CS273603B2 - Method of high-molecular electroconductive material production - Google Patents

Method of high-molecular electroconductive material production Download PDF

Info

Publication number: CS273603B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; group; denotes; weight; polymer
Prior art date: 1983-12-30

Application number

CS1065684A

Other languages

Czech (cs)

English (en)

Other versions

CS1065684A2 (en

Inventor

Marian Prof Dr Kryszewski

Janusz Dr Pecherz

Original Assignee

Polska Akad Nauk Centrum

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.)

1983-12-30

Filing date

1984-12-29

Publication date

1991-03-12

1983-12-30 Priority claimed from PL24545083A external-priority patent/PL139037B1/pl

1984-11-15 Priority claimed from PL25043684A external-priority patent/PL142693B1/pl

1984-12-29 Application filed by Polska Akad Nauk Centrum filed Critical Polska Akad Nauk Centrum

1990-08-14 Publication of CS1065684A2 publication Critical patent/CS1065684A2/cs

1991-03-12 Publication of CS273603B2 publication Critical patent/CS273603B2/cs

Links

238000004519 manufacturing process Methods 0.000 title claims abstract description 8
238000000034 method Methods 0.000 title claims description 19
239000000463 material Substances 0.000 title abstract description 19
229920000642 polymer Polymers 0.000 claims abstract description 21
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims abstract description 14
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 12
PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 claims abstract description 11
230000007935 neutral effect Effects 0.000 claims abstract description 8
IXHWGNYCZPISET-UHFFFAOYSA-N 2-[4-(dicyanomethylidene)-2,3,5,6-tetrafluorocyclohexa-2,5-dien-1-ylidene]propanedinitrile Chemical compound FC1=C(F)C(=C(C#N)C#N)C(F)=C(F)C1=C(C#N)C#N IXHWGNYCZPISET-UHFFFAOYSA-N 0.000 claims abstract description 7
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 7
VRGCYEIGVVTZCC-UHFFFAOYSA-N 3,4,5,6-tetrachlorocyclohexa-3,5-diene-1,2-dione Chemical compound ClC1=C(Cl)C(=O)C(=O)C(Cl)=C1Cl VRGCYEIGVVTZCC-UHFFFAOYSA-N 0.000 claims abstract description 6
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 6
239000004020 conductor Substances 0.000 claims abstract description 6
229910052698 phosphorus Inorganic materials 0.000 claims abstract description 6
239000011574 phosphorus Substances 0.000 claims abstract description 6
229910052785 arsenic Inorganic materials 0.000 claims abstract description 5
RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims abstract description 5
125000001424 substituent group Chemical group 0.000 claims abstract description 5
125000003118 aryl group Chemical group 0.000 claims abstract description 3
125000005842 heteroatom Chemical class 0.000 claims abstract description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims abstract 2
239000000654 additive Substances 0.000 claims description 17
239000002904 solvent Substances 0.000 claims description 13
230000000996 additive effect Effects 0.000 claims description 9
150000002605 large molecules Chemical class 0.000 claims description 7
239000000178 monomer Substances 0.000 claims description 7
239000000758 substrate Substances 0.000 claims description 6
238000001704 evaporation Methods 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 4
239000011593 sulfur Substances 0.000 claims description 4
239000000370 acceptor Substances 0.000 abstract description 6
230000005670 electromagnetic radiation Effects 0.000 abstract description 2
239000005416 organic matter Substances 0.000 abstract description 2
125000004429 atom Chemical group 0.000 abstract 2
239000005864 Sulphur Substances 0.000 abstract 1
238000012216 screening Methods 0.000 abstract 1
150000003839 salts Chemical class 0.000 description 13
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
230000007704 transition Effects 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
239000011521 glass Substances 0.000 description 4
229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
229920002239 polyacrylonitrile Polymers 0.000 description 4
239000004926 polymethyl methacrylate Substances 0.000 description 4
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
239000006229 carbon black Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000002131 composite material Substances 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
239000006259 organic additive Substances 0.000 description 2
GMVPRGQOIOIIMI-DODZYUBVSA-N 7-[(1R,2R,3R)-3-hydroxy-2-[(3S)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]heptanoic acid Chemical compound CCCCC[C@H](O)C=C[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(O)=O GMVPRGQOIOIIMI-DODZYUBVSA-N 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
229920005601 base polymer Polymers 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229920001940 conductive polymer Polymers 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
239000011888 foil Substances 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
239000010931 gold Substances 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000000203 mixture Substances 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1

Classifications

- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K9/00—Screening of apparatus or components against electric or magnetic fields
- H05K9/0073—Shielding materials
- H05K9/0081—Electromagnetic shielding materials, e.g. EMI, RFI shielding
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- 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
- C08G85/00—General processes for preparing compounds provided for in this subclass
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/121—Charge-transfer complexes

Landscapes

Chemical & Material Sciences (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Physics & Mathematics (AREA)
General Chemical & Material Sciences (AREA)
Spectroscopy & Molecular Physics (AREA)
Electromagnetism (AREA)
Engineering & Computer Science (AREA)
Microelectronics & Electronic Packaging (AREA)
Compositions Of Macromolecular Compounds (AREA)
Electroluminescent Light Sources (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

CS1065684A 1983-12-30 1984-12-29 Method of high-molecular electroconductive material production CS273603B2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
PL24545083A PL139037B1 (en)	1983-12-30	1983-12-30	Method of obtaining high polymer material exibiting electric current conducting properties
PL25043684A PL142693B1 (en)	1984-11-15	1984-11-15	Method of obtaining a macromolecular material exibiting electrically conductive properties

Publications (2)

