DD141678B1 - Siliziumhaltige nitrofarbstoffe - Google Patents
Siliziumhaltige nitrofarbstoffe Download PDFInfo
- Publication number
- DD141678B1 DD141678B1 DD20458878A DD20458878A DD141678B1 DD 141678 B1 DD141678 B1 DD 141678B1 DD 20458878 A DD20458878 A DD 20458878A DD 20458878 A DD20458878 A DD 20458878A DD 141678 B1 DD141678 B1 DD 141678B1
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- dyes
- general formula
- fibers
- silicone
- radical
- Prior art date
Links
- -1 siloxanes Chemical class 0.000 claims description 12
- 238000004043 dyeing Methods 0.000 claims description 9
- 239000000835 fiber Substances 0.000 claims description 9
- 229910052710 silicon Inorganic materials 0.000 claims description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000001005 nitro dye Substances 0.000 claims description 8
- 239000010703 silicon Substances 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 229910010272 inorganic material Inorganic materials 0.000 claims description 3
- 239000011147 inorganic material Substances 0.000 claims description 3
- 125000004999 nitroaryl group Chemical group 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- 150000003254 radicals Chemical class 0.000 claims description 3
- 239000000985 reactive dye Substances 0.000 claims description 3
- 150000004756 silanes Chemical class 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 239000006103 coloring component Substances 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 239000012209 synthetic fiber Substances 0.000 claims description 2
- 229920002994 synthetic fiber Polymers 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims 1
- 125000005375 organosiloxane group Chemical group 0.000 claims 1
- 239000000975 dye Substances 0.000 description 22
- 229920001296 polysiloxane Polymers 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 229920002379 silicone rubber Polymers 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000004945 silicone rubber Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 229940024463 silicone emollient and protective product Drugs 0.000 description 5
- 229920002050 silicone resin Polymers 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- VYZAHLCBVHPDDF-UHFFFAOYSA-N Dinitrochlorobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 VYZAHLCBVHPDDF-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000987 azo dye Substances 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 150000002828 nitro derivatives Chemical class 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- FXMKXMJLXRTQSW-UHFFFAOYSA-N 2,4-dinitroiodobenzene Chemical compound [O-][N+](=O)C1=CC=C(I)C([N+]([O-])=O)=C1 FXMKXMJLXRTQSW-UHFFFAOYSA-N 0.000 description 1
- FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical class NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 description 1
- KQIKKETXZQDHGE-FOCLMDBBSA-N 4,4'-diaminoazobenzene Chemical compound C1=CC(N)=CC=C1\N=N\C1=CC=C(N)C=C1 KQIKKETXZQDHGE-FOCLMDBBSA-N 0.000 description 1
- IJJWOSAXNHWBPR-HUBLWGQQSA-N 5-[(3as,4s,6ar)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-n-(6-hydrazinyl-6-oxohexyl)pentanamide Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)NCCCCCC(=O)NN)SC[C@@H]21 IJJWOSAXNHWBPR-HUBLWGQQSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- OBFQBDOLCADBTP-UHFFFAOYSA-N aminosilicon Chemical class [Si]N OBFQBDOLCADBTP-UHFFFAOYSA-N 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- YQGOWXYZDLJBFL-UHFFFAOYSA-N dimethoxysilane Chemical compound CO[SiH2]OC YQGOWXYZDLJBFL-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000001016 thiazine dye Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 239000001003 triarylmethane dye Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
- 239000011787 zinc oxide Substances 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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/008—Dyes containing a substituent, which contains a silicium atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Silicon Polymers (AREA)
- Coloring (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD20458878A DD141678B1 (de) | 1978-04-05 | 1978-04-05 | Siliziumhaltige nitrofarbstoffe |
| DE19792908205 DE2908205A1 (de) | 1978-04-05 | 1979-03-02 | Siliziumhaltige nitrofarbstoffe |
