴ 染料,或是當使用水可互溶溶劑時而形成之式⑴染料都 可藉以水稀釋及添加水可溶鹽,如氣化鈉或氯化鉀,選擇 地在氯化辞或氣化鑷之存在下,以可藉過濾分離之固體產 物形式獲得。 根據本發明式⑴之染料可用於供喷墨印刷之油墨及用 於光寫入數據儲存介質。 因此,本發明之另一主題為印刷油墨,其包含至少一種 式⑴之陽離子性聯苯胺染料,及彼等用作喷墨記錄系統之 記錄液體。一較佳形式包括式⑴之染料、該等式(1)染料 之混合物、或式(I)染料與其他適合製造青藍色印刷之較 佳陽離子性染料之混合物。 ·.? 根據本發明方法之喷墨法意指將油墨滴液喷霧至基質上 之喷墨記錄法。微細油墨滴液可藉各種方法產生。彼等較 佳係藉一般的熱力喷氣、泡沫喷氣、壓力喷氣或閥門喷墨 法來產生。這些方法可由例如丁丄.]^奶〇11,^^.卩1^(^.€:〇1〇-ration,22,22(1992)中獲知。 油墨為水性染料配方。一種安定、濃縮之水性染料配方 的製傷可以習知方式進行,例如在添加或不添加一種或多 ________—19— 本紙張尺度適用中國國家標準(CNS) A4規格(21〇><297公 {謂先閲讀背面之注意事項再填苟本頁,> 、-0 L» 473512 A7 B7 五、發明説明(18 ) 種輔助劑(如水溶增溶化合物或安定劑)的情況下,將染 料溶解於水中。 水性染料配方通常包含由約0.5至2〇重量%之一或多 種式(I)之染料及由80至99.5重量%的水及/或溶劑,及 若需要,其他的習用成分。 於本案情況中,較佳之有機溶劑為醇類及彼等之醚類或 醋類,幾基酿胺類、脒,亞硪及颯尤其是具有分子量<2〇〇 者。特別適合溶劑之實例為甲醇、乙醇、丙醇、異丙醇; 乙一醇、丙二醇、二乙二醇、硫代二乙二醇、二丙二醇、 戊二醇、三乙二醇及聚乙二醇;丁二醇、込^戊二醇、丨,2_ 二羥基丙烷;甘油、1,3,6·己三醇;β_羥基丙腈;乙二醇單 乙基及丙基謎、伸乙基二乙二醇單乙謎、三乙二醇丁醚、 丁基聚二醇、1-曱氧基-2-丙醇、2-甲氧暴_1,丙醇;甲醯 胺' Ν,Ν_二甲基甲醯胺、吡咯啶酿j、己内醯胺' Ν_甲基_ 己内醯胺、丁内酯、己内酯;2-羥基乙酸乙酯、2-(2,-羥 乙基)-乙酸乙酯、乙酸二醇酯;服、四甲基脒、丨,3_二甲 基-2-四氫咪唑酮、N,N_二羥甲基伸丙基雎;二甲亞砜、 ^一甲减、環丁石風0 經浐部中夹榀準而只Jr.消Φ;合作私卬^ _(誚先閱讀背面之注意事項再填寫本頁) 、-'° 其他用於水性染料配方(特別是用於印刷油墨)之適合 及習知的添加劑為擒離子性或非離子性物質,其可藉諸如 陰離子、陽離子戒中性表面活性劑(如分散劑及黏度調整 劑)來調整彼等之黏度及/或表面張力至應用所需的範 圍。黏度調整劑之功能可被例如有機溶劑所取代。 根據本發明之染料配方亦可包含其他非式⑴之染料e
A7 B7 五、發明説明(19 經浐部中央榀準而只工消货合作^卬^ 水性染料配方(特別是染料溶液)之較佳例包括·· -由0.5至20重量%,特別是由1至15重量%之一種或 多種染料,其中至少一種為式(1), -由50至99.5重量%,特別是由85至99重量%之水, 由0至30重量%,特別是由〇至重量%之一種或多 種有機溶劑, 由〇至30重量%,特別是由0至10重量%之可影響黏 度及/或表面張力之添加劑, 這些成分之合總計為1〇〇重量%。 水性染料配方可藉將式⑴之染料溶於水中,或將式(II) 之脫水鹼溶於水中,並添加一當量之如上述之酸11又而製 備。於此情況下,在溫度如由20至100oc,選擇地在由30 至100°C,特別在由30至50χ之高溫下選擇地可添加 一或多種上述之有機溶劑及/或添加劑且/或選擇地可 添加無機酸或有機酸。 適且之酸為乙酸、經基乙酸或乳酸,但特別是式取之 酸,其中X為式(I)染料之陰離子。 油墨為適幹噴墨印刷在普通紙上及在塗覆紙和塗覆塑膠 膜上者。制塗該為較獲得較㈣的表面較高的光 澤度及/或改料刷之H此包括改良耐水性、耐光性 及/或明亮度。所使用之塑膠臈特別是具有可印刷、最好 是透明的塗膜之透明薄膜,就包含式⑴染料之油墨而言, 特別適合之紙或薄膜為可攜帶酸性塗膜者。此種酸性材 料,例如可為酸性黏土或料鹽(特別是具有片狀構造 (讀先閱讀背面之注意事項再填寫本頁〕 __________________^. -Φ i· —21— 473512 广五、 發明説明(20 者)、苯酚-甲醛樹脂或水楊酸之鹽類。這些材料可與一結 合劑及選擇地之其他物質(如填料)一起被塗覆至紙或薄 膜上。 