SU604502A3 - Способ получени полимеров, содержащих триазиновые кольца - Google Patents
Способ получени полимеров, содержащих триазиновые кольцаInfo
- Publication number
- SU604502A3 SU604502A3 SU752120692A SU2120692A SU604502A3 SU 604502 A3 SU604502 A3 SU 604502A3 SU 752120692 A SU752120692 A SU 752120692A SU 2120692 A SU2120692 A SU 2120692A SU 604502 A3 SU604502 A3 SU 604502A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- triazine
- mixture
- polymer
- secondary amine
- solid
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims description 40
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 title claims description 12
- 238000000034 method Methods 0.000 title claims 4
- 238000010438 heat treatment Methods 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 5
- -1 cyanamide compound Chemical class 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- 150000003573 thiols Chemical class 0.000 claims description 2
- 150000003335 secondary amines Chemical class 0.000 claims 4
- 150000002894 organic compounds Chemical class 0.000 claims 3
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 43
- 239000007787 solid Substances 0.000 description 24
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000011343 solid material Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 229960001755 resorcinol Drugs 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- CFLAKPREKITGNE-UHFFFAOYSA-N cyanamide;triazine Chemical compound NC#N.C1=CN=NN=C1 CFLAKPREKITGNE-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 201000003704 mandibulofacial dysostosis with alopecia Diseases 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- UITKHKNFVCYWNG-UHFFFAOYSA-N 4-(3,4-dicarboxybenzoyl)phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 UITKHKNFVCYWNG-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 208000020329 Zika virus infectious disease Diseases 0.000 description 1
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- JLXXLCJERIYMQG-UHFFFAOYSA-N phenylcyanamide Chemical compound N#CNC1=CC=CC=C1 JLXXLCJERIYMQG-UHFFFAOYSA-N 0.000 description 1
- VBOZZYDXKHSARC-UHFFFAOYSA-N phenylcyanamide;sodium Chemical compound [Na].N#CNC1=CC=CC=C1 VBOZZYDXKHSARC-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/0622—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms
- C08G73/0638—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms with at least three nitrogen atoms in the ring
- C08G73/0644—Poly(1,3,5)triazines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/456,916 US3960783A (en) | 1974-04-01 | 1974-04-01 | Novel polymers from s-triazine cyanamide compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU604502A3 true SU604502A3 (ru) | 1978-04-25 |
Family
ID=23814666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU752120692A SU604502A3 (ru) | 1974-04-01 | 1975-03-31 | Способ получени полимеров, содержащих триазиновые кольца |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3960783A (enExample) |
| JP (1) | JPS5845454B2 (enExample) |
| AU (1) | AU7964375A (enExample) |
| BE (1) | BE827421A (enExample) |
| CA (1) | CA1068438A (enExample) |
| DD (1) | DD117471A5 (enExample) |
| DE (1) | DE2513731A1 (enExample) |
| ES (1) | ES436152A1 (enExample) |
| FR (1) | FR2265795B1 (enExample) |
| GB (1) | GB1500522A (enExample) |
| NL (1) | NL7503764A (enExample) |
| SU (1) | SU604502A3 (enExample) |
| ZA (1) | ZA751974B (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2457081A1 (de) * | 1974-12-03 | 1976-06-10 | Bayer Ag | S-triazin-vorpolymerisate |