Publication Number	Publication Date
CS1065684A2 CS1065684A2 (en)	1990-08-14
CS273603B2 true CS273603B2 (en)	1991-03-12

Family

ID=26652996

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS1065684A CS273603B2 (en)	1983-12-30	1984-12-29	Method of high-molecular electroconductive material production

Country Status (3)

Country	Link
EP (1)	EP0147871A3 (fr)
CS (1)	CS273603B2 (fr)
HU (1)	HUT37523A (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DD301547A7 (de) *	1987-04-09	1993-03-04	Leipzig Tech Hochschule	Verfahren zur herstellung leitfaehiger strukturen in poly(organylheteroacetylenen)
EP0353760A3 (fr) *	1988-08-03	1991-01-16	TDK Corporation	Eléments à cristaux liquides et mélanges conducteurs de composés organiques filmogènes
US5231523A (en) *	1988-08-03	1993-07-27	Tdk Corporation	Liquid crystal elements and conductive organic compound film-forming compositions
FR2666438B1 (fr) *	1990-08-30	1993-12-31	Commissariat A Energie Atomique	Procede de fabrication en phase vapeur d'un ecran a base de polymere conducteur et ecran obtenu par ce procede.
FR2666439B1 (fr) *	1990-08-30	1994-03-18	Commissariat A Energie Atomique	Ecran absorbant a base de polymere conducteur electronique.
RU2256967C1 (ru) *	2004-02-03	2005-07-20	Кольцова Анастасия Андриановна	Электроактивный полимер и материал на его основе

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1241302A (en) *	1967-08-03	1971-08-04	Matsushita Electric Industrial Co Ltd	Heat-sensitive high molecular weight resistors
FR2102832A5 (en) *	1970-08-25	1972-04-07	California Inst Tech	Alkylated pyridine aldehyde in conductive c - ompositions
JPS4825041A (fr) *	1971-08-04	1973-04-02
US4206308A (en) *	1976-06-11	1980-06-03	Matsushita Electric Industrial Co., Ltd.	Organic heat-sensitive semiconductive materials
DE3133738A1 (de) *	1981-08-26	1983-03-10	Bayer Ag, 5090 Leverkusen	Neue komplexsalze mit hoher elektrischer leitfaehigkeit

1984
- 1984-12-29 CS CS1065684A patent/CS273603B2/cs unknown
- 1984-12-29 HU HU489584A patent/HUT37523A/hu unknown
- 1984-12-31 EP EP84116513A patent/EP0147871A3/fr not_active Withdrawn

Also Published As

Publication number	Publication date
CS1065684A2 (en)	1990-08-14
EP0147871A3 (fr)	1986-01-08
EP0147871A2 (fr)	1985-07-10
HUT37523A (en)	1985-12-28

Publication	Publication Date	Title
US4798685A (en)	1989-01-17	Production of base-type conducting polymers
Kanazawa et al.	1979	‘Organic metals’: polypyrrole, a stable synthetic ‘metallic’polymer
Hotta et al.	1987	Conducting polymer composites of soluble polythiophenes in polystyrene
US4935163A (en)	1990-06-19	High service temperature conductive polymers and method of producing same
Elsenbaumer et al.	1982	Electrically conducting polyaromatic sulfides
US20080241390A1 (en)	2008-10-02	Insulating polymers containing polyaniline and carbon nanotubes
FR2536079A1 (fr)	1984-05-18	Polymeres electro-actifs et leur procede de production
JPH06508874A (ja)	1994-10-06	開始剤による予備処理を採用しての導電性ポリマーフィルムの形成
Lee et al.	1997	Synthesis and characterization of soluble polypyrrole
Goh et al.	1996	Miscibility of polyaniline/poly (vinyl acetate) blends
JP3400404B2 (ja)	2003-04-28	溶融加工または溶液加工可能な高度に導電性のポリアニリンおよびその製造方法並びにｐｖｃおよびｅｖａとこれとのブレンド
CS273603B2 (en)	1991-03-12	Method of high-molecular electroconductive material production
Výprachtický et al.	2017	New copolymers with thieno [3, 2‐b] thiophene or dithieno [3, 2‐b: 2′, 3′‐d] thiophene units possessing electron‐withdrawing 4‐cyanophenyl groups: Synthesis and photophysical, electrochemical, and electroluminescent properties
Wan et al.	1995	Transparent and conducting coatings of polyaniline composites
Keller	1987	Phthalonitrile‐based conductive polymer
US4374048A (en)	1983-02-15	Electrically conductive polymeric compositions
Bhandari et al.	2009	Influence of reaction conditions on the formation of nanotubes/nanoparticles of polyaniline in the presence of 1‐amino‐2‐naphthol‐4‐sulfonic acid and applications as electrostatic charge dissipation material
US5776370A (en)	1998-07-07	Charge transfer complexes between polyaniline and organic electron acceptors and method of fabrication
US5407987A (en)	1995-04-18	Polycyclic aromatic group - pendant polysilanes and conductive polymers derived therefrom
Jeszka et al.	1985	Surface-conductive polymer films by reticulate doping with organic metals
SU1466650A3 (ru)	1989-03-15	Способ получени полимерного пленочного материала
Jayalakshmi et al.	2021	Polychalcones based on triphenylamine and carbazole building blocks via Claisen–Schmidt route
Son et al.	1998	Condensation polymerization of triphenylamine derivatives with paraformaldehyde
Yasuda et al.	1984	Novel semiconducting organometallic polymers containing M (CO) 3 (1, 3-diene) groups (M= Fe, Ru)
Rao et al.	2000	Studies on the optical properties and stability in dc: Conductivity of PTSA-I2 doped poly-4-vinyl pyridine