當根據本發明之染料以其如上所詳細敘述之水性配方的 形式被用作喷墨記錄系統之印刷油墨時,將導致下列之優 點’物理性質(如黏度、表面張力等)為在適當範圍内; 記錄液體不會造成喷墨記錄設備之細小輸出喷嘴的阻塞; 提供高光學密度的影像;於貯存時,不會改變物理特性及 /或不會有固體成分沉澱於記錄液體中;記錄液體為適合 記錄於各種記錄介質上,不會因記錄介質的性質而受到限 制;記錄液體快速地固定且提供具優越抗水性、耐光性、 耐磨餘性及解析度之影像。 本發明之另一主題為包含至少一種式⑴之陽離子性聯 苯胺染料之光寫入數據儲存介質。 此等數據儲存介質為帶有吸光層之光學記錄材料。將此 層曝露於光,如利用適當波長之雷射光,會導致曝露面積 的加熱,結果於其間造成改變。例如,加熱可導致溶化, 藉此使此層之表面起變化而形成例如小凹陷孔(crater)。 此種加熱亦可能使部t分材料蒸發,同樣形成凹陷孔。吸光 層之染料亦可為熱及>或光化學所破壞。此層之折射指數 亦可能改變。於各情況中,依此方式改變之層即包含貯存 形式之數據。這些數據可藉一較弱的光源再次被讀出。 此種吸光層之製備及彼等於儲存介質令之用途,被描述 於例如 WO 84/02795 及 EP-A 0 023 736 中。 ‘(諳先閱讀背面之注意事項 — 項再填寫 裝— Γ本頁} 、-6 Φ 本紙張尺度適用中國國家標準() A4規格(2!〇χ297公羡) 473512 Α7 Β7 五 '發明説明(21) ~ 此種數據儲存介質於基材上帶有一層吸光塗膜,該基材 通常為具有顯著光學特性(高透明度、無雙折射)且係由 例如聚碳酸酯所組成之塑膠板。此塗膜通常不僅包括染 料,亦包括黏結劑。塑縢板亦可利用鋁而為可反射的。塗 膜有利地可藉由如旋塗法’由溶液來塗敷β塗媒必須非常 薄、非常均勻且具高度光學品質&此外,其在光源之範固 内必須有強烈吸收。所使用之光源為雷射,如雷射二極體, 其在600至7〇〇nm之範圍内作用。 由於根據本發明之式(I)染料在此波長範圍内有顯著吸 收,彼等特別適合用於此種數據儲存介質中。此等染料之 混合物亦同樣適合。他們在習用塗膜溶劑中為易溶的。這 些;谷劑必須不會攻擊塑膠板。此種溶劑之實例為酿j類及醇 類,如丁酮、環己酮、甲醇、乙醇、丁醇或二丙酮醇或其 混合物。 經沪部中央榀苹而Κ工消贽合作拉卬" ·(讀先閱讀背面之注意事項再填寫本頁) 適當之結合劑為所有成膜性(較佳為聚合性)之材料, 例如聚笨乙稀、聚-α-甲基苯乙烯、聚甲基丙稀酸酯、聚 甲基丙烯酸甲酯、聚氯乙烯、聚乙酸乙烯酯、聚(乙酸乙 烯酯/乙烯吡咯啶酮)、聚碳酸酯、硝酸纖維素、乙酸丁 酸纖維素,或其混合物或共聚物。 此外,根據本發明之式(I)染料亦特別適合用於染色及印 刷陽離子性可染纖維,較佳為丙烯腈及二氰乙烯之聚合物 及共聚物,及聚醯胺和聚酯之酸修飾之纖維,並提供耐色 度(fast shades )。此染料夺可被用於染色及印刷輮製的 纖維素材料、紙、絲及皮革。他們另外適合供製造書寫液、 ___ _ —23— 不,..氏浓人中關家襟準(CNS ) A4規格⑺〇χ297公 經"部中央枝^·^只工消贽合作拍印來 473512 A7 -----------------------B7___ 五、發明説明(22 ) ~ 打印液及筆芯油,亦可用於橡皮印刷中。 丙烯腈之聚合物及共聚物之染色,可將其在較佳為4〇 至6〇°C下浸入染浴,且在沸點之溫度下施行染色而由弱 酸液中發生。亦能在高於100〇C之溫度及於壓力下實施染 色。此外,亦可能使用棒據本發明之染料來製備用於染色 含聚丙烯腈纖維之旋塗溶液。 根據本發明之式(I)染料對於聚丙烯腈材料之染色,有極 佳的耐光、耐濕及耐磨性,且對纖維有高度親和性。 根據本發明之式(II)的脫水鹼可用於喷墨印刷之油墨或 用於染料擴散轉移技術。 因此,本發明之另一主題為包含至少一種式(π)之脫水 鹼的印刷油墨,及其作為噴墨記錄系統用之記錄液體的用 途 較佳形式包括式(II)之脫水驗、此種式(Π)之脫水驗 之混合物、或式(II)之脫水鹼與其他脫水鹼或可質子化染 料或其先質(其在質子化後適合製造藍綠色印料)之混合 物。 噴墨記錄法已於上文敘述。 包含式(Π)脫水鹼之油墨一般非為水性的Ρ然而,若式(Η) 之脫水鹼為在分散態形式,則他們可包含水作為基質。 於包含式(II)脫水鹼之油墨中,溶解形式之使用係由溶 劑或其混合物製得。