| SU797770488A SU1017706A1 (ru) | 1978-04-05 | 1979-03-07 | Способ получени кремнийсодержащих нитрокрасителей |
| CS791667A CS218886B1 (en) | 1978-04-05 | 1979-03-12 | Method of preparation of the new azodyes containing the silicon |
| GB7910304A GB2018797B (en) | 1978-04-05 | 1979-03-23 | Silicon-containing nitro dyestuffs |
| BE0/194271A BE875160A (fr) | 1978-04-05 | 1979-03-28 | Colorants nitres contenant du silicium et leur procede de preparation |
| FR7908521A FR2421935A1 (fr) | 1978-04-05 | 1979-04-04 | Colorants nitres contenant du silicium |
| JP4152679A JPS54148023A (en) | 1978-04-05 | 1979-04-05 | Siliconncontaining nitro dye |
| US06/391,657 US4405801A (en) | 1978-04-05 | 1982-06-24 | Silicon-containing nitro dyes and process for making the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD20458878A DD141678B1 (de) | 1978-04-05 | 1978-04-05 | Siliziumhaltige nitrofarbstoffe |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DD141678A1 DD141678A1 (de) | 1980-05-14 |
| DD141678B1 true DD141678B1 (de) | 1980-12-24 |
Family
ID=5512075
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD20458878A DD141678B1 (de) | 1978-04-05 | 1978-04-05 | Siliziumhaltige nitrofarbstoffe |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4405801A (fr) |
| JP (1) | JPS54148023A (fr) |
| BE (1) | BE875160A (fr) |
| CS (1) | CS218886B1 (fr) |
| DD (1) | DD141678B1 (fr) |
| DE (1) | DE2908205A1 (fr) |
| FR (1) | FR2421935A1 (fr) |
| GB (1) | GB2018797B (fr) |
| SU (1) | SU1017706A1 (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5070158A (en) * | 1987-03-12 | 1991-12-03 | Hewlett-Packard Company | Covalently labeled siloxane polymers |
| EP0283206A3 (fr) * | 1987-03-12 | 1990-08-22 | Hewlett-Packard Company | Polysiloxanes ayant des groupes de marquage liés par des liaisons covalentes |
| FR2746102B1 (fr) * | 1996-03-18 | 1998-04-30 | Colorants siloxaniques, compositions les contenant et utilisations | |
| US5789515A (en) * | 1997-03-13 | 1998-08-04 | Milliken Research Corporation | Polysiloxane-poly(oxyalkylene) copolymer-substituted colorant |
| DE102006027533A1 (de) * | 2006-06-14 | 2007-12-20 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbige Organopolysiloxane |
| DE102006046465A1 (de) * | 2006-09-29 | 2008-04-03 | Dystar Textilfarben Gmbh & Co. Deutschland Kg | Farbige Organopolysiloxane |
| EP2155805A2 (fr) * | 2007-05-11 | 2010-02-24 | Basf Se | Colorants polymériques |
| JP5851336B2 (ja) * | 2012-05-09 | 2016-02-03 | オリンパス株式会社 | 複合ゴム材料、成形体、複合ゴム材料の製造方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2756246A (en) * | 1954-02-08 | 1956-07-24 | Gen Electric | Nitro derivatives of organosilicon compounds |
| US2985680A (en) * | 1959-08-03 | 1961-05-23 | Union Carbide Corp | Nitro and nitrito derivatives of organosilicon compounds |
| US3375218A (en) * | 1962-12-07 | 1968-03-26 | Union Carbide Corp | Nitroarylsilanes and siloxanes |
| US3731205A (en) * | 1972-03-23 | 1973-05-01 | Embhart Corp | Sequence detector circuit |
| US4139403A (en) * | 1977-08-19 | 1979-02-13 | The United States Of America As Represented By The Secretary Of The Navy | Dinitroalkyl and fluorodinitroalkyl silicon compounds |
-
1978
- 1978-04-05 DD DD20458878A patent/DD141678B1/de not_active IP Right Cessation
-
1979
- 1979-03-02 DE DE19792908205 patent/DE2908205A1/de not_active Withdrawn
- 1979-03-07 SU SU797770488A patent/SU1017706A1/ru active
- 1979-03-12 CS CS791667A patent/CS218886B1/cs unknown
- 1979-03-23 GB GB7910304A patent/GB2018797B/en not_active Expired
- 1979-03-28 BE BE0/194271A patent/BE875160A/fr unknown
- 1979-04-04 FR FR7908521A patent/FR2421935A1/fr not_active Withdrawn
- 1979-04-05 JP JP4152679A patent/JPS54148023A/ja active Pending
-
1982
- 1982-06-24 US US06/391,657 patent/US4405801A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| GB2018797A (en) | 1979-10-24 |
| BE875160A (fr) | 1979-07-16 |
| CS218886B1 (en) | 1983-02-25 |
| DE2908205A1 (de) | 1979-10-18 |
| US4405801A (en) | 1983-09-20 |
| FR2421935A1 (fr) | 1979-11-02 |
| DD141678A1 (de) | 1980-05-14 |
| GB2018797B (en) | 1982-08-04 |
| JPS54148023A (en) | 1979-11-19 |
| SU1017706A1 (ru) | 1983-05-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |