JPH0329244B2 - - Google Patents

Info

Publication number: JPH0329244B2
Authority: JP; Japan
Prior art keywords: polymer; sulfide; pyridine ring; dihalogenated; ethylene
Prior art date: 1985-06-07
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 - Lifetime

Application number

JP60122565A

Other languages

English (en)

Japanese (ja)

Other versions

JPS61281130A (ja

Inventor

Yukihiro Ikeda

Masaru Ozaki

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

National Institute of Advanced Industrial Science and Technology AIST

Original Assignee

Agency of Industrial Science and Technology

Priority date (The priority date 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 date listed.)

1985-06-07

Filing date

1985-06-07

Publication date

1991-04-23

1985-06-07 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1985-06-07 Priority to JP60122565A priority Critical patent/JPS61281130A/ja

1986-12-11 Publication of JPS61281130A publication Critical patent/JPS61281130A/ja

1991-04-23 Publication of JPH0329244B2 publication Critical patent/JPH0329244B2/ja

Status Granted legal-status Critical Current

Links

229920000642 polymer Polymers 0.000 claims description 39
-1 ethylene, 1,2-ethylene Chemical group 0.000 claims description 19
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 18
238000004519 manufacturing process Methods 0.000 claims description 8
150000003222 pyridines Chemical class 0.000 claims description 6
229910052783 alkali metal Inorganic materials 0.000 claims description 3
150000001340 alkali metals Chemical group 0.000 claims description 2
238000007334 copolymerization reaction Methods 0.000 claims 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 20
229920001197 polyacetylene Polymers 0.000 description 14
125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
238000000034 method Methods 0.000 description 6
238000000862 absorption spectrum Methods 0.000 description 5
238000005452 bending Methods 0.000 description 5
150000004770 chalcogenides Chemical class 0.000 description 5
238000000921 elemental analysis Methods 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000000706 filtrate Substances 0.000 description 4
239000000203 mixture Substances 0.000 description 4
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 4
230000004580 weight loss Effects 0.000 description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
238000005227 gel permeation chromatography Methods 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
239000011630 iodine Substances 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
FEYDZHNIIMENOB-UHFFFAOYSA-N 2,6-dibromopyridine Chemical compound BrC1=CC=CC(Br)=N1 FEYDZHNIIMENOB-UHFFFAOYSA-N 0.000 description 2
FILKGCRCWDMBKA-UHFFFAOYSA-N 2,6-dichloropyridine Chemical compound ClC1=CC=CC(Cl)=N1 FILKGCRCWDMBKA-UHFFFAOYSA-N 0.000 description 2
SOSPMXMEOFGPIM-UHFFFAOYSA-N 3,5-dibromopyridine Chemical compound BrC1=CN=CC(Br)=C1 SOSPMXMEOFGPIM-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical group [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
230000009102 absorption Effects 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
238000005266 casting Methods 0.000 description 2
230000008602 contraction Effects 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000002798 polar solvent Substances 0.000 description 2
238000012643 polycondensation polymerization Methods 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
UKDOTCFNLHHKOF-FGRDZWBJSA-N (z)-1-chloroprop-1-ene;(z)-1,2-dichloroethene Chemical group C\C=C/Cl.Cl\C=C/Cl UKDOTCFNLHHKOF-FGRDZWBJSA-N 0.000 description 1
AKAIWNDBVZJOAJ-UHFFFAOYSA-N 1,4-dithiine Chemical compound S1C=CSC=C1 AKAIWNDBVZJOAJ-UHFFFAOYSA-N 0.000 description 1
ZHXUWDPHUQHFOV-UHFFFAOYSA-N 2,5-dibromopyridine Chemical compound BrC1=CC=C(Br)N=C1 ZHXUWDPHUQHFOV-UHFFFAOYSA-N 0.000 description 1
GCTFDMFLLBCLPF-UHFFFAOYSA-N 2,5-dichloropyridine Chemical compound ClC1=CC=C(Cl)N=C1 GCTFDMFLLBCLPF-UHFFFAOYSA-N 0.000 description 1
WPGHPGAUFIJVJF-UHFFFAOYSA-N 3,5-dichloropyridine Chemical compound ClC1=CN=CC(Cl)=C1 WPGHPGAUFIJVJF-UHFFFAOYSA-N 0.000 description 1
238000006418 Brown reaction Methods 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
229910001508 alkali metal halide Inorganic materials 0.000 description 1
150000008045 alkali metal halides Chemical class 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
KFUSEUYYWQURPO-UPHRSURJSA-N cis-1,2-dichloroethene Chemical group Cl\C=C/Cl KFUSEUYYWQURPO-UPHRSURJSA-N 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
238000011835 investigation Methods 0.000 description 1
238000000465 moulding Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229920000620 organic polymer Polymers 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000007157 ring contraction reaction Methods 0.000 description 1
238000006049 ring expansion reaction Methods 0.000 description 1
229910052711 selenium Inorganic materials 0.000 description 1
239000004065 semiconductor Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
125000004436 sodium atom Chemical group 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
238000001228 spectrum Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
238000005979 thermal decomposition reaction Methods 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000011345 viscous material Substances 0.000 description 1

Landscapes

Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

JP60122565A 1985-06-07 1985-06-07 スルフィド系高分子重合体及びその製造方法 Granted JPS61281130A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP60122565A JPS61281130A (ja)	1985-06-07	1985-06-07	スルフィド系高分子重合体及びその製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP60122565A JPS61281130A (ja)	1985-06-07	1985-06-07	スルフィド系高分子重合体及びその製造方法

Publications (2)

Publication Number	Publication Date
JPS61281130A JPS61281130A (ja)	1986-12-11
JPH0329244B2 true JPH0329244B2 (cs)	1991-04-23

Family

ID=14839036

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP60122565A Granted JPS61281130A (ja)	1985-06-07	1985-06-07	スルフィド系高分子重合体及びその製造方法

Country Status (1)

Country	Link
JP (1)	JPS61281130A (cs)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR20130018236A (ko) *	2010-02-09	2013-02-20	수스 마이크로텍 리소그라피 게엠바하	얇은 웨이퍼 캐리어

1985
- 1985-06-07 JP JP60122565A patent/JPS61281130A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR20130018236A (ko) *	2010-02-09	2013-02-20	수스 마이크로텍 리소그라피 게엠바하	얇은 웨이퍼 캐리어

Also Published As

Publication number	Publication date
JPS61281130A (ja)	1986-12-11

Legal Events

Date	Code	Title	Description
2005-06-07	EXPY	Cancellation because of completion of term

Publication	Publication Date	Title
Ueda et al.	1991	Synthesis of poly (3-phenyl-2, 5-thiophene) by nickel-catalyzed coupling polymerization of 3-phenyl-2, 5-dichlorothiophene
CA1265295A (en)	1990-01-30	Conductive polymers
TW200418864A (en)	2004-10-01	Preparation of 2,2'-di(3,4-ethylenedioxythiophene)s
JPH0784524B2 (ja)	1995-09-13	芳香族スルフィドアミド重合体の製造法
US5338823A (en)	1994-08-16	Lithium/HMPA-promoted synthesis of poly(phenylenes)
JPH0329244B2 (cs)	1991-04-23
Subramanyam et al.	1993	Conjugated ionic polyacetylenes. 6. Polymerization of 2-ethynylpyridinium triflates
Zhou et al.	2007	Synthesis and characterization of tris (2, 2′‐bipyridine) ruthenium‐cored star‐shaped polymers via RAFT polymerization
Kodaira et al.	1979	Cyclopolymerization. VIII. Polymerization of sym-Dimethacryloyldimethylhydrazine and Related Compounds
US5300625A (en)	1994-04-05	Heteroaromatic polyether
JPH02189333A (ja)	1990-07-25	自己ドーピング機能を有する導電体の製造方法
US5530090A (en)	1996-06-25	Reductive method for preparation of macrocyclic oligomer mixtures
JP6726521B2 (ja)	2020-07-22	光学活性基を有する置換ポリアセチレン及びその製造方法
JP3164671B2 (ja)	2001-05-08	アリーレンビニレン重合体およびその製造方法
Liu et al.	2008	Synthesis and properties of polysilanes with tetrathiafulvalene as pendant group
JP2730757B2 (ja)	1998-03-25	導電性複素環式重合体およびその製造方法
JPH04108784A (ja)	1992-04-09	ポリエチレンのチオフェン誘導体およびエチレンのチオフェン誘導体
Sarker et al.	1994	Syntheses of new poly (arylene vinylene) analogues: Poly (4, 7‐benzofuran vinylene) and poly (4, 7‐benzothiophene vinylene)
Shouji et al.	1994	Synthesis of poly (sulfonium cation) as an alkylating reagent
JPS6243421A (ja)	1987-02-25	カルコゲナイド系重合体及びその製造法
KR920009684B1 (ko)	1992-10-22	가공성 폴리아조메틴수지 및 그 제조방법
JPH04283231A (ja)	1992-10-08	芳香族ポリエーテルケトン共重合体およびその製造方法
Shimomura et al.	1998	Synthesis and properties of novel polymers having S‐methyldibenzothiophenium salt moieties
Sergeyev et al.	1975	Synthesis and certain properties of soluble polyphenylene sulphides
JPH01168735A (ja)	1989-07-04	芳香族スルフィドアミド重合体及びその製造方法

JPH0329244B2 - - Google Patents

Info

Links

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Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=14839036

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Also Published As

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