| DE2457154A1 (de) * | 1974-12-04 | 1976-06-10 | Bayer Ag | S-triazin-vorpolymerisate und ein verfahren zu deren herstellung |
| DE2533121A1 (de) * | 1975-07-24 | 1977-02-10 | Bayer Ag | Hochmolekulare polytriazine aus loeslichen polymeren n-cyan-isoharnstoffaethern |
| DE2533124A1 (de) * | 1975-07-24 | 1977-02-10 | Bayer Ag | Verfahren zur herstellung von polytriazinen in gegenwart hochsiedender ester |
| JPS5879017A (ja) * | 1981-11-04 | 1983-05-12 | Hitachi Ltd | イソメラミン環を有するポリマ |
| JPS5934226A (ja) * | 1982-08-19 | 1984-02-24 | 松下電器産業株式会社 | 自動炊飯装置 |
| US4650867A (en) * | 1985-03-26 | 1987-03-17 | Ciba-Geigy Corporation | Process for the preparation of 2,4,6-tris(aminophenylamino)triazines |
| US4734457A (en) * | 1987-05-07 | 1988-03-29 | R. T. Vanderbilt Company, Inc. | Rubber compositions containing polymeric phenol derivatives of 1,3,4-thiadiazole |
| US4818778A (en) * | 1987-05-07 | 1989-04-04 | R. T. Vanderbilt Company, Inc. | Rubber compositions containing phenol derivatives of 1,3,4-thiadiazole |
| US9603848B2 (en) * | 2007-06-08 | 2017-03-28 | Senomyx, Inc. | Modulation of chemosensory receptors and ligands associated therewith |
| US8492509B2 (en) * | 2009-05-12 | 2013-07-23 | Chemnano Materials, Ltd. | Sulfur functionalized polymers for separation of metals from gas and liquid and methods for preparation thereof |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3053796A (en) * | 1958-09-30 | 1962-09-11 | Dal Mon Research Co | Polymerization products of unsaturated triazine derivatives |
| US3308101A (en) * | 1963-09-24 | 1967-03-07 | Du Pont | Novel polymeric materials |
| DE1200314B (de) * | 1963-10-26 | 1965-09-09 | Bayer Ag | Verfahren zur Herstellung von substituierten s-Triazinen |
| DE1595651B2 (de) * | 1966-04-23 | 1977-01-20 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung polymerer produkte |
| US3654192A (en) * | 1968-08-19 | 1972-04-04 | Minnesota Mining & Mfg | Poly(arylene s-triazines) |
| US3779997A (en) * | 1972-06-12 | 1973-12-18 | Minnesota Mining & Mfg | Poly(hexasubstituted melamines) |
-
1974
- 1974-04-01 US US05/456,916 patent/US3960783A/en not_active Expired - Lifetime
-
1975
- 1975-03-27 AU AU79643/75A patent/AU7964375A/en not_active Expired
- 1975-03-27 ZA ZA00751974A patent/ZA751974B/xx unknown
- 1975-03-27 NL NL7503764A patent/NL7503764A/xx unknown
- 1975-03-27 DE DE19752513731 patent/DE2513731A1/de not_active Ceased
- 1975-03-27 CA CA223,226A patent/CA1068438A/en not_active Expired
- 1975-03-31 SU SU752120692A patent/SU604502A3/ru active
- 1975-03-31 DD DD185107A patent/DD117471A5/xx unknown
- 1975-03-31 ES ES436152A patent/ES436152A1/es not_active Expired
- 1975-04-01 JP JP50039729A patent/JPS5845454B2/ja not_active Expired
- 1975-04-01 BE BE154973A patent/BE827421A/xx unknown
- 1975-04-01 GB GB13225/75A patent/GB1500522A/en not_active Expired
- 1975-04-01 FR FR7510124A patent/FR2265795B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2265795A1 (enExample) | 1975-10-24 |
| FR2265795B1 (enExample) | 1977-04-15 |
| DE2513731A1 (de) | 1975-10-09 |
| CA1068438A (en) | 1979-12-18 |
| NL7503764A (nl) | 1975-10-03 |
| AU7964375A (en) | 1976-09-30 |
| DD117471A5 (enExample) | 1976-01-12 |
| GB1500522A (en) | 1978-02-08 |
| JPS5845454B2 (ja) | 1983-10-11 |
| JPS50138100A (enExample) | 1975-11-04 |
| US3960783A (en) | 1976-06-01 |
| BE827421A (fr) | 1975-10-01 |
| ZA751974B (en) | 1976-02-25 |
| ES436152A1 (es) | 1977-02-01 |
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