JPH0353326B2 - - Google Patents
Info
- Publication number
- JPH0353326B2 JPH0353326B2 JP18213587A JP18213587A JPH0353326B2 JP H0353326 B2 JPH0353326 B2 JP H0353326B2 JP 18213587 A JP18213587 A JP 18213587A JP 18213587 A JP18213587 A JP 18213587A JP H0353326 B2 JPH0353326 B2 JP H0353326B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- polymer
- polymerization
- groups
- group
- Prior art date
- 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
Links
- 238000006116 polymerization reaction Methods 0.000 claims description 14
- 125000000962 organic group Chemical group 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 56
- 229920000642 polymer Polymers 0.000 description 14
- LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 description 13
- 239000007787 solid Substances 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- 229910052794 bromium Inorganic materials 0.000 description 7
- 239000004952 Polyamide Substances 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000004760 aramid Substances 0.000 description 4
- 229920003235 aromatic polyamide Polymers 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 2
- IOSGANIYBODQTB-UHFFFAOYSA-N 2-ethynylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C#C IOSGANIYBODQTB-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000005691 oxidative coupling reaction Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- VNQABZCSYCTZMS-UHFFFAOYSA-N Orthoform Chemical compound COC(=O)C1=CC=C(O)C(N)=C1 VNQABZCSYCTZMS-UHFFFAOYSA-N 0.000 description 1
- -1 amide compounds Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 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
- 150000004985 diamines Chemical class 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000008204 material by function 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
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000015 polydiacetylene Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyamides (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18213587A JPS6426635A (en) | 1987-07-23 | 1987-07-23 | Polyamide containing diacetylene group |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18213587A JPS6426635A (en) | 1987-07-23 | 1987-07-23 | Polyamide containing diacetylene group |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6426635A JPS6426635A (en) | 1989-01-27 |
| JPH0353326B2 true JPH0353326B2 (enrdf_load_stackoverflow) | 1991-08-14 |
Family
ID=16112950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18213587A Granted JPS6426635A (en) | 1987-07-23 | 1987-07-23 | Polyamide containing diacetylene group |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6426635A (enrdf_load_stackoverflow) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0198627A (ja) * | 1987-10-12 | 1989-04-17 | Agency Of Ind Science & Technol | ジアセチレン基含有ポリアミド成形体 |
| JPH01115928A (ja) * | 1987-10-29 | 1989-05-09 | Agency Of Ind Science & Technol | ジアセチレン基含有ポリアミドの製造方法 |
-
1987
- 1987-07-23 JP JP18213587A patent/JPS6426635A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6426635A (en) | 1989-01-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2006520840A (ja) | 水溶性高分子の活性化形 | |
| JP2017160164A (ja) | ロタキサン化合物 | |
| JPH0353326B2 (enrdf_load_stackoverflow) | ||
| CN115353476A (zh) | 一种马来酰亚胺-酰胺-低聚乙二醇-丙酸的合成方法 | |
| JP3031036B2 (ja) | 含フッ素芳香族ジアミン化合物、アミノ基が保護された含フッ素ジアミン化合物及びそれらの製造法 | |
| JPH0338297B2 (enrdf_load_stackoverflow) | ||
| JPH0623242B2 (ja) | ジアセチレン基含有ポリエステル | |
| JP2916614B2 (ja) | カルバゾール系ポリアミド及びカルバゾール系ポリアミドの製造方法 | |
| JP3018643B2 (ja) | フッ素含有ジアミノベンゼン化合物及びフッ素含有芳香族ジアミン化合物の製造法 | |
| US4115367A (en) | Perfluoroalkylene ether bibenzoxazole polymers | |
| JPH05239208A (ja) | ポリアミド・イミド類の製造方法 | |
| KR102605275B1 (ko) | 아미드 칠량체 및 이의 제조 방법 | |
| RU2697529C1 (ru) | Способ получения ациклических полиимидов | |
| JP3911705B2 (ja) | アゾビスシアノカルボン酸クロリドの製造方法 | |
| Hsiao et al. | Synthesis and properties of polyamides based on a spirobichroman bis (ether‐carboxylic acid) | |
| JPH0525874B2 (enrdf_load_stackoverflow) | ||
| JPS6344736B2 (enrdf_load_stackoverflow) | ||
| JPH0552831B2 (enrdf_load_stackoverflow) | ||
| JPH0580932B2 (enrdf_load_stackoverflow) | ||
| JP4806858B2 (ja) | 開環重合体の製造方法 | |
| KR20220054018A (ko) | 아미드 오량체 및 이의 제조 방법 | |
| JPS62288628A (ja) | ジアセチレン基含有芳香族性ポリアミド | |
| JPH01186852A (ja) | アミド基含有ジフェニルジアセチレン | |
| JPH07252223A (ja) | カルバゾール誘導体及びその製造方法 | |
| JP2590430B2 (ja) | カルバゾール誘導体、カルバゾール系ポリアミド及びカルバゾール系ポリアミドの製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |