JPH0555524B2 - - Google Patents

Info

Publication number: JPH0555524B2
Authority: JP; Japan
Prior art keywords: formula; group; polymer; spectrum; present
Prior art date: 1986-05-16
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

JP11090786A

Other languages

English (en)

Japanese (ja)

Other versions

JPS62267249A (ja

Inventor

Jinichiro Kato

Katsuyuki Nakamura

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.)

1986-05-16

Filing date

1986-05-16

Publication date

1993-08-17

1986-05-16 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1986-05-16 Priority to JP11090786A priority Critical patent/JPS62267249A/ja

1987-11-19 Publication of JPS62267249A publication Critical patent/JPS62267249A/ja

1993-08-17 Publication of JPH0555524B2 publication Critical patent/JPH0555524B2/ja

Status Granted legal-status Critical Current

Links

229920000015 polydiacetylene Polymers 0.000 claims description 18
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 14
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 4
125000003368 amide group Chemical group 0.000 claims description 3
125000001246 bromo group Chemical group Br* 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims 2
229920000642 polymer Polymers 0.000 description 36
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
229910052739 hydrogen Inorganic materials 0.000 description 19
125000003277 amino group Chemical group 0.000 description 15
238000000034 method Methods 0.000 description 14
239000000178 monomer Substances 0.000 description 10
238000006116 polymerization reaction Methods 0.000 description 10
239000002994 raw material Substances 0.000 description 10
238000001237 Raman spectrum Methods 0.000 description 9
238000002329 infrared spectrum Methods 0.000 description 9
238000010521 absorption reaction Methods 0.000 description 8
LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 description 8
229910052801 chlorine Inorganic materials 0.000 description 7
239000000460 chlorine Substances 0.000 description 7
150000002430 hydrocarbons Chemical group 0.000 description 7
238000000371 solid-state nuclear magnetic resonance spectroscopy Methods 0.000 description 7
239000002904 solvent Substances 0.000 description 7
238000001228 spectrum Methods 0.000 description 7
238000001069 Raman spectroscopy Methods 0.000 description 6
229910052794 bromium Inorganic materials 0.000 description 6
239000000463 material Substances 0.000 description 6
FRIJYOLUYSXHRS-UHFFFAOYSA-N n-(6-acetamidohexa-2,4-diynyl)acetamide Chemical compound CC(=O)NCC#CC#CCNC(C)=O FRIJYOLUYSXHRS-UHFFFAOYSA-N 0.000 description 6
-1 but in the process Chemical class 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
230000000704 physical effect Effects 0.000 description 5
150000001875 compounds Chemical class 0.000 description 4
238000005259 measurement Methods 0.000 description 4
125000004433 nitrogen atom Chemical group N* 0.000 description 4
230000009257 reactivity Effects 0.000 description 4
238000000944 Soxhlet extraction Methods 0.000 description 3
QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
238000005481 NMR spectroscopy Methods 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
239000013078 crystal Substances 0.000 description 2
125000004185 ester group Chemical group 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
238000000279 solid-state nuclear magnetic resonance spectrum Methods 0.000 description 2
238000012719 thermal polymerization Methods 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
238000000862 absorption spectrum Methods 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
WHVXVDDUYCELKP-UHFFFAOYSA-N butatriene Chemical group C=C=C=C WHVXVDDUYCELKP-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
WRJWRGBVPUUDLA-UHFFFAOYSA-N chlorosulfonyl isocyanate Chemical compound ClS(=O)(=O)N=C=O WRJWRGBVPUUDLA-UHFFFAOYSA-N 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000004020 conductor Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
238000001514 detection method Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000010894 electron beam technology Methods 0.000 description 1
239000012776 electronic material Substances 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
230000005251 gamma ray Effects 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
239000012761 high-performance material Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000006698 induction Effects 0.000 description 1
230000009878 intermolecular interaction Effects 0.000 description 1
229920002521 macromolecule Polymers 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000015654 memory Effects 0.000 description 1
238000000465 moulding Methods 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
238000001225 nuclear magnetic resonance method Methods 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000007790 solid phase Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1

Landscapes

Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP11090786A 1986-05-16 1986-05-16 アミノ基含有ポリジアセチレン Granted JPS62267249A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP11090786A JPS62267249A (ja)	1986-05-16	1986-05-16	アミノ基含有ポリジアセチレン

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP11090786A JPS62267249A (ja)	1986-05-16	1986-05-16	アミノ基含有ポリジアセチレン

Publications (2)

Publication Number	Publication Date
JPS62267249A JPS62267249A (ja)	1987-11-19
JPH0555524B2 true JPH0555524B2 (fr)	1993-08-17

Family

ID=14547679

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11090786A Granted JPS62267249A (ja)	1986-05-16	1986-05-16	アミノ基含有ポリジアセチレン

Country Status (1)

Country	Link
JP (1)	JPS62267249A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH08124769A (ja) *	1994-10-20	1996-05-17	Hanshin Electric Co Ltd	内燃機関用点火コイル

1986
- 1986-05-16 JP JP11090786A patent/JPS62267249A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH08124769A (ja) *	1994-10-20	1996-05-17	Hanshin Electric Co Ltd	内燃機関用点火コイル

Also Published As

Publication number	Publication date
JPS62267249A (ja)	1987-11-19

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Legal Events

Date	Code	Title	Description
2006-05-16	EXPY	Cancellation because of completion of term