此種溶劑之實例為網類,如亇纲或環 己酮;腈類,如乙腈、丙腈或戊二腈;醯胺類,如二甲醯 胺、Ν-甲基毗咯啶酮或&己内醯胺;酯類,如乙酸乙酯、 乙酸丁酯、苯甲酸甲酯或酞酸二丁酯;天然油類,如向日 ____ —24—_ 本μΓ張尺度適/fl巾關家標準(CNS ) Α4規格(21()χ297公楚) — —~ _(諳先閲讀背面之注意事項再填寫本頁) 訂 A7 B7 473512 五、發明説明(23) 葵油椰H㈣油、㈣& 1 肪酸之酯類(其為此4汽旦油,及脂 於、諸田 類之基質),*菜籽油脂肪酸甲 酯、油酸甲酯、2-椰早酿7 w 曰奶敗丫 硬脂酸甲酿。 基己酯、肉豆謹酸異丙醋或異 將為分散_式。為此目的,可 是㈣之溶齡散於水不互溶之溶 劑::實例為上述之酿類或天然油類)、分散於水或水盘 =其:>谷之溶劑的混合物中(實例為上述之醯胺類或二 醇,U,6_己三醇或1,5-戊三醇)。分散液可利用習 知非離子性或料性分散劑予以安定。 油墨為適於喷墨印刷在塗覆紙或轉膜上,但亦可在非 不吸水的平滑表面,如金屬或塑膠上1包含式(π)脫水 驗之油墨而。’特別適合之紙或薄膜為帶有酸性塗蹲者。 此種酸性材料可為酸性黏土切酸鹽(特別是具有片狀構 造者)、苯酚·甲醛樹脂或水揚酸之鹽類。這些材料可與— 結合劑及選擇地之其他物f (如㈣)—起被塗覆至紙或 薄膜上。此種塗膜被用來改善印刷之特性,此包括改^耐 水14耐光性及/或明亮度。式(π)之脫水驗在這些酸性 塗膜材料上為部分或完全質子化的,以提供式⑴之染料。 本發明之另一主題為式(11)脫水鹼用於染料擴散轉移技 術之用途。 於此情況中,將式(II)之脫水鹼、其混合物或其與其他 非離子性、易擴散或昇華染料之混合物組合於一層狀物 中’該層狀物係位於一由聚酯所製成之薄支持材料上。若 -25- 本紙張尺度適用中國國家標率(CNS ) A4規格(21〇χ297公釐 • - >- *二 _ in I I -- i I nn - - ml '1:01 ϋ^ϋ . I I I 11 (諳先閲讀背面之注意事項再填iss本頁j 經浐部中戎榀率^工消贽合竹il卬欠 Η/二):> 丄 z A7 -------------------B7五、發明説明(24) 此提供顏色層與接受層(其同樣位於一支持材料上)接觸, 則藉由電k號控制之熱印字頭,即能夠將提供顏色之脫水 驗(單獨或混合其他染料)由提供顏色層轉移至接受層上, 於該處形成對應於電信號之圖型。此種程序被描述於例如 ΕΡ-Α-0 384 040 中。 接文層可位於纺織材料上,但特別是位在紙、塑膠膜或 聚合網上。此等層狀物較佳為酸性層。他們包括如酸性黏 土或矽酸鹽(特別是具有片狀構造者)、苯酚-甲醛樹脂或 水楊酸之鹽類。這些材料可與一結合劑及選擇地之其他物 質(如填料)一起被塗覆至紙或薄膜上。式(II)之脫水鹼 在這些酸性塗膜材料中為部分或完全質子化的以提供式 (I)之染料。此種接受層及對應之印刷技術被描述於例如 ΕΡ-Α-0 273 307 中。 另,本發明之主題為供記錄的材料,特別是由塗覆或未 塗覆之紙或塑膠膜所構成且已用包含至少一種式(1)之染 料或至少一種式(II)之脫水鹼的油墨所寫入或印刷,或已 藉染料擴散轉移法,用式(II)之脫水鹼所寫入者;以及_ 據儲存介質,其吸光層包含至少一種式(I)之染料。 (讀先閱讀背面之注意事項再填寫本頁} I裝 麫方—部中央枒^^:"二消贽合作^印剩 _ —26— 中國國家標準(CNS ) A4規格(2ΪΟΧ297公釐) 4/3M2 A7 —----- — B7五、發明説明(25 ) 實施例 -實蒌例1 (式(I)之染料) 將10.7克下式之染料 , Μ 經沪部中央榀4,-^只工消费合作社印繁 ι-Γ fed (川)理 jET人 (其被描述於EP-AO 717 082中)、20.0克4-胺基-4,-甲氧 基聯苯胺氣化氫和6.6克醋酸鈉,在5〇°C下,於110毫 升之甲醇中攪拌6小時。以13公升醋酸乙酯稀釋混合物, 以抽吸過濾,及將固體產物以醋酸乙酯洗滌並在真空中乾 燥。然後攪拌於500毫升水中,以抽吸過濾混合物且將固 體產物以水洗滌,再次在真空中乾燥。獲得12.2克(85 %理論值)之式(I)中1^=:^=異丙基,r3=甲基,尺4=甲氧 基,R3=R6=R8=R9=氫,R7=t=4-曱氧笨胺基且x-=ZnCl3_之染 料。 於9:1之甲醇/冰醋酸中之溶液,在639nm中顯示最 ·? 大吸收度。 實施例2 (式(II)之脫水鹼) 將2.6克實施例1之染料溶解於200毫升甲醇中,逐滴 加入30毫升之1〇重量%之氫氧化鈉溶液。於攪拌2小時 後,以抽吸過濾混合物且將固體產物以甲醇洗滌。將其攪 拌於200毫升水中,抽吸過濾混合物且將固體產物以水洗 一 27— 0、
CH, Ο \ CH,
ZnCL (讀先閱讀背面之注意事項再填寫本頁) ▼裝. 、1 本紙張尺度適用中國國家摞準(CNS ) A4規格(210X297公釐) 473512 A7 B7 五、發明説明(26 ) 滌及在真空中乾燥。獲得1.9克(96%理論值)之式(Π) 中RLRk異丙基,R3=甲基,R4=甲氧基,R5=R6=R8=r9= 氫,R7=4-甲氧苯胺基之脫水鹼。 於二甲醯胺中之溶液,在526 nm中顯示最大吸收度。 實施例3 (式(I)染料之溶液的製備) 將0.9克實施例2之脫水鹼懸浮於6毫升之92/8二丙 酮醇/丁醇混合物中。加入0.25克之四氟甲烷磺酸。將混 合物在70°C下加熱5分鐘,然後再予以冷卻。獲得式(I) 中RLRL異丙基,R3=甲基,R4=甲氧基,R5=R6=R8=R9= 氫,R7=4-甲氧苯胺基且X-=F3CS03-之澄清、深藍綠色之 染料溶液6 將一滴此溶液塗佈於一玻璃板上,蒸發溶液後獲得一鍵 接在玻璃上且可抗磨耗之透明、藍綠色的薄膜。 於下表中所提出的染料為以類似於實施例1之方式製 備: (諳先閱讀背面之注意事項 Γ本頁) 、-° 經 部 中 央 消 f: 合 作 印 -28— 本紙張尺度適州中國國家標準(CNS ) A4規格(210X297公釐) 473512 A7 _________ B7 五、^.明説明(27 ) 輕沪部中央"4,-^θ工消贽合作私印製 «Τ Ο 〇 〇 υ t 5 X 〇 E c H c B c E c E c E c E c E c • H c B c ε c C3 1 s忑 NO ro VD 菩 SO oo ro 卜 fN \〇 «〇 s «〇 v〇 O s oo s «η \〇 X ZnCI3- 1 r< G 1 G 1 r< g £ u 1 s 壬 u • ⑺ Ο ΐ u V D M k CH30S03· « oo 〇 £ u CH30S03· X a: a: rr X X re X a: 3: 0CH3 oo a: X X X X X X X X X I U 〇 9 i 工 X ΐ u 〇 〇 0 1 £ (J 〇 ό r £ U z. 9 〇 X a 〇 0CH3 1 o ό u o v〇 οά r X ΐ a 〇 r·· u o r· G o X u r*· u 0 U rr x X IE re X ΐ u 0 CJ 1 X. n: 0 X T* X X X re 5 土 y X u i X X X X CJ X och3 〆 a: u 〇 r·" X u o u o u o u X CJ u X o £ u 〇 £ 0 r u 〇 0CH3 rn^ u c*· u r< U 壬 u X u Γ u Γ u V X CJ 3E"1 u X u ^=5" € <N^ ch(ch3)2 工 Γ* u X u c- ;£ U U r u Γ u r u f u • X X u u 1 i CH(CH3)2 工 r u u r u X a r U Γ o Γ u f· re u u m U f CJ m S lt- rj fh弋 H « v〇 卜 oo O o = CN 寸 H八: 乂諳先閱讀背面之注意事項再填寫本頁) —29— 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐)
Claims (1)
- 473512 經濟部智慧財產局員工消費合作社印製 A8 B8 C8 D8 六、申請專利範圍 專利申請案第87107921號 ROC Patent Appln. No.87107921 -修兵之申請專利範圍中文本一附件(一) Amended Cliaims in Chinese - Enel. (I) t T民p 90年3月2曰送呈) (Submitted on March 2 , 2001) 種式(I)陽離子性噻二唑二苯胺染料N 5 R Na 4r.R7 R o c (請先閱讀背面之注意事項再填寫本頁) •裝 χ· 其特徵為 R1及R2,互相獨立地代表Cb烷基或C3-6環烷基, 或 R1及R2,與其所鍵接之氮原子一起代表吡咯啶基, R3代表Cl-4烧基或C2-6稀基5 R4代表Cw烷氧基, R5代表氫或Cl-4烧幾胺基, R6代表氫或Cl-4炫氧基, R7代表Cl-4烧氧苯胺基、二-(Cl-4院基)胺基、Cl-4烧氧 基、苯胺基或笨氧基, -30 - 87165b ·! — — — — — — % 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 六 、申請專利範 圍 A8 B8 C8 D8 或 及R7,一起形成Cw伸烷二氧基, R8代表氫或(^-4烷氧基, R9代表氫或Cl-4烧氧基, X 代表陰離子。 2. 如申請專利範圍第1項之式(I)陽離子性噻二唑二苯胺 染料,其中: R1及R2互相獨立地於各情況中為C!-4烷基、環戊基或環 己基, 或 R1及R2與其所鍵接之氮原子一起代表吡咯啶基, R3代表G-4烷基,或代表烯丙基, R4代表烷氧基, R5代表氫、鹵素或Ch烷羰胺基, P代表Ch烷氧基, R7代表Cw烷氧苯胺基、二-(G-4烷基)胺基、Ch烷氧 基,苯胺基或苯氧基, 或 R6及R7,一起形成G-4伸烷二氧基, R8代表氫或G-4烷氧基, R9代表氫或G-4烷氧基, Γ代表陰離子。 3. 如申請專利範圍第1項之式(I)陽離子性σ塞二σ坐二苯胺 染料,其中: _ -31 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閲讀背面之注音2事項再填寫本頁) ▼-裝—·— η.—訂---------. 經濟部智慧財產局員工消費合作社印製經濟部智慧財產局員工消費合作社印製 、申請專利範圍 R1及R2互相獨立地代表曱基、乙基、丙基、異丙基、丁 基、甲丙基、戊基、甲丁基、二甲基丙基、己基、 環己基; 或 R及R,與其所鍵接之氮原子一起代表吡咯啶基; R3代表T基、乙基、丙基、丁基或烯丙基; R4代表曱氧基或乙氧基; R 代表氫或氣; R6代表f氧基或乙氧基; 或 R8及R9互相獨立地代表氫; R代表曱氧基、乙氧基、丙氧基、丁氧基、苯氧基、 Ci-4烷氧苯胺基、二-(Ch烷基)胺基或苯胺基; 或 , R及R,一起形成-0-CH2-0-架橋.; t 代表陰離子。 4.如申请專利範圍第1項之式(I)陽離子性^塞二唾二苯胺 染料,其中: R及R2互相獨立地代表甲基、乙基、丙基、異丙基或丁 基’或R1及R2與介於其間之氮原子一起代表吡咯啶 基, R3代表曱基、乙基、丙基或丁基; R4代表甲氧基; R5代表氫; ’ -32 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先間讀背面之注意事項再填寫本頁) 裝 > I H n 1 ϋ^1·^ 1 1 I -ϋ I 473512 A8B8C8D8 經濟部智慧財產局員工消費合作杜印製 六、申請專利範圍 R6代表曱氧基; R7代表甲氧基、乙氧基、苯氧基、二曱基胺基、二乙 基胺基、二丁基胺基、苯胺基、2-、3-或4-曱氧基 苯胺基、2, 4-或3, 4-二曱氧基苯胺基; 或 R6及R7 —起形成-0-CH2-0-架橋; R8及R9代表氫,及 Γ代表陰離子。 5.如申請專利範圍第1項之式(I)陽離子性噻二唑二苯胺 染料,其中: R1及R2互相獨立地代表曱基、乙基、丙基、異丙基、或 丁基; 或 R1及R2與其所鍵接之氮原子一起代表吡咯啶基; R3代表曱基、乙基、丙基或丁基; R4代表曱氧基; R5代表氮或乙醯胺基; R6代表氫或甲氧基; R7代表二甲基胺基、二乙基胺基、二丁基胺基、苯胺 基、2-、3-或4-甲氧基苯胺基、2, 4-或3, 4-二甲氧 基苯胺基; 或 R6及R7 —起形成-0-CH2-0-架橋; -33 - 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) (請先閱讀背面之注咅?事項再填寫本頁) 裝 .——訂---------. 473512 A8 B8 C8 D8六、申請專利範圍 R8及R9代表氫,及 Γ代表陰離子。 6. 一種式(II)之脫水驗, 經濟部智慧財產局員工消費合作社印製其特徵為 R1至R9具有申請專利範圍第1項所述之定義。 7. 如申請專利範圍第1項之陽離子性噻二唑二苯胺染料, 其用於噴墨油墨。 8. 如申請專利範圍第6項之脫水鹼,其用於喷墨油墨。 9. 如申請專利範圍第1項之陽離子性噻二唑二苯胺染料, 其用於光寫入數據儲存介質。 10. 如申請專利範圍第6項之脫水鹼,其用於染料擴散轉移 法之染料擴散轉移薄膜。 (請先閱讀背面之注意事項再填寫本頁) 裝---.---^--訂--------- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)
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DE19724583A DE19724583A1 (de) | 1997-06-11 | 1997-06-11 | Kationische Diphenylaminfarbstoffe und deren Anhydrobasen |
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TW087107921A TW473512B (en) | 1997-06-11 | 1998-05-22 | Cationic thiadiazolediphenylamine dyes and their anhydro bases |
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US (1) | US5952475A (zh) |
EP (1) | EP0884367B1 (zh) |
JP (1) | JPH11228852A (zh) |
KR (1) | KR19990006836A (zh) |
DE (2) | DE19724583A1 (zh) |
TW (1) | TW473512B (zh) |
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US6200370B1 (en) * | 1998-09-30 | 2001-03-13 | Fuji Photo Film Co., Ltd. | Jet printing ink and ink-jet recording method |
US6143061A (en) * | 1999-04-26 | 2000-11-07 | Eastman Kodak Company | Delocalized cationic azo dye for ink jet ink |
JP4099301B2 (ja) * | 1999-09-29 | 2008-06-11 | 富士フイルム株式会社 | 色素化合物 |
JP2004524201A (ja) | 2001-03-28 | 2004-08-12 | バイエル アクチェンゲゼルシャフト | 情報層中に吸光性化合物としてジアザヘミシアニン色素を含有する光学データ記憶媒体 |
CN1545700A (zh) * | 2001-03-28 | 2004-11-10 | 在信息层中包括阳离子胺基杂环染料作为光吸收剂化合物的光学数据载体 | |
US7497878B2 (en) * | 2005-06-30 | 2009-03-03 | L'oreal, S.A. | Azo dyes containing a sulphonamide or amide function for the dyeing of human keratin fibers and method of dyeing and dyeing compositions containing them |
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DE2811258C2 (de) * | 1978-03-15 | 1982-12-30 | Bayer Ag, 5090 Leverkusen | Kationische 1,3,4-Thiadiazol-Farbstoffe, Verfahren zu deren Herstellung sowie Verfahren zum Färben und Bedrucken natürlicher und synthetischer Materialien |
NL7905914A (nl) * | 1979-08-01 | 1981-02-03 | Philips Nv | Kleurstof bevattend laagje van een filmvormend polymeer bindmiddel en toepassing ervan in een informatie- registratieeelement. |
WO1984002795A1 (en) * | 1982-12-31 | 1984-07-19 | Minnesota Mining & Mfg | Recording medium for optical data storage |
DE3644369A1 (de) * | 1986-12-24 | 1988-07-07 | Basf Ag | Verfahren zur uebertragung von kationischen farbstoffen in ihrer deprotonierten, elektrisch neutralen form |
EP0384040B1 (en) * | 1989-02-24 | 1994-01-26 | Agfa-Gevaert N.V. | Dye-donor element for thermal dye sublimation transfer |
DE4100810A1 (de) * | 1991-01-12 | 1992-07-16 | Bayer Ag | Kationische 1,3,4-thiadiazolfarbstoffe |
DE4205632A1 (de) * | 1992-02-25 | 1993-08-26 | Bayer Ag | Azinneutromethine |
DE4222257A1 (de) * | 1992-07-07 | 1994-01-13 | Bayer Ag | Kationische Thiadiazoldiphenylaminfarbstoffe |
DE4444861A1 (de) * | 1994-12-16 | 1996-06-20 | Bayer Ag | Verfahren zur Herstellung von kationischen 1,3,4-Thiadiazolfarbstoffe |
DE19524134A1 (de) * | 1995-07-03 | 1997-01-09 | Bayer Ag | Verfahren zum Reduzieren der Toxizität von Restflotten und neue kationische Farbstoffe |
-
1997
- 1997-06-11 DE DE19724583A patent/DE19724583A1/de not_active Withdrawn
-
1998
- 1998-05-22 TW TW087107921A patent/TW473512B/zh active
- 1998-05-29 EP EP98109914A patent/EP0884367B1/de not_active Expired - Lifetime
- 1998-05-29 DE DE59809257T patent/DE59809257D1/de not_active Expired - Fee Related
- 1998-06-04 US US09/090,744 patent/US5952475A/en not_active Expired - Fee Related
- 1998-06-08 JP JP10173815A patent/JPH11228852A/ja active Pending
- 1998-06-10 KR KR1019980021455A patent/KR19990006836A/ko not_active Withdrawn
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EP0884367A2 (de) | 1998-12-16 |
KR19990006836A (ko) | 1999-01-25 |
EP0884367A3 (de) | 2000-05-17 |
EP0884367B1 (de) | 2003-08-13 |
DE19724583A1 (de) | 1998-12-17 |
US5952475A (en) | 1999-09-14 |
JPH11228852A (ja) | 1999-08-24 |
DE59809257D1 (de) | 2003-09-18 |
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