JPS62195025A - ニセレン化炭素重合体の製造方法 - Google Patents
ニセレン化炭素重合体の製造方法Info
- Publication number
- JPS62195025A JPS62195025A JP3501286A JP3501286A JPS62195025A JP S62195025 A JPS62195025 A JP S62195025A JP 3501286 A JP3501286 A JP 3501286A JP 3501286 A JP3501286 A JP 3501286A JP S62195025 A JPS62195025 A JP S62195025A
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- carbon
- diselenide
- carbon diselenide
- electromagnetic wave
- 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.)
- Granted
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 40
- JNZSJDBNBJWXMZ-UHFFFAOYSA-N carbon diselenide Chemical compound [Se]=C=[Se] JNZSJDBNBJWXMZ-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 230000001678 irradiating effect Effects 0.000 claims description 2
- XIMIGUBYDJDCKI-UHFFFAOYSA-N diselenium Chemical compound [Se]=[Se] XIMIGUBYDJDCKI-UHFFFAOYSA-N 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 abstract description 11
- 238000009835 boiling Methods 0.000 abstract description 5
- 238000000034 method Methods 0.000 description 16
- 239000000843 powder Substances 0.000 description 11
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 8
- -1 polyphenylene Polymers 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 6
- 238000000921 elemental analysis Methods 0.000 description 6
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 5
- 229910052753 mercury Inorganic materials 0.000 description 5
- 229910052711 selenium Inorganic materials 0.000 description 5
- 239000011669 selenium Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229920001940 conductive polymer Polymers 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 229920001197 polyacetylene Polymers 0.000 description 3
- 239000002861 polymer material Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 150000003346 selenoethers Chemical class 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920000265 Polyparaphenylene Polymers 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000002019 doping agent Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000006418 Brown reaction Methods 0.000 description 1
- GXGJIOMUZAGVEH-UHFFFAOYSA-N Chamazulene Chemical group CCC1=CC=C(C)C2=CC=C(C)C2=C1 GXGJIOMUZAGVEH-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
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005251 gamma ray Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3501286A JPS62195025A (ja) | 1986-02-21 | 1986-02-21 | ニセレン化炭素重合体の製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3501286A JPS62195025A (ja) | 1986-02-21 | 1986-02-21 | ニセレン化炭素重合体の製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62195025A true JPS62195025A (ja) | 1987-08-27 |
| JPH0349296B2 JPH0349296B2 (enExample) | 1991-07-29 |
Family
ID=12430162
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3501286A Granted JPS62195025A (ja) | 1986-02-21 | 1986-02-21 | ニセレン化炭素重合体の製造方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62195025A (enExample) |
-
1986
- 1986-02-21 JP JP3501286A patent/JPS62195025A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0349296B2 (enExample) | 1991-07-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR20150000860A (ko) | 그라펜 나노리본 전구체 및 그의 제조에 적합한 단량체 | |
| Antoun et al. | Synthesis and electrical conductivity of poly (arylene vinylene). I. Poly (2, 5‐dimethoxyphenylene vinylene) and poly (2, 5‐dimethylphenylene vinylene) | |
| Pan et al. | Regiospecific, functionalized poly (phenylenevinylene) using the Heck coupling reaction | |
| Nandgaye et al. | An Expeditious Synthesis of Near‐Infrared‐Absorbing Imide‐Based Graphene Nanoribbons and Their Photothermal Properties | |
| Massoumi et al. | Chemical and electrochemical grafting of polythiophene onto polystyrene synthesized via ‘living’anionic polymerization | |
| JPS62195025A (ja) | ニセレン化炭素重合体の製造方法 | |
| Lahouel et al. | Green Synthesis Method of Poly [(2, 5-diyl pyrrole)(4-hydroxy-3-methoxy benzylidene)] Semiconductor Polymer Using an Ecologic Catalyst | |
| Pomerantz et al. | Poly (benzo [1, 2-b: 4, 5-b'] dithiophene-4, 8-diylvinylene). Synthesis, Properties, and Electronic Structure of a New Dithiophene-Fused p-Phenylenevinylene Conducting Polymer | |
| Kijima et al. | Syntheses and properties of conjugated polymers with cumulenic bond in the main chain | |
| Wu et al. | Intercalation of polyfuran in FeOCl. | |
| Pavlović et al. | Controlled synthesis of unsubstituted high molecular weight poly (para-phenylene) via Suzuki polycondensation-thermal aromatization methodology | |
| JPS61231031A (ja) | 二硫化炭素重合体の製造方法 | |
| Yokota et al. | Alternating copolymerization of carbonyl sulfide with aziridines | |
| JPH0725869B2 (ja) | ポリ−p−フェニレンビニレンの製造方法 | |
| Kobayashi et al. | Novel conjugated polymer containing aromatic ring and selenium in backbone: Addition polymerization of 1, 4‐benzenediselenol to 1, 4‐diethynylbenzene | |
| Tanaka et al. | Preparation and electrical properties of poly (3‐thienylacetylene) | |
| Iván et al. | Cyclopentadienylation of PVC | |
| JPS6354436A (ja) | 導電性塗料およびその製造方法 | |
| Bertinelli et al. | Poly (m‐phenylene disulfide): Antimony pentafluoride doping and infrared spectroscopy | |
| JPS5945323A (ja) | ポリフエニレンスルフイド | |
| Paganin et al. | Synthesis and Characterization of a Highly Soluble Poly [3‐(10‐hydroxydecyl) thiophene] | |
| Carotenuto et al. | Polyacetylene Prepared by Chemical Dehydration of Poly (Vinyl Alcohol). Coatings 2024, 14, 1216 | |
| SU487912A1 (ru) | Способ получени азотсодержащих полимеров | |
| SU1154292A1 (ru) | Способ получени полиарилентиохинодиимидов | |
| KR910007467B1 (ko) | 전기 전도성 폴리머를 이용한 광학디스플레이 및 광전지의 제조방